painful toes: hi, I was diagnosed with... - Multiple System A...

Multiple System Atrophy Trust

1,774 members1,425 posts

painful toes

Trudy2020 profile image
9 Replies

hi, I was diagnosed with Parkinson’s in2020. This changed to MSA-P in 2022 . My main problem is no balance and unsteady walking.I use a walker.I have very painful toes with pins and needles. Does anyone suffer from that ? Any other remedies you’ve tried that work ? TIA

Written by
Trudy2020 profile image
Trudy2020
To view profiles and participate in discussions please or .
9 Replies
Epace profile image
Epace

my hwp since 2016 going into hospital for possible msa diagnosis’s / suffers from very sore legs now takes 2 tramadol- does the trick. Anything for peace.

I hope this might help you too / good luck 🤞

Trudy2020 profile image
Trudy2020 in reply toEpace

thanks . I’ll try that

Sounds like nerve pain, you need to chat to Parkinson nurse as they can advise which medication would work best. They also have ways of contacting your neurologist and are probably better than the GP. As the GP usually will refer back to them anyway. Xx

Trudy2020 profile image
Trudy2020 in reply to

thanks, I’ll do that

LadyLins profile image
LadyLins

hello I suffer with sore feet and pins and needdles as well as being unsteady. I have found exercise does help and you can do sitting down pilates which is great for balance and as you can break pilates down you only need to do 10 minutes a day. It really helps. Also exercising in water is fantastic if you can such as a hydro pool or just the local swimming pool. As for the pins and needles ita weird but you actually get used to them but I also take Gabapentin which helps. The best person to talk to is your PD nurse or you MSA nurse specialist. I have Katie Rigg and she is fantastic to talk to and to get advice from. There is also fact sheets on the MSA Trust webpage which may help.

Trudy2020 profile image
Trudy2020 in reply toLadyLins

thanks

Hi

That's how my wife's condition started nearly 14 years ago...

She was prescribed a nerve pain inhibitor such as Gabapentin and we are still using the tablets today.

Chat with the consultant and pain team to see if that is suitable fro yourself.

Paul

Trudy2020 profile image
Trudy2020 in reply toPaul_and_Sue_Wood

thanks Paul , I’ll do that but gabapentin has bad side effects, no?

All drugs have side effects. And they all effect people differently.

Sue had no side effects.

Not what you're looking for?

You may also like...

Help!!

My brother was admitted to hospital before Christmas and his stay lasted 4 weeks. During that time...
Cory0407 profile image

Emotional outbursts

Hello can I ask how you all cope with the emotional outbursts that come with MSA? My wife (Jackie)...
Derek1uk profile image

Needing opinions or facts with MSA-C

I need opinions. My husband has MSA-C, his sister is a chiropractor. She has started John on...
Andrashko profile image

My heart is aching...

My husband Carl passed away last evening, very unexpectedly! I am still in shock. He had a regular...
heysunshine profile image

Carers

Hi, just wondering if anyone has had any trouble finding carers for someone with MSA. The carers we...
Keycode profile image

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.