NUMB BUM: Hi All Can anyone recommend... - Multiple System A...

Multiple System Atrophy Trust

1,773 members1,423 posts

NUMB BUM

6 Replies

Hi All

Can anyone recommend a seat cushion?

M keeps getting a numb bum whilst sat in his rise and recliner chair and as he is now immobile he unfortunately has to spend a lot of time on it.

I’ve looked at purchasing one but there are so many different ones available it’s a bit of a minefield.

Any suggestions/recommendations would be greatly appreciated

Many thanks

Sharon

6 Replies
Yanno profile image
Yanno

Hello Sharon, You don’t say where you are in your bio but if in the Uk then the OT’s should provide a suitable cushion for M. Jackie has one called Roho. It’s inflatable with lots of little cushions within the outer casing. It’s been fabulous for her and we’ve tried a few.

I would try and get the OT’s to provide as they’re quite expensive

Take care, Ian

Photo of Roho cushion with cover pulled back.
in reply toYanno

Thanks Ian. Yes we are in the UK (north Lincolnshire) Don’t have much involvement with OT but have a fabulous physio who has sorted all the other equipment M needs so will have a chat with her. Thanks again. Sharon

in reply to

hi, I agree you need to have OT support. They have access to lots of good options and supply what you need. If you haven't got one, contact your parkinson team or GP. Xx

in reply to

Thanks for your advice

Kaye31 profile image
Kaye31

hi

Our OT gave us a square of something i would liken to large bubble wrap but full of gel. Just sits on the chair

in reply toKaye31

Thank you. M’s physio popped round the other day and I mentioned to her (we don’t see anyone from OT but physio lady is fab arranging equipment etc)and she is arranging a foam cushion to start (as M only has low level soreness) with a view to moving to the gel and air cushions when required. Thanks again for your input. Sharon x

Not what you're looking for?

You may also like...

Leg half numb

Hiya diagnosed Feb 2016 probable MSA-C gone downhill since then no longer drive or can keep my...
Mick3849 profile image

CHC funding

Hello, just wondering how many people with MSA have been able to get CHC funding? I appreciate...
K8chris profile image

I don’t understand

hi My husband was diagnosed with Parkinson’s in 2021 after a few years of dizziness and balance...
DeeMilo25 profile image

My dad

I know that every case is different but my dad has been living with MSA for quite a few years but...
Becca9019 profile image

Saddest of News

It is with immense sorrow, I tell you that, My darling husband, Tony, passed away on Monday 30th...

Moderation team

See all
MSATKirsten profile image
MSATKirstenAdministrator
JamesMSAT profile image
JamesMSATAdministrator
NicoleMSA profile image
NicoleMSAAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.