Does Mucuna pruriens help: I want to try... - Cure Parkinson's

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Does Mucuna pruriens help

Joanne_Joyce profile image
15 Replies

I want to try Mucuna pruriens to reduce my dyskinesia. What is the experience of anyone using it.

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Joanne_Joyce profile image
Joanne_Joyce
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15 Replies
Juliegrace profile image
Juliegrace

Mucuna gave me dyskinesia the same as c/l.

Farooqji profile image
Farooqji in reply toJuliegrace

Do you use mucuna extract or raw powder

Juliegrace profile image
Juliegrace in reply toFarooqji

It was a long time ago, but I tried every extract from 15% to 100%.

Farooqji profile image
Farooqji in reply toJuliegrace

Try raw powder if possible. It contains other ingredients which act synergetically with Ldopa content

Edge999 profile image
Edge999

trying it for the last few weeks but im only 1.5 years into Parkinson . Doesn’t make me sick like madopar but doesn’t seem to do alot yet. Theres a good facebook site on it

Tayogi profile image
Tayogi

check out this group on facebook m.facebook.com/groups/32883...

Joanne_Joyce profile image
Joanne_Joyce in reply toTayogi

Thanks. I found it and it is very encouraging.

Rscott profile image
Rscott

it did not work for me. We tried increasing the dosage slightly each week for several weeks until my head started swimming and I couldn’t think clearly. I decided to stop since I would rather enjoy life. By the way, it was part of a so-called amino therapy protocol, but they gave me excessive doses of B6, which caused me permanent nerve damage.

Despe profile image
Despe in reply toRscott

See my reply above.

Despe profile image
Despe

Did you ever add 1/2 t of carbidopa to your MP?

JohnPepper profile image
JohnPepper

I don't use anything other than common sense! I was diagnosed in 1992 and started to do fast walking for up to one hour, every second day and have been symptom-free since 1996. I am now 89 and still living a good life.

Speak to me!

Joanne_Joyce profile image
Joanne_Joyce in reply toJohnPepper

Hi John. We have communicated over the years but you share your experience with so many people it is understandable that you don't remember me . I am happy to learn that you are doing well. I am 83 years old and I live in Nigeria. Three years ago I fell and broke my hip and am now a wheelchair user. I admire your determination to encourage fast walking despite the rude and insulting reactions you sometimes receive. I believe there are many people who have benefited from your experience.

JohnPepper profile image
JohnPepper in reply toJoanne_Joyce

Yes! There are hundreds, if not thousands of other PD patients all over the world who do what I am doing and many have written to tell me of their experiences.

CV119 profile image
CV119 in reply toJohnPepper

Could you kindly recommend any specific supplements you take or anything outside the standard medical care you do that has helped you kept going with good quality of life?

Despe profile image
Despe

I did leave it to the pros, "Dr. Isaacs/ MDS, at Vanderbilt. :) He recommended it as he was/is very knowledgeable of all natural levodopa available! :) He doesn't just push meds!!!

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