Question:
Hi, all! That’s about all I have to say. I generally find denial to be one of my most useful tools when dealing with MS, so I avoid the group — but I do lurk, and I felt like saying hello. So… hello! Keith http://www.woollymammoth.com/keith
Response:
<gig friendly wave
Hi Keith! ((U)) M "Keith Snyder" <ke…@woollymammoth.com
wrote in message
news:BAA3407D.69E01%keith@woollymammoth.com… – Hide quoted text — Show quoted text -
Hi, all! That’s about all I have to say. I generally find denial to be one of my most useful tools when dealing with MS, so I avoid the group — but I do lurk, and I felt like saying hello. So… hello! Keith http://www.woollymammoth.com/keith
Response:
Hello back at ya. Any new books? Gaylan "Keith Snyder" <ke…@woollymammoth.com
wrote in message
news:BAA3407D.69E01%keith@woollymammoth.com… – Hide quoted text — Show quoted text -
Hi, all! That’s about all I have to say. I generally find denial to be one of my most useful tools when dealing with MS, so I avoid the group — but I do lurk, and I felt like saying hello. So… hello! Keith http://www.woollymammoth.com/keith
Response:
Hello to you, too, Keith. Denial is a comfortable place to be when dealing with this disease. Stay there a little while longer, if you wish. We still have some snow on the ground, summer might be a good time to poke out your nose and check for your shadow. :-) — From: watchman (watch…@nucleus.com) [Now ironjust...@aol.com] Newsgroups: alt.support.thyroid Date: 2002-01-12 15:56:30 PST "Look lady .. if you don’t know what you are talking about ‘medically’ .. then stay out of it .. The man has had three miscarriages/spontaneous abortions."
Response:
Hi Keith! Hello backatcha! Anything new with you? New books, travels, adventures? Updates, please! Sylvia
Response:
Sylv772…@yahoo.com (Sylvia) wrote in message <news:e43f7f84.0303231845.244bd958@posting.google.com
… Anything new with you? New books, travels, adventures?
No new books. I’ve been working on a screenplay for most of the last year, and it’s getting close to being done. I was in Pasadena, CA a couple of weeks ago for a mystery convention, and then I went to Louisville, KY to teach a writing workshop last week. Unfortunately, it was a bad MS week (well, bad compared to my usual, anyway; compared to a lot of people’s, it was good), so I came back pretty fried. Better now, though. Keith http://www.woollymammoth.com/keith
Response:
Keith Snyder <ke…@woollymammoth.com
wrote in message <news:BAA3407D.69E01%keith@woollymammoth.com… Hi, all! That’s about all I have to say. I generally find denial to be one of my most useful tools when dealing with MS, so I avoid the group — but I do lurk, and I felt like saying hello. So… hello! Keith http://www.woollymammoth.com/keith
Hello , Keith! Glad to have you peeping in. What eve happene with your book discussions? Jayne
Response:
Ja…@Planet-Save.com (Jayne Adler) wrote in message <news:60223b1e.0303251015.1ebda3c8@posting.google.com
… Glad to have you peeping in. What eve happene with your book discussions?
There wasn’t all that much of a response, so they just kind of fizzled. Keith http://www.woollymammoth.com/keith
Response:
At 02:58 PM 3/14/96 +0200, you wrote:
Hi to all May I introduce myself. My name is Dotty and I live in Surrey, England I am getting on a bit now, but I have had MS for nearly 50 years. This comes from Dotty’s Den, somewhere in the heart of Surrey Internet E mails ecstatically received at do…@ooh.dircon.co.uk welcome and then some! to tired to write much more, my folks used to live
in south croyden, now they live in gerard’s cross. i just love england, and scottland, oh well and turkey, and canada, and so on a laugh a day keeps the blues away
susan
Response:
Marcello Brocchi <pcs…@venus.devetir.qld.gov.au
wrote: Heloo everyone… I have just discovered that I have internet mail and news at work so I have decided to have a look. When I saw this group I almost cried. My very good friend that I love very very much may have MS.. thankyou. Marcello.
hello marcello! sounds like your friend is lucky to have you in her life! is there a ms society in australia? if you do have access to a ms society office, they will be able to give you pamphlets to read. if not, let us know and someone in this group can mail you these. i sound like a salesperson for multiple sclerosis! peggy
Response:
Hi Susan
May I introduce myself. My name is Dotty and I live in Surrey, England
I am getting on a bit now, but I have had MS for nearly 50 years.
This comes from Dotty’s Den, somewhere in the heart of Surrey
Internet E mails ecstatically received at do…@ooh.dircon.co.uk
welcome and then some! to tired to write much more, my folks used to live
S_
in south croyden, now they live in gerard’s cross. i just love
S_
england, and scottland, oh well and turkey, and canada, and so on
I live only a few miles from South Croydon so we could have been neighbours:) Look after yourself and write again .E ___ Blue Wave/DOS v2.21 [NR] ___ _ _ / _ ___ | |__ | | Internet: do…@ooh.dircon.co.uk | | | |/ _ | ‘_ | | FidoNet : Dorothy Denn 2:254/233 | |_| | (_) | | | |_| ___/ ___/|_| |_(_) Ooh! BBS London +44-181-395-3108 [MULTI-LINE]
Response:
Hullo BJ Bj
Welcome Dotty,
Bj
Of course you can, I will look forward to hearing from you.
Bj
((((((((((((((((((((hugs)))))))))))))))))))))))))))))))))))))))
May I introduce myself. My name is Dotty and I live in Surrey, England
I am getting on a bit now, but I have had MS for nearly 50 years.
I did have large spells of remission, but now I appear to be going
downhill faster than I would like. May I please join this very caring
company
Thank you for your welcome. Our BBS has only taken this echo for a few weeks, so it is all very strange. I am surprised and sad at the number of people that suffere from this crippling disease. Look afer yourself .E This comes from Dotty’s Den, somewhere in the heart of Surrey Internet E mails ecstatically received at do…@ooh.dircon.co.uk ___ Blue Wave/DOS v2.21 [NR] ___ _ _ / _ ___ | |__ | | Internet: do…@ooh.dircon.co.uk | | | |/ _ | ‘_ | | FidoNet : Dorothy Denn 2:254/233 | |_| | (_) | | | |_| ___/ ___/|_| |_(_) Ooh! BBS London +44-181-395-3108 [MULTI-LINE]
Response:
Hi Thel, Th
Hello Dotty,
Th
Welcome! So glad to have you joining us. I am sorry that you
Th
are going downhill more quickly these days but I am sure you have many
Th
happy memories of those good remissions. I look forward to hearing
Th
more from you. (Is ‘Dotty’ short for ‘Dorothy’? – don’t answer unless
Th
you want to… I hope people are too polite to guess what my name is
Th
short for…) Oh, yes, we have someone on this list (Bill in
Th
New Mexico, where are you???) who just might have something to say
Th
about being ‘chronologically disadvantaged’. (ggg)
Th
Sunshine,
Th
Thel
Age has a lot of problems itself without having the MS dumped on top it it. But I get by, one has too, very frustrating though<g
Yes my name is Dorothy, but I thought Dotty sounded more friendly, and that is also how I am known on my BBS. I come from Sutton in Surrey, England, just a few miles south of London. Where do you hail from? I have not yet heard from Bill in New Mexico, that pleasure I hope still to come. Sorry this is brief, but I have had such a lot of welcoming messages, it is taking all my time (and strength) to answer them Speak to you soon .E This comes from Dotty’s Den, somewhere in the heart of Surrey Internet E mails ecstatically received at do…@ooh.dircon.co.uk … To whom the gods destroy, they first teach Windows… ___ Blue Wave/DOS v2.21 [NR] ___ _ _ / _ ___ | |__ | | Internet: do…@ooh.dircon.co.uk | | | |/ _ | ‘_ | | FidoNet : Dorothy Denn 2:254/233 | |_| | (_) | | | |_| ___/ ___/|_| |_(_) Ooh! BBS London +44-181-395-3108 [MULTI-LINE]
Response:
Hi Peggy Ab
hi dotty!
Ab
please join in the fun anytime your heart desires!
Nice to hear from you, I do like this echo, everyone is so friendly. Where are you, and how are you Speak to you soon .E This comes from Dotty’s Den, somewhere in the heart of Surrey Internet E mails ecstatically received at do…@ooh.dircon.co.uk … Health is merely the slowest possible rate at which one can die. ___ Blue Wave/DOS v2.21 [NR] ___ _ _ / _ ___ | |__ | | Internet: do…@ooh.dircon.co.uk | | | |/ _ | ‘_ | | FidoNet : Dorothy Denn 2:254/233 | |_| | (_) | | | |_| ___/ ___/|_| |_(_) Ooh! BBS London +44-181-395-3108 [MULTI-LINE]
Response:
Hi Jan Js
Hi, Dorothy! Welcome to this group! We are always sad for the
Js
_reason_ people join us, but always glad to have a new friend! It
Js
sounds like you are still enjoying life…that’s what it’s all about,
Js
eh? When I was 30, I was quite healthy, but my life was a mess, full
Js
of fear, anger, and mental pain. Now I am 49, have MS, and am happier
Js
than I have ever been in my life! Just goes to show you, mental
Js
attitude is all! And you seem to have it. Hope to hear more from
Js
you, about your "den", Surrey, et al. Hugs and lots of warm
Js
fluffies–JAN
How lovely to hear from you, so may people have answered my message, I feel quite flattered<g
Yes I still enjoy life, if one can enjoy life
spending most of the day in a wheelchair. But it is only after reading some of the postings here, I realise how much worse some other people are so I don’t grumble. Sorry to hear how things are for you, there were time that I felt I could not go on, and people do not understand the mental torture one goes through. I started having walking and sight problems when I was 16 – 17 years, but nobody took any notice. The doctors and hospitals didn’t know what the matter was either. Luckily I had long bouts of remission when everything seemed to be back to normal, then I would have a relapse. But I managed to have two children (although I lost 4) aand have now 3 granchildren. I was finally diagnosed 15 years ago, when my husband promptly left me. Some people can be so stupid, I was sure he thought I would be in a wheelchair the next day, barmy and dribbling, and him having to look after me 24 hours a day. I am much better off without him. So cheer up if you can, I know it can’t be easy sometimes life can be a proper b****r at times, but don’t let it win:)) Cheers .E This comes from Dotty’s Den, somewhere in the heart of Surrey Internet E mails ecstatically received at do…@ooh.dircon.co.uk … * Denn: Noun. A small cubby hole or place to hide. ___ Blue Wave/DOS v2.21 [NR] ___ _ _ / _ ___ | |__ | | Internet: do…@ooh.dircon.co.uk | | | |/ _ | ‘_ | | FidoNet : Dorothy Denn 2:254/233 | |_| | (_) | | | |_| ___/ ___/|_| |_(_) Ooh! BBS London +44-181-395-3108 [MULTI-LINE]
Response:
At 06:27 AM 3/14/96 GMT, you wrote:
Heloo everyone… I almost cried. My very good friend MS.. Every 5 years or so she has experienced some MS symptoms.
hi, you came to a very good place. i’ve had symptoms for almost 20 years, but just got diagnosed 6 years ago. it can be terrible, but livable. at least in my mind. i have days i’m depressed, days i’m angry, days i’m sad, sometimes all three. but i have so much to live for. even with my left sided paralysis i get along, not like i used to but i do. the checkers at the grocery store know i want paper, instead of plastic, there are 3 men that squabble about who will help me to the car, all sorts of good things. and i haven’t even mentioned the most wonderful guy i’m married to. yes that’s rightr my husband. so yes it’s a disturbing and frustrating disease, but can be lived through. we all here on the list are doing it. treat your friend as you would have anyway, but when weird things happen, let her laugh or cry, or do both. if you are at a loss for words, the greatest thing for me to hear is: I AM HERE. hope this helps, good luck a laugh a day keeps the blues away
susan
Response:
Hi Cathy Cm
Cheers Dotty! Nice to ‘ear from someone from over ‘ome, as my dad
Cm
calls it. My rellies hail from Faversham, Kent – is that close to
Cm
Surrey? Sorry to year you’ve been going downhill, but glad you’ve
Cm
found us. We’ll have to teach all these ‘mercans how to spell
Cm
neighbour and theatre and how to say "schedule", eh what?
Nice of you to answer my call. Yes Kent is very close to Surrey, do you ever get over here at all. I think I’m going downhill a bit faster now because I am OLD, I don’t want to be old, but the years are creeping up<sob
Suppose it comes to us all sometime<g Now be careful how you try
to teach these Yanks to spell, you don’t know who’s looking in, they might try and make fun of the English spellings. BTW I was speaking to a Lorraine Phillips in Calgary some time back. She has never answered my netmail, she too has MS, do you know her at all? Cm
Hope you’re well
I’m keeping my pecker up <g
Cheers .E This comes from Dotty’s Den, somewhere in the heart of Surrey Internet E mails ecstatically received at do…@ooh.dircon.co.uk … Ground Beef – a cow with no legs ___ Blue Wave/DOS v2.21 [NR] ___ _ _ / _ ___ | |__ | | Internet: do…@ooh.dircon.co.uk | | | |/ _ | ‘_ | | FidoNet : Dorothy Denn 2:254/233 | |_| | (_) | | | |_| ___/ ___/|_| |_(_) Ooh! BBS London +44-181-395-3108 [MULTI-LINE]
Response:
do…@ooh.dircon.co.uk (Dorothy Denn) wrote:
Hi to all May I introduce myself. My name is Dotty and I live in Surrey, England I am getting on a bit now, but I have had MS for nearly 50 years. I did have large spells of remission, but now I appear to be going downhill faster than I would like. May I please join this very caring company Bye
hi dotty! please join in the fun anytime your heart desires! peggy
Response:
Hello Dotty, Welcome! So glad to have you joining us. I am sorry that you are going downhill more quickly these days but I am sure you have many happy memories of those good remissions. I look forward to hearing more from you. (Is ‘Dotty’ short for ‘Dorothy’? – don’t answer unless you want to… I hope people are too polite to guess what my name is short for…) Oh, yes, we have someone on this list (Bill in New Mexico, where are you???) who just might have something to say about being ‘chronologically disadvantaged’. (ggg) Sunshine, Thel – Hide quoted text — Show quoted text -
May I introduce myself. My name is Dotty and I live in Surrey, England I am getting on a bit now, but I have had MS for nearly 50 years. … I’m not old – just chronologically disadvantaged do…@ooh.dircon.co.uk
Response:
At 02:58 14/03/96 +0200, you wrote:
Hi to all May I introduce myself. My name is Dotty and I live in Surrey, England I am getting on a bit now, but I have had MS for nearly 50 years. I did have large spells of remission, but now I appear to be going downhill faster than I would like. May I please join this very caring company
Cheers Dotty! Nice to ‘ear from someone from over ‘ome, as my dad calls it. My rellies hail from Faversham, Kent – is that close to Surrey? Sorry to year you’ve been going downhill, but glad you’ve found us. We’ll have to teach all these ‘mercans how to spell neighbour and theatre and how to say "schedule", eh what? Hope you’re well. Cathy in Calgary (Alberta, Canada)
Response:
Hi, Dorothy! Welcome to this group! We are always sad for the _reason_ people join us, but always glad to have a new friend! It sounds like you are still enjoying life…that’s what it’s all about, eh? When I was 30, I was quite healthy, but my life was a mess, full of fear, anger, and mental pain. Now I am 49, have MS, and am happier than I have ever been in my life! Just goes to show you, mental attitude is all! And you seem to have it. Hope to hear more from you, about your "den", Surrey, et al. Hugs and lots of warm fluffies–JAN On 12 Mar 1996, Dorothy Denn wrote: – Hide quoted text — Show quoted text -
Hi to all May I introduce myself. My name is Dotty and I live in Surrey, England I am getting on a bit now, but I have had MS for nearly 50 years. I did have large spells of remission, but now I appear to be going downhill faster than I would like. May I please join this very caring company Bye .E This comes from Dotty’s Den, somewhere in the heart of Surrey Internet E mails ecstatically received at do…@ooh.dircon.co.uk … I’m not old – just chronologically disadvantaged ___ Blue Wave/DOS v2.21 [NR] ___ _ _ / _ ___ | |__ | | Internet: do…@ooh.dircon.co.uk | | | |/ _ | ‘_ | | FidoNet : Dorothy Denn 2:254/233 | |_| | (_) | | | |_| ___/ ___/|_| |_(_) Ooh! BBS London +44-181-395-3108 [MULTI-LINE]
Response:
Hi to all May I introduce myself. My name is Dotty and I live in Surrey, England I am getting on a bit now, but I have had MS for nearly 50 years. I did have large spells of remission, but now I appear to be going downhill faster than I would like. May I please join this very caring company Bye .E This comes from Dotty’s Den, somewhere in the heart of Surrey Internet E mails ecstatically received at do…@ooh.dircon.co.uk … I’m not old – just chronologically disadvantaged ___ Blue Wave/DOS v2.21 [NR] ___ _ _ / _ ___ | |__ | | Internet: do…@ooh.dircon.co.uk | | | |/ _ | ‘_ | | FidoNet : Dorothy Denn 2:254/233 | |_| | (_) | | | |_| ___/ ___/|_| |_(_) Ooh! BBS London +44-181-395-3108 [MULTI-LINE]
Response:
We are ok. Thanks. It *does* hurt, what these bastards do. Somebody
brainwashed those suicide ‘living bombs’ that they will go straight to
paradise. Disgusting.
Love to all,
Chanoch Weil
ccan…@ALUF.TECHNION.AC.IL
Chanoch, I take it you are in The Holy Land…my prayers are with you and your family. On the humorous side (we must look for humor in the worst of situations!) Picture the ‘living bombs’ waking up and realizing that ‘paradise is on fire!!!!’
May God bless and protect you, Karlyn
Response:
Dear Chanoch and Tamari: I am so glad you wrote and told us you were okay. Since I’m not familiar with where each town is located, I don’t know who is getting the bombings. It’s very scary for those of us who know people there. They show everything on television, even the 5 yo’s who will replace the dead human bombs! It is disgusting! Somehow, they, the Muslims, must realize that for each human they kill, it does NOT mean going to their Paradise! Please take good care of yourselves, and try not to let the stress get to you both:-) We all care about you! Circles Of Love Around The World, Stelle
Response:
Heloo everyone… I have just discovered that I have internet mail and news at work so I have decided to have a look. When I saw this group I almost cried. My very good friend that I love very very much may have MS.. Every 5 years or so she has experienced some MS symptoms. A few years ago she almost lost her vision became blurry for a short time and lately her left arm has been ‘dieing’ on and off to put it in her words. She has been checked in to have a MS test performed. I think it is called MIA test. Please excuss my ignorance. Well my ignorance is really the reason for my posting here. Can someone please mail me some information about MS. whats it like living with it and how I should approach the problem with her. I really would like to hear it from someone who has MS rather than reading it in some med. journal. thankyou. Marcello. email : pcs…@devetir.qld.gov.au
Response:
Welcome Dotty, Of course you can, I will look forward to hearing from you. ((((((((((((((((((((hugs)))))))))))))))))))))))))))))))))))))))
May I introduce myself. My name is Dotty and I live in Surrey, England I am getting on a bit now, but I have had MS for nearly 50 years. I did have large spells of remission, but now I appear to be going downhill faster than I would like. May I please join this very caring company
B.J. M.S.- THE DISEASE OF USED TO BE. *HUGS* For those looking for first-hand accounts of experiences with MS, try: http://stripe.colorado.edu/~leonarm/ms and don’t forget to leave your experiences too! Take charge of your health-care, you are the boss and you are the one the meds./treatments affect.
Response:
if…@cleveland.Freenet.Edu (Mary Johnson) wrote:
Well, I guess I’m not up to much more right now – excuse my typos -I just don’t have the energy to fix them – it sure is great to talk to people who understand that! See you! Mary in Seattle
Hi Mary: Don’t worry about the typos and conserve your energy. I’m glad you joined in with the group–Welcome! ((((Hugs)))) and o/ o/ Blessings o/ o/ Millie Ser…@pacificnet.net
Response:
Mary in Seatle, Welcome to the group – as I’ve seen a very caring group! I didn’t see any "typos" – I got a spell checker turned on, but sometimes I don’t agree with it
"Joint pain" I’m in that group too!,
You and I have two things in common – I have an 8 yr old daughter
and I’ve had MS for 22 years
Time sure flys doesn’t it? The other day I had a conversation with an older gentleman and he was talking about how old he was feeling – got me thinking, I’ve been feeling old for a while now and I’m only 38. I don’t know how growing old feels – it just happened. I guess the saying really applies "young at heart"
Anyway, hope to hear more from you. Eddie B
what you can do well today will be envied tomorrow <<
———- From: owner-mslist-l To: Multiple recipients of list MSLIST-L Subject: Hello Date: April 17, 1996 6:06PM Hi – I just started reading this ng (just sarted with computers for that matter). I’ve had ms for 22yrs, been unable to work (except for being a single parent to my eight year old daughter) for the last eight. I’m really glad to be joining this group, especially since I’ve never been part of a ms suport group. I was interested to read several people saying they had joint pain similar to mine, since my dr. always says its nor considtent with ms. I had all the arthritis tests also. Well, I guess I’m not up to much more right now – excuse my typos -I just don’t have the energy to fix them – it sure is great to talk to people who understand that! See you! Mary in Seattle – x x
Response:
Mary Johnson (if…@cleveland.Freenet.Edu) wrote:
: Hi – I just started reading this ng (just sarted with computers : for that matter). I’ve had ms for 22yrs, been unable to work : (except for being a single parent to my eight year old daughter) Thats a full time job. I was single parent to two boys and it was definitely an adventure. : for the last eight. I’m really glad to be joining this group, : especially since I’ve never been part of a ms suport group. I : was interested to read several people saying they had joint pain : similar to mine, since my dr. always says its nor considtent with : ms. I had all the arthritis tests also. Well, I guess I’m not : up to much more right now – excuse my typos -I just don’t have : the energy to fix them – it sure is great to talk to people who : understand that! See you! Mary in Seattle Joint pain is very consistent with MS. Its because we adapt the ways we do things to match our abilities. These adaptations cause us to use our skeleton in ways contrary to its design adding stress to the joints. If I have to walk a lot I get pain in my hip because of my gait, I have no feeling in my lower leg so the lower leg and foot muscles do not cushion my landing like they are supposed to. Bill in New Mexico
Response:
Hi – I just started reading this ng (just sarted with computers for that matter). I’ve had ms for 22yrs, been unable to work (except for being a single parent to my eight year old daughter) for the last eight. I’m really glad to be joining this group, especially since I’ve never been part of a ms suport group. I was interested to read several people saying they had joint pain similar to mine, since my dr. always says its nor considtent with ms. I had all the arthritis tests also. Well, I guess I’m not up to much more right now – excuse my typos -I just don’t have the energy to fix them – it sure is great to talk to people who understand that! See you! Mary in Seattle — x x
Response:
Pauline wrote :
I’m in the UK & have PPMS so no meds. I have worsening symptoms but not as disabled as some and fortunate to have little pain. I have had only 1 MRI scan but am claustrophobic and had a panic attack after only 1 min. inside the tube. Take care, Pauline
Have you ever thought about sedation for the MRI? You have to get there earlier, stay later, and have someone drive you, but it sounds like you had a bad time of it before. Good luck. Vincent
Response:
| Pauline wrote : |
I’m in the UK & have PPMS so no meds. I have worsening
|
symptoms but not as disabled as some and fortunate to
|
have little pain. I have had only 1 MRI scan but am
|
claustrophobic and had a panic attack after only 1 min.
|
inside the tube.
"Vincent" <show…@ev1.net
wrote in message |
| Have you ever thought about sedation for the MRI? You have to get there | earlier, stay later, and have someone drive you, but it sounds like you had | a bad time of it before. | Good luck. Thanks but I doubt that I will ever have need for another scan but if I’m asked intend to spend the whole of it asleep. I didn’t realise how claustrophobic I was until I was enclosed inside the tube, although I did once spend a sleepless night in a windowless hotel room in Amsterdam. How Anne Frank and others stayed imprisoned for years in those tiny garrets without going mad I don’t know. Perhaps they did but then the alternative was much worse. Take care, Pauline
Response:
Nice to meet you. Dx 12-98. Copaxone. Take care, Vincent
Response:
"Ron" <nal…@comcast.net
wrote in message …
| Hello everyone | My name is Ron I was dx’d 2 years ago with 1 major attack (my neuro is | pretty good) on Avonex pretty good so far side effects all but gone I am | also in a study in Boston where I went for my second opinion they say I am | a classic case and wanted me in this study it is a natural history study 10 | years long I go twice a year tons of blood work physco stuff and an Mri and | a damn long one too it’s a 3d mri and each one I do is over 2 hours long | 1/2 without gad and the other half with gad…. | As far as meds go I’m on provigil (a life saver)Zoloft,neurontim 1200mg a | day for some pain in my head which is kinda bad and various drugs for the | pain but so far nothing really good I am trying not to go for the narcotics | like Vicodin cause I work full time and I’d like to continue and do not want | to be doped too bad but other than that I am married to a wonderful | woman last year was 20 years and a daughter 18 who is ok (you know | haha) Anyway pleased to meet all of you. Pleased to meet you too Ron but sorry that any of us have reason to be here. I’m in the UK & have PPMS so no meds. I have worsening symptoms but not as disabled as some and fortunate to have little pain. I have had only 1 MRI scan but am claustrophobic and had a panic attack after only 1 min. inside the tube. Take care, Pauline
Response:
Hello everyone My name is Ron I was dx’d 2 years ago with 1 major attack (my neuro is pretty good) on Avonex pretty good so far side effects all but gone I am also in a study in Boston where I went for my second opinion they say I am a classic case and wanted me in this study it is a natural history study 10 years long I go twice a year tons of blood work physco stuff and an Mri and a damn long one too it’s a 3d mri and each one I do is over 2 hours long 1/2 without gad and the other half with gad…. As far as meds go I’m on provigil (a life saver)Zoloft,neurontim 1200mg a day for some pain in my head which is kinda bad and various drugs for the pain but so far nothing really good I am trying not to go for the narcotics like Vicodin cause I work full time and I’d like to continue and do not want to be doped too bad but other than that I am married to a wonderful woman last year was 20 years and a daughter 18 who is ok (you know haha) Anyway pleased to meet all of you. Ron
Response:
Hi, my name is Don Anders and after a month of lurking in the background I thought it was time to introduce myself. I have gained more knowledge this month about what it means and doesn’t mean to have MS than ever before. I have also come to realize the importance of support among friends. Because of the slow course of my illness I had decided to ignore it for many years. I is just resently that I have come out of the closet. When I was a freshman in college I had my first symptom: a slight loss of vision in my right eye. The doctors at Johns Hopkins called it an idiosyncrasy and sent me on my merry way. Since I was 18 and invincible that was fine for me. By the time I was a senior I went to another eye doctor who told me that my optic neuritis could be an early sign of MS. This was just two weeks before my marriage. I scared the hell out of me. What to do while waiting for a dx? In my case get married, have two children, finish graduate school, change jobs several times, move and work in three states: all the stuff people do. By the time I was 40 nothing had happened; so I concluded that second doctor was an idiot. There was nothing wrong with me, after all, I had heard that MS was diagnosed in young people and I was now 42. Too old, right? Then at the end of my 42nd year the next set of symptoms hit. It was a year of stress for me. I sold one business and started another, we renovated a house built in 1824, and then my wife died. I guess stress sure does influence the course of MS. For the next ten years I have had a few more symptoms but they have progressed slowly. I am now back teaching at a local college, am in a wonderful relationship, and am the grandfather of a 14 month old boy. MS has not stopped me from enjoying life to the best that I can. Sorry if this is long posting, but this is the first time that I have openly talked about this stuff to anyone other than my children and my SO.
Response:
Welcome Don!
Response:
Hi, I posted on this website recently and found the responses I received very helpful. I had written in that I had fallen and was concerned that it was related to the MS and could happen again. Of course there’s no way to know for sure; the doctor feels that since I have a slight weakness in my left side, I may have tripped and not felt it. But for now, I wear shoes with good support(As suggested) and go at a slower pace. Hannah
Response:
Hannah1…@webtv.net wrote:
<< I had written in that I had fallen and was concerned that it was related to the MS and could happen again.
You are correct, this fall may have been related to weakness on one side, or some other aspect of your MS, or it may have ben the result of a momentary loss of focus on what you were doing! This happens to EVERYONE MS or no MS. Many times we attribute to MS a problem that may be due to other issues, or due to nothing in particular, that is one of the … lovely … things about MS it’s unpredictability! Since starting on Copaxone I fall down a lot less often, but I have done my share of Chevy Chase initato pratalls as well, some years ago long preceding diagnosis! My friend jane Vessey ued to refer to this as," there was a thread on the carpet that needed tripping over", and that is as good of a reason as any. Be well! LarryC (Who used to be dadman@erols but now is larcrav…@aol.com
Response:
Hi Ron Sorry you have MS but this group is great ~ (I had trouble with my server and am still working on it.) I take neurontin as well for pain ~ think it’s a brilliant drug but so expensive (my GP got me $600 worth free recently via the rep!!!) I hope you get good results from the trial you are on. Welcome to a group of fun and info.I live in Australia. Barb "Giganews" <nal…@comcast.net
wrote in message
news:TvOcnbZI1scAzk-jXTWcpA@comcast.com… – Hide quoted text — Show quoted text -
Hello everyone My name is Ron I was dx’d 2 years ago with 1 major attack (my neuro is pretty good) on Avonex pretty good so far side effects all but gone I am also in a study in Boston where I went for my second opinion they say I am
a
classic case and wanted me in this study it is a natural history study 10 years long I go twice a year tons of blood work physco stuff and an Mri
and
a damn long one too it’s a 3d mri and each one I do is over 2 hours long
1/2
without gad and the other half with gad…. As far as meds go I’m on provigil (a life saver)Zoloft,neurontim 1200mg a day for some pain in my head which is kinda bad and various drugs for the pain but so far nothing really good I am trying not to go for the
narcotics
like Vicodin cause I work full time and I’d like to continue and do not
want
to be doped too bad but other than that I am married to a wonderful woman last year was 20 years and a daughter 18 who is ok (you know haha) Anyway pleased to meet all of you. Ron
Response:
Hi, Ron, There are many ideas floating around this group and most are very, very useful. I have found out so many things from this eclectic bunch. I assume you have seen Paul Jones’ website? It is the first thing I usually refer people to because of the wealth of information – real information, not quackery. http://www.mult-sclerosis.org/ Read and post. We need you. We want you. – Lynne "Giganews" <nal…@comcast.net
wrote in message
news:TvOcnbZI1scAzk-jXTWcpA@comcast.com… – Hide quoted text — Show quoted text -
Hello everyone My name is Ron I was dx’d 2 years ago with 1 major attack (my neuro is pretty good) on Avonex pretty good so far side effects all but gone I am also in a study in Boston where I went for my second opinion they say I am
a
classic case and wanted me in this study it is a natural history study 10 years long I go twice a year tons of blood work physco stuff and an Mri
and
a damn long one too it’s a 3d mri and each one I do is over 2 hours long
1/2
without gad and the other half with gad…. As far as meds go I’m on provigil (a life saver)Zoloft,neurontim 1200mg a day for some pain in my head which is kinda bad and various drugs for the pain but so far nothing really good I am trying not to go for the
narcotics
like Vicodin cause I work full time and I’d like to continue and do not
want
to be doped too bad but other than that I am married to a wonderful woman last year was 20 years and a daughter 18 who is ok (you know haha) Anyway pleased to meet all of you. Ron
Response:
Ron, hi and welcome. You’re lucky to be near a center where they have a study going. But that MRI sounds like a doozy. Hope you’re not claustrophobic. They’ve never bothered me, but I know a lot of people have problems with them. It sounds like you’re dealing with your dx pretty well, and that you have a good support system. That’s crucial. And not taking any more meds than absolutely necessary is a good thing, as each med, though fixing one symp, gives you a side effect. Check in with us whenever with questions/comments. There are as many opinions here as there are people! — Shirley B. ASMS List #6 http://come.to/ASMS-Lists "Making a way out of No Way is sometimes the Only way" Dr. Johnnetta B. Cole TO REPLY BY EMAIL REMOVE ’NICK’ "Giganews" <nal…@comcast.net
wrote in message
news:TvOcnbZI1scAzk-jXTWcpA@comcast.com… – Hide quoted text — Show quoted text -
Hello everyone My name is Ron I was dx’d 2 years ago with 1 major attack (my neuro is pretty good) on Avonex pretty good so far side effects all but gone I am also in a study in Boston where I went for my second opinion they say I am
a
classic case and wanted me in this study it is a natural history study 10 years long I go twice a year tons of blood work physco stuff and an Mri
and
a damn long one too it’s a 3d mri and each one I do is over 2 hours long
1/2
without gad and the other half with gad…. As far as meds go I’m on provigil (a life saver)Zoloft,neurontim 1200mg a day for some pain in my head which is kinda bad and various drugs for the pain but so far nothing really good I am trying not to go for the
narcotics
like Vicodin cause I work full time and I’d like to continue and do not
want
to be doped too bad but other than that I am married to a wonderful woman last year was 20 years and a daughter 18 who is ok (you know haha) Anyway pleased to meet all of you. Ron
Response:
Hello everyone My name is Ron I was dx’d 2 years ago with 1 major attack (my neuro is pretty good) on Avonex pretty good so far side effects all but gone I am also in a study in Boston where I went for my second opinion they say I am a classic case and wanted me in this study it is a natural history study 10 years long I go twice a year tons of blood work physco stuff and an Mri and a damn long one too it’s a 3d mri and each one I do is over 2 hours long 1/2 without gad and the other half with gad…. As far as meds go I’m on provigil (a life saver)Zoloft,neurontim 1200mg a day for some pain in my head which is kinda bad and various drugs for the pain but so far nothing really good I am trying not to go for the narcotics like Vicodin cause I work full time and I’d like to continue and do not want to be doped too bad but other than that I am married to a wonderful woman last year was 20 years and a daughter 18 who is ok (you know haha) Anyway pleased to meet all of you. Ron
Response:
Sorry the first one went out under my boyfriend e-mail had to change disregaurd Tim Ridolfi it should be from Terri.I have been reading this since I was dx on april fools day this year some joke hey. Since then I have had a course of IV steriods and I am taking a 20 day steriods oral no and I am on Amantadine and lots of other things. Now that we know what is wrong I think I have had it all my life just little relaps now and then. But I have been though the ring for the last 3 years and it finally got so bad they couldn’t deni it anymore and so 3 mris and a year off work they said you have MS. Now what happens How do you keep stress out of your life and not make you sick? I wish there ws someone to tell me what to exspect my doc and nero say that it is differnent for everyone. I have enjoyed the group and reading your stories it has help when I am down. I would like to take part now in the group.
Response:
Hi Terri, Welcome to the group (sorry for the reason). How you keep stress out of your life? That’s a question which has both easy and hard answers. What’s necessary is to remodel your personality and life such that they accommodate your MS problems (and limit potential stressors). That sounds good but it’s a process of making small changes a little at a time. The first thing to try is to make sure you do 1 thing for YOURSELF every day! Z http://www.mindspring.com/~cczimmer/ +————————————————————————+ + Carolyn C. Zimmer | "I’ve been warped by the rain, | + Duluth, GA | driven by the snow, I’m drunk and dirty, | + cczim…@mindspring.com | don’t you know, But I’m still…willin’" | + STANDARD DISCLAIMER | Lowell George | +————————————————————————+
Response:
Welcome aboard!! Sorry MS is so individualistic and so different at different times of day or weeks it’s hard to know what a doctor should tell you. Stress: I use hypnosis, relaxation tapes, now I think spring is here in NH i can start working on my landlady’s window box, I do deep breathing and watch funny videos, and of course there’s the list to let my feelings out, be they scared, angry, funny, sad, etc. Glad you are here sorry for the reason. At 09:57 PM 5/1/97 -0500, you wrote:
Sorry the first one went out under my boyfriend e-mail had to change disregaurd Tim Ridolfi it should be from Terri.I have been reading this since I was dx on april fools day this year some joke hey. Since then I have had a course of IV steriods and I am taking a 20 day steriods oral no and I am on Amantadine and lots of other things. Now that we know what is wrong I think I have had it all my life just little relaps now and then. But I have been though the ring for the last 3 years and it finally got so bad they couldn’t deni it anymore and so 3 mris and a year off work they said you have MS. Now what happens How do you keep stress out of your life and not make you sick? I wish there ws someone to tell me what to exspect my doc and nero say that it is differnent for everyone. I have enjoyed the group and reading your stories it has help when I am down. I would like to take part now in the group.
| _,,,—,,_ luv susan /,`.-’`’ -. ;-;;,_ s_guzie…@conknet.com |,4- ) )-,_..; ( `’-’ ’—”(_/–’ `-’_) fL The mind is its own place, and in itself, can make heaven of Hell, and a hell of Heaven. -John Milton
Response:
Thank you so much for you support it always helps to know that there is someone out there. Since I can do this with anyone in my family. At 05:45 PM 5/5/97 +0300, you wrote: – Hide quoted text — Show quoted text -
Welcome aboard!! Sorry MS is so individualistic and so different at different times of day or weeks it’s hard to know what a doctor should tell
you.
Stress: I use hypnosis, relaxation tapes, now I think spring is here in NH i can start working on my landlady’s window box, I do deep breathing and watch funny videos, and of course there’s the list to let my feelings out, be they scared, angry, funny, sad, etc. Glad you are here sorry for the reason. At 09:57 PM 5/1/97 -0500, you wrote: Sorry the first one went out under my boyfriend e-mail had to change disregaurd Tim Ridolfi it should be from Terri.I have been reading this since I was dx on april fools day this year some joke hey. Since then I have had a course of IV steriods and I am taking a 20 day steriods oral no and I am on Amantadine and lots of other things. Now that we know what is wrong I think I have had it all my life just little relaps now and then. But I have been though the ring for the last 3 years and it finally got so bad they couldn’t deni it anymore and so 3 mris and a year off work they said you have MS. Now what happens How do you keep stress out of your life and not make you sick? I wish there ws someone to tell me what to exspect my doc and nero say that it is differnent for everyone. I have enjoyed the group and reading your stories it has help when I am down. I would like to take part now in the group. | _,,,—,,_ luv susan /,`.-’`’ -. ;-;;,_ s_guzie…@conknet.com |,4- ) )-,_..; ( `’-’ ‘—”(_/–’ `-’_) fL The mind is its own place, and in itself, can make heaven of Hell, and a hell of Heaven. -John Milton
Response:
Hello. I’m new at this so I hope I’m doing it right. This is my first mailing list. I’m really enjoying the letters I read. They have quite a bit of information in them about meds and coping with this wonderful illness we all share. I also enjoy reading the jokes some of you have written. It’s nice to hear that others are dealing with this M.S. with a sense of humor. I have Chronic Progressive, and am pretty much wheelchairbound. I find that trying not to take this illness too seriously and looking at the fact that there is always someone worse of than I am helps.I am very grateful and fortunate that I am blessed with such a supportive family and friends. It sure helps beat the depression that comes with this illness and the meds. The one thing l learned is that you can sure tell who your friends are real quick. Anyway I am glad I joined this list. You folks seem very kind, warm and friendly. I look forward to more. Sincerely……………..Gwendolyn.
Response:
Hi Gwendolyn, Welcome to the group. I am also cp and wheelchair bound. This group is a lifesaver. Most of my friends walked out on me also. They didn’t even want to try to understand. It’s so sad this…but you’re right about one thing…You quickly find out who your friends are. My only consolation in regards to this miserable illness, are groups like this. Here you find caring, warmth, support, and information. Everyone is in the same boat, so at least we understand each other. Take care!!!!! Dawn ******************* – Hide quoted text — Show quoted text -
Hello. I’m new at this so I hope I’m doing it right. This is my first mailing list. I’m really enjoying the letters I read. They have quite a bit of information in them about meds and coping with this wonderful illness we all share. I also enjoy reading the jokes some of you have written. It’s nice to hear that others are dealing with this M.S. with a sense of humor. I have Chronic Progressive, and am pretty much wheelchairbound. I find that trying not to take this illness too seriously and looking at the fact that there is always someone worse of than I am helps.I am very grateful and fortunate that I am blessed with such a supportive family and friends. It sure helps beat the depression that comes with this illness and the meds. The one thing l learned is that you can sure tell who your friends are real quick. Anyway I am glad I joined this list. You folks seem very kind, warm and friendly. I look forward to more. Sincerely……………..Gwendolyn.
Response:
At 12:56 PM 5/25/97 -0400, you wrote:
Hello. I’m new at this so I hope I’m doing it right. This is my first mailing list. I’m really enjoying the letters I read. They have quite a bit of information in them about meds and coping with this wonderful illness we all share. I also enjoy reading the jokes some of you have written. It’s nice to hear that others are dealing with this M.S. with a sense of humor.
Hi Gwendolyn: Welcome aboard and your coming through loud and clear. Lots of really nice people who are willing to share their information, support and most important a sense of humor!!!!! Toodles, Pam McHenry Indianapolis, IN
Response:
On 5/25/97 you wrote:
Hello. I’m new at this so I hope I’m doing it right. This is my first
mailing
list. I’m really enjoying the letters I read. They have quite a bit of information in them about meds and coping with this wonderful illness we
all
share. I also enjoy reading the jokes some of you have written. It’s nice
to
hear that others are dealing with this M.S. with a sense of humor.
Gwendolyn, Hi & welcome to the list! Although I’m not glad you need to be here, I’m glad you found us. There are a lot of great folks, info & humor here. Post whenever you like. And whatever you did, it worked just fine!! Lyse
U, ,U Doggies are just kids in fur! ==o==
Response:
Hi Gwendolyn, Welcome to the group — especially with your positive attitude. The other day I was discussing mobility aids with a friend (his wife has other problems and really needs to be using a cane but won’t), and came to a startling conclusion about them — MOBILITY AIDS ARE TOOLS, and what humans are particulary good at (besides language) is making and using TOOLS! If you require a wheelchair for mobility (as I did for 1 1/2 years, and still do for long distance, shorter I just use my cane), then be thankful that you are able to get one! Z http://www.mindspring.com/~cczimmer/ +————————————————————————+ + Carolyn C. Zimmer | "I’ve been warped by the rain, | + Duluth, GA | driven by the snow, I’m drunk and dirty, | + cczim…@mindspring.com | don’t you know, But I’m still…willin’" | + STANDARD DISCLAIMER | Lowell George | +————————————————————————+
Response:
THIS IS MY FIRST TIME ON THE NET. I’VE HAD M.S. NOW FOR 7 YEARS, AND BECAME WHEELCHAIR BOUND IN JUST THE LAST YEAR. I’VE BEEN BATTLING DEPRESSION SINCE I WAS DIAGNOSED. I’VE TRIED TO COMMIT SUICIDE MANY TIMES. I FINALLY ACCEPTED MY CONDITION JUST LAST YEAR, AND AM COPING ON A DAY TO DAY BASIS. I HAVE 2 CHILDREN ONE 10 AND ONE 4. MY HUSBAND IS THERE BUT DOESN’T UNDERSTAND OR EVEN TRY. I HOPE I CAN FIND SUPPORT AND UNDERSTANDING FROM THIS GROUP. SUSAN DEMELLO CALIFORNIA
Response:
SUSAN, Welcome to the MS List. I firmly believe that you will find all the understanding and warm-hearted support you seek here. There are a lot of great people here. Don’t be shy. Please make comments and ask all the questions you like. You can’t possibly ask too many. You will receive answers and support from a variety of kindly people who have experienced many of your MS problems, so they will understand what you are going through. Whenever you do not receive the specific information you are after, please be persistent. Ask again and again until you receive what you need. You won’t offend anybody by being persistent and you will be amply rewarded. You will also have the opportunity to pass on to others what you have learned about how to deal with your MS. Please try to feel like one of the family. You’ll be surprised at the warmth you will find. I’m sorry to learn that your husband is not being as supportive as he should be. Those of us who have supportive spouses are, indeed, fortunate. Maybe there is some way that you can encourage your spouse to learn more about MS and to be more supportive. Ask others on this list if they have found any way to accomplish that. Maybe you can find a way. I sincerely hope you can. In the meantime and forever, we will be you family. With the hope that you will find the support you need here, best wishes, Paul Bruce From: SUSAN DEMELLO, carsdn…@aol.com (CARSDNTED), Date: 13 Jun 1997 18:36:15 GMT: THIS IS MY FIRST TIME ON THE NET. I’VE HAD M.S. NOW FOR 7 YEARS, AND BECAME WHEELCHAIR BOUND IN JUST THE LAST YEAR. I’VE BEEN BATTLING DEPRESSION SINCE I WAS DIAGNOSED. I’VE TRIED TO COMMIT SUICIDE MANY TIMES. I FINALLY ACCEPTED MY CONDITION JUST LAST YEAR, AND AM COPING ON A DAY TO DAY BASIS. I HAVE 2 CHILDREN ONE 10 AND ONE 4. MY HUSBAND IS THERE BUT DOESN’T UNDERSTAND OR EVEN TRY. I HOPE I CAN FIND SUPPORT AND UNDERSTANDING FROM THIS GROUP. SUSAN DEMELLO CALIFORNIA Path: lobby01.news.aol.com!newstf02.news.aol.com!newstf01.news.aol.com!audrey02. news.aol.com!not-for-mail From: carsdn…@aol.com (CARSDNTED) Newsgroups: alt.support.mult-sclerosis Subject: Re: Hello Date: 13 Jun 1997 18:36:15 GMT Lines: 11 Message-ID: <19970613183600.OAA14…@ladder02.news.aol.com
NNTP-Posting-Host: ladder02.news.aol.com X-Admin: n…@aol.com Organization: AOL http://www.aol.com References: <199705261618.MAA09…@jacinet.johnabbott.qc.ca
Response:
Dear Susan, Oh honey, have you come to the right place! You’ll get all the love and understanding and support you could possibly ask for and then some. You can feel free to ask any questions or express any feelings you could possibly have. Here you can rant, rave, laugh, cry, learn and love. Folks here know what you’re going thru and know how you feel. Somebody, if not several somebodies, has been there, done that and can help you along the way. Thank God your suicide attempts failed. Life ain’t over just cuz you’ve got MS. It’s just different that’s all. You can also get meds that will help with your depression. Sometimes depression comes just from being diagnosed and sometimes it’s actually caused by the MS itself, but there IS help for it. And you’ve got two little kids who need their Mom – no matter what shape she’s in. Besides, there are so many new things today to help treat the symptoms – things that weren’t around even 7 yrs. ago when you were diagnosed. They’re closer to a cure now than ever before. We also have some hubbies here whose wives have MS. It’s possible that they can help you help your husband. Kevin, Nik, Robert – give this lady a hand please! Carolyn might be able to help too – she’s the wife of an MSer who now has it too. She’s seen the picture from both sides. As for me, I’m just part of the welcoming committee when I can be. My daughter has MS – dx’d at 19, gonna be 25 next week and is getting married in October. I’ve also got big shoulders if ya need ‘em, or I can give a good swift kick in the butt if that’s called for.
If you read the thread "Getting to Know You" you’ll get to meet a number of us and maybe feel comfortable enough to tell us some more about yourself and your family. We’re here for you, individually and as a whole. Welcome to the family. Very glad you found us. Hugs n prayers, P. At 18:36 6/13/97 GMT, you wrote:
THIS IS MY FIRST TIME ON THE NET. I’VE HAD M.S. NOW FOR 7 YEARS, AND BECAME WHEELCHAIR BOUND IN JUST THE LAST YEAR. I’VE BEEN BATTLING DEPRESSION SINCE I WAS DIAGNOSED. I’VE TRIED TO COMMIT SUICIDE MANY TIMES. I FINALLY ACCEPTED MY CONDITION JUST LAST YEAR, AND AM COPING ON A DAY TO DAY BASIS. I HAVE 2 CHILDREN ONE 10 AND ONE 4. MY HUSBAND IS THERE BUT DOESN’T UNDERSTAND OR EVEN TRY. I HOPE I CAN FIND SUPPORT AND UNDERSTANDING FROM THIS GROUP. SUSAN DEMELLO CALIFORNIA
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ Some days you’re the pigeon and some days you’re the statue.
PamY Spokesmom for Jennie who has MS. ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Response:
Susan, You came to the right group for support and understanding. Please realize that your children and family need you. Whatever questions you have, we have some answers or can point you in the right direction to get the help you need. Of course, sometimes we may not have *the* answer you want or need, but we are here for you, none the less. I think you will realize that just having this group around is going to make a *big* difference in your life and the way you deal with your disease. Not only can you glean useful, scientific information about MS, you have the opportunity to hear from people who are in your shoes – they can tell you what works (and doesn’t work) for them in regards to daily living. Please write often and let us know how we can help. Sincerely Cathy from Illinois
THIS IS MY FIRST TIME ON THE NET. I’VE HAD M.S. NOW FOR 7 YEARS, AND BECAME WHEELCHAIR BOUND IN JUST THE LAST YEAR. I’VE BEEN BATTLING DEPRESSION SINCE I WAS DIAGNOSED. I’VE TRIED TO COMMIT SUICIDE MANY TIMES. I FINALLY ACCEPTED MY CONDITION JUST LAST YEAR, AND AM COPING ON A DAY TO DAY BASIS. I HAVE 2 CHILDREN ONE 10 AND ONE 4. MY HUSBAND IS THERE BUT DOESN’T UNDERSTAND OR EVEN TRY. I HOPE I CAN FIND SUPPORT AND UNDERSTANDING FROM THIS GROUP. SUSAN DEMELLO CALIFORNIA
Cathy Ashmore Information Technology Services Eastern Illinois University Charleston, IL 61920 217.581.2727
Response:
Hi Susan – I’m very sorry about the difficulties you are having emotionally. This group is a wonderful place to get information and support. Many of us have had MS with various degrees of disability (and many, many different symptoms), for a long time. Please feel free to vent your frustration and ask questions. I certainly hope that you have a good neurologist that is knowledgeable about the drugs currently available. Let us know a little about you when you become comfortable with us. Someone may have suggestions that will help you cope. And as PamY said, there are people here to help your husband too. I contacted the National Multiple Sclerosis Society (NMSS), and went to their counseling for newly diagnosed people. This included one session that my husband and father attended. It really helped them understand better what I was going through. I strongly recommend counseling of some sort for both of you!! Where abouts in California do you live? I live in Ventura County (Oxnard) and there are several others here from California too…LaVonne is in San Diego, Marilyn is in Oakland, Sharon in Guadalupe, Stelle in Agoura….let us know where you are. Welcome aboard. Let us help you if we can. Candace PS Your email address is intriguing. Sounds like an auto body shop, or demolition derby, or junk yard or something. (Oh yeah, just so you know, most people don’t use all capital letters when they send Email – it is considered the equivalent of yelling!)
Response:
Well I’m sure glad you found us. yes coping on a day to day basis is about all we can do. Maybe you and your husband can find a support group that you could visit together. He might be reacting to fear. At least this group offers understanding, empathy, share what you are comfortable with we are here to support one another. It’s like a family and do have the minor squabbles from time to time. Here’s a heartfelt welcome to the group, I hope you make use of us. (((((((hugs))))) At 06:36 PM 6/13/97 GMT, you wrote:
THIS IS MY FIRST TIME ON THE NET. I’VE HAD M.S. NOW FOR 7 YEARS, AND BECAME WHEELCHAIR BOUND IN JUST THE LAST YEAR. I’VE BEEN BATTLING DEPRESSION SINCE I WAS DIAGNOSED. I’VE TRIED TO COMMIT SUICIDE MANY TIMES. I FINALLY ACCEPTED MY CONDITION JUST LAST YEAR, AND AM COPING ON A DAY TO DAY BASIS. I HAVE 2 CHILDREN ONE 10 AND ONE 4. MY HUSBAND IS THERE BUT DOESN’T UNDERSTAND OR EVEN TRY. I HOPE I CAN FIND SUPPORT AND UNDERSTANDING FROM THIS GROUP. SUSAN DEMELLO CALIFORNIA
| _,,,—,,_ luv susan /,`.-’`’ -. ;-;;,_ s_guzie…@conknet.com |,4- ) )-,_..; ( `’-’ ’—”(_/–’ `-’_) fl The mind is its own place, and in itself, can make heaven of Hell, and a hell of Heaven. -John Milton
Response:
On Fri, 13 Jun 1997 21:57:55 -0400, PamY <den…@EQUINOX.NET
wrote:
(snip) : We also have some hubbies here whose wives have MS. It’s possible :that they can help you help your husband. Kevin, Nik, Robert – give this :lady a hand please! (snip) Susan, Sometimes the social side effects of MS are as difficult to deal with as the disease itself. Because many of the symptoms of MS are not visible from the outside, it is hard for someone who doesn’t have MS to understand. See the message from chantel…@aol.com, subject "Hidden MS — You Look So Good (Invisible MS symptoms)", posted 6/14/97. Your husband doesn’t understand. As a husband of someone with MS, neither do I. The difference is, I _know_ I don’t understand. Reading the messages from this group, and thinking about the way Nella acted, I found that she has many of the symptoms described here that she never told me about. She didn’t want to be a whiner. When I asked her about some of them, she said, "Oh, that’s been happening for two or three years. But you can’t do anything about it anyway, so I just learned to live with it." While Nella’s attitude of not wanting to bother me is admirable in its way, it does not foster good communication between spouses. If I don’t know she gets exhausted easily, she looks lazy to me. If I don’t know that she has cognitive problems from MS, she looks thoughtless. If I don’t know she has coordination problems, she looks careless. If I don’t know that her condition can get worse unexpectedly, she looks unreliable. As in any marriage, the secret is communication, communication, communication. If communication doesn’t happen, you get misunderstandings. Misunderstandings range from trivial through nuisance, annoyance, and pain in the rear to major problem. Example of misunderstanding from poor communication: I spent months or years being annoyed with Nella over her insistence on using towels where hot pads would be appropriate. I could never find the hot pads, the towels would soak with liquid and weren’t practical, she was just being silly and inconveniencing me. It turns out that she needs to use towels because she has lost temperature sensation in her hands. Using hot pads, she can burn herself by not noticing that she misses the pad part, The towels have greater area to cope with this, and are thinner and easier to deal with for her reduced coordination. I didn’t know this till I saw some posts here about loss of temperature sensation. Recalling some things I had observed in Nella, I asked her about this symptom and we talked about it for a few minutes. This got rid of a long-standing, if minor, emotional conflict between us. Communication, communication, communication! Even if I understand the fatigue, coordination problems, cognitive difficulties, etc., as well as can be understood from the oustide, MS still presents difficulties for me as the spouse of the affected person. The difficulties of MS interact with every other challenge life throws our way and seem to make many of them more difficult to deal with. You have two children, ages 10 and 4. Anyone who has had kids knows that small children take a lot of parental energy. MS causes (among other things) fatigue and lack of energy. Given that you have had MS for 7 years, I expect that the last 4 of them (at least) have been a process of moving from one crisis to the next in child rearing, frequently having to ask your husband to help out in ways that other husbands don’t have to. If he has been trying at all to be a good father and husband, he is likely emotionally exhausted, stressed, and unable to cope with the situation. Been there, done that. If you both keep working on it, eventually things get better. (I have war stories, but this message is already long.) If your husband is still there, he may be trying more than you think. He will have his problems, too. One of them is that you have worse problems, so he will feel he has no right to complain. Much of the work of adjusting your household to accomodate a wheelchair will fall on his shoulders; this is in addition to earning a living, being a good father, and whatever else is going on in his life. It’s tough, just not as tough as what you are going through. Free advice, worth what it costs: Think about how this is for him. Show him messages from people about how they cope, and discuss how your experience is similar or different. Show him this message and talk about where I’ve hit the mark and what I’ve guessed that doesn’t apply to your situation. Don’t assume he can see how you are doing just because it’s so obvious to you. Keep coming back to the online support group and let us know how you’re doing; the people here can be very supportive. Kevin : :At 18:36 6/13/97 GMT, you wrote: :
THIS IS MY FIRST TIME ON THE NET. I’VE HAD M.S. NOW FOR 7 YEARS,
AND :
BECAME WHEELCHAIR BOUND IN JUST THE LAST YEAR. I’VE BEEN BATTLING
:
DEPRESSION SINCE I WAS DIAGNOSED. I’VE TRIED TO COMMIT SUICIDE MANY
:
TIMES. I FINALLY ACCEPTED MY CONDITION JUST LAST YEAR, AND AM
COPING ON :
A DAY TO DAY BASIS. I HAVE 2 CHILDREN ONE 10 AND ONE 4. MY HUSBAND
IS :
THERE BUT DOESN’T UNDERSTAND OR EVEN TRY. I HOPE I CAN FIND SUPPORT
AND :
UNDERSTANDING FROM THIS GROUP.
:
:
SUSAN DEMELLO
:
CALIFORNIA
:
:~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ :Some days you’re the pigeon and :some days you’re the statue.
: PamY :Spokesmom for Jennie who has MS. :~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ kclnfltr @ frontiernet.net It is impossible to make anything foolproof, because fools are so ingenious. — Eleventh Corollary to Murphy’s Law
Response:
Well I’m sure glad you found us. yes coping on a day to day basis – Hide quoted text — Show quoted text -
is about all we can do. Maybe you and your husband can find a support group that you could visit together. He might be reacting to fear. At least this group offers understanding, empathy, share what you are comfortable with we are here to support one another. It’s like a family and do have the minor squabbles from time to time. Here’s a heartfelt welcome to the group, I hope you make use of us. (((((((hugs))))) At 06:36 PM 6/13/97 GMT, you wrote: THIS IS MY FIRST TIME ON THE NET. I’VE HAD M.S. NOW FOR 7 YEARS, AND BECAME WHEELCHAIR BOUND IN JUST THE LAST YEAR. I’VE BEEN BATTLING DEPRESSION SINCE I WAS DIAGNOSED. I’VE TRIED TO COMMIT SUICIDE MANY TIMES. I FINALLY ACCEPTED MY CONDITION JUST LAST YEAR, AND AM COPING ON A DAY TO DAY BASIS. I HAVE 2 CHILDREN ONE 10 AND ONE 4. MY HUSBAND IS THERE BUT DOESN’T UNDERSTAND OR EVEN TRY. I HOPE I CAN FIND SUPPORT AND UNDERSTANDING FROM THIS GROUP. SUSAN DEMELLO CALIFORNIA | _,,,—,,_ luv susan /,`.-’`’ -. ;-;;,_ s_guzie…@conknet.com |,4- ) )-,_..; ( `’-’ ’—”(_/–’ `-’_) fl The mind is its own place, and in itself, can make heaven of Hell, and a hell of Heaven. -John Milton
Gee, Susan, depression and suicidal thoughts seems to be a big part of the emotional side of MS. I was very depressed (from lack of a diagnosis for a long time, and then anxiety attacks after that), but fortunately my neuro early on prescribed elavil on a daily basis (40 mg at bedtime, but I could take up to 100 mg daily he said–I don’t think I could stand it). But it helps me a lot and if i start worrying or getting anxious, I usually realize I’ve forgotten to take my elavil. Good luck. We care. My sustaining thought is by Robert Frost: "One thing I’ve learned about life: it goes on." Brenda S.
Response:
Welcome to our group Susan!!! I’m so sorry MS is the reason you have to come here, but also so very glad you chose to do so. We all try to help each other in both good times and bad. I too suffer from depression, and also live in California. I’m in the Santa Monica Mountains, 8 miles to Malibu. If you’re close by, I’ll send you my phone number, if you’d like, and you can call me. My husband is there for me, and we went to a couples group from the MS Society, which helped us a lot. I also went to the Newly Dx’ed Group and also was a Peer Counseler for 4 years. Plus I ran a support group in Thousand Oaks for 4 years too. That group also helped me. We have to have places and people to turn to, who know what we’re going through. It must be very hard for our spouses to understand. Especially, when "we look so good"! I tried Prozac and became very suicidal on it. So, I changed to Zoloft and it works great for me. I now take 200mg/day. Otherwise, not only would I be depressed, but I would be crying at inappropriate times, like with tv commercials and funny movies. I also take Effexor too. I have to see a Psychiatrist in order to get these anti-depressant meds. I see her about 4 times a year. I do hope your husband will either read some of the newly dx’ed info, or join you in a couples group. Another choice is for him and you too, to have separate Peer Counselers, provided for free, just by asking, from the MS Society. Let me know if I can be of further assistance. Warm hugs, Stelle
Response:
Welcome to Gwen and all the other new people who’ve joined our wonderful group. I’m so sorry that MS is the reason, but very happy you chose to join us. Let me know if I can be of any assistance. Warm Hugs, Stelle
Response:
Thank you, Kevin! I printed out your post for my grown daughters. It helped me understand that by being stoic I am NOT being brave, I am hindering communication and exacerbating misunderstanding. What a wonderful lesson. Again, thank you! (((hugs))) to you and your wife. Jeanie
Response:
Hi there Susan, Just wanted to add my welcome to everyone else’s and to say how much I have valued this group since becoming a part of it some months ago. Hope you will feel able to participate and enjoy it too. Jim is here in the background – reading posts, learning a lot, and generally being supportive to me. He doesn’t usually post up to the group but I know he would be delighted to reply to any individual e-mails from anyone who might like his perspective. Kevin is absolutely right in his comments about ongoing communications – when we first found this group Jim was hurt and a bit cross because he said he was finding out more about me from reading my postings to the group than he was from living with me daily(!); and so he was, because for the first time I had found somewhere I could be open and honest instead of conveying the impression that all was ok all the time. Good luck and warm wishes from us both Helen and Jim
Response:
THIS IS MY FIRST TIME ON THE NET. I’VE HAD M.S. NOW FOR 7 YEARS, AND BECAME WHEELCHAIR BOUND IN JUST THE LAST YEAR. I’VE BEEN BATTLING DEPRESSION SINCE I WAS DIAGNOSED. I’VE TRIED TO COMMIT SUICIDE MANY TIMES. I FINALLY ACCEPTED MY CONDITION JUST LAST YEAR, AND AM COPING ON A DAY TO DAY BASIS. I HAVE 2 CHILDREN ONE 10 AND ONE 4. MY HUSBAND IS THERE BUT DOESN’T UNDERSTAND OR EVEN TRY. I HOPE I CAN FIND SUPPORT AND UNDERSTANDING FROM THIS GROUP. SUSAN DEMELLO CALIFORNIA
Susan, you’ve come the right place. I have never fnd a more supportive group than here. We are here to help everyone, but in doing so, we help ourselves. I think you’ll find a very helpful loving group right here. Cyberhugs, Cyd :) ~~~~~~~~|~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ `~-._| I love being alive ` ~ ) and I will be the best man I possibly can. – // I will take love wherever I find it ,,.–(_ ("""^==–* and offer it to everybody who will take it. ;;( ,___, ,/~; Seek knowledge from those who are wiser ;’ )/
/ ’–, and teach those who wish to learn from me.
| ` |" -Unknown ~~ " " " ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ c…@eden.rutgers.edu c…@rci.rutgers.edu c…@pilot.njin.net
Response:
Hi there, This is the first time I have posted anything anywhere on the ‘net and I am not sure that it will work. I was diagnosed as having MS about 15 months ago and have not joined any support group before now. I have found some of the postings both supportive and informative. Thanks to all in the group. Chris
Response:
Linda Landre <linda_lan…@bendnet.com
wrote: I’m trying to learn how to post to the newsgroup. Hope it works this time.
linda, it worked! are you surprised?? welcome aboard! peggy
Response:
In article <4e6knd$…@news0.rain.rg.net
,
Linda Landre <linda_lan…@bendnet.com
wrote: I’m trying to learn how to post to the newsgroup. Hope it works this time.
You did something right this time. Welcome! Lois.
– Hide quoted text — Show quoted text –
Response:
In article <7uk95k$t7…@news.hitter.net
, "Marianne" <major1nos…@hitter.net
writes:
The doctor has the wait and see attitude for good reason. My mom had a serious attack (hospitalized & diagnosed) and didn’t have a second for 10 years! My MS, unfortunately, was rapid progression. I wish you well. Marianne
How rapidlydid yours progress? I am PPMS, diagnosed in 93 but had it 20 yrs before that I’m in a w/c 75% of the time right now. Bummer. Major bummer. Kathi
Response:
In article <19991020133836.27098.00000…@ng-cr1.aol.com
,
flowofs…@aol.compote (Keith Snyder) writes:
I do intend to ask my neurologist more about her decision not to start drug treatment, but my understanding so far is that she just doesn’t want to begin what would be a lifetime course of injection if it’s not unambiguously necessary.
If you have ms, it is not ambiguous and your doctor is way behind the times. Get a second opinion. Please do not wait until it is too late. Kathi
Response:
Thanks again for the welcomes and the advice. I’ll be speaking to my doctor soon about why she’s not putting me on ABC drugs. Thanks, Keith http://www.woollymammoth.com/keith
Response:
How rapidlydid yours progress? I am PPMS, diagnosed in 93 but had it 20 yrs before that I’m in a w/c 75% of the time right now. Bummer. Major bummer. Kathi
My first symptoms (optic neuritis & numbness) 1989. Diagnosed after leg weakness so severe I used crutches, 1991. 1992 Canadian Crutches, PT Wheelchair, hand breaks in the car, Stiffness and Balance problems. 1993 Wheelchair (total paralysis in legs), Rigidity and Tremors. 1999 Assisted Slide Board transfers Wheelchair to Hospital Bed. Trunk involvement, hand tingling & closing, arms weakening, Shallow Breathing. Very Progressive (No Remissions), but I can still think, speak, and contribute valuable input in my 13 year old daughter’s life while she helps keep me at home. Marianne
Response:
Hello Keith, I’m new to this too but I recently read a health letter by the Mayo Clinic and they said "Scientists now understand that even when MS seems to be in remission, it may be silently attacking the central nervous system. For this reason, physicians are initiating treatment for MS at an earlier stage than in the past. Best wishes Frank
Response:
I’ve been lurking for about a day and figured I’d say hello. I was hospitalized with double vision a week and a half ago after my flu symptoms escalated, and came out with an MS diagnosis. Lesions on the MRI, positive oligoclonal banding test. No insurance, of course — I’ve always been healthy, and I’m a starving artist. The hospital bill will total more than last year’s gross income. My symptoms are gradually getting better, and I’m obviously in better shape than a lot of the people whose posts I’ve been reading here. (And pretty lucky that my diagnosis took about three days, total, as opposed to the many years of frustration I’ve been reading about. I got lucky in wandering into an ER at a hospital with an MS center.) The neurologist wants to keep me off the ABC drugs until I have a second episode, but I’m not quite clear on why that is. Anyway, hello, nice to meet you. I don’t think I have much to contribute here yet, but I wanted to say hello. Keith http://www.woollymammoth.com/keith
Response:
Hello Keith- The doctor has the wait and see attitude for good reason. My mom had a serious attack (hospitalized & diagnosed) and didn’t have a second for 10 years! My MS, unfortunately, was rapid progression. I wish you well. Marianne Keith Snyder wrote in message <…
My symptoms are gradually getting better, and I’m obviously in better shape than a lot of the people whose posts I’ve been reading here. (And pretty
lucky
that my diagnosis took about three days, total, as opposed to the many
years of
frustration I’ve been reading about. I got lucky in wandering into an ER
at a
hospital with an MS center.) The neurologist wants to keep me off the ABC drugs until I have a second episode, but I’m not quite clear on why that
is.
Response:
Hi Keith! << The neurologist wants to keep me off the ABC drugs until I have a second episode, but I’m not quite clear on why that is.
Get another opinion on this! The general consensus on the ABC drugs is: start as soon as you are diagnosed. Why wait to get worse? Sorry you have joined us, but welcome to the group! Let us know how you are doing! Sylvia
Response:
Welcome (unfortunately). I was recently DX in Aug. This was my 4th episode in 10 years and have just started on Avonex. I too have been lurking around in this newgroup and am just starting to contribute (although I feel I am receiving more info than I’m giving). SB
Response:
Hi Keith! Well, as you can see, the concensus about starting one of the ABC’s is divided! Most likely the reason yer neuro wants to wait until you have a 2nd attack before starting one of these is because, the general "standard" for positively dx-ing MS is, 2 seperate attacks of differing symptoms. Having said that, I know someone who had their first attack in 1987, was dx’d right away, & hasn’t had an attack since! Sucks to have to be here, but welcome!
Lin ~~ If you can’t be nice, at least have the decency to be vague ~~
Response:
Thanks for the warm welcomes. My vision is finally to where I can start researching this stuff, so I’m reading web sites, newsgroups, and whatever I can find. I do intend to ask my neurologist more about her decision not to start drug treatment, but my understanding so far is that she just doesn’t want to begin what would be a lifetime course of injection if it’s not unambiguously necessary. Anyway, nice to meet you all. Keith http://www.woollymammoth.com/keith
Response:
Hi all I have been wondering around and this seems to be a comfortable place. This is an unfortunate Dx. But if I had the opportunity to be able to start from the beginning. I would start eating a low fat no fat diat. the (Shank diet ) stanleystone Keith Snyder wrote in message
<19991020133836.27098.00000…@ng-cr1.aol.com
…
– Hide quoted text — Show quoted text -
Thanks for the warm welcomes. My vision is finally to where I can start researching this stuff, so I’m reading web sites, newsgroups, and whatever
I
can find. I do intend to ask my neurologist more about her decision not to start drug treatment, but my understanding so far is that she just doesn’t want to
begin
what would be a lifetime course of injection if it’s not unambiguously necessary. Anyway, nice to meet you all. Keith http://www.woollymammoth.com/keith
Response:
<< if I had the opportunity to be able to start from the beginning. I would start eating a low fat no fat diat
I’ve actually been on Atkins, or at least something like it, for several months. My family has an inherited blood sugar thing (we just call it "the curse"), and low-carb eating, along with a little exercise, helps keep my mind from fogging. I’d hope I could continue to eat this way. Why do you recommend low-fat for MS? Thanks, Keith http://www.woollymammoth.com/keith
Response:
Hi Keith, sorry you have to be here, but it’s a great place, Very knowledgable, sharing and supportiive people. I’m new too.
Response:
Hello Keith…..Welcome and have fun here. Let your hair done and say whatever you want. It is extremely scary to know you have this stuff and even more so if you dont have someone to listen to you. Everybody hear listens to everybody. I for one just respond to the ones I can relate to and I am sure you will get the hang of it real quick. You are quite lucky you got diagnosed so soon. You have no idea how much stress you go through with that waiting game. As far as you next episode, I dont think they can predict those. I know mine didnt match up with others and different things happen to different people. You will find all the support you need here… Stick around
Response:
Hi Keith, Welcome to the group, you have discovered the most wonderful bunch of people. No matter what you need, question or want to share you are accepted. While it sucks that ms is a common thread joining us it is also something that brought everyone together. Laura Keith Snyder <flowofs…@aol.communist
wrote in article
<19991020095537.27084.00000…@ng-cr1.aol.com
…
– Hide quoted text — Show quoted text -
I’ve been lurking for about a day and figured I’d say hello. I was hospitalized with double vision a week and a half ago after my flu symptoms escalated, and came out with an MS diagnosis. Lesions on the
MRI,
positive oligoclonal banding test. No insurance, of course — I’ve
always been
healthy, and I’m a starving artist. The hospital bill will total more
than
last year’s gross income. My symptoms are gradually getting better, and I’m obviously in better
shape
than a lot of the people whose posts I’ve been reading here. (And pretty
lucky
that my diagnosis took about three days, total, as opposed to the many
years of
frustration I’ve been reading about. I got lucky in wandering into an ER
at a
hospital with an MS center.) The neurologist wants to keep me off the
ABC
drugs until I have a second episode, but I’m not quite clear on why that
is.
Anyway, hello, nice to meet you. I don’t think I have much to contribute
here
yet, but I wanted to say hello. Keith http://www.woollymammoth.com/keith
Response:
My Name is Moishe Pipik & I come from Palestine My mother brought me up on ManIScHewitz Kosher Wine
Response:
At 04:36 PM 3/23/96 -0500, you wrote:
My Name is Moishe Pipik & I come from Palestine My mother brought me up on ManIScHewitz Kosher Wine
Moishe, Welcome to the group. It is nice to have you here. I hope you will tell us a bit more about yourself. I hope we can help you here and that you will feeel free to ask questions and offer help to others when you wish to. I will look forward to seeing you here again. Take care. CL Spuhler _________________________ | ~ ^ ^ | Cheryl and Dana Spuhler | ~ ()() /( | spuh…@bright.net | ~ / / | / ( | Beware of Dragon | ~00/ | |___/ ( | | ^^ | ( | |____________________(___|
Response:
My Name is Moishe Pipik & I come from Palestine My mother brought me up on ManIScHewitz Kosher Wine
Hello Moishe, Welcome to the group. My name is Fernando and I live in Tarragona (Spain). I’m married with 2 sons. Since 10 years ago I have MS. If you like, tell me about yourself. My best wishes from Spain Fernando f…@tinet.fut.es
Response:
WELCOME CHRIS! Look forward to hearing from you! <C
Christine ______________________________ Reply Separator _________________________________ Subject: Hello Author: Multiple Sclerosis Discussion/Support <MSLIS…@TECHNION.TECHNION.AC.IL
at umkc-smtpgate
Date: 1/30/96 4:12 PM Hi there, This is the first time I have posted anything anywhere on the ‘net and I am not sure that it will work. I was diagnosed as having MS about 15 months ago and have not joined any support group before now. I have found some of the postings both supportive and informative. Thanks to all in the group. Chris
Response:
At 01:00 AM 1/25/96 GMT, Linda Landre wrote:
I’m trying to learn how to post to the newsgroup. Hope it works this time.
Guess What Linda, it worked! I’ve been off the group, or at least hanging low due to illness and I will assume that you are fairly new to the group. Welcome, and hope you get something from this forum. Gary Stone gst…@genesee.freenet.org
Response:
I’m trying to learn how to post to the newsgroup. Hope it works this time.
Hi Linda, I can certainly identify with "trying to learn". It worked – Welcome Aboard!
Response:
I’m trying to learn how to post to the newsgroup. Hope it works this time. Hi!
It worked. Take it from someone who has problems connecting sometimes,just keep posting away. Welcome. Karen in Alaska
Response:
Hooray Linda! It worked and welcome. Strawberries, Watermelon & Lollipops (and hugs, smiles and sunshine) Eric Eric Weinberg a0020…@bcfreenet.seflin.lib.fl.us – Hide quoted text — Show quoted text -On Thu, 25 Jan 1996, Linda Landre wrote:
I’m trying to learn how to post to the newsgroup. Hope it works this time.
Response:
"Gary L. Stone" <gst…@GENESEE.FREENET.ORG
wrote: I’ve been off the group, or at least hanging low due to illness and I will assume that you are fairly new to the group. Welcome, and hope you get something from this forum. Gary Stone
gar, i do hope you are feeling better! miss ya! peggy
Response:
At 09:44 PM 1/23/96 GMT, you wrote:
Hi there, This is the first time I have posted anything anywhere on the ‘net and I am not sure that it will work. I was diagnosed as having MS about 15 months ago and have not joined any support group before now. I have found some of the postings both supportive and informative. Thanks to all in the group. Chris
Chris, I hope you stay with us and post more often now that you have started. Welcome to the group. I am glad that you have found both support and information here. Please fell free to ask questions or offer some support yourself. Take care. CL Spuhler _________________________ | ~ ^ ^ | Cheryl and Dana Spuhler | ~ ()() /( | spuh…@bright.net | ~ / / | / ( | Beware of Dragons | ~00/ | |___/ ( | | ^^ | ( | |____________________(___|
Response:
Subject: Hello From: "[ Doc Jeff ]" m…@privacy.net Date: 9/18/2004 7:57 PM Mountain Daylight Time Message-id: <Xns9568C0B4222A64…@127.0.0.1 I worry about how tired she is even after doing mundane things like bringing in groceries.
Multiple sclerosis has been genetically linked to iron excess. Iron overload has been shown to cause extreme fatigue . Iron has been hypothesized to be involved in multiple sclerosis. Cites for all of the above .. Duck because this thread is about to be attacked .. Who loves ya. Tom Who loves ya. Tom Jesus Was A Vegetarian! http://jesuswasavegetarian.7h.com Man Is A Herbivore! http://pages.ivillage.com/ironjustice/manisaherbivore DEAD PEOPLE WALKING http://pages.ivillage.com/ironjustice/deadpeoplewalking
Response:
In <news:20040918223020.08241.00000696@mb-m10.aol.com
,
doe said:
Duck because this thread is about to be attacked ..
It wouldn’t be attacked if you’d just keep your fat, fatuous, flatulent ass the hell out of it.
Response:
ON 9/18/04 8:57 PM [ Doc Jeff ] actually said this about that ;
The lady with whom I am in love has MS. I’ve read much about it and how it works. I even listened to some online lectures about it to help educate myself. Is there anything I should pay particular attention to? Any advice from other guys who are in love with a woman with MS? (or women who are in love with a guy who has it) I worry about how tired she is even after doing mundane things like bringing in groceries. Any comments are appreciated (other than more of the political stuff which bores me to death) :)
Bring chocolates. Learn massage. Practice listening. (Just relax. Everybody has something.) Lo Oh! Remember to tip your server.
Response:
Subject: Re: Hello From: "Michael" muirh…@haidagwaii.net Date: 9/18/2004 8:45 PM Mountain Daylight Time Message-id: <2r4a67F153rq…@uni-berlin.de In <news:20040918223020.08241.00000696@mb-m10.aol.com, doe said: Duck because this thread is about to be attacked .. It wouldn’t be attacked if you’d just keep your fat, fatuous, flatulent ass the hell out of it.
Very nice .. You must be able to cure yourself with your .. command .. of the English language .. eh .. ? Oh .. yeah .. that’s right .. You .. can’t .. —————————————————– Iron in multiple sclerosis .. Read and absorb .. http://tinyurl.com/3w584 Who loves ya. Tom Jesus Was A Vegetarian! http://jesuswasavegetarian.7h.com Man Is A Herbivore! http://pages.ivillage.com/ironjustice/manisaherbivore DEAD PEOPLE WALKING http://pages.ivillage.com/ironjustice/deadpeoplewalking
Response:
<chuckling
does joan know you’re telling us about her encounters? three a month eh. rofl – Hide quoted text — Show quoted text -Jim Carter wrote:
on 19 Sep 2004 01:57:07 GMT, "[ Doc Jeff ]" <m…@privacy.net wrote in alt.support.mult-sclerosis: I worry about how tired she is even after doing mundane things like bringing in groceries. My wife and I both had MS when we were married 3 1/2 years ago. I do not get the MS fatigue. Drugs called Amantadine and Evening Primrose Oil reduce Joan’s encounters to about three times per month.
Response:
On Fri, 24 Sep 2004 17:57:04 +1000, jils <j…@spambegone.net.au
wrote in
alt.support.mult-sclerosis:
<chuckling does joan know you’re telling us about her encounters? three a month eh. rofl
Each encounter lasts about 10 days. February is hell. — Spelling and grammatical errors are deliberate to catch copyright violators.