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Amantadine
Hi Everybody, Hope you don't get tired of me always posting here and asking questions. It's just the best site for information I know of. My neurologist prescribed Amantadine for MS related fatigue, but I've been afraid to take it because of the possibility of insomnia which I can't tolerate because
Hi Everybody, Hope you don't get tired of me always posting here and asking questions. It's just the best site for information I know of. My neurologist prescribed Amantadine for MS related fatigue, but I've been afraid to take it because of the possibility of insomnia which I can't tolerate because
Ikeeptrying
in
My MSAA Community
7 years ago
I AM A HOT MESS
Im starting to think I will never be even as good as I was even before my last med change, on the 28th of Nov my Dr took me off the Azilect and wants to add amantadine and Lexapro ins is questioning the amantadine but I did start the Lexapro on day 2 I started having panic attacks now I feel so out
Im starting to think I will never be even as good as I was even before my last med change, on the 28th of Nov my Dr took me off the Azilect and wants to add amantadine and Lexapro ins is questioning the amantadine but I did start the Lexapro on day 2 I started having panic attacks now I feel so out
Boomercd
in
Cure Parkinson's
7 years ago
Let me introduce myself.
I was diagnosed with Early Onset PD at the age of 49. I am now 67. Will fill in more another day. It's 11:00 am & time to get moving. Thank you all for the hearty welcome!! This seems to be a very user-friendly (and friendly user) forum. ```````````````````````````````````````````````````````````````
I was diagnosed with Early Onset PD at the age of 49. I am now 67. Will fill in more another day. It's 11:00 am & time to get moving. Thank you all for the hearty welcome!! This seems to be a very user-friendly (and friendly user) forum. ```````````````````````````````````````````````````````````````
BLinNJ
in
Cure Parkinson's
7 years ago
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Shouting out during sleep
Hi everyone my name is Shelley G. I was diagnosed with PD just last month , but truly think I have had it longer and was just not discovered till now. I have a question about sleeping, I have been having very vivid dreams and shout out and kick a lot lately and have never done it before, ( I only take
Hi everyone my name is Shelley G. I was diagnosed with PD just last month , but truly think I have had it longer and was just not discovered till now. I have a question about sleeping, I have been having very vivid dreams and shout out and kick a lot lately and have never done it before, ( I only take
Shakinginnc
in
Cure Parkinson's
7 years ago
Paying for having fun.
I sure enjoyed my time hunting the last couple of days with my son and nephews but of course it came with a cost. Today my fatigue has me kicked to the curb. In so darn tired and weak its an effort to make it to the bathroom. But if that's the cost of being normal so be it. God willing I will do it
I sure enjoyed my time hunting the last couple of days with my son and nephews but of course it came with a cost. Today my fatigue has me kicked to the curb. In so darn tired and weak its an effort to make it to the bathroom. But if that's the cost of being normal so be it. God willing I will do it
Doubled51
in
My MSAA Community
7 years ago
PD individual evolution
Few days ago I posted about my PD under the title "New PD owner". I got my diagnostic in august after three doctors before said I have ET. It started 2-3 years ago with random right hand shaking which got worse this year. Recently I noticed random shaking in my right foot. Other than these I do not
Few days ago I posted about my PD under the title "New PD owner". I got my diagnostic in august after three doctors before said I have ET. It started 2-3 years ago with random right hand shaking which got worse this year. Recently I noticed random shaking in my right foot. Other than these I do not
ion_ion
in
Cure Parkinson's
7 years ago
New PD owner
Starting two years ago I noticed a tremor in my right hand when holding a spoon with soup and moving from the plate to the mouth. This was happening very rarely, like 2-3 times a month when I was tired or stressed. The tremor was more intense when reaching the mouth. In March my mom passed away and I
Starting two years ago I noticed a tremor in my right hand when holding a spoon with soup and moving from the plate to the mouth. This was happening very rarely, like 2-3 times a month when I was tired or stressed. The tremor was more intense when reaching the mouth. In March my mom passed away and I
ion_ion
in
Cure Parkinson's
7 years ago
Confused and overwhelmed
I’m currently 59 and 7 years dx. I currently take only the prescription drugs directed by my neurologist which consist of rytary, amantadine, ropinerole, methylphenidate. I exercise daily but it’s not enough and my progression downward continues, I’m freezing up more often, my tremors are getting worse
I’m currently 59 and 7 years dx. I currently take only the prescription drugs directed by my neurologist which consist of rytary, amantadine, ropinerole, methylphenidate. I exercise daily but it’s not enough and my progression downward continues, I’m freezing up more often, my tremors are getting worse
Sleeplessparki
in
Cure Parkinson's
7 years ago
dyskinesias levodopa induced
excerpt dyskinesias, and dizziness. In some individuals, levodopa may cause confusion, hallucinations, or psychosis. Motor fluctuations develop in about 40% of people treated for 4-6 years. copy Which medications are right for me? Medications that are effective for one person with Parkinson's disease
excerpt dyskinesias, and dizziness. In some individuals, levodopa may cause confusion, hallucinations, or psychosis. Motor fluctuations develop in about 40% of people treated for 4-6 years. copy Which medications are right for me? Medications that are effective for one person with Parkinson's disease
Hidden
in
Cure Parkinson's
7 years ago
15 Years on Mirapex
I just found you yesterday. My name is Marcia, I am now 66, and I have had symptoms since 1997, but took until 2003 to get dx. It was a long, embarrassing process. Have taken Mirapex, then Mirapex ER the entire time. Also, Amantadine . I am an oddity. No one even notices. Few tremors. No shuffle
I just found you yesterday. My name is Marcia, I am now 66, and I have had symptoms since 1997, but took until 2003 to get dx. It was a long, embarrassing process. Have taken Mirapex, then Mirapex ER the entire time. Also, Amantadine . I am an oddity. No one even notices. Few tremors. No shuffle
Marcia1951
in
Cure Parkinson's
7 years ago
Nervous
Today has been odd to say the least. Typically I take 3-4 Ext Rls C/L, 2 Amantadine and maybe throw in 1 imm rls c/l... My last dose of any c/l was at 1:30 yesterday ( Thursday nov 2) ?!?!? By 3 pm after that dose , I was super on. My toes & left leg were screaming by 6:30pm Now here I am Friday nov
Today has been odd to say the least. Typically I take 3-4 Ext Rls C/L, 2 Amantadine and maybe throw in 1 imm rls c/l... My last dose of any c/l was at 1:30 yesterday ( Thursday nov 2) ?!?!? By 3 pm after that dose , I was super on. My toes & left leg were screaming by 6:30pm Now here I am Friday nov
Cbgs
in
Cure Parkinson's
7 years ago
Michael J Fox dyskinesia gone?
When I was at the supermarket in line I saw a magazine that claimed he was cured , inside it's not a cure but he is quoted as saying he "stumbled" upon a new combination of medications that greatly reduced his dyskinesia. (Not an exact quote but close) I find dyskenisia one of the most difficult parts
When I was at the supermarket in line I saw a magazine that claimed he was cured , inside it's not a cure but he is quoted as saying he "stumbled" upon a new combination of medications that greatly reduced his dyskinesia. (Not an exact quote but close) I find dyskenisia one of the most difficult parts
ConnieD
in
Cure Parkinson's
7 years ago
Medicine when to start and w/ what
copy: Which medications are right for me? Medications that are effective for one person with Parkinson's disease, may not work well for another person. The best way for a person to identify the right medications is through an evaluation by a doctor or nurse practitioner who is knowledgeable about
copy: Which medications are right for me? Medications that are effective for one person with Parkinson's disease, may not work well for another person. The best way for a person to identify the right medications is through an evaluation by a doctor or nurse practitioner who is knowledgeable about
Hidden
in
Cure Parkinson's
7 years ago
is there an interaction between amantadine and mirapex ,,,, is there aside effect of coconut oil , what vitamins can i take?
is there an interaction between amantadine and mirapex ,,,, is there aside effect of coconut oil , what vitamins can i take?
is there an interaction between amantadine and mirapex ,,,, is there aside effect of coconut oil , what vitamins can i take?
jack-carpenter
in
Cure Parkinson's
7 years ago
amantadine . coconut oil & parkinson?
hello.i diagnosed with parkinson from 6 years and now im suffering from tremor and slow movment im on mirapex and sinemet i heard that amantadine is good for sinemet induced dyskinesia wich appear up to 1 hour after taking my dose is there an intreactions between mirapex and amantadine .does amantadine
hello.i diagnosed with parkinson from 6 years and now im suffering from tremor and slow movment im on mirapex and sinemet i heard that amantadine is good for sinemet induced dyskinesia wich appear up to 1 hour after taking my dose is there an intreactions between mirapex and amantadine .does amantadine
jack-carpenter
in
Cure Parkinson's
7 years ago
Vision Problems with PD
I've recently started to have some vision problems - suddenly cloudy eyes, difficulty focusing on near objects. The ophthalmologists have not found anything wrong with my eyes except that cataracts are growing. I'm wondering if it is a side effect of my meds and if anyone else has experienced it. My
I've recently started to have some vision problems - suddenly cloudy eyes, difficulty focusing on near objects. The ophthalmologists have not found anything wrong with my eyes except that cataracts are growing. I'm wondering if it is a side effect of my meds and if anyone else has experienced it. My
Joanne_Joyce
in
Cure Parkinson's
7 years ago
YOUR INPUT
https://youtu.be/C3xM8sHGoiQ I have come to the conclusion that you will not be able to use symptoms to category Parkinson.s. The next step would be to categorize medications and are they helping your symptoms. You should be diagnosed for at least 3-4 years and there should also be the question are you
https://youtu.be/C3xM8sHGoiQ I have come to the conclusion that you will not be able to use symptoms to category Parkinson.s. The next step would be to categorize medications and are they helping your symptoms. You should be diagnosed for at least 3-4 years and there should also be the question are you
Serenity_finaly-1
in
Cure Parkinson's
7 years ago
Vegetative State Coma
Hello everyone, My son is in a VS for the last 31 months as a result of a automobile accident. He has severe brain damage. His general health is good, however he currently has Aspiration Pneumonia caused by the g-tube feed and flushing that goes on with the medications and food. I found a drug called
Hello everyone, My son is in a VS for the last 31 months as a result of a automobile accident. He has severe brain damage. His general health is good, however he currently has Aspiration Pneumonia caused by the g-tube feed and flushing that goes on with the medications and food. I found a drug called
Hidden
in
Headway
7 years ago
Amantadine time-released - drug for dyskinesia has been approved
https://www.google.com/url?hl=en&q=http://click.michaeljfox-email.org/?qs%3D228cf19966fbaf4117435863205b40b4189fb5b19458e3c2005a1042bbae41967fa2ad63afbe153bf0623f79ca247e13cebaf5abbeea9d76&source=gmail&ust=1504133212509000&usg=AFQjCNEyg1ZKAjRwvUIop5dy2hzF8npOYg
https://www.google.com/url?hl=en&q=http://click.michaeljfox-email.org/?qs%3D228cf19966fbaf4117435863205b40b4189fb5b19458e3c2005a1042bbae41967fa2ad63afbe153bf0623f79ca247e13cebaf5abbeea9d76&source=gmail&ust=1504133212509000&usg=AFQjCNEyg1ZKAjRwvUIop5dy2hzF8npOYg
parkie13
in
Cure Parkinson's
7 years ago
What is considered the latter stages of MSA?
Hi my name is Kelly! I have been caring for my Mother for over a year now who was first diagnosed with Parkinson's in Aug 2015 but then rediagnosed with MSA January 2017. She has really went down hill fast. She is strickened to a wheelchair and has no balance what so ever which makes is very hard for
Hi my name is Kelly! I have been caring for my Mother for over a year now who was first diagnosed with Parkinson's in Aug 2015 but then rediagnosed with MSA January 2017. She has really went down hill fast. She is strickened to a wheelchair and has no balance what so ever which makes is very hard for
Klk4475
in
Multiple System Atrophy Trust
7 years ago
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