Are you taking Mannitol? : To those of you... - Cure Parkinson's

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Are you taking Mannitol?

Parkie- profile image
10 Replies

To those of you on Mannitol NOT taking Parkinson meds, do you see improvement? If so, how long and what improvement did you get? Thank you in advance, need a bit of encouragement...

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Parkie- profile image
Parkie-
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10 Replies
alexask profile image
alexask

It eliminated my internal tremor, restored my sense of smell and helped me sleep better. And obviously eliminated constipation. I take it with Coconut oil, Curcumin and (now) PQQ (in coffee though I am ambivalent whether coffee helps or hinders). Note am at the early stages of Parkinson's (see my profile).

wilson4343 profile image
wilson4343 in reply toalexask

how much mannitol do you take and how many times a day?

alexask profile image
alexask in reply towilson4343

I take a slightly heaped teaspoon ( I am 70 Kg) in the morning. Depending on how you process it and your weight you may need to take more or less. I might take tiny bits in tea or coffee around lunchtime.

wilson4343 profile image
wilson4343 in reply toalexask

Thanks

Parkie- profile image
Parkie- in reply toalexask

Thank you for your reply Alexask. Since there is no one else responding, we can probably think Mannitol works mostly for those taking PD meds. You are maybe an exception to the rule.

If anyone has had positive results using it without PD meds, please feel free to write it down in this post later on: it would be usefull to confirm or infirm the info. Thank you.

alexask profile image
alexask in reply toParkie-

I think it is more likely to just work on a sub-set of Parkinson's patients. It might depend on the type and cause of Parkinson's that you have. And/or it may help with other supplements that are being taken.

Parkie- profile image
Parkie- in reply toalexask

Absolutely. I wish there was a way to gather and analyse type of PD, and so on, from people saying they had benefits from Mannitol on this Website...

I know several members wrote about great benefits but their history of PD type, meds, etc is often not listed in their profile and reading their posts or replies and gathering the info is almost impossible.

I know CliniCrowd is working on it but it will be a while.

Too bad because the precious info IS available, hidden somewhere in the posts...

AmyLindy profile image
AmyLindy in reply toalexask

Me too! Funny, something so simple seems to have done the trick. Can’t fake the results (returning sense of smell). On low dose 5mg/d of Selegiline, too, however, so it’s not isolated/definitive. Rx helps stave off depression, so not willing to discontinue at present.

AmyLindy profile image
AmyLindy

Clinicrowd is 👍🏻

AmyLindy profile image
AmyLindy

I use a tablespoon w coffee ☕️ and some w tea later in the day. Low dose Selegiline seems to reduce arm tremor and improve swing & gait on effected side. I attribute returned sense of smell (and maybe more, to be determined) to mannitol x 4 months.

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