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Messages 5 - 36 of 331   Oldest  |  < Older  |  Newer >  |  Newest
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5
Thanks so much for organizing this group. I suffer from LGMD. I've noticed problems since 1993, but it wasn't until last year that doctors were able to...
Jamal Davis
gbmee_1999@...
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Jun 3, 2001
2:17 pm
6
hi! I'm the second spanish in this group (It's not a bad average). I'm afected by a muscular dystrofhy since i was a child. Now I'm 29 years old and I haven't...
clavilenho@...
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Jun 6, 2001
10:08 pm
7
thanks to María José for leading me to the site of the upcoming XVII World Congress of Neurology, to be held in London, 17-22 June The conference webpage is ...
BWilliams16@...
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Jun 9, 2001
5:44 pm
8
I thought I would see what experiences others have had... When I first started to have symptoms (20 years ago) it seemed to be very difficult to find a...
BWilliams16@...
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Jun 9, 2001
5:53 pm
9
... Hi Brad, and also to the rest of the group. For those who don't know me (who I guess is everyone except Brad), I'm a student doing research into dysferlin...
Daniel MacArthur
mesk125@...
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Jun 11, 2001
10:27 am
10
Hi, I'm Suzi from Surrey, England. I was originally diagnosed approximately 7-8 years ago with Polymyositis. After high dose steroids, Cyclosporin and a...
joesuzi.croft@...
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Jun 15, 2001
6:33 pm
11
Hi Suzi, nice to hear from you! Your diagnosis story sounds quite difficult. I was somewhat fortunate in that, although some doctors I had consulted while I...
BWilliams16@...
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Jun 16, 2001
5:04 pm
12
As I discovered yesterday, the default in sending a reply to a message is to send it only to the author of the original message, not the group. To send it to...
BWilliams16@...
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Jun 16, 2001
5:17 pm
13
While I realize that this forum is about dysferlin, I have a question about LGMD -- which I have. Does anyone know if there are any sort of exercises that...
Jamal Davis
gbmee_1999@...
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Jun 26, 2001
5:13 am
14
(the first time I sent this message back to the author only and not to the board) Oops! Hi Jamal; Your question is very good one, and I've been asked that by...
BWilliams16@...
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Jul 1, 2001
2:33 am
15
This was originally a reply to Jamal's message (13), but I (also) neglected to select the option to send it to the board: There is a website, rehabinfo.net,...
jerrywilliams2@...
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Jul 6, 2001
5:30 am
16
Hi everyone; The following is a "preview" of a new pamphlet on distal MD being prepared by the US MDA. This was sent to me by Sharon Hesterlee, who invites...
BWilliams16@...
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Aug 1, 2001
3:03 am
17
the dysferlin website has a new address: http://www.dysferlin.org the site still exists on the previous address for the moment (if the server is functioning,...
BWilliams16@...
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Aug 27, 2001
5:08 am
18
Hello, My name is Vikram. My brother in India is suffering from Miyoshi myopathy since 1996. Several docs have tried and given up on any kind of treatment. We...
vgokhale@...
vgokhale.rm
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Nov 27, 2001
1:56 pm
19
Hi Vikram, Welcome to the group. As far as the prognosis of Miyoshi myopathy goes, the symptoms are progressive, although rather slowly. Typically patients...
BWilliams16@...
baw1064
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Nov 27, 2001
9:58 pm
20
I am a final year student at Brighton University (UK), studying social science. For my dissertation I am investigating how individuals with Muscular Dystrophy...
jades_fireuk
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Dec 31, 2001
6:04 pm
21
Just wanted to say Hi to everyone here. I'm not sure yet but we are testing for LGMD Type2B. I've had a diagnosis of Polymyositis since 1997 and saw a...
dad4dogs33
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Jan 10, 2002
11:51 pm
22
Welcome to the group, BillG. I appreciate how frustrating it must be awaiting a diagnosis--it certainly was for me. From what I've read and also heard from...
baw1064
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Jan 14, 2002
4:48 am
23
I just came across the following abstract, which reports a way of diagnosing dysferlin deficiency from a blood sample. The caution is that this test still...
baw1064
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Jan 14, 2002
5:01 am
24
I am so glad to know that you all are here. This has been such a long, emotionally and physically draining ordeal for me and my family. I was told 2 weeks ago...
khurte
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Jan 16, 2002
1:43 am
25
Welcome to the group, Kendra. I can definitely relate to the thoughts and feelings you express. I imagine you are kind of overwhelmed right now trying to come...
baw1064
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Jan 16, 2002
8:04 pm
26
Hi ! I've been diagnosed with type 2b for about a year now and I hope to learn as much as possible. Info is sparse on 2b and myoshi. I did learn quite a bit...
fretmaster6
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Jan 31, 2002
7:04 am
27
Welcome New Guy-- Brad Williams is usually online to greet newcomers to this list, but he has been incapacitated recently (I understand that he is on the mend...
Sharon Hesterlee
shesterlee
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Feb 1, 2002
6:06 pm
28
Hi again folks and thanks for the greeting Sharon! Please forgive me for not pointing out that my name is Dave and I am the inquisitive type. To that end, I'd...
fretmaster6
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Feb 2, 2002
5:08 am
30
... I've also read that the number is very low at "end stages" . What's the scoop? CK (or CPK) is a muscle enzyme which leaks into the bloodstream when muscles...
baw1064
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Feb 3, 2002
12:52 am
31
Hi everyone, and thanks for filling in, Sharon! Well, I managed to fall down last week and break my leg...specifically, the upper portion of the tibia. I...
baw1064
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Feb 3, 2002
1:00 am
32
Thanks for the info Brad and I hope you have a speedy recovery. It must smart horribly to break a leg. I have another question. Has anyone here experienced any...
fretmaster6
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Feb 3, 2002
5:31 am
33
Hi, everyone, My name is Phalevi. I'm a french medical student interested in distal myopathies and of course dysferlinopathies. (so be lenient with the...
natalisan
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Feb 7, 2002
1:38 am
35
... nor ... de ... in ... the ... heart ... the ... the ... a ... begin. ... usually ... complementary ... this ... of ... vaccines ... some ... other...
dad4dogs33
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Feb 8, 2002
8:04 am
36
Hi All, Just thought I would point out that Dr. Bob Brown has developed an antibody-based test for dysferlin deficiency that can be used on blood samples (no...
shesterlee
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Feb 22, 2002
5:31 pm
Messages 5 - 36 of 331   Oldest  |  < Older  |  Newer >  |  Newest
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