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Madopar
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Madopar dosage
Is there any limit of dosage? What is the maximum?
Is there any limit of dosage? What is the maximum?
suetdumpling
in
Cure Parkinson's
11 years ago
Modopar
just met with my consultant and he has asked me to increase dosage through the night by taking slower release tablet to help me sleep, i take three times a day every five hours anyway. he says taking at correct time really important to halt progression of parkinsons anybody got any comments
just met with my consultant and he has asked me to increase dosage through the night by taking slower release tablet to help me sleep, i take three times a day every five hours anyway. he says taking at correct time really important to halt progression of parkinsons anybody got any comments
charlton
in
Cure Parkinson's
11 years ago
Selegiline a new drug for me!
I'm already taking
madopar
and reprinerole. Is anyone else taking selegiline and what are your thoughts on this drug?.
I'm already taking
madopar
and reprinerole. Is anyone else taking selegiline and what are your thoughts on this drug?.
camper
in
Cure Parkinson's
11 years ago
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Anxiety attacks with Parkinson's making my life hell.
Since September when I went on stalevo and mirapexin my panic attacks have got very bad,.i wake op and feel I cann't move the panic sets in and takes me hours to get out of that freezing state it has got so bad it's effects most part of the day I also take 1 sinimrt ,a half sinimet ,
madopar
3 times
Since September when I went on stalevo and mirapexin my panic attacks have got very bad,.i wake op and feel I cann't move the panic sets in and takes me hours to get out of that freezing state it has got so bad it's effects most part of the day I also take 1 sinimrt ,a half sinimet ,
madopar
3 times
doddy
in
Cure Parkinson's
11 years ago
which is better... madopar or sinemet?
poloman
in
Cure Parkinson's
11 years ago
In 7 years of PD, never heard of Apokinin pump!
Hi, am living in France, have been treated for PD for nearly 7 years (am 48 y. old) with Requip (2X 8) and Modopar 125 (4 pills a day). This is not really effective so when I heard that the Apokinin pump could be efficient (TV news tonight) according to the person who gave the testimony, I began searching
Hi, am living in France, have been treated for PD for nearly 7 years (am 48 y. old) with Requip (2X 8) and Modopar 125 (4 pills a day). This is not really effective so when I heard that the Apokinin pump could be efficient (TV news tonight) according to the person who gave the testimony, I began searching
lydko
in
Cure Parkinson's
11 years ago
strange but true
hello all - it us very odd but i am now back on modoar and it seems to be having some effect- for thise who dont know me -i was on tons of drugs for PD and then told i had PSP IN NOVEMBER SO WAS OFF ALL MEDS UNTIL I WENT BACK TO SEE MY NEURO LAST WEEK - I TOLD HIM MY NECK WAS HURTING AND HE SAID
hello all - it us very odd but i am now back on modoar and it seems to be having some effect- for thise who dont know me -i was on tons of drugs for PD and then told i had PSP IN NOVEMBER SO WAS OFF ALL MEDS UNTIL I WENT BACK TO SEE MY NEURO LAST WEEK - I TOLD HIM MY NECK WAS HURTING AND HE SAID
shasha
in
Cure Parkinson's
11 years ago
Medications
Does anyone have any suggestions as to what to take for these necessary breaks from
Madopar
.
Does anyone have any suggestions as to what to take for these necessary breaks from
Madopar
.
Pabula
in
Restless Legs Syndrome
12 years ago
Change
i have just reduced requip and increased modopar to deal with OCD behaviour. Ive been warned about becoming depressed as a result anybody had similar experience?
i have just reduced requip and increased modopar to deal with OCD behaviour. Ive been warned about becoming depressed as a result anybody had similar experience?
charlton
in
Cure Parkinson's
12 years ago
is anybody having troube leaning
My neurologist said its the "Pizza Syndronme"and it is do do with the
Madopar
that I am taking so he has got me to come off them. I am down to two a da y now but I don't feel any better. I am still leaning over and in fact I feel worse if anything.
My neurologist said its the "Pizza Syndronme"and it is do do with the
Madopar
that I am taking so he has got me to come off them. I am down to two a da y now but I don't feel any better. I am still leaning over and in fact I feel worse if anything.
pokoono
in
Cure Parkinson's
12 years ago
bit scared staggered bumped head freezing episode
i staggered backwards doing it a lot scarey bumped head very dizzy twice then froze luckily was at friends she tried to help had freezing episode scared in case happens wen on my own keep on staggering not good does anyone take
madopar
for freezing worry about side effects thanks
i staggered backwards doing it a lot scarey bumped head very dizzy twice then froze luckily was at friends she tried to help had freezing episode scared in case happens wen on my own keep on staggering not good does anyone take
madopar
for freezing worry about side effects thanks
kath33
in
Cure Parkinson's
12 years ago
HI IS THERE AWAY OF PAYING FOR SOME MADOPAR , NO QUESTIONS ASK,T
I get my drugs weekly very weekly . If I get constipation the pills don't work .so need more. try'd talking to GP . Also if one pill last 3 hours it do not mean the next one will. Feel its time to go on the black market yours EXPORT
I get my drugs weekly very weekly . If I get constipation the pills don't work .so need more. try'd talking to GP . Also if one pill last 3 hours it do not mean the next one will. Feel its time to go on the black market yours EXPORT
export
in
Cure Parkinson's
12 years ago
Anyone know how long the waiting list is for DBS at the National Hospital for Neurology and Neurosurgery, Queen Square, London?
I am adding in Amantadine to my daily regime of
Madopar
CR and
Madopar
dispersible every 5 hours. Any feedback on this? Has anyone had their DBS done through Queen Square Neurology?
I am adding in Amantadine to my daily regime of
Madopar
CR and
Madopar
dispersible every 5 hours. Any feedback on this? Has anyone had their DBS done through Queen Square Neurology?
Yogibear
in
Cure Parkinson's
12 years ago
2 x Madopar CR, 100mg taken 11pm tonight - ambulance called at 2am? Why did this happen?
My GP suggested that I try 2 x
Madopar
CR for bedtime dose to see if that helped. I took them at about 11:30pm (I also had Baclofen in my system to calm painful leg dystonia). I fell asleep.
My GP suggested that I try 2 x
Madopar
CR for bedtime dose to see if that helped. I took them at about 11:30pm (I also had Baclofen in my system to calm painful leg dystonia). I fell asleep.
Yogibear
in
Cure Parkinson's
12 years ago
No tremor-just sticking and losing balance
I'm on 6
madopar
a day but it doesn't seem to be helping. What medication are you on?
I'm on 6
madopar
a day but it doesn't seem to be helping. What medication are you on?
camper
in
Cure Parkinson's
12 years ago
madopar patches
But I keep getting conflicting advice from his doctors regarding
Madopar
patches. Can anyone tell me how well they have worked for them. B needs his night time
Madopar
to be slow release. He also has Rivastigmine; anyone know if this can be delivered via patches?
But I keep getting conflicting advice from his doctors regarding
Madopar
patches. Can anyone tell me how well they have worked for them. B needs his night time
Madopar
to be slow release. He also has Rivastigmine; anyone know if this can be delivered via patches?
mattiesmum
in
Cure Parkinson's
12 years ago
suggestions please? anyone?
anyway after reading some of these posts i thought about asking my doc if i could switch to
madopar
and the neupro patch. and possibly one tab of a CR (controlled release) to help me to get thru nite bec i cant move around in bed and i always have to get up at least once in middle of nite to use restroom
anyway after reading some of these posts i thought about asking my doc if i could switch to
madopar
and the neupro patch. and possibly one tab of a CR (controlled release) to help me to get thru nite bec i cant move around in bed and i always have to get up at least once in middle of nite to use restroom
tmhiggs
in
Cure Parkinson's
12 years ago
Drugs for Parkinson's- how do you spell their names?
The most commonly used drugs seem to be
Madopar
Sinemet Mirapexin also known as pramipexole Requip also known as ropinerole Symmetrel also known as amantadine CR after the first two means controlled release There are many other drugs that might be used, and it's confusing
The most commonly used drugs seem to be
Madopar
Sinemet Mirapexin also known as pramipexole Requip also known as ropinerole Symmetrel also known as amantadine CR after the first two means controlled release There are many other drugs that might be used, and it's confusing
Cerelia
in
Cure Parkinson's
12 years ago
anyone take madopar and use the neupro patch. how well does it work? thinking about asking doc to switch from sinemet n mirapax.
suggestions please?
suggestions please?
tmhiggs
in
Cure Parkinson's
12 years ago
Side effects of Pramipexole and Madopar or the disease itself ??
I used to be a really outgoing self confident person but in the 4 years since diagnosis and taking the prescrbed Pramipexole for 3½ years and also
Madopar
for the last 6 months I have lost all my self confidence. I feel edgy, nervy and a bit scared all the time.
I used to be a really outgoing self confident person but in the 4 years since diagnosis and taking the prescrbed Pramipexole for 3½ years and also
Madopar
for the last 6 months I have lost all my self confidence. I feel edgy, nervy and a bit scared all the time.
bass123
in
Cure Parkinson's
12 years ago
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