Parkinson's Disease Tulip


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Old 08-04-2009, 03:43 PM #11
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Default If I knew then what I know now....

I've been on meds for nine years now. Started with Requip and added Sinemet. Used selegeline for a while but it is heavy on the liver and poses a potential problem with some of the alternative stuff I try so I dropped it. I am at max dose of Requip of 24 mg but was up to 32 mg for awhile. I seem to tolerate it extremely well. Add 700 mg of Sinemet and you have my med history.

In retrospect, I wish that I had hit things like turmeric, etc earlier and harder, but hindsight is always better. For me, the bottom line is to resist adding or increasing a drug as long as possible.
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Born in 1953, 1st symptoms and misdiagnosed as essential tremor in 1992. Dx with PD in 2000.
Currently (2011) taking 200/50 Sinemet CR 8 times a day + 10/100 Sinemet 3 times a day. Functional 90% of waking day but fragile. Failure at exercise but still trying. Constantly experimenting. Beta blocker and ACE inhibitor at present. Currently (01/2013) taking ldopa/carbadopa 200/50 CR six times a day + 10/100 form 3 times daily. Functional 90% of day. Update 04/2013: L/C 200/50 8x; Beta Blocker; ACE Inhib; Ginger; Turmeric; Creatine; Magnesium; Potassium. Doing well.
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Old 08-04-2009, 10:18 PM #12
girija girija is offline
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Default

Charlie,
I was taking 3mg per day and managed to cut down to 1mg in the morning and 0.5 in the evening. I have both physical and psychological symptoms. Muscles ache and the pain is hard to describe, deep inside the muscle and feel restless;
I have to try very hard not take my usual dose, some days I give up, thats the routine for the last 3 months, However, when i have other things on my mind and forget to take meds, none of these symptoms show up! thats why I call it addiction, clearly psychological need for Dopamine high and in its absence physical pain. Thats my analysis........Lucky for you, you didnt have to deal with that!
girija

Quote:
Originally Posted by chasmo View Post
interesting you are having withdrawal issues with Mirapex. I quit cold turkey after my DBS. (Max dose of 4.5 mgs daily) My question is; do you think your
"addiction" is physical or pyschological? I never had any yearnings to go back on it myself.

Charlie

Last edited by girija; 08-05-2009 at 06:27 AM.
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Old 08-05-2009, 05:13 AM #13
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Default My experience

I was diagnosed 3 years ago at the age of 63. Main symptom slight tremor and rigidity on the right side. From day 1 the neurologist wanted to put me on cinemet but I refused.
Helped by this forum and my own search I have been taking a load of supplements including mucuna , creatine and whey and a strict routine of exercise about 1 hour in the morning and 1 hour in the afternoon. Quality of life is good enough. To deal with tremor I started Kemadrin about 6 months ago which seemed to help. I visited same neurologist after 3 years and he said I should be on cinament but he said that he will not object if I am happy with my own "invented" regime !
I must add that I have the support of a wonderful wife and I do some work from home and I try zero stress ..and listen to music

Imad
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Old 08-05-2009, 07:28 AM #14
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Default addiction has its place

Good Morning Friends,

Just to play the devil's advocate: As PWP we all have in common a deficiency of dopamine. So many of us look for something to help us out with that. For me, it's Requip XL (now 12 mg) and Fava Bean Extract, which is a natural source of L-dopa that crosses the BBB.

How is this different than a diabetic who is dependent on insulin to function within the range of normal (say, conscious, for example)? Or people with bipolar who stay well on lithium and get really sick without it? Should these folks break their addiction? Of course, they should do whatever they are up for with diet and exercise, but if they need insulin or lithium, they need it.

Similarly, people with unrelenting pain, say cancer patients or some of us with PD such as, well, moi. Under the care of a pain management specialist, I take hydrocodone daily. It allowed me to work (until the PD overtook me), to parent (on good days), to clean my house (do people still do that?) and to not let the pain overwhelm me. Do I suffer if I skip a few doses because I forgot to pack my meds when going out of town? Yes, like hell.

What's the lesson? That I'm addicted? No. It's don't leave the painkiller at home. Don't leave home without it.

BTW, I am also addicted to air. Water. My family. Poetry. And, apparently, this forum!

What are YOU addicted to?

Rose

Last edited by rose of his heart; 08-05-2009 at 07:36 AM. Reason: proofreading
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Old 08-08-2009, 07:39 AM #15
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Default There was no effect from Requip XL ...

Quote:
Originally Posted by EugeneS View Post
I am a new one diagnosed with PD. Even maybe not diagnosed but assumed by my neurologist to have early stage of PD. Tremor in left hand (from end of last year), some stiffness in face muscles and neck…
He proposed to start Requip XL 2mg daily and see what happen with symptoms. But I hesitate…

Thanks
Finally I took Requip XL 2mg during the week (as a drug test)...
There were no side effects observed...
There were no improvements with symptoms (left hand tremor, some face rigidity..)
What can be the next step in this research?

Thanks
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Old 08-11-2009, 10:38 AM #16
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Default requip xl didn't work as well 4 me

i have been on requip for roughly 8 yrs. when we switched to XL it didn't really work and made me feel "speedy". back to plain requip - much better for me. 5mg 3x daily.
stevie
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