If you are not a registered member of our community, please click here to register...

 Home Message Boards Health Guide Join for Free Testimonials About Us
Search
   
  


PDA

View Full Version : Symtoms of PD


 

 

 
cactus wren
07-16-2006, 12:12 AM
My neurologist started out diagnoising me w/essential tremors, two months ago. (a few years back family doctor diagnoised the same) Then a month later he said I show signs of PD, but he is sticking with ET. I was treated w/beta blocker it did no good. Now I am on primidone. Not yet helping much. (we keep increasing the dose) My MRI showed low calvarial marrow. (doctor not sure why) Blood work fine. I get muscle cramps in my legs & hands. I'm always tired and don't sleep well. The tremors are in my legs & hands. I have always been active and healthy. I am 47. I am not sure what to do next. Any suggestions would be greatly appreciated.:angel:

Sponsor
 



debbiem425
07-16-2006, 11:23 AM
I was just recently diagnosed with Parkinson's so I don't know a lot about what combinations of symptoms are or are not Parkinson's. Regardless, I think you should get a second opinion. I have been to a general neurologist, then a movement disorder neurologist and am now waiting for an appointment at second movement disorder neurologist. This disease involves a lot of medication and I want to be sure I get the best care possible.
Good Luck!

solution
07-17-2006, 04:13 PM
My neurologist started out diagnoising me w/essential tremors, two months ago. (a few years back family doctor diagnoised the same) Then a month later he said I show signs of PD, but he is sticking with essential tremors. I was treated w/beta blocker it did no good. Now I am on primidone. Not yet helping much. (we keep increasing the dose) My MRI showed low calvarial marrow. (doctor not sure why) Blood work fine. I get muscle cramps in my legs & they hurt, my hands hurt too. I'm more stiff in the mornings. I'm always tired and don't sleep well. The tremors are alfull, mostly hands. I have always been active and healthy. I am 47. I am not sure what to do next. Any suggestions would be greatly appreciated.:angel:

I've found the following combination of vitamins and supplements to help greatly:
-vit. B1: 200-250 mg three times daily, with breafast, lunch and dinner
- vit. B2: 30 mg three times daily, with breafast, lunch and dinner
- vit. B complex, once daily, with breakfast, lunch and dinner (B1 and B2 will be duplicated some, but never mind)
- vit C: 1000 mg three times daily, with breafast, lunch and dinner
- melatonin, 10 mg, once daily, half an hour before bed time
- A multivitaminic: once daily, with breakfast
- CDP Choline: 250 mg, twice daily, with breakfast and lunch.

Get them cheap at your local pharmacy and/or on the internet.
In my experience, benefits are felt immediately.
Let me know if they help.

cactus wren
07-26-2006, 10:39 PM
[Thank you for the suggestion. Have you been using the vit. for awhile. ]I've found the following combination of vitamins and supplements to help greatly:
-vit. B1: 200-250 mg three times daily, with breafast, lunch and dinner
- vit. B2: 30 mg three times daily, with breafast, lunch and dinner
- vit. B complex, once daily, with breakfast, lunch and dinner (B1 and B2 will be duplicated some, but never mind)
- vit C: 1000 mg three times daily, with breafast, lunch and dinner
- melatonin, 10 mg, once daily, half an hour before bed time
- A multivitaminic: once daily, with breakfast
- CDP Choline: 250 mg, twice daily, with breakfast and lunch.

Get them cheap at your local pharmacy and/or on the internet.
In my experience, benefits are felt immediately.
Let me know if they help.[/QUOTE]

solution
07-31-2006, 07:13 PM
[Thank you for the suggestion. Have you been using the vit. for awhile. ]I've found the following combination of vitamins and supplements to help greatly:
-vit. B1: 200-250 mg three times daily, with breafast, lunch and dinner
- vit. B2: 30 mg three times daily, with breafast, lunch and dinner
- vit. B complex, once daily, with breakfast, lunch and dinner (B1 and B2 will be duplicated some, but never mind)
- vit C: 1000 mg three times daily, with breafast, lunch and dinner
- melatonin, 10 mg, once daily, half an hour before bed time
- A multivitaminic: once daily, with breakfast
- CDP Choline: 250 mg, twice daily, with breakfast and lunch.

Get them cheap at your local pharmacy and/or on the internet.
In my experience, benefits are felt immediately.
Let me know if they help.[/QUOTE]

Several years, but for cdp-choline (recently).

Oldbat
08-19-2006, 01:12 AM
Hi, I was treated for Essential tremours for 4 years and just in April I finally found a Neurologist who proved I had
adult stage parkinsons by watching me walk, by checking arms for cogwheeling, by testing brain (MRI) and starting me on low dose Mirapex from 0.125mg 3x/day to current dose of 0.50mg 3x/day and I use Parcopa 25mg/100m sometimes between. Some symptoms are, walking without swinging arms, shuffling feet, short steps, pokerface, monatone voice, hard to keep balance when walking. But i have gained in somethings with Mirapex. I now eat corn and peas with a fork instead of a spoon by taking dose before eating and I don't have to use a cane except on long walks, But I still get scared about stairs and I just get depressed. Parkinsons affects my typing too.I also have an ID bracelet. hope I helped witth the symptoms. Good luck.

JCitron
08-22-2006, 06:37 PM
CactusWren,

I'm 45 and I have similar symptoms. My doctor says I have dystonia because of the cramps, but I also I have the other symptoms including the tremors (very slight), the cogwheeling in my arms and legs, and the stiffness and slowness. I sometimes freeze when I move, and this has caused me to trip a few times. The last time I did this I thought I broke my left foot, but I had only bruised the toes instead.

I take regular Sinemet 4x per day plus 1 Sinemet CR for night along with Mirapex, which was recently increased to 2x per day. I've tried to stay positive, even though it's very difficult at times, and I am grateful that I can still move around rather well, and don't dwell on what I can't do or may never be able to do.

This magic mixture has helped me gain back a lot of what I lost. Prior to this, I had stopped playing the piano, which is something I have always done because I was too stiff. I don't play a lot of fast things like I used to, but now enjoy the slower works that I can play accurately. In general this mixture has made me feel almost normal again, and there are days when I question whether I really need it.

John

cactus wren
10-05-2006, 01:04 AM
Thank you, I have finally found an MDS dr. I can't get in till Jan. I really feel the Specialist opinion is needed. My symtoms have not improved at all. I am being treated for ET only. Thanks for your reply. (sorry for the late response)





Site owned and operated by HealthBoards.com (TM)
Copyright and Terms of Use © 1998-2009 HealthBoards.com (TM) All rights reserved.
Do not copy or redistribute in any form!