Ok I too am scared, this week for the last few days my brain has been backfireing I have trouble remembering what store I'm in, the name of the person I just talked to on the phone(my mom), my sisters name ect. about 2 times a day I forget something like that only for a second then after I've blurted out the wrong name or the wrong place I usally know its not right. I am starting to not trust my self, Im not sure if its PD or the Azilect (sp?) but something is off I take no other meds and have only been taking it for 2 months started with .5mg and went to 1mg for the last month Im waiting on my MRI and return to the Dr Nov 30 I continue to hang on but I feel my life crumbling around me.
bad week: Ok I too am scared, this week for... - Cure Parkinson's
bad week
It could be some bad things but PD is one of the least bad. I hope you are ok.
When I was on azilect I thought I was losing my mind. I couldn't even remember four numbers together. I went off it by myself probably should have talked to doctor first. I had not comfortable couple weeks were I felt mad at everything. After that I was back to normal.
I was on .5 mg for 2 months and then the third month I went to 1 mg and then it's got really worse. I would get up and go to get something when I got there I couldn't remember what it was. When I get off the azilect. I definitely noticed that my movements were worse so I guess it was doing something however not worth the side effects. Also, my driving was really spaced out.
Same here. Although I started on Rasagiline (generic for Azilect) 1mg/day but then was so spacey that had to focus really hard to accomplish anything which was very depressing as I was used to doing a few things at once. So, after being in a brain fog for a few weeks, fortunately, I still got enough brain power to figure out that I need to cut my dose to 0.5mg which I did and my brain started working again. However, 5 months later I developed daily headaches and since this was listed as one of side effects, I gradually got myself off rasagiline. It's been about a month since I stopped taking it and so far I have not noticed any difference in my symptoms, but I understand that Azilect/rasagiline is not for symptomatic relief but to slow progression of PD - just mentioning that because of your experience of movements getting worse.
What I keep on forgetting to mention is that I got one of the really bad side effects it was malaise slash flu like. Till I got off azilect I really did not make the connection of losing my mind and the azilect till I stopped.
Sorry to hear that. If you look at rasagiline's clinical pharmacology, there is a statement:
"In vitro metabolism studies showed that CYP1A2 was the major enzyme responsible for the metabolism of rasagiline"
I personally don't have variants in CYP1A2 but have plenty variants in other CYP genes which also may affect clearance of rasagiline, hence the difference between individuals taking it.
I hear you, and my heart goes out to you. My brain's in the same place.
I know it doesn't help...but no matter how bad I've got it, there's always someone worse. It is what it is. Try to make lemonade out of the lemons.
Update MRI was normal, dr stopped Azilect started lexapro and amitadine not sure of the spelling but that's where I am at insurance is questioning the amitadine but I have weaned of the Azilect and 2 days on lexapro and today I had what they say is a panic attack. Shot of Ativan fixed that but my tremors are horrible now this is a wild ride hope I have what it takes to live with PD