HI: I agree with Antes that every individual is different, with reference to the response to Sinemet or any other drug for that matter. Early on I decidedd to stay away from medications as long as I can. Come to think of it, my decision in 1999 was the right one. However, I was seeking other sources for some relief. Extensive reading helped me to decide what can I do to help myself fro my predicamnt. On top of my problems, my movement disorder spoecialist refused to see me becuase I sought a second opinion. I decided to give a try at Ayurvedic medicine. I went and interviewed Dr. Paneri in Ahmedabad, I tried his medications for two years. At he same time, I was actively pursuing my own knowledge about anti-oxidants (AOs). I added 1/2 a pill of celebrex (Since we know that this will inhibit n enzyme that will aid in PD development) to my AOs, which I think was a mistake. In 2005 or so, I had a block in my coranary artery and I went through two angioplasties in one year. My cariologist told me that No Celebrex any more. As a result, I stopped Dr. Paneri's medications since at that time I did not kjnow what caused my heart problems. Now I am taking the following medications (Mostly nutritional supplements) which are helping me and I am still functional, even though I am 74. Swanson's condition specific brain esentials (This is esentially some B vitamins and Gotu kola - an ayurvedic herb.) This is the only PD medicine I was taking everyday 1 cps in the morning and 1 caps, in the evening for some time. Others are simply nutritional upoplements such as turmeric (1 x 500 mg capsule 3 timees day) Aspirin 81 mg pill 1 a day (this is for my heart trouble, But I am sure this also inhibits the same enzyme as celebrex does, which I aM confident is helping me in my fight against PD. Synthroid 50 mcg Co E Q10 200 mg caps 3x a day (This is known to retard PD and also is required for heart function by providing energy, since I am taking Lipitor for my heart trouble. I am lso taking motoprolal and attacand for my heart trouble). N-acetyl cysteine 600 mg one caps in the morning Multivitamin pill 1 in the morning Goji extract caps. 1 in the morning and 1 in the evening Blue berry extract caps 3 in the evening Pomogranate extract 1 caps. in the evening Grape seed extract 1 in the morning Since Sinamet is supposed to protect L-dopa producing cells, I added 2 pills per day: 1 in the morning and 1/2 pill in the evening and 1/2 pill in the night, I am sure that Sinamet and the condition specific Brain essentials are keeing me going the whole day. My PD doctor tells me that I should take more sinamet pills. But I am content with what I am taing right now. I don't want to take more sinamet, if i can help it. The story's take home lesson is that sinamet and my Ayurvedic Brain Essentials are together effective in helping through out the day. I am on the second year of using sinamet. So far, I do not have dyskenasia. This is for your info. Dr. R. Rajaraman ****************************************************************************** ----- Original Message ----- From: "Scott E. Antes" <[log in to unmask]> To: <[log in to unmask]> Sent: Friday, June 27, 2008 11:43 AM Subject: Re: Sinemet CR & Dyskinesia ???? > No matter how much has been researched and written on L-Dopa and other > meds, > no matter what our individual experiences are, the bottom line (again) is > that > every PD patient is unique and responds differently to meds and other > treatments. This is what makes this malady so frustrating. I have been > astounded to hear neurologists ask Laureen, "What do you want to try > next?" > One neurologist even wrote her half a dozen prescriptions, so that she > could > decide for herself what to experiment with! > > As we've already discussed, neurologists take their own approaches to PD. > Some have a lot of experience with PD, others have little more than a > clue. > Some unbelievably overmedicate their patients. Some take a more cautious > approach. Some say it's better to start medication early, others later, > etc. > As a scholar, I have read the literature on medications over and over and > over > and over, only to conclude that very little exists (to date, and to my > knowledge) that applies to everyone in the PD community. One thing we can > say > for sure is that PD medications have side effects, whether it be > hallucinations, diskinesia, gastric distress, or whatever. > > What makes a list like this one so valuable is that fact that it enables > PDers > to compare their experiences and share information that hopefully will > apply > to others on the list. One researcher commented to me that everyone on > this > PD list is lost, that everyone is just grabbing at straws! (That > researcher > by the way, does not have the answers, either.) As insulting as that > comment > sounds, it seems to me that the world of PD is, indeed, an easy one in > which > to get lost, because everyone who's trusted to know what he or she is > doing > gives different directions. At least here on the List, people have found > *something* important; they've found each other. I don't need to go into > how > helpful that is. Scott > > Scott E. Antes > Department of Anthropology > Northern Arizona University > Flagstaff, AZ 86011-5200 > > ---------------------------------------------------------------------- > To sign-off Parkinsn send a message to: > mailto:[log in to unmask] > In the body of the message put: signoff parkinsn -------------------------------------------------------------------------------- No virus found in this incoming message. Checked by AVG. Version: 8.0.101 / Virus Database: 270.4.2/1523 - Release Date: 28/06/2008 7:00 AM ---------------------------------------------------------------------- To sign-off Parkinsn send a message to: mailto:[log in to unmask] In the body of the message put: signoff parkinsn