Legs work?: Do folks sometimes have trouble... - Ataxia UK

Ataxia UK

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Legs work?

Litty profile image
21 Replies

Do folks sometimes have trouble making their legs work? x

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Litty profile image
Litty
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21 Replies
LOUISASAM profile image
LOUISASAM

I love this post 😊. I'm wobbly at times

Litty profile image
Litty in reply to LOUISASAM

yey! I am so glad not alone - unfortunately happening more often - so embarrassing they just will not work - some days fine x

springlove profile image
springlove

Kitty, my legs don’t take notice of my brain! In fact my body goes in a different direction sometimes. I feel like I’m being possessed lol, I stop and let each catch up with the other. People stop and ask if I’m alright 😦

Litty profile image
Litty in reply to springlove

Glad you are ok - good they notice lol x

pollybanana profile image
pollybanana

Yes, often when I try to walk after sitting down my legs won't work. Its as if they don't know what to do.

Edward1943 profile image
Edward1943

Tell me about it!!

neta profile image
neta

There r times when one foot seems glued to the ground and wont budge. Ive been told by PTs that this can be a body's way of expressing fear or a case of the foot carrying too much weight. My legs wont jump, jog but they will march, walk (slow ly ) and climb stairs (very awkwardly) The automatic pilot is off definately xxx N

Litty profile image
Litty

Really very sorry to hear so many experience the same but so pleased to hear normal for us lol xx

margieboo22 profile image
margieboo22

Sometimes feel like I'm made off jelly 😁😁

Capricorn9157 profile image
Capricorn9157

Hi Litty. Yep, everyday. Feel like a baby learning to walk. Legs splayed (as if I am wearing a nappy!!!), one foot 'drags' etc. :( Sometimes when I stand I have to wait to get control before I start to walk. Also, balance is off and use stick indoors and crutches when out else I am like a 'sober drunk'...lol.

GOOD LUCK :)

hsilverman1 profile image
hsilverman1

Dear Litty,

What you are experiencing is the Ataxia kicking in. I have EA 2 (episodic Ataxia) and it is very common. When I used to teach and had to chair an IEP meeting for over an hour; I would lose my balance getting up from the conference table. Very stressful and upsetting. Parents and colleagues would think that I was drunk 😵.

Take care,

HS

ddmagee1 profile image
ddmagee1

It is problematic and embarrassing, at times, when my legs just won’t work well for me. Ataxia, combined with Parkinson’s, sometimes makes it very difficult for me to walk very far, if, at all.

Woodturnerman profile image
Woodturnerman

Hi Litty

All part of Ataxia. The part of your brain that controls your body movements is not sending the right messages, if any.

I am falling over all the time.

Dave

neta profile image
neta

One more thing....Dr Thomas Clouse makes the point that intensive exercise can override the damage. N Some PTs also seem to believe this.

Vert profile image
Vert

Yes I have that problem, especially when I have been still for a prolonged period. I was diagnosed as having 'Hereditory Spastic Parapresis' and Ataxia (lucky me). Apparently it's a rare genetic condition that I got from my mom & dad. No treatment yet. Speak with your Neulologist about testing if you want.

peterallison profile image
peterallison in reply to Vert

I have exactly the same condition, well thats what the Sheffield hospital specialist worded it. And I am the same, sat down for long periods, manage to get of the sofa, stand there for a moment, the try and get my foot to turn, and wobble of to make a half cup of coffee, half a cup, as I used to spill most of it before. And had too pack in work (58 yrs old), as being a butcher, it was getting dangerous, especially on the wet floors we had

Vert profile image
Vert in reply to peterallison

Hi, I live in West Mids, where are you? Your the first person with the same condition that I have ever spoken to.

peterallison profile image
peterallison in reply to Vert

welcome to the club, its small but there are a few of us. I live up in Harrogate, north yorkshire. I was diagnosed back in 2014, I was told then that there were just a few in the area

Peter

Vert profile image
Vert in reply to peterallison

No I gather there aren’t that many of us are there! Do you know of anyone else?

peterallison profile image
peterallison in reply to Vert

not a soul, there is just me and the family, and they kind of understand it (SPG7)

Vert profile image
Vert in reply to peterallison

That’s exactly the same as me.

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