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Azatadine
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Amantadine
I had my appointment with my new neurologist today, she is very nice and took her time with me She gave me a very thought exam, more than my other movement specialist did (she my third one but I believe she's a keeper ) she lowered my neupo patch decreased cl which was just change due to rotary not being
I had my appointment with my new neurologist today, she is very nice and took her time with me She gave me a very thought exam, more than my other movement specialist did (she my third one but I believe she's a keeper ) she lowered my neupo patch decreased cl which was just change due to rotary not being
Justme4
in
Cure Parkinson's
4 years ago
My "PD" is modulated by three factors. Dysautonomia is one.
My "PD" is modulated by: Norepinehrine loss in CNS. Amantadine helps. Dysautonomia (ANS pathologies). Eg, elevated norepinephrine in periphery. Midface hypoplasia (eg, severe malocclusion, high arched palate). Also, I've come to believe: distorted development of my insular cortices and interconnected
My "PD" is modulated by: Norepinehrine loss in CNS. Amantadine helps. Dysautonomia (ANS pathologies). Eg, elevated norepinephrine in periphery. Midface hypoplasia (eg, severe malocclusion, high arched palate). Also, I've come to believe: distorted development of my insular cortices and interconnected
aspergerian
in
Cure Parkinson's
4 years ago
Symmetrel (Amantadine)
Hello to All, Has anyone taken the drug Amantadine, brand name Symmetrel, to treat MS fatigue? I’ve been on it for a few days but unfortunately I had a pretty bad adverse reaction today and I will have to stop taking it. I’m interested to know if you had any side effects while on it or withdrawal issues
Hello to All, Has anyone taken the drug Amantadine, brand name Symmetrel, to treat MS fatigue? I’ve been on it for a few days but unfortunately I had a pretty bad adverse reaction today and I will have to stop taking it. I’m interested to know if you had any side effects while on it or withdrawal issues
Lara1
in
My MSAA Community
4 years ago
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Amantadine
I’ve been on Amantadine for about 6 weeks and have felt worse than ever. Symptoms were worst I’ve ever had. Dry. Mouth, very dry eyes to the point of not being able to see. Starting seeing images all over my house, bad dreams. D/C per MDS, but.nothing to replace. Has anyone else had these issues?
I’ve been on Amantadine for about 6 weeks and have felt worse than ever. Symptoms were worst I’ve ever had. Dry. Mouth, very dry eyes to the point of not being able to see. Starting seeing images all over my house, bad dreams. D/C per MDS, but.nothing to replace. Has anyone else had these issues?
Foncie
in
Cure Parkinson's
4 years ago
Amantadine for…
"Amantadine is an antiviral medicine that blocks the actions of viruses in your body. Amantadine is used to treat or prevent influenza A in adults and children. Amantadine may not be effective during every flu season because certain strains of the virus may be resistant to this medicine. Amantadine
"Amantadine is an antiviral medicine that blocks the actions of viruses in your body. Amantadine is used to treat or prevent influenza A in adults and children. Amantadine may not be effective during every flu season because certain strains of the virus may be resistant to this medicine. Amantadine
kaypeeoh
in
Cure Parkinson's
4 years ago
Amantadine
Hi, if you’ve had experience with taking Amantadine please share your information with me. I was doing well and had first appointment with MDS and she decreased my Rytary and took me off QUEtiapine Fumarate. I haven’t felt well since. Appreciate any feedback. Thank you.
Hi, if you’ve had experience with taking Amantadine please share your information with me. I was doing well and had first appointment with MDS and she decreased my Rytary and took me off QUEtiapine Fumarate. I haven’t felt well since. Appreciate any feedback. Thank you.
Foncie
in
Cure Parkinson's
4 years ago
RASAGILINE........PWP have you tried it with good results??
My Neurologist just prescribed, I am currently on 1 1/2 of 25/100 C/L 2x day and I was also on amantadine, but it was causing very bad back pain, so my neuro put me in RASAGILINE. But I am afraid to start it. Any advice would be much appreciated. 🙏🏽
My Neurologist just prescribed, I am currently on 1 1/2 of 25/100 C/L 2x day and I was also on amantadine, but it was causing very bad back pain, so my neuro put me in RASAGILINE. But I am afraid to start it. Any advice would be much appreciated. 🙏🏽
Chicafromchitown
in
Cure Parkinson's
4 years ago
Vitamin C , Vitamin D 3 & Coconut Oil
Does anyone know the effects of taking the tablets daily on Carbidopa - Levodopa, Amantadine & Rasagilne?
Does anyone know the effects of taking the tablets daily on Carbidopa - Levodopa, Amantadine & Rasagilne?
NewHope1961
in
Cure Parkinson's
4 years ago
Orthostatic hypotension
I am trying to deal with being dizzy and sometimes fainting. I am transitioning from Sinemet to mucuna . My dosage was 7 1/2 pills a day. 1 extended at night and 1 amantadine in the morning and 1 at night I have increased my water intake and taking essential oils to increase my blood pressure. My neurologist
I am trying to deal with being dizzy and sometimes fainting. I am transitioning from Sinemet to mucuna . My dosage was 7 1/2 pills a day. 1 extended at night and 1 amantadine in the morning and 1 at night I have increased my water intake and taking essential oils to increase my blood pressure. My neurologist
Bowling55
in
Cure Parkinson's
4 years ago
VERY HIGH THIAMINE blood levels
Routine bloodwork last week in hubby has turned up surprising. His THIAMINE blood level is 378.9 with the lab's maximum range being 200.0. I know B1 is not supposed to be toxic. His kidney functions are fine, but his liver enzymes are extremely high, too. The Dr. is running more tests to determine
Routine bloodwork last week in hubby has turned up surprising. His THIAMINE blood level is 378.9 with the lab's maximum range being 200.0. I know B1 is not supposed to be toxic. His kidney functions are fine, but his liver enzymes are extremely high, too. The Dr. is running more tests to determine
Boyce3600
in
Cure Parkinson's
4 years ago
Switching to Mucuna from c/ levodopa
This past week I switch from CL to MP I also take a man to die amantadine one at 7 a.m. and one at 7 p.m. is there a supplement to replace this medication. Thanks
This past week I switch from CL to MP I also take a man to die amantadine one at 7 a.m. and one at 7 p.m. is there a supplement to replace this medication. Thanks
Bowling55
in
Cure Parkinson's
4 years ago
Experienced some tremor relief
Dx Jan 2017, 72 yrs old, Tremor dominate. I tremor intermittently, that is daily for the past 2+ years. When I perform certain movements with my good side, such as wiping down shower (with left arm), my right arm tremors consistently. I walk 2.5-3 miles daily. Whenever I walk steep ascents, tremor is
Dx Jan 2017, 72 yrs old, Tremor dominate. I tremor intermittently, that is daily for the past 2+ years. When I perform certain movements with my good side, such as wiping down shower (with left arm), my right arm tremors consistently. I walk 2.5-3 miles daily. Whenever I walk steep ascents, tremor is
ParlePark
in
Cure Parkinson's
4 years ago
Creatine, StemEnhance, B1 Thiamine & Amantadine
I received a bonus container of “Pure Creatine” with a mail order, a couple months ago. I decided to go to the internet to see what it was used for and was surprised to see claims that some people feel it has been helpful for PwP. I use an electrolyte drink mix recommended by my primary care doctor.
I received a bonus container of “Pure Creatine” with a mail order, a couple months ago. I decided to go to the internet to see what it was used for and was surprised to see claims that some people feel it has been helpful for PwP. I use an electrolyte drink mix recommended by my primary care doctor.
blogger_7
in
Cure Parkinson's
4 years ago
How is PD connected to Restless Leg Syndrome?
Or is it? I had a mild degree of RLS for several years. It wasn't enough of a problem to warrant medical help. Over the past few months the restless leg has gotten worse. Coincidentally two years I was diagnosed with PD. I was on Sinemet for over a year. Stopped it and switched to amantadine
Or is it? I had a mild degree of RLS for several years. It wasn't enough of a problem to warrant medical help. Over the past few months the restless leg has gotten worse. Coincidentally two years I was diagnosed with PD. I was on Sinemet for over a year. Stopped it and switched to amantadine
kaypeeoh
in
Cure Parkinson's
4 years ago
Is there withdrawal from not taking the medicines?
I've been on ropinirole, amantadine, mybetriq and atorvastatin for a few months. Yesterday I didn't take anything. During the evening I developed a miserable headache that kept me up much of the night. Woke up with it but Tylenol helped. Is withdrawal an effect of not taking the medicines?
I've been on ropinirole, amantadine, mybetriq and atorvastatin for a few months. Yesterday I didn't take anything. During the evening I developed a miserable headache that kept me up much of the night. Woke up with it but Tylenol helped. Is withdrawal an effect of not taking the medicines?
kaypeeoh
in
Cure Parkinson's
4 years ago
Difficult to don a face mask
I got really upset yesterday regarding my physical limitations with PD. I wanted to go out for a walk, needed exercise to help we with my PD symptoms. I suffer severe chronic bilateral hamstring muscle spasms with severe chronic right leg sciatica. Not sure if the pain is secondary to the PD or the Spondylolisthesis
I got really upset yesterday regarding my physical limitations with PD. I wanted to go out for a walk, needed exercise to help we with my PD symptoms. I suffer severe chronic bilateral hamstring muscle spasms with severe chronic right leg sciatica. Not sure if the pain is secondary to the PD or the Spondylolisthesis
Shaky-hand
in
Cure Parkinson's
4 years ago
should i sleep with my husband
Hi all, I am 62 with mental health issues, my husband has PD dx 8 years ago, he is self isolating just going in the garden for a walk round and does a bit of gardening. I am only going out in a crisis ie collect a few bits from shop,chemist, etc but staying in most of the time. When i return from being
Hi all, I am 62 with mental health issues, my husband has PD dx 8 years ago, he is self isolating just going in the garden for a walk round and does a bit of gardening. I am only going out in a crisis ie collect a few bits from shop,chemist, etc but staying in most of the time. When i return from being
allofatremor
in
Cure Parkinson's
5 years ago
Promising drug could treat debilitating movement problems in people with Parkinson's
https://eurekalert.org/pub_releases/2020-03/pu-pdc022820.php Monday 02 March 2020 - Results from a study looking at an experimental drug to tackle the debilitating side effect of dyskinesia, have offered hope that it may have potential as a future treatment for people with Parkinson's. Research carried
https://eurekalert.org/pub_releases/2020-03/pu-pdc022820.php Monday 02 March 2020 - Results from a study looking at an experimental drug to tackle the debilitating side effect of dyskinesia, have offered hope that it may have potential as a future treatment for people with Parkinson's. Research carried
John_morris71
in
Cure Parkinson's
5 years ago
Hallucinations
My husband is recently on a feeding tube following a hospital stint brought on by an outside catalyst ( removal of amantadine with movement disorder specialists guidance). The hospital sent him to a rehab once establish infection with MDS’s that he titrating back in Med. Once at rehab speech & movement
My husband is recently on a feeding tube following a hospital stint brought on by an outside catalyst ( removal of amantadine with movement disorder specialists guidance). The hospital sent him to a rehab once establish infection with MDS’s that he titrating back in Med. Once at rehab speech & movement
Aurala
in
PSP Association
5 years ago
Possible causes of Ataxia
🙂 This is a ‘long read’ and may be difficult to interpret, but never the less it’s interesting. What processes can cause ataxia? The pathophysiology of cerebellar ataxias is as diverse as the various neurological and systemic diseases affecting the cerebellum. Broadly classifying ataxias into genetic
🙂 This is a ‘long read’ and may be difficult to interpret, but never the less it’s interesting. What processes can cause ataxia? The pathophysiology of cerebellar ataxias is as diverse as the various neurological and systemic diseases affecting the cerebellum. Broadly classifying ataxias into genetic
wobblybee
in
Ataxia UK
5 years ago
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