Does anyone feel like they are shaking inside. Almost like adrenaline rushing but its not.

Hi the Beep and others,. I know that Botox injections are used frequently now by physicians to stop or lessen excessive sweating.;; I wondered if a drug like Botox could interfere with PD and its meds.. My research revealed it is used often, including for people PD. I used. to get Botox for cosmetic reasons . I had a wonderful doctor; 3-4 times a year. It works magic cosmetically.

But with Covid,. my doctor retired. But it is apparently considered safe, although things can go wrong with any drug, of course.I would have to search more to find a doctor who. does it, but. it's definitely being used for excessive sweating problems, approved by the. US .public health agencies.I
I would li.ke to restart it for cosmetic use .I have an appointment tomorrow just for a consult .

First consults with cosmetic docs are usually free. Let us know if anyone tries it. I am SO 🥶, right now at 77 degrees in my.house.

I have both sweat & chills at the same time. But remember the shortrst sermon on a sultry, hot Sunday morning::"If you think it's hot now, what do you it will like
for the Christless people?

@A MyParkinsonsTeam Member. Well i guess we are both still here. Praise God! How are you doing?

Mentioned Users

A MyParki...

I thought if i keep my room cold, i could sleep with the comforter...but that doesn't work...need to buy a blanket...