Cerebella Atrophy: I have recently been diagnosed... - Ataxia UK

Ataxia UK

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Cerebella Atrophy

Jacqui-A profile image
16 Replies

I have recently been diagnosed with Cerebella Atrophy, I am reaching out for your support.

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Jacqui-A profile image
Jacqui-A
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16 Replies
BlanketTime1 profile image
BlanketTime1

welcome!

Meekster profile image
Meekster

Welcome Maridale! What a Cute picture! I’m glad you found this site. I’m sure you’ll find it helpfull and usefull as many of us have. Finding out you have ataxia can be overwhelming. Please tell us more about yourself.

Jacqui-A profile image
Jacqui-A in reply to Meekster

I was diagnosed two weeks ago but went to GP 3 or 4 years ago with balance issues and she dismissed it. I saw another GP last year and she dismissed it. I don't get on with the walking sticks I had issued me by the physio, my coordination isn't that good, it is so embarrassing to go out and I feel I'm fall.

Going to

ConfusedAtaxian profile image
ConfusedAtaxian in reply to Jacqui-A

Get a good walker, Maridale x

Jacqui-A profile image
Jacqui-A in reply to ConfusedAtaxian

Yes I have bought one thanks for that

Happyfacexx profile image
Happyfacexx

Welcome to our group 💐

Jacqui-A profile image
Jacqui-A in reply to Happyfacexx

Thank you!

margieboo22 profile image
margieboo22

Hi,I was told ataxia about 3months ago,so much to take in! Xx

Jacqui-A profile image
Jacqui-A in reply to margieboo22

I had never heard of it before, have seen the physio and he's given me exercises to do hope they keep me mobile. I was distraught and in floods of tiers when I first learned fearing what's round the corner.

margieboo22 profile image
margieboo22 in reply to Jacqui-A

I know,I already use a wheelchair and sticks, what's next? Xx

suzie44na profile image
suzie44na

Hi, I have brain atrophy too, but I have no positive diagnosis, which is most stressful, as I am always hoping for a diagnosis. Sometimes you do just need someone to talk to about your problems, so this is a helpful site to ask anything you like and feel less lonely. Welcome and wishing you all the best

Suzie

Jacqui-A profile image
Jacqui-A in reply to suzie44na

Hi Suzie

After two visits to two different doctors I eventually found a GP who took me seriously and started by seeing an ENT specialist who recommended an MRI scan. Of course there was nothing wrong with my ears, but when I saw the neurologist He was able to diagnose me so ask for an MRI scan

suzie44na profile image
suzie44na in reply to Jacqui-A

Hi Maridale, I have had MRI scans, my neurologist told me I had brain atrophy on my scan,but the report never said this

Suzie

swtb profile image
swtb

Welcome Maridale. You hv come to the right place for support, important info, and understanding. You are not alone. I too was diagnosed wi Cerebellar Ataxia and i am learning so much more from this platform than any GP or even my 2 neurologists, who basically said good luck. Glad yu are here.

Jacqui-A profile image
Jacqui-A in reply to swtb

Thank you, when were you diagnosed, can you still use your legs?

Jacqui-A profile image
Jacqui-A in reply to Jacqui-A

Yes I can still use my legs, not well though, I have a mobility scooter for walking the dogs and I find one walking stick is better than two because of the lack of coordination.

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