Hydrotherapy : Has anyone tried this, love to know... - Ataxia UK

Ataxia UK

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Hydrotherapy

Angelcake1 profile image
17 Replies

Has anyone tried this, love to know if you would recommend as a therapy for Ataxia.

We have a pool close by which is open to hire for the public, which my husband whom has idiopathic Cerebellar Ataxia.

TIA

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Angelcake1 profile image
Angelcake1
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17 Replies
ray-wiffen-1958 profile image
ray-wiffen-1958

hi I have ataxia type 2 ive had hydro on and off for the last 6 or 7 years and

it helped quite well but being nhs I only got 1 appointment a week for 6 weeks

then I had to wait about 4 months for another 6 sessions if they had of continued

with it that would have done more good , but it did help,

best wishers

ray

Angelcake1 profile image
Angelcake1 in reply to ray-wiffen-1958

Thank for your reply. I asked because the neuro physio has said it wouldn’t be a good thing for him because it would make his muscles floppy. In what way did it help you please?

We have a local pool which is only £10 for half an hour. Did you need the physio to be in the pool with you.

ray-wiffen-1958 profile image
ray-wiffen-1958 in reply to Angelcake1

hi no the physio gave me exersisers to do in the pool and let me

get on with it, having hydro built my muscles up and made me a lot

stronger all so it improved my balance.

Helenc76 profile image
Helenc76

My daughter has FA and like Ray gets sessions from the Nhs now and then. She goes to the hospital pool with her physio and gets loads of benefits. She gets stronger and it really boosts her confidence. It’s lovely to see her enjoying herself whilst exercising

Angelcake1 profile image
Angelcake1

The theory behind the neuro physio judgement is that it will make his muscles floppy, which is ok if he’s was a hoist transfer, but because he can weightbear for very short periods to transfer from and to his power, it will be unsafe, so he can’t get it through the NHS. Your answers are great great thank you, I’m thinking of asking the Ataxia nurses at Sheffield if they will recommend him for the hydrotherapy and perhaps get a budget for it. Thanks again

Ginger1 profile image
Ginger1

Hi. I have CA & via my neurologist I experienced the hydrotherapy pool a few times. I personally didn't feel the heated water was of any benefit but certain exercises they taught me ie jogging on the spot without looking at my feet & walking in a figure of 8 i did in an ordinary pool & they helped. I wud say give it a go. Ur husband may find it helps. Everyone is different.

I cudnt swim at 1st & perservered. I used 'toggles' (long foam tubes) for buoyancy. Swimming in general is supposed to be a great exercise for ataxia. It's great to walk in the water too as you've the water resistance. A foam tube can go around ur body or can be held to aid if ur frightened of falling but at least you can't hurt yourself when falling!😜

Angelcake1 profile image
Angelcake1

Hi Ginger

Thanks for your post, are you still able to walk? I ask because you said about jogging in the water and wondered if this was something you can do if not able to walk on dry land. My husband does the gym three times a week so his muscle power is good, he can't walk tho.

maryrose46 profile image
maryrose46

Hi Angelcake ... I love hydro but find just using a swimming pool as beneficial. I can walk in water unaided ( I use a rollator & wheelchair ) I swim with a toggle and can move my entire body, which is the most amazing feeling. I even do rolly pollys much to my own amusement. Being in the water I feel alive & free. Fab that your hubby goes to the gym , the water whichever you decide will be great for him and you(.

Have fun

Mary

Angelcake1 profile image
Angelcake1

Hi Mary

He used to swim 3 times a week but his coordination is very poor now, the main reason he stopped going was because his swallow is very poor and he aspirates causing pneumonia. Left to him he would still go but I had to intervene as his breathing was out of sinc and would inhale as he put his face into the water. That’s why I would so love him to go to hydrotherapy but was worried about going against the neuro physio advice. I asked here because to me you are the experts x

suzie44na profile image
suzie44na

Hi Angelcake1, I used to go to neuro hydrotherapy and it did make me feel stronger, because I am weak. They only let me have 20 to 30 minutes in the pool because of how warm it is and then give you a drink on coming out. On coming out of the pool I did find it difficult at first because I felt my legs were really heavy to move, so I was quite off balance, but it did make me feel stronger in the end, worth going, take it easy at first and do not stay in too long.

Enjoy, Suzie

Angelcake1 profile image
Angelcake1

Thank you suzie, that’s s great help x

Cubsfan profile image
Cubsfan

Yes. It is great therapy! My ataxia mostly in lower legs and core and my. GP and PT both recommend. I try to do in warm salt water.

Angelcake1 profile image
Angelcake1

Great thank you, I’m going to show these posts to the NHS, if they won’t let him go

stedman profile image
stedman

Hello, I have used hydrotherapy solely for relaxing.

I find that a hot shower, as hot as can be tolerated directed at the top of the spine allowing the water to run down the back ia a great relief and sets me up for a good part of the day 😃

Angelcake1 profile image
Angelcake1

Thanks for your reply, my husband love a really got shower. He’s always very cold did runs a low body temperature so I’m sure he’ll like the hydro pool

neta profile image
neta

I went with my son to a local pool. He was very enthusiastic. I went in the baby pool but i couldn't find a way to prevent the water from entering my mouth and thus drowning

Angelcake1 profile image
Angelcake1 in reply to neta

Hi Neta

Thanks for your reply, in an older post Litty said she uses an inflatable collar to keep her head above water💧 maybe something you could try.

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