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Messages 4678 - 4717 of 4787   Oldest  |  < Older  |  Newer >  |  Newest
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4678
Hello all - Over the past few years I've had some symptoms that have me a bit concerned, and I thought I'd see if anyone else came up on MS this way. It...
Katherine
katherine_n_...
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Aug 2, 2007
10:07 am
4680
Hello My name is Dan and I am 43yr. I live here in Georgia and I have a 14yr son who lives with me. I have had MS for 4yrs now. I have been divorced about the...
Dan
about_ms
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Aug 2, 2007
10:20 am
4681
I have had all of the same things and you are the first I remember hearing of like me. I have had MS for 2.5 years now. I was on every medicine possible for...
dotjiris
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Aug 4, 2007
5:54 pm
4682
I have secondary progressive MS and the neuro claims the pain+fevers I also have is severe Fibromyalgia (every point is painful) but the Rheumatologist says...
mummyratnz
Send Email
Aug 4, 2007
5:54 pm
4683
Hi there, my name is Terry and I've been dx'd with MS for 2 yrs now so I know what many of you are going through. I was wondering if anyone here has been put...
nightwolf8955
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Aug 19, 2007
1:48 am
4684
Hi- I am a 35 year old mother of three that just with in the last two weeks has been told that I have MS along with a list of other medical issues. I am scared...
bodacious7279
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Aug 19, 2007
1:52 am
4686
Hello! This is my first post. My name is Linda and I was diagnosed with MS in April. I am still in the "research" stage - where I am researching as much as I...
mrsmcentee
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Sep 4, 2007
7:17 am
4687
Hi My name is Terry, also with MS going on 3 yrs now. Mother of 5 girls, grandmother 4, married 24 yrs, can't work anymore. I manage a support group and stay...
nightwolf8955
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Sep 4, 2007
7:17 am
4688
Thanks so much for getting this group up and running again. I much appreciate getting messages, but I won't always chime in. I hope that's OK. I'll be happy...
gaild1975
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Sep 4, 2007
7:20 am
4689
Will anyone with significant experience with Tysabri please post about your experience. I am a person with MS now for more than 31 years and am now looking at...
regnignam
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Sep 10, 2007
4:45 am
4690
Hi all !! I'm new to this group but not new to MS. I've been diagnosed with MS for about 6 years now and currently having one of my worse exacerabations (been...
angelicagrin
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Sep 19, 2007
1:28 pm
4691
Hi, my name is Gwen. I have a long medical history that I wont bore you with the details, however I have recently been told I might have Autoimmune...
neldatinker
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Sep 19, 2007
1:49 pm
4692
I would refer you to look up Dr. Vince Macaluso on Google or any other search engine. You'll find pages and pages about him on the net. He is a neurologist who...
giwkhd
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Sep 22, 2007
6:58 pm
4693
One thing to remember the prednisone is not given to cure or fix anything. Only your body can naturally heal itself. The purpose of the prednisone is to...
fogle25
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Sep 22, 2007
7:02 pm
4694
The last exaserbation, I had, started 3 1/2 years ago. The Solumedrol did nothing to help me whatsoever, but I hope that it was worth the try? Hoping it...
knitkin
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Sep 22, 2007
7:02 pm
4695
Hang in there! Don't worry cuz it isn't good for you. It'll get better, have faith. Samantha...
fourtsranch
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Sep 25, 2007
3:12 am
4697
http://www.novartisclinicaltrials.com/webapp/portals/MSClinicaltrials/...
about_ms
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Oct 21, 2007
8:39 pm
4703
Hi I am Laura and I have just been dx'd with MS about a week ago. Hoping someone can please help me understand how Copaxone will help and your take on what...
lauralonelyheart777
lauralonelyh...
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Feb 6, 2008
10:05 pm
4704
Hi , Iım new to this group, but old to MS ‹ I was diagnosed exactly 10 years ago this month, but think I had it much longer than that. I donıt think there...
Josie
josiebyzek
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Feb 7, 2008
11:02 pm
4705
I was Dx oct 06 but it was suspected in 1989. I LOVE Copaxone!!! There is relatively no or few side effects!! All the interferons you feel like a super bad...
giwkhd
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Feb 7, 2008
11:04 pm
4706
Hi, My name is Charlene. I've lived with MS for 13 years. I'm sorry I won't be of any help with Copaxone. I don't take any drugs. I treat my MS with...
ct_christen
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Feb 7, 2008
11:05 pm
4707
It has been awhile ...since I have been here! This has been a really rough couple of months. Have been trying to be really tough. Here are details. On Dec. 18,...
sunshiner61
knitkin
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Feb 8, 2008
11:09 pm
4708
I'm so sorry to hear you have MS. It's such a shock, all your preconceived ideas about MS come up although these days with the new medications it's not the...
kfryk1
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Feb 8, 2008
11:11 pm
4709
Hi, I'm sorry to read about your DX :( Eight years ago, I remember when my neurologist put the films from my MRI on the light-box and I looked at them and...
Jayne
jayne_alexander
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Feb 8, 2008
11:12 pm
4710
Hello, I noticed Laura's message. This is the place for the questions you have! I have been diagnosed and have lived with M.S. for almost 10 years now. Please...
Olga
olgamogilev
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Feb 11, 2008
2:19 am
4711
Sunshiner61 - I am so sorry to hear about your relapse...I know it's got to be scary. I know that I could wake up with new symptoms or a relapse with no...
tonidances
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Feb 11, 2008
2:19 am
4712
Hi all, I was DX with MS in 2002. In the beginning I was hit pretty hard. My vision was gone, had Trigeminal Neuralgia on the right side of my face, balance...
reginas
gina120402
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Feb 11, 2008
2:20 am
4714
Hello everyone. My name is Lisa and I joined this sight to get more information about my mother who was diagnosed with MS in 1984. I myself am a high...
alaskanquad
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Mar 31, 2008
10:24 pm
4715
I am Melissa. The group description said it is for anyone open to with an interest in Multiple Sclerosis. I have interest in this matter. I was certain...
mjshook1974
xmelax43
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Mar 31, 2008
10:29 pm
4717
Hi, I was diagnosed back in '98, but I'm pretty sure had MS for much longer than that. My own MS is more relapsing-remitting than any other type (although to...
Josbyz
josiebyzek
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Apr 3, 2008
3:18 am
Messages 4678 - 4717 of 4787   Oldest  |  < Older  |  Newer >  |  Newest
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