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Non-dysferlin LGMD   Message List  
Reply | Forward Message #483 of 592 |
Re: [dysferlin] Re: Non-dysferlin LGMD

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 started to notice that my symptoms worsened with my pregnancies. But I think God everyday for Husband and children. Like you I think If I did not have them in my life. I would have given up! My whole life is about them. I live in a small town in Texas and work part-time for an eye doctor. The girls that I work with are very supportive of me. Especially If I have fallen or don't feel good they will do most of the walking tasks for me while a sit and answer phone and other stationary office tasks. So that really helps alot. I probably have a least one person per day ask me if Im Ok or If hurt my self.  Usually I will tell them that I have Musclar Dystropy . Most of patients have been great about it. They will start to ask question about it I that kind of makes me feel like it's Ok to be different. Just remember that your not alone and always keep your focus on God.


From: Suzanne Croft <joesuzi.croft@...>
To: dysferlin@yahoogroups.com
Sent: Wednesday, April 22, 2009 4:05:10 AM
Subject: Re: [dysferlin] Re: Non-dysferlin LGMD

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 didn't notice any more worsening than the usual during this time. In fact, being a mum has helped me to realise that I'm not the most important peron now in my life and has given me a real focus.  I think that if i hadn't have had kids then I might have been tempted to "give in" a bit and let the disease win!
 
I still work part-time, managing a dental practice so i have a lot of contact with the public.  I use a wheelchair when I go out of the house with the exception of when I'm at work (where I use an elbow crutch to help get around). At work I am constantly hearing the phrase "what have you done" and I honestly think they are expecting the answer like "i've torn a muscle" or "i've cracked a bone".  For this reason, and because I'm unlikely to see them again socially, I usually just reply "oh nothing much!".  This is not because I'm embarrased or ashamed of the truth but because I find that usually the truth is too shocking to a stranger who is just being polite.  If they persist in question asking, or if it is someone I've met socially, I would just say that I have Muscular Dystrophy.  If they are interested to know more they will usually ask at this stage & I will answer their questions honestly.  I also find that when I'm in my wheelchair, far fewer people ask!  Children are the best. They just come out and ask what they're thinking and I find that a really simple answer like " my legs don't work very well" satisfies them without scaring them (their parents are usually coweriing in embassment that their child has asked!"
 
I hope I haven't rambled on too much but I feel sooooo strongly that positive advice and thinking is the key to winning!
 
Take Care
 
Suzanne, Surrey UK
----- Original Message -----
From: DeejLouise
Sent: Sunday, April 19, 2009 9:29 PM
Subject: [dysferlin] Re: Non-dysferlin LGMD

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 that I have many of the same symptoms as those that do. Along with my tip-toe issue, I have a lot of fatty infiltration in my back muscles as well as muscle weakness in my calves, thighs and arms. I mentioned that my brother is showing symptoms, but he hasn't gone through any of the tests that I have been through. I don't know of anyone else on my mother's side of the family that had this, so it must have been a long ways down the family tree. Because this is on the recessive gene, no one really thought about it being passed down, since my mom was definitely not related to my dad.

I'm very interested in how pregnacey affected your mother. I would still like to have children, but because of my age (39) and not knowing how pregnancy would affect my body, I wonder what I could possibly expect to happen. I know that LGMD affects people differently so I know that how pregnancy affected her, may not affect me in the same way, but being prepared would make it easier to accept. I shouldn't have waited so long to start a family. :) I'm not totally convinced that pregnancy has anything to do with the progression of LGMD since my grandfather suffered quite severely from this and obviously he didn't give birth! You cannot assume that because your mother had you, that she was worse off. Also, how old was you mother when her knees began bending crazy? How old is your aunt that suffers with this?

Regards,

Donna

--- In dysferlin@yahoogrou ps.com, Louise Needham <louiseneedham@ ...> wrote:
>
>
> 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@yahoogrou ps.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@yahoogrou ps.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 23, 2009 1:48 pm

trkt04
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Message #483 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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