Posts - Multiple System Atrophy Trust | HealthUnlocked

Multiple System Atrophy Trust

1,635 members • 1,295 posts

All posts for August 2019

Sensitive nose ?

My partner with MSA has experienced a very sensitive nose all his life - seeing anything prickly like a cactus or pointy made his nose feel odd. I know this...

My partner with MSA has experienced a very sensitive nose all his life - seeing ...

•5 years ago

🐝 🐝 Birds and bees 🐝 🐝 and just a little about bums and bladders!

At the Three Counties, we had an interesting support group this week - we talked for some time about birds and bees. It turns out that one of our carer...

At the Three Counties, we had an interesting support group this week - we talked...

•5 years ago

Stairlifts

Hi, we live in a Housing Association house and applied for adaptations but were refused a stair lift because of Alan's condition. Since then there has been...

Hi, we live in a Housing Association house and applied for adaptations but were ...

•5 years ago

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Hydrotherapy

Has anyone tried this ? Has it helped ? Where do you do it ? Thanks

Has anyone tried this ? Has it helped ? Where do you do it ? Thanks

•5 years ago

Three Counties Support Group meeting in Tewkesbury next week

Just a quick reminder that on Tuesday, 27th of August 1:30 – 3:30pm we will be meeting at the Boys' Brigade Community Centre, Canterbury Leys, Newtown,...

Just a quick reminder that on Tuesday, 27th of August 1:30 – 3:30pm we will be m...

•5 years ago

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Hello - new here

Hello everyone My husband was diagnosed with MSA 9 months ago at the age of 47. We had noticed slowness in his movements and slurring in his speech, and had a...

Hello everyone My husband was diagnosed with MSA 9 months ago at the age of 47. ...

•5 years ago

The tricky subject of dying

I really recommend ‘With the End in Mind : Dying, Death and Wisdom in an Age of Denial’ by Kathryn Mannix. She is a former palliative care consultant and I...

I really recommend ‘With the End in Mind : Dying, Death and Wisdom in an Age of ...

•5 years ago

Multiple system atrophy??

Hi everyone well I think I might have MSA and don’t know what to do - about any of it! So had MS for a long time - 2odd years, but in 2013 my balance just...

Hi everyone well I think I might have MSA and don’t know what to do - about any ...

•5 years ago

Just introducing myself

My name is Jan and I am the carer for my husband Alan who has MSA - C. Alan was first diagnosed with atypical Parkinsons and then probable MSA. After...

My name is Jan and I am the carer for my husband Alan who has MSA - C. Alan was...

•5 years ago

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