Tapering off sinemet replacement of Mucuna - Cure Parkinson's

Cure Parkinson's

26,583 members27,899 posts

Tapering off sinemet replacement of Mucuna

Jenzo profile image
7 Replies

Good day,

I'm 48 and recently switched to a vegan diet. I suffer from Parkinson's but take only the min dose of sinemet daily. Half 100/25 x 3 daily. Since moving to veganism (my doctor provided pretty convincing evidence it helps a Parkinson's brain) my negative side effects from the sinemet are quite noticeable. I would like to try switching to Mucuna pruriens but work full time and I'm worried about withdrawal symptoms. I think I can manage my disease at least currently with the supplement. Any advice on dosage and how I may best transition or your experience with withdrawal. My neurologist is not a natural guy (believes in the gold standard) and unfortunately can't help me very much. I find our disease does leave you in trial and error anyhow on your own. Any advice I would really appreciate.

Written by
Jenzo profile image
Jenzo
To view profiles and participate in discussions please or .
Read more about...
7 Replies
WinnieThePoo profile image
WinnieThePoo

Take a look at these posts

healthunlocked.com/parkinso...

healthunlocked.com/parkinso...

Jenzo profile image
Jenzo in reply toWinnieThePoo

Thanks 😊

Niggs profile image
Niggs

Perhaps the diet is providing an environment that allows more of your meds to reach the brain? An increase in side effects, for me personally. is because of either an increase or decrease in drug levels and can take 3months + to settle. Re: withdrawals, it will be dependent on your own body, length of time on sinemet, sadly like all else in pd so many variables and as you say you have to suck 'it and see'. Maybe ask your Dr about reducing sinemet to see if it eases the side effects but still gives you sufficient symptom control. If so, you're on the right track but under a Dr's care.

Good luck

Jenzo profile image
Jenzo in reply toNiggs

Thank you 😙

trishtheteacher profile image
trishtheteacher

Hi Jenzo,

I’m 48 also. Diagnosed about five years ago. My neurologist originally put me on carbidopa/levodopa 100-25, 3 times a day. Unfortunately, I started getting dyskinesia after just a few months. I cut back on the c/l and am now down to 1 tablet a day (1/2 when I wake up, the other half in the evening, BUT it took a long time (years) to get down to this (headaches and nausea during withdrawal). Unfortunately, mucuna gives me dyskinesia as well, so my doctor (functional medicine… I gave up on the neurologist about three years ago), put me on amantadine, 100mg, twice a day. I still get dyskinesia, but it’s not as strong and, if I watch what I eat, I don’t get it at all.

A few other things that might interest you:

•Purchasing mucuna: I use Mucuna Pruriens powder, Zandopa, which is available on Amazon. I also take mucuna capsules by Now when I’m not able to prepare the powder version. It’s also available on Amazon.

•Dosage: Mucuna powder- ¾ tsp every 2.5- 3 hours; Capsules- 1 capsule every 2.5- 3 hours.

•Other supplements I take: Thiamin HCL (B-1), CoQ10, fish oil (I’ve got a zillion others, but these are the ones I take most consistently. If I had to pick only one to take, it would be the B-1.)

•Diet: I’ve tried them all- paleo, keto, raw, vegan, vegetarian, anti-inflammatory, fasting. What seems to work best for me is a mostly vegetarian diet (but I eat fish and use half and half in my coffee). I think the most helpful things for me, diet-wise, are limiting sugar (I really should eliminate it), no refined/processed foods, lots of veggies, lots of healthy fats (EV organic coconut oil, Almonds, and walnuts, mostly) and limited grain.

•Inflammation- I worked with a functional medicine doctor (Eric Potter, Sanctuary Medical, in Franklin, TN, USA) for two years before we figured out that #1) my inflammation was sky high (C4a was 26,000+), and #2) inflammation was probably caused by toxic levels of mold in my house—yikes! Dr. Potter diagnosed CIRS (Chronic Inflammatory Response Syndrome), which means my body does not appropriately get rid of toxins. I am doing much better since totally remodeling my house and detoxing the mold out of my body (under Dr. Potter’s supervision). I highly recommend functional medicine.

•The more exercise I get, the better I feel. 😊

Hope this helps,

Trish

Jenzo profile image
Jenzo in reply totrishtheteacher

Thanks so much for this. I really appreciate it.

interpreters profile image
interpreters

Purchase L-Dopa from: nutrivitashop.com/cart.php

They will tell you the equivalent to your pharma sinemet. Mine cam to 1/8th spoonful.

It helps to purchase a measuring 1/8 spoon, to be exact, from Amazon. There is no side effects from the product or from transitioning. Sometimes I will take half an old pill because I may need it in night and it's slightly easier to take a pill but I don't need the sinemet pills,

Not what you're looking for?

You may also like...

Mucuna sinemet equivalent?

We have successfully been reducing my dad's sinemet intake and replacing it with mucuna. We started...
pdkid profile image

Tapering Sinemet

I have been taking Sinemet in a very low dosage of 6/25-25 for the last 2 months for the first time...
Kia17 profile image

Not diagnosed but recommended Sinemet.

Hello, Over the last few years I have suffered from fatigue, cramp in the hands, calves and feet,...
spuddy profile image

Underprescribing Sinemet for PD?

In 'The New PD Treatment Book' (2015) by Eric Ahlskog he says on page 164, start with one...
ramotswe profile image

Mucuna Pruriens (MP) vs Sinemet

I am getting bad side effects from Sinemet mono therapy. Basically, dystonia. Has anyone replaced...

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.