Search
Search
About
Log in
Join
Experiences with
Naturopathy
Posts
Communities
2,561 public posts
Filter results
Results are in
A couple of weeks ago, I joined this community after experiencing High Heart Rates (HHR) and faced the possibility of an Ablation. I was waiting to see my PCP for some lab work and discuss other possible causes of my HHR. Since then, the HHRs have stopped. Just as fast as they started, they stopped.
A couple of weeks ago, I joined this community after experiencing High Heart Rates (HHR) and faced the possibility of an Ablation. I was waiting to see my PCP for some lab work and discuss other possible causes of my HHR. Since then, the HHRs have stopped. Just as fast as they started, they stopped.
MartyVA
in
Atrial Fibrillation Support
3 years ago
Monoamine Oxidase Inhibitors: A Review of Their Anti-Inflammatory Therapeutic Potential and Mechanisms of Action
Article from 30 April 2021 https://www.frontiersin.org/articles/10.3389/fphar.2021.676239/full
Concluding Remarks and Future Perspectives
MAO inhibitors have a long history of successful clinical use to manage CNS diseases such as depression, Parkinson’s, and Alzheimer’s.
There is also an
Article from 30 April 2021 https://www.frontiersin.org/articles/10.3389/fphar.2021.676239/full
Concluding Remarks and Future Perspectives
MAO inhibitors have a long history of successful clinical use to manage CNS diseases such as depression, Parkinson’s, and Alzheimer’s.
There is also an
Hidden
in
Cure Parkinson's
3 years ago
Nebivolol
I have started taking this for my AF but I am concerned that there may be a problem as I take a very small dose of Amitriptyline for restless legs at night . I wonder what might be the best time to take the Nebivolol ? Many thanks Best wishes to all
I have started taking this for my AF but I am concerned that there may be a problem as I take a very small dose of Amitriptyline for restless legs at night . I wonder what might be the best time to take the Nebivolol ? Many thanks Best wishes to all
linc2u
in
Atrial Fibrillation Support
3 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Pain relief
Hhi there. I'm currently taking MST for pain relief and I've been told in passing from a GP that I may be better on subutex. I was wondering if anyone can h help me.. Will it be a straight forward transition to subutex or will I have to have a break from the morphine before starting subutex
Hhi there. I'm currently taking MST for pain relief and I've been told in passing from a GP that I may be better on subutex. I was wondering if anyone can h help me.. Will it be a straight forward transition to subutex or will I have to have a break from the morphine before starting subutex
Peggysue12345
in
Pain Concern
3 years ago
Alpha Lipoic Acid
Hi I've been taking the above for a number of weeks as I'd read its good for neuropathy. I have fibro and one of my most persistent and annoying symptoms is pins and needles in my feet and hands. In recent months it had spread to my head and other areas and was driving me nuts. I have a suspicion it's
Hi I've been taking the above for a number of weeks as I'd read its good for neuropathy. I have fibro and one of my most persistent and annoying symptoms is pins and needles in my feet and hands. In recent months it had spread to my head and other areas and was driving me nuts. I have a suspicion it's
Sparklingsunshine
in
Thyroid UK
3 years ago
Anyone tried a homeopath
My mum has suffered with rls for about 10 years. She's tried ropinerole, pamiprexole, skin patches, gabapentin and pregablin. All of this gave her relief at first and then symptoms returned. Next the doctor gave her topiremade, with this her rls went away however she had really bad depression symptoms
My mum has suffered with rls for about 10 years. She's tried ropinerole, pamiprexole, skin patches, gabapentin and pregablin. All of this gave her relief at first and then symptoms returned. Next the doctor gave her topiremade, with this her rls went away however she had really bad depression symptoms
Bejwo50
in
Restless Legs Syndrome
3 years ago
Physical Therapist Management of Parkinson Disease: A Clinical Practice Guideline from the American Physical Therapy Association
Resistance Training gets 4 Diamonds: Physical therapists should implement resistance training to reduce motor severity, improve strength, power, nonmotor symptoms, functional outcomes, and QOL in PD. Evidence Quality: High; Recommendation Strength: Strong https://academic.oup.com/ptj/advance-article/
Resistance Training gets 4 Diamonds: Physical therapists should implement resistance training to reduce motor severity, improve strength, power, nonmotor symptoms, functional outcomes, and QOL in PD. Evidence Quality: High; Recommendation Strength: Strong https://academic.oup.com/ptj/advance-article/
Farooqji
in
Cure Parkinson's
3 years ago
Phantom Pain
I have suffered with this since a BKA (Below Knee Amputation) in 2020. The last few days it has tended to start after I go to bed. I am tied and want to sleep yet suffer various pains (cramp, pain in ankle, burning in big toe area). It may take a couple of hours to drift off. I am on 3 x 300mg Gabapentin
I have suffered with this since a BKA (Below Knee Amputation) in 2020. The last few days it has tended to start after I go to bed. I am tied and want to sleep yet suffer various pains (cramp, pain in ankle, burning in big toe area). It may take a couple of hours to drift off. I am on 3 x 300mg Gabapentin
MichaelJH
in
Pain Concern
3 years ago
Plasmapheresis treatments
Just received my 5th treatment. Doc saying not seeing the results they expected. Anyone else have this Tx and can give me idea, how many, when you saw results? Will be discussing options with docs Monday after they discuss…IVIG or another IV tx starts with an R (sorry, brain 🧠🙄). New here, trying
Just received my 5th treatment. Doc saying not seeing the results they expected. Anyone else have this Tx and can give me idea, how many, when you saw results? Will be discussing options with docs Monday after they discuss…IVIG or another IV tx starts with an R (sorry, brain 🧠🙄). New here, trying
Byourownadvocate
in
Hughes Syndrome APS Forum
3 years ago
why I feel so hot after taking b12 timed release?
My symptoms was started to develop fast because Cyanocobalamin didn't work for me and I was in agonizing situation I couldn't stand on my feet and my pain was unbearable. then I found my Ferritin is low and helped a lot after taking that but my weakness was phenomenal and extreme weakness along with
My symptoms was started to develop fast because Cyanocobalamin didn't work for me and I was in agonizing situation I couldn't stand on my feet and my pain was unbearable. then I found my Ferritin is low and helped a lot after taking that but my weakness was phenomenal and extreme weakness along with
Hamayeshguy
in
Pernicious Anaemia Society
3 years ago
Spacing out injections
Tried to go from weekly injections to every two weeks…make it one day past my normal shot day and horrible small fiber neuropathy in my feet that I haven’t had since doing weekly injections. 😫 Anyone else get symptoms back if they try to extend just a day or two past their normal spacing?
Tried to go from weekly injections to every two weeks…make it one day past my normal shot day and horrible small fiber neuropathy in my feet that I haven’t had since doing weekly injections. 😫 Anyone else get symptoms back if they try to extend just a day or two past their normal spacing?
lambuth_eagle
in
Pernicious Anaemia Society
3 years ago
Levodopa‐Induced Neuropathy: A Systematic Review
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384168 Conclusions Over one third of PD patients in treatment with l‐dopa may develop PNP, with a significantly higher prevalence of acute and subacute forms in those receiving LCIG. Pathogenic mechanisms remain unclear, but possibly related to a complex
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384168 Conclusions Over one third of PD patients in treatment with l‐dopa may develop PNP, with a significantly higher prevalence of acute and subacute forms in those receiving LCIG. Pathogenic mechanisms remain unclear, but possibly related to a complex
Thal
in
Cure Parkinson's
3 years ago
Swapping Gabapentin for Pregabalin
Can I just ask a question regarding swapping 1200 Gabapentin taken in two doses (7pm and 9pm) for Pregabalin, which has stopped working for me. I also take, most nights, 50mg Tramadol. My doctor has agreed to the swap, however, says I will need to wean off the Gabapentin before taking Pregabalin. I
Can I just ask a question regarding swapping 1200 Gabapentin taken in two doses (7pm and 9pm) for Pregabalin, which has stopped working for me. I also take, most nights, 50mg Tramadol. My doctor has agreed to the swap, however, says I will need to wean off the Gabapentin before taking Pregabalin. I
Mulberry100
in
Restless Legs Syndrome
3 years ago
RLS and Parkinson's
Hi everyone, I'm new here but have been reading a lot of posts and find it very helpful. Great to find this community that support each other. I wanted to tell about my mother’s condition to see if anyone has any helpful tips or insights. My mum has been diagnosed with Parkinson recently and has started
Hi everyone, I'm new here but have been reading a lot of posts and find it very helpful. Great to find this community that support each other. I wanted to tell about my mother’s condition to see if anyone has any helpful tips or insights. My mum has been diagnosed with Parkinson recently and has started
Fernando80
in
Restless Legs Syndrome
3 years ago
Needle size and dosage
Hi everyone, thanks so much for support and advice. It's been invaluable and given me the confidence to purchase vit b12. Could someone tell me which needles to use for intramuscular injections. Thank you
Hi everyone, thanks so much for support and advice. It's been invaluable and given me the confidence to purchase vit b12. Could someone tell me which needles to use for intramuscular injections. Thank you
Mrsmr
in
Pernicious Anaemia Society
3 years ago
Peripheral Neuropathy
I was diagnosed with PBC around 6 years ago. Due to the current Covid -19 situation here in the UK I haven't had any contact my Gastroenterologist for almost 2 years. I understand, one of the symptoms associated with PBC is Peripheral Neuropathy. I have this condition in both feet, numbness, burning
I was diagnosed with PBC around 6 years ago. Due to the current Covid -19 situation here in the UK I haven't had any contact my Gastroenterologist for almost 2 years. I understand, one of the symptoms associated with PBC is Peripheral Neuropathy. I have this condition in both feet, numbness, burning
suzycatt1
in
PBC Foundation
3 years ago
Is it just me?
Hi, is it just me that can’t tolerate the smell of perfume or aftershave ( any fragrance brand) at all? It makes me want to rip my skin off. I was never like this before lupus. ( diagnosed about 7 years ago but lived with it for about 15) I didn’t have this issue before lupus I’ve had to tell my daughter
Hi, is it just me that can’t tolerate the smell of perfume or aftershave ( any fragrance brand) at all? It makes me want to rip my skin off. I was never like this before lupus. ( diagnosed about 7 years ago but lived with it for about 15) I didn’t have this issue before lupus I’ve had to tell my daughter
joanneM200
in
LUPUS UK
3 years ago
New ache in wrists
Hi all - wishing everyone the best of health (or at least some relief) for the holidays. I have a new or worsening symptom & wondering if it‘s familiar to anyone. I have developed an unrelenting ache in my wrists & hands. I have had issues with neuropathy - shooting pains, numbness, & iciness, but
Hi all - wishing everyone the best of health (or at least some relief) for the holidays. I have a new or worsening symptom & wondering if it‘s familiar to anyone. I have developed an unrelenting ache in my wrists & hands. I have had issues with neuropathy - shooting pains, numbness, & iciness, but
SigNi
in
Pernicious Anaemia Society
3 years ago
Anterior prolapse?
Hi everyone, I am new to this group. Joined today after I started doing some research on Anterior Prolapse. I visited the physiotherapist today and was told that my pelvic muscles were really tight. Towards the end of the session, she mentioned to me that my bladder is too low. She specifically said
Hi everyone, I am new to this group. Joined today after I started doing some research on Anterior Prolapse. I visited the physiotherapist today and was told that my pelvic muscles were really tight. Towards the end of the session, she mentioned to me that my bladder is too low. She specifically said
Sweettear74
in
Pelvic Pain Support Network
3 years ago
Increasing self doses
After recent diagnosis and poor care from doctors, I am self injecting as I have said in a few previous posts. My plan was once every 2 weeks - boy I was wrong. Symptoms return like a total crash, really bad. I am now on 3 times a week just to keep the symptoms away, bearing in mind it takes 2 days from
After recent diagnosis and poor care from doctors, I am self injecting as I have said in a few previous posts. My plan was once every 2 weeks - boy I was wrong. Symptoms return like a total crash, really bad. I am now on 3 times a week just to keep the symptoms away, bearing in mind it takes 2 days from
Vitali-ep
in
Pernicious Anaemia Society
3 years ago
1
...
24
25
26
...
100
Next page
10
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Fibromyalgia Action UK
283 results
Restless Legs Syndrome
260 results
Pernicious Anaemia Society
259 results
View top 10 communities
Sort by
Most Relevant
Newest