HEREDITARY ATAXIA: My Ataxia has just been... - Ataxia UK

Ataxia UK

4,055 members4,607 posts

HEREDITARY ATAXIA

judithrolfe2 profile image
9 Replies

My Ataxia has just been confirmed by neurologist. Hereditary. Familiarl.

Any information please would be apprecated.

Written by
judithrolfe2 profile image
judithrolfe2
To view profiles and participate in discussions please or .
9 Replies
wobblybee profile image
wobblybee

Hi Judith, welcome😊

If you weren't already aware, there are numerous types of Ataxia, it can be genetic, or have other causes. Basically, no matter what the type or cause, most of us cope with similar debilitating symptoms😏 These can vary enormously in severity and progression, even between family members.

Generally, Neurologists are not renowned for giving information. Often on initial diagnosis the exact type or cause is still being researched but if you already know it's genetic, perhaps you know the type🤔

Helpful, reliable information can be found on ataxia.org.uk and ataxia.org

😊xBeryl

Litty profile image
Litty

Sorry never heard of it but other reply good : )

Regina75 profile image
Regina75

My ataxia is heriditary. Its autosomal recessive. Both parents have the same faulty bit of DNA and unfortunately passed it on to me.

Pashka013 profile image
Pashka013

Do BOTH parents have to have the faulty gene to be called`hereditary ataxia`?

Ginger1 profile image
Ginger1 in reply to Pashka013

Hi paska13. In answer to your question. No It doesn't,. It can be autosomal dominant- one parent passes faulty gene - or autosomal recessive- both parents pass on faulty gene.

popepjp profile image
popepjp

If I understand mine is one parent

Pashka013 profile image
Pashka013

I think i am the same its one parent but of the three children only one has got it , is that normal

MBubble profile image
MBubble

Mine is hereditary, one parent, 2 out of 3 children have it

peterallison profile image
peterallison

this is what I was diagnosed by the specialist at hallam hospital in sheffield. I was confused at first, because here is no family history of it, but saying that, I am the ONLY person to have had a TIA, which started it. And it only affects males of the family, faulty gene,,,,, thanks mum and dad ha ha ha .

I have been getting gradually worse, over the last couple of years, to the extent, were in the last week, have just been in touch with the social services here, and am at the job centre, (as am unable to do my job properly now) next week, and its with regards to going now long term sick, on grounds of the ataxia...... I just really hope they have heard about it, and understand about it

Peter

You may also like...

Pregnant with ataxia

balance will be affected by my growing bump. Has anyone been in the same position?

Ataxia and depression

unstable at the moment, my Ataxia has always effected my speech so the depression has meant I've...

fundraising for ataxia

I just thought I would mention that I am holding a nearly new sale in two weeks time. Here in Hull,

3yo undiagnosed ataxia

neuroligist is suggesting she has episodic ataxia. Anyone here with episodic ataxia who can tell...

New to Ataxia diagnosis

recently been diagnosed with ataxia, they have not found which type yet, my neurologist has taken...