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Non-dysferlin LGMD   Message List  
Reply | Forward Message #464 of 592 |
RE: [dysferlin] Re: Non-dysferlin LGMD

Hi Donna,
 
Thanks for replying so quickly!  You're the first family I've heard of who are dysferlin-positive as well, and it sounds like you have similar symptoms.  My mum was the first one in the family who had this (as far back as we know), but now that my aunt has it at least we can assume it's recessive and not a new mutation.  It seems like such a rare thing, the specialist kept asking if my grandparents were related since they must have both been carriers! (They weren't though).
Since the muscles in my mum's thighs are so wasted, she can't support herself with her knees bent the right way.  So I think it just started happening when she was walking, her knees started hyperextending backwards because she couldn't support them.  The specialist we saw a couple of years ago said if she carried on walking like that, eventually her knees would dislocate.  He gave her braces to wear that stopped her knees bending, but after walking like that for so many years she couldn't get used to them.  My aunt seems to be affected much less severely, her knees don't bend back, but her muscles are a bit weak and she can't stand on tip-toes.  I think it affects you worse if you've had children, which makes me feel awful!
My mum has used walking sticks as long as I can remember (I'm 21), and her walking has gotten gradually worse over the years.  She still manages to go short distances, but I was worried she was exerting herself too much, and now she uses a wheelchair for the more strenuous things like shopping.  My mum still stays active - swimming is a good thing for her to do because she can use her arms mostly.
Just out of interest, where abouts are you?  I'm in Newcastle, England.
 
Best wishes,
Louise

 

To: dysferlin@yahoogroups.com
From: deejlouise@...
Date: Thu, 16 Apr 2009 00:13:08 +0000
Subject: [dysferlin] Re: Non-dysferlin LGMD



Hi Louise,

What your mum and aunt suffer from sounds exactly what my grandfather suffered from. They didn't have a diagnosis for him back when he first started showing signs. They just diagnosed him with muscular dystrophy. He started showing symptoms when he was in his late 30's and was wheelchair bound by his 60's. When I was a little girl, he was already using a cain to walk. His knees would bend back too. I wasn't close to my grandfather as my folks were divorced and he lived in a different state. But I do remember those few things. I now am suffering from some non-dysferlin LGMD. I'm 39 years old and started noticing symptoms about 2 years ago. I've under gone several tests, but all tests show that dysferlin is present and functioning. I have 4 brothers and one of them (a year older than me) is also developing symptoms. I only seem to have issues with toe walking as my calf muscles have wasted away to practically nothing. My brother, however, mentioned burning sensations around his knees, which I'm wondering if this is perhaps the beginnings of the crazy bending of the knee. He has also mentioned issues with tip-toe. I would be interested in keeping up with your mother's progress, as she seems to be on the same path of progression I'm heading towards.

I'll stop rambling now...

Donna
--- In dysferlin@yahoogroups.com, "louiseneedham21" <louiseneedham@...> wrote:
>
> Hi I'm Louise, this is my first post.
> I don't have LGMD, but my mum has suffered with it for about 25 years now. Interestingly, she only started to show symptoms during her first pregnancy, aged 28. Now at 53, she is making the transition from walking sticks to wheelchair, but hopefully she won't be completely dependent on the chair.
> I'm trying to find out more information, because my mum has one of the rare types of LGMD where her dysferlin function is normal. It is not known what gene mutation causes her condition, but they assume it is recessively inherited and that me and my sister will not be affected. My aunt is just starting to show symptoms now, at 56 and going through menopause! I was just wondering if anyone knows anything about it, or even knows someone that has this.
> My mum has a lot of muscle wastage on her thighs, and when she walks her knees bend back at a horrible angle. However, her arms don't seem to be affected. Like most of you, she can't stand on her tip-toes and falls over a lot.
> Any information would mean a lot,
> Thanks, Louise.
>




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Thu Apr 16, 2009 9:27 am

louiseneedham21
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Message #464 of 592 |
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Hi I'm Louise, this is my first post. I don't have LGMD, but my mum has suffered with it for about 25 years now. Interestingly, she only started to show...
louiseneedham21
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Apr 15, 2009
11:16 pm

Hi Louise, What your mum and aunt suffer from sounds exactly what my grandfather suffered from. They didn't have a diagnosis for him back when he first...
DeejLouise
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Apr 16, 2009
12:13 am

Hi Donna, Thanks for replying so quickly! You're the first family I've heard of who are dysferlin-positive as well, and it sounds like you have similar...
Louise Needham
louiseneedham21
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Apr 16, 2009
9:27 am

Louise, I live in Iowa, USA. You are also the first family I've come across that has what I have. Doctors just know that I don't have dysferlin deficiency and...
DeejLouise
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Apr 19, 2009
8:30 pm

Hi Donna, I guess I assumed that having children made things worse because my mum started showing symptoms at her first pregnancy, and they got worse after her...
Louise Needham
louiseneedham21
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Apr 19, 2009
10:21 pm

Louise, I can understand your paranoia about being suspect of your pains. Take comfort in how rare this is and that it is a recessive trait not likely to...
DeejLouise
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Apr 20, 2009
2:09 am

Hi I have Miyoshi type LGMD and am now 40 for starters! My symptoms started in my early 20s. I married at 23 and i have two kids which I had at 30 and 33. I...
Suzanne Croft
craftycroftyuk
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Apr 22, 2009
9:05 am

Hi, Suzanne Thank-You so much for your posting, I am now 31. My symptoms also started in my early 20's. I am married with 2 children  ages 6 and 3. I really...
Roxanne Kraft
trkt04
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Apr 23, 2009
1:48 pm

Hi Roxanne Our lives seem quite similar don't they? A great husband, 2 lovely kids, a job in the health sector, supportive friends and colleagues. We even...
Suzanne Croft
craftycroftyuk
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Apr 26, 2009
10:53 am

Our lives do seem similar. I think thats pretty cool! May God continue to give us strength to do our daily activities though out this week. God Bless and have...
Roxanne Kraft
trkt04
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May 4, 2009
4:26 am

Hello, This is Casey 30. I can still walk with pain with my Dysferlinopathy. When I was reading the post it made me think about one of the most interesting...
bowieinc
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Apr 24, 2009
5:59 pm

wondering why dint test this procedure in humans with muscle disorders. http://www.reuters.com/article/scienceNews/idUSTRE53E4WJ20090415 ...
MATHEW anas
vlacas2002
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Apr 25, 2009
6:09 pm

Louis, I read recently through DNA study that 17 variations of LGMB exists. Some over next years will be renamed. Stephen...
luv2cruz49
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Apr 17, 2009
9:05 pm

Hi Louise   I was reading your post about how children have affected people with lgmd. I have 2 boys one age 11 and the other 4  I really didn't notice much...
patty martinez
pattymartine...
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Apr 21, 2009
3:47 am

Hi Patty, Before posting on this group I hadn't heard of any other family who have the dysferlin-positive type LGMD. I was trying to find an explanation as to...
Louise Needham
louiseneedham21
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Apr 21, 2009
2:26 pm

I'm so sorry that as a child you had to carry the guilt of your mothers physical condition.  My children don't know why this has happened but my older son has...
patty martinez
pattymartine...
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Apr 21, 2009
4:47 pm
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