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Madopar controlled release
Hi , has anyone had good results from madopar controlled release? Thanks Joanne
Hi , has anyone had good results from madopar controlled release? Thanks Joanne
joe45
in
Cure Parkinson's
10 years ago
Neupropatch
Hi just wondered as I mentioned in previous posts , I'm reducing/coming off neupropatch did anyone's walking improve after coming off patch ? I'll be only on madopar Thanku
Hi just wondered as I mentioned in previous posts , I'm reducing/coming off neupropatch did anyone's walking improve after coming off patch ? I'll be only on madopar Thanku
joe45
in
Cure Parkinson's
10 years ago
New information on sinemet
The End for Levodopa Phobia: New Study Shows Sinemet is a Safe Initial Therapy for Treatment of Parkinson’s Disease You can find out more about NPF's National Medical Director, Dr. Michael S. Okun, by also visiting the NPF Center of Excellence, University of Florida Center for Movement Disorders & Neurorestoration
The End for Levodopa Phobia: New Study Shows Sinemet is a Safe Initial Therapy for Treatment of Parkinson’s Disease You can find out more about NPF's National Medical Director, Dr. Michael S. Okun, by also visiting the NPF Center of Excellence, University of Florida Center for Movement Disorders & Neurorestoration
Hidden
in
Cure Parkinson's
10 years ago
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Neupropatch
Hi. I've been on neupropatch for a while can't quite remember how long and on madopar but now I think the doctors told me to up patch each visit because I'm getting wearing off but it just doesn't seem to solve wearing off its just making me dizzy unbalanced slurred speech can't always sleep and I've
Hi. I've been on neupropatch for a while can't quite remember how long and on madopar but now I think the doctors told me to up patch each visit because I'm getting wearing off but it just doesn't seem to solve wearing off its just making me dizzy unbalanced slurred speech can't always sleep and I've
joe45
in
Cure Parkinson's
10 years ago
Curcumin and CoQ10
My husband has PSP and is taking the drugs sinemet CR, Apo-levocarb, gabapentin, tyrazodone and magnesium glycinate. Is it safe to take curcumin and CoQ10 along with these drugs?
My husband has PSP and is taking the drugs sinemet CR, Apo-levocarb, gabapentin, tyrazodone and magnesium glycinate. Is it safe to take curcumin and CoQ10 along with these drugs?
Hidden
in
PSP Association
10 years ago
15years taking Ibuprofen, Parkinson's has plateaued!
I was diagnosed PWP way back in 1991 - at the age of 45. I was prescribed Beta blockers only for a couple of years, then a small levodopa - MADOPAR 125mg once a day. This intake is now 8 x 125mg together with Entacapone plus Pramipexole. Around 1993, I used to have lots of friends who drank quite a lot
I was diagnosed PWP way back in 1991 - at the age of 45. I was prescribed Beta blockers only for a couple of years, then a small levodopa - MADOPAR 125mg once a day. This intake is now 8 x 125mg together with Entacapone plus Pramipexole. Around 1993, I used to have lots of friends who drank quite a lot
rob26387
in
Cure Parkinson's
10 years ago
DBS and madopar. Any one taking more than 12 -125mg tablets a day with a DBS. I would like to here from .
export
in
Cure Parkinson's
10 years ago
Does anyone have problems with feet especially big toes? Have had a numb tingling feeling on top of both feet and inflamed painful big toe
Was diagnosed Parkinsons January 2013 ..on Madopar and Entacapone. Does anyone else experience this?
Was diagnosed Parkinsons January 2013 ..on Madopar and Entacapone. Does anyone else experience this?
rosea1946
in
Cure Parkinson's
10 years ago
My neurologist wants me to go to Madopar CR instead of just Madopar, I'm a bit dubious - has anyone had experience with this drug ? Thanks.
kirleyvall
in
Cure Parkinson's
10 years ago
Is there anyone with DBS taking Madopar or Sinemet and then added Azilect?
This question is for a friend who is not 'online'. He has DBS and on Madopar several times a day. His DBS specialist prescribed him Azilect, several months ago, which he took for about one week, but stopped because he perceived no benefit. His specialist told him that he did not give it enough time
This question is for a friend who is not 'online'. He has DBS and on Madopar several times a day. His DBS specialist prescribed him Azilect, several months ago, which he took for about one week, but stopped because he perceived no benefit. His specialist told him that he did not give it enough time
Norton1
in
Cure Parkinson's
10 years ago
Has anyone suffered hair loss whilst on madopar and amantadine
I take 250 mgs madopar 4 times a day and amantadine tablets twice a day. Also I take 4 adcal ( calcium tablets) a day for bone strength. I did take alendronic tablet once a week but stopped taking it 2 months ago as I thought that was causing my hair loss. As I'm still losing hair has anyone else had
I take 250 mgs madopar 4 times a day and amantadine tablets twice a day. Also I take 4 adcal ( calcium tablets) a day for bone strength. I did take alendronic tablet once a week but stopped taking it 2 months ago as I thought that was causing my hair loss. As I'm still losing hair has anyone else had
camper
in
Cure Parkinson's
10 years ago
Anyone having problems with Madopar? Or more specifically Levodopa in particular?
My neurologist has taken me off Madopar because the Levodopa that it contains is causing me extreme problems with impulsive behaviour. The problem is now my tremor has started to get worse again in the last week since stopped the Madopar and I am due a review in 3 months once the Madopar has left my
My neurologist has taken me off Madopar because the Levodopa that it contains is causing me extreme problems with impulsive behaviour. The problem is now my tremor has started to get worse again in the last week since stopped the Madopar and I am due a review in 3 months once the Madopar has left my
2Chrissie4
in
Cure Parkinson's
10 years ago
My neurologist has taken me off Madopar after being on it for 7 months because it contains Levadopa. What can I have instead?
I have been on Madopar for about 6 months and saw my neurologist for a review last week. The I told him of my problems with impulse buying that has gone out of control for which I am having help from a psychologist to help me control these impulses. My neurologist told me off in that should have called
I have been on Madopar for about 6 months and saw my neurologist for a review last week. The I told him of my problems with impulse buying that has gone out of control for which I am having help from a psychologist to help me control these impulses. My neurologist told me off in that should have called
2Chrissie4
in
Cure Parkinson's
10 years ago
Exercise if you can!
I find going to the gym 3 times a week very theraputic. My consultant says vigorous exercise has shown a positive effect in lots of PD cases, has anybody got any comments? I was diagnosed 4 yrs ago i take, modopar, azilect and ropinerole and am still leading a normal (!) life.
I find going to the gym 3 times a week very theraputic. My consultant says vigorous exercise has shown a positive effect in lots of PD cases, has anybody got any comments? I was diagnosed 4 yrs ago i take, modopar, azilect and ropinerole and am still leading a normal (!) life.
charlton
in
Cure Parkinson's
10 years ago
pd & us
my husbands had pd 28yrs dx aged 37yrs.coped well for years.began to get hallucinations 2yrs ago & had to be taken off most of his meds, which has caused him to lose his mobility.Now needs my care full time.hospital will not risk putting him back on meds, they say hallucinations will return,been left
my husbands had pd 28yrs dx aged 37yrs.coped well for years.began to get hallucinations 2yrs ago & had to be taken off most of his meds, which has caused him to lose his mobility.Now needs my care full time.hospital will not risk putting him back on meds, they say hallucinations will return,been left
macelott
in
Cure Parkinson's
10 years ago
Does anyone have any reliable information about ZANDOPA?
I have been on Sinemet for six years - 800 mg currently - and now that the s/e are severely impacting on my life I am keen to find a way of reducing it. In particular, the dyskinesias are getting much worse. I can't be prescribed a dopamine agonist because of ICD previously. I have received a 200g
I have been on Sinemet for six years - 800 mg currently - and now that the s/e are severely impacting on my life I am keen to find a way of reducing it. In particular, the dyskinesias are getting much worse. I can't be prescribed a dopamine agonist because of ICD previously. I have received a 200g
batwing7
in
Cure Parkinson's
11 years ago
Extended Release Medications
I have read some posts where Extended Release medication forms such as Sinemet CR and Stalevo are being cut in half. These medications are meant to be swallowed whole as cutting them (or chewing them) defeats the purpose of the dose.....a gradual slow release of the active medication so that large "spikes
I have read some posts where Extended Release medication forms such as Sinemet CR and Stalevo are being cut in half. These medications are meant to be swallowed whole as cutting them (or chewing them) defeats the purpose of the dose.....a gradual slow release of the active medication so that large "spikes
ozepook47
in
Cure Parkinson's
11 years ago
Hi all I suffer with PD and was diagnosed about 18 months ago, I take 2 x 125 mg madopar 3 times a day and 1 x 0.7 mg of pramipexole 3 time
martinn1962
in
Cure Parkinson's
11 years ago
I have horrid nightmares and often wake myself up screaming......3 times in the one night last week. On Madopar and Sifrol ER.
Usual other symptoms........an imaginary wind at my back pushes me faster than I would like........light headed........jerking arm movements, one side only and only when its at rest and I am trying to relax.
Usual other symptoms........an imaginary wind at my back pushes me faster than I would like........light headed........jerking arm movements, one side only and only when its at rest and I am trying to relax.
Hidden
in
Cure Parkinson's
11 years ago
SLEEP PROBLEMS
This has no doubt been discussed before but I haven't really used this site much yet and so haven't found it. My PD is reasonably controlled during the day but I dread going to bed! As soon as I get in to bed I am uncomfortable, mainly because of my leg which has the tremor. The tremor gets less
This has no doubt been discussed before but I haven't really used this site much yet and so haven't found it. My PD is reasonably controlled during the day but I dread going to bed! As soon as I get in to bed I am uncomfortable, mainly because of my leg which has the tremor. The tremor gets less
Janew
in
Cure Parkinson's
11 years ago
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