← Return to Living with Parkinson's Disease - Meet others & come say hi

Discussion
Comment receiving replies
@lisalucier

Hello, @psvantx - I wanted to add my welcome to Mayo Clinic Connect along with @hopeful33250. That sounds really hard having your biggest fear come true with getting a Parkinson's disease (PD) diagnosis recently after watching your mother and brother suffer and die from the disease. I have never had a PD diagnosis, but have had high anxiety before with high-stress situations. I recognize that is a difficult way to live.

Since you are currently thinking over the side effects you read about the medications prescribed for your Parkinson's, rasagiline and carbidopa-levodopa, I'm hoping that others can come in and talk about their (or a loved one's) experiences with these medications. @psvantx, please meet @susan62 @jdb @ggopher @trouble4343 @anna1060.

I'd also like to invite other members who've talked about these two medications in various Mayo Clinic Connect discussions —@safari1949 @mjfelder1 @maxaz1 @stephenmcelroy @justinian @gwgrover — to share any side effects or lack thereof they (or someone close to them) has had with taking rasagiline and/or carbidopa-levodopa.

psvantx, you talked about your anxiety being through the roof at this point. Is this due to the diagnosis, what you read about potential medication side effects, or something else?

Jump to this post


Replies to "Hello, @psvantx - I wanted to add my welcome to Mayo Clinic Connect along with @hopeful33250...."

Thank-you. My anxiety was raised by my PD diagnosis, but was already there. I stopped Zoloft due to dry mouth.....which has led to $13,000 worth of dental bills (3 implants) with no dental insurance. I need to avoid a repeat if possible! Certainly need to find anti-anxiety drug that will work w/o the dry mouth....haven’t had any luck asking drs. As for symptoms, I’m sure I’m in the early stages if PD....still able to move around with no probs. Have occasional drooling and infrequent balance issues (at 75, is it due to age or PD 🤷‍♀️)? The neurologist I need to see is booked out to July! Finally got in to see one who first told me I did NOT have PD, but a datscan in Dec. showed otherwise. He did prescribe the 2 meds,....haven’t started due to travel during holidays, but need to start! Meeting with a nurse tomorrow to discuss my concerns. Then wait for July! Thanks for listening....very encouraged to be in this group!