Prednisone and Parkinson’s: Has anyone... - Cure Parkinson's

Cure Parkinson's

26,583 members27,901 posts

Prednisone and Parkinson’s

Friend70 profile image
12 Replies

Has anyone noticed their Parkinson’ symptoms have improved if they received prednisone (or other corticosteroid) for an autoimmune condition? It happened to me, although the details are a bit hard to explain.

Written by
Friend70 profile image
Friend70
To view profiles and participate in discussions please or .
Read more about...
12 Replies
Dap1948 profile image
Dap1948

Might this be because it reduces inflammation?

DianeF profile image
DianeF

My regular doctor told me years ago, before diagnosis, that prednisone makes everyone feel better, no matter what. The problem is the side effects, unfortunately, no one can take it long term.

Friend70 profile image
Friend70 in reply toDianeF

Thanks for your reply Diane. I think, as with any treatment, it’s a matter of balancing benefit vs. risk. if one has terrible PD symptoms that are greatly helped by prednisone (but not by standard PD treatment), why is that any riskier than a patient with MS getting therapy with prednisone? The contributions of inflammatory processes to Parkinson’s are now being studied more intensely, but I don’t think the knowledge is being applied to patient care as quickly as it could be.

KemptonD profile image
KemptonD

I came across a case study that reported that short term use of prednisolone helped one women with 'dropped head syndrome.'

I would be curious to know if this steroid helped anybody else with neck dystonia.

See:

researchgate.net/publicatio...

Friend70 profile image
Friend70 in reply toKemptonD

Thanks so much for the reference to this publication.

maryalice profile image
maryalice in reply toKemptonD

Thank you..

maryalice profile image
maryalice

I would also be interested in knowing more about this. I have neck and foot dystopia really bad. Any help would be greatly appreciated

maryalice profile image
maryalice

Thanks for the information. I have neck and foot dystonia. Do you?

Friend70 profile image
Friend70 in reply tomaryalice

I don’t have dystonia. Prednisone helped my bradykinesia, stiffness and balance problems (which levodopa did not), but I didn’t get it long enough to really assess it properly. My neurologist wouldn’t prescribe it for me.

maryalice profile image
maryalice

Thanks

ConnieD profile image
ConnieD

I found this to be true, I had an allergic rash this summer and was on Prednisone for about 2 weeks I felt like my PD symptoms were better. Specifically my off periods were better. I think it may be due to being an anti inflammatory, just my thoughts

Friend70 profile image
Friend70 in reply toConnieD

Thanks for the info!

Not what you're looking for?

You may also like...

Tapeworms and Parkinson’s

I don't know what to make of this but it is true and I wanted to share it in case it sparks...
AGH_1966 profile image

autophagy and Parkinson’s

Please take the time to watch this video. I think this might be one of the most effective ways to...
38yroldmale profile image

Febuxostat and Parkinson’s

Hi all this is my first post in the community. I am recently diagnosed with Parkinson’s, it seems...
William321 profile image

Parkinson’s and eyes

Yesterday, I had an eye test and my vision has improved. This is great but I spent a lot of money...
forest1 profile image

Sweating and Parkinson’s

If you or your person with Parkinson’s has excessive sweating issues (afternoon and evening) what...
jcavana profile image

Moderation team

See all
CPT_Aleksandra profile image
CPT_AleksandraAdministrator
CPT_Anaya profile image
CPT_AnayaAdministrator

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.