I have discovered a valuable tool regarding the drugs I use. It is called "First Word" and comes to me daily at no charge from The P/S/L Group. It up-dates...
Hello to All, We are all aware of the results of a scientific study conducted by giving PDers high daily dosages of coenzyme Q10. The results were very...
I am looking for someone who has had the DBS surgery. My mother is considering the surgery but would feel more comfortable is she spoke with someone who has...
Hi, I was wondering what new prescriptions were given to your husband for his Parkinson Physcoisis. My husband has these episodes from very severe to "mild"....
HI there i have had parkinson's for 15 yrs i am now 54. every time i go to my neurologist he ask me i am having hallucinations. I had none until he put me on...
Hi
My name is David Willard .... i don't have any information to share on DBS
Surgey... but i'm 39 and facing this same decision...for myself ..if you
get...
1088
Mrlauer@...
Jun 15, 2003 1:24 am
"OntheDock@..." (Ruth) has had a successful DBS and is willing to discuss it with anyone who is seriously considering having the procedure done. Just tell...
Hello group, Just an introduction.....I'm a 55 year old male who was just diagnosed with Parkinsons this past week. Hopefully you members can give me advice on...
I am 55 and had PD for at least 2- 3 years. PD is not the end of the world. Alcohol slows the tremours down for a couple of hours. A couple of half nips of...
I only have mild tremors in a couple of fingers at this point, along with mild balance problems and fatigue. I was prescribed Mirapex, which I haven't yet...
Hi Terry - I have PD myself - dx in 3 - 2001 - i was in bad shape - falling down - tremors - dr put me on sinement right away and it helped for a while. I...
Tips on living with PD: 1. Keep a good mental attitude - It is not the end of the world, it just sometimes seems like it. 2. Do, do, do stretching exercises...
It is nice to get some feed back about creative edevours. Everything in this world started with a single thought. Mandkind is a creative being, as we a made in...
June 18, 2003 Parkinson Action Network Texas Grass-Roots Movement Dear friend, neighbor, care partner and fellow parkinsonian, It is being called the Texas...
Have any of you gone for a second opinion after your initial PD diagnoses? I got the approval from my health insurance yesterday for a second opinion, in fact...
Saturday, August 2, 2003 at Silver Park in Alliance, Ohio. live entertainment, clowns, food, games, prizes, horse shoe tournament. please bring covered dish or...
I need 10 people with Parkinson's disease to participate in paid interviews about treatment preferences in Manhattan this week. Compensation $50. Please...
1100
parkinsons@yahoogroup...
Jun 22, 2003 12:03 am
Hello, This email message is a notification to let you know that a file has been uploaded to the Files area of the parkinsons group. File : /JGHERB ...
ATTENTION: PEOPLE WITH PARKINSON'S DISEASE WE MOVE, a not-for-profit organization dedicated to education and awareness of movement disorders, has an...
My sister has been looking into rehab centers to see if this help. She has been having serious tremors and sore backs all the time. She has emotional tremors...
what does her neurologist say.......it is normal for many of us parkinsons suffers to feel depressed at times...i doubt if a rehab cetre can help her.....
does anyone here experience what i call a "blackout syndrome" wherein all of a sudden, you feel sleepy and then lie down and then blackout with associated...
I have exact same reactions. I take amantadine as well for PD. It was the first drug I started on about 6 yrs ago. It didn't affect me like that at first....
