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Depression Takes a Toll on Parkinson's Patients
As a patient or caregiver, have you found this to be true? If you have faced depression, how are you managing it? (therapy, medication, lifestyle changes like nutrition or exercise, etc.)
HaylenView Thread
On occasion, I have tremors in my left hand and some involuntary leg and arm jerks, however, I have had a skin condition that has been getting worse over the last couple of years. I believe it is plaque Psoriasis.
I've wondered whether there is a link with my skin condition and Parkinson's disease.
I welcome your comments!
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1. Azilect in 11/2010 1 mg per day
2. Sinemet in 9/2011 6-1/2 pills per day every 3 hours - I take 1-1/2 at 6 am the the remainder of day I take 1 pill at 9 am, 12 pm, 3 pm, 6 pm and then 9 pm and no more until in the morning.
3. Neupro 2mg which I just started taking last week.
My Neuro has told me that I have a "mild" case of pd. I have body jumps. I cannot remember if I had them before I started the meds or not, but I do not think so. I am now wondering if they are from the meds or not. Either my arm or leg will jump up high by itself. It happens usually when I am relaxing and my body is still. It just happens and I don't know when it is going to happen. Mostly my leg but also my arm seems to jump up on its own. Each time my body jumps it does it only one time. I wish I could see it happen but as I say I don't know when it is going to happen. The jumps do not happen a lot just every now and then. What do you think? Do you think it is dyskinsia? Someone on my support group said that is how his dyskinsia started. Also, when I happen to doze off especially if I am falling asleep in the day time sitting up my lips smack or move as if they are taking a bite of something.
I do not want to start getting dyskinsia so early in my disease. Do yo think I am over medicated? Although each time I started using more sinemet it was because my symptoms would start up again - the rigidity, tremors, paranoia, I especially have trouble with my vision. And so far the meds make me even forget I even have PD except that I take the meds every 3 hours.
My Neuro has said that I have a mild case of PD. I have had a lot of stress for the past year trying to take car of my very aggressive mother who has dementia (finally had to put her in a nursing home), my job merged with our NY office had to start commuting too NYC which adds 3 hours each day to my commute and now my job has added another partner to my work load and I am working for 3 partners (2 very busy) and an of counsel and a very busy associate. I'm trying to cope with everything.
I was agreeable to taking the sinemet because I work and didn't want to stop working and when I started taking the sinement it was because I could no longer type with my left hand. The sinement solved all of my pd problems. I have no tremors because of the meds.
As always, thank you for your help Dr. Stacy. It is so great that we have the opportunity to come to this website and be heard!!!!! You are appreciated!!! Even though I do not post a lot I am a lurker.View Thread
Can stress induced tremors cause prominent low dopamine levels on a Datscan? Or does early onset and being a woman change the presentation in any way of Parkinson's?
ThanksView Thread
I know little or nothing about this disease at all. The neurologist that saw me wasn't even the same guy that I was scheduled to see. All he did was confirm that I had it, he asked me if I had any questions which I was just too floored to think of any, and that was it. I've used WEB MD for other things so I thought I would check but I'm still confused, VERY uninformed, and I have to tell you, very scared at this point. I'm totally on my own here so please forgive my asking so many questions......but I need help FAST.......View Thread
I know little or nothing about this disease at all. The neurologist that saw me wasn't even the same guy that I was scheduled to see. All he did was confirm that I had it, he asked me if I had any questions which I was just too floored to think of any, and that was it. I've used WEB MD for other things so I thought I would check but I'm still confused, VERY uninformed, and I have to tell you, very scared at this point. I'm totally on my own here so please forgive my asking so many questions......but I need help FAST.......View Thread
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I am so tired and doing the least amount ot activity wears me out. I am noticing some increase in my Parkinson's complaints, mostly the chest pain and shortness of breath. I assume this can be called a "flare" or is there another name for it?
I also wanted to ask the other ladies on this site something that I have noticed the past few months and keep forgetting to ask. I rarely feel the "need" to urninate unless my bladder is really full. Even then, I am finding that I need to "push" to initiate the stream and keep it going. Anyone else experience this?View Thread
Thank You for all that you do for Parkinson's
Jo HView Thread
Thanks for any help you might be able to provide.
I hope all of you or your loved ones are doing well; my prayers go out to all of you.
God BlessView Thread
He was very understanding and the evidence for what I have come up with supports my findings and he agrees with me and told me he had to run one test that did not get completed and one test that needs to be current before he can give me a Definate Diagnossis of PSP....He is the head Neurologist for both the V.A. hospital and the University Hospital and sgreed that four years of testing and retesting and still no diagnossis or trearment is way too long....
I'll have to continue this Because this site times out on me and I loose everything I type...So Cont.....View Thread
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