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interesting stuff!
Some of you have mentioned behaviours that I have, but have not looked at them in the light of OC before. For example, I draw and do colored pencil work...my work has become very detailed and that has occurred since I started mirapex. I find it interesting that I can be so captivated by the veins on a leaf (observing myself). Where did this subtle change in "me" come from. You have certainly made me think with all your comments. I totally relate to the post that talks about keeping your house etc. neat and tidy before PD and now being totally unconcerned. I have noticed when I am "off" I become quite distressed about the disorder around me and make lists of what I MUST do as soon as my meds kick in....then they kick in and I go do something else, ignoring the list as if it were made by some other person (my mother maybe) but she's not around to make me do it!!! I'm stranger than I think I am:eek:
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mirapex
i was taking mirapex about 1 year i got to where i was on my computer. i would say iam done on it and before i new it i was right back on it i quit meripex and requip i dont have any complulsive behaver. as soon as i quit it stoped.donna
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Well the most damning evidence, for me at least, was when CNN (Paula Zahn) did a segment on Mirapex and the connection with compulsive gambling. The doctors (of the manufacturer B.I.) very non-chalantly said "Yes, we know it's the drug that's causing this". Case Closed! http://www.kintera.org/site/pp.asp?c...BKlF&b=1293531 Boehringer Ingelheim makes the most prescribed agonist, Mirapex. The company told us in a statement that two years ago it started warning in its package inserts about reports of compulsive gambling and that it is working with Parkinson's experts to "investigate the relationship, if any, between Parkinson's drugs and compulsive behavior." __The company suggested we call two of those experts. Drs. Matthew Stern and Daniel Weintraub at the University of Pennsylvania. Surprisingly, both doctors told us there is no question the drugs are behind the compulsive behavior. In addition, since being diagnosed with breast cancer on top of all my PD woes, and going through treatment for same, one can say I'm a wee bit depressed.......but I somehow don't have the urge to gamble. Interesting, isn't it. |
Dear blue Dahlia,
I am so sorry, no wonder you feel depressed, having one serious illness is already one too many.
About agonists, the Doctors you mentioned, at University of Pennsylvania, are conducting the survey in which I participated this past December. The survey is sponsored by the drug companies that produce Mirapex and Requip. They are pairing up patients who experience obsessive behaviour for a long term study. Obviously they are still taking the problem very seriously. I wish you strength and courage and thorough mending from the illness that is mendable. I hope all the very best for you. birte |
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The breast cancer is gone and with the hormone treatment I am currently on, should not return. We can only do so much. The rest is in God's hands. I can't emphasize enough about some of the dangers of Mirapex. I don't want anyone to have to suffer the way I did. Thanks again. |
my mom developed an organizing and cleaning compulsion on mirapex, and now seems to have the same trouble with Azilect. 8-12 hours a day organizing drawers, putting things in baggies, rubber bands around everything. I'm wondering if agonists in general do this to her.
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I was on Requip for 2 months and not even close to the therapeutic dosage. Taking it made me feel like I was on a medium to mild psychodelic drug. I never wrote poetry, but on Requip it just came out. Like in the previous post about the veins in the leaves, I had the same experience to anything visual.
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Carolyn,
I think the OCD problem varies from person to person. I have been on Mirapex since 1997, Starting with 0.375 mg 3 X per day, gradually increasing to the maximum of 1.5 mg 3 X per day in 2005. From that point I have stayed at the same dose until now. Although, OCD and hallucinations are listed as side effects, I haven't experienced any. The closest I have come is maybe more vivid dreams. I can tell you that without the Mirapex, I could not function. Have a nice day!:) Salvator |
Hi, at a slight tangent here, I'm on my 6th week of Mirapexin (as we call it here in Blighty), maximum dose for last 2 weeks and the daytime drowsiness doesn't get any better, compounded by night-time insomnia (which obviously makes the next day's drowsiness a lot worse). In addition, it's definitely affected my mental state, and not in a good way. I feel jittery and anxious and depressed and generally "weird", for want of a better term (which is odd as this drug is supposed to be an anti-depressant). On the plus side, it certainly improves some of the physical symptoms. However, I'm seeing the PD Nurse next week and will either ask to change meds or get something for the anxiety/depression. Not that I want to be popping dozens of pills. Anyone else had a similar experience?
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Welcome to NeuroTalk Bob...:Wave-Hello:
Goodness, I never thought this thread would go on for so long, but nice to see it has. Bob, I have noted that my anxiety has increased to a point of needing medication for it from time to time, but never considered that Mirapex might be a culprit Salvador, I am sure you are quite right, everyone will have a different reaction to meds. I was to have seen my MovementNeurologist last Thursday, but here in the PA we were iced in with 4 to 12 inches of ices everywhere. So, I had to move my appt to March. I will mention the anxiety to her, in addition to the OCD issues. At least I am not gambling my car away...:holysheep: |
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