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Any ideas on sleep issues
Hi all, hope everyone is doing as well as they can be. Been a while since I posted. My WBC is now up to 25.67, Lymph% 77.3 and Lymph # 19.84. Still on W&W. Wondering if anyone else is having a similar sleep issues. Even with taking Melatonin 20mg before bed, I fall asleep feeling fine. I wake up
Hi all, hope everyone is doing as well as they can be. Been a while since I posted. My WBC is now up to 25.67, Lymph% 77.3 and Lymph # 19.84. Still on W&W. Wondering if anyone else is having a similar sleep issues. Even with taking Melatonin 20mg before bed, I fall asleep feeling fine. I wake up
CBME
in
CLL Support
2 years ago
weighted vest
I’m pretty new to this group but am very grateful to be part of this forum. I was diagnosed with osteoporosis in 2017 and started sodium risedronate around 2018. I took it until about 4 months ago when my Endocrinologist took me off to put me on Prolia, which she assured me had no contraindications
I’m pretty new to this group but am very grateful to be part of this forum. I was diagnosed with osteoporosis in 2017 and started sodium risedronate around 2018. I took it until about 4 months ago when my Endocrinologist took me off to put me on Prolia, which she assured me had no contraindications
Uncertain2
in
Bone Health and Osteoporosis UK
2 years ago
I lost a day
This morning I woke and showered and prepared for two appointments. One at Hartford Health for Tai chi and one with my primary care doc. At 2PM I was back . An hour later I went to bed. When I next woke I thought it was 4AM. That explained why it was still dark out. I started coffee then turned
This morning I woke and showered and prepared for two appointments. One at Hartford Health for Tai chi and one with my primary care doc. At 2PM I was back . An hour later I went to bed. When I next woke I thought it was 4AM. That explained why it was still dark out. I started coffee then turned
kaypeeoh
in
Cure Parkinson's
2 years ago
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medication that makes RLS worse
I need to know which medications , especially pain relief and sleeping meds, make RLS worse. Some years ago I was given pain relief and sleeping meds after rotator cuff surgery and spent the whole night walking around my room. I have another procedure coming up and want to avoid a repeat. I know
I need to know which medications , especially pain relief and sleeping meds, make RLS worse. Some years ago I was given pain relief and sleeping meds after rotator cuff surgery and spent the whole night walking around my room. I have another procedure coming up and want to avoid a repeat. I know
Stelladevico
in
Restless Legs Syndrome
2 years ago
Some words of encouragement
We all know that PD is a degenerative disease. It should however not mean that everything necessarily gets worse all the time. I am sharing the information below as an encouragement to all. I am currently on holiday close to Syracuse in Sicily and was amazed to find out this morning that I could
We all know that PD is a degenerative disease. It should however not mean that everything necessarily gets worse all the time. I am sharing the information below as an encouragement to all. I am currently on holiday close to Syracuse in Sicily and was amazed to find out this morning that I could
Michel0220
in
Cure Parkinson's
2 years ago
fitful sleeps
I have cardiomyopathy with no symptoms at this point. The only issue is my interrupted sleeping with fidgeting and the need to stretch my hamstrings .( bizarre I know) .I am on telmisartin plus for BP and Plavix and Crestor.Also sertraline which is for anxiety.My question is and I would ask the Dr. This
I have cardiomyopathy with no symptoms at this point. The only issue is my interrupted sleeping with fidgeting and the need to stretch my hamstrings .( bizarre I know) .I am on telmisartin plus for BP and Plavix and Crestor.Also sertraline which is for anxiety.My question is and I would ask the Dr. This
Darcy2000
in
British Heart Foundation
2 years ago
Oxidative Stress (ROS), Sleep and the Gut Microbiome: Staying Alive
I am just back from a challenging (humbling) multiday backpack in the High Sierras of California. Very beautiful but drought conditions, dry stream water sources made it more difficult. Here is a pre-note on my own regimen: After completing my two phase radiation treatments for oligometastatic PC:
I am just back from a challenging (humbling) multiday backpack in the High Sierras of California. Very beautiful but drought conditions, dry stream water sources made it more difficult. Here is a pre-note on my own regimen: After completing my two phase radiation treatments for oligometastatic PC:
MateoBeach
in
Advanced Prostate Cancer
2 years ago
melatonin
hello all. Today 13 July 2022 my doctor has told me to read up about melatonin. Saying she was unable to prescribe melatonin, as it’s not available on the NHS. We, that’s her and I, are trying a program to help with my insomnia. Which I’ve suffered for many years. This is going to be a start asking for
hello all. Today 13 July 2022 my doctor has told me to read up about melatonin. Saying she was unable to prescribe melatonin, as it’s not available on the NHS. We, that’s her and I, are trying a program to help with my insomnia. Which I’ve suffered for many years. This is going to be a start asking for
StJulian1305
in
Sleep Matters
2 years ago
Melatonin for PD
Melatonin (5-methoxy-N-acetyltryptamine): powerful antioxidant that treats abnormalities in sleep-wake cycle, jet lag, cancer, and Parkinson’s disease. Epileptic children have a higher incidence of sleep problems; epilepsy is exacerbated by sleep deprivation. Melatonin has antiepileptic activity. Mechanism
Melatonin (5-methoxy-N-acetyltryptamine): powerful antioxidant that treats abnormalities in sleep-wake cycle, jet lag, cancer, and Parkinson’s disease. Epileptic children have a higher incidence of sleep problems; epilepsy is exacerbated by sleep deprivation. Melatonin has antiepileptic activity. Mechanism
Farooqji
in
Cure Parkinson's
2 years ago
MY COVID, HOSPITAL, LOW SODIUM, Vaccines
Dear all, I’m 57, ET. Was harmed by the Pfizer vaccine (veins and Vagus Nerve) and after a year, do not count as vaccinated. I was treated for these problem with bioresonance and the Quint system which finally gave me my brain and energy back. Covid hit my family: My husband 60 is vaccinated 3x. My
Dear all, I’m 57, ET. Was harmed by the Pfizer vaccine (veins and Vagus Nerve) and after a year, do not count as vaccinated. I was treated for these problem with bioresonance and the Quint system which finally gave me my brain and energy back. Covid hit my family: My husband 60 is vaccinated 3x. My
Anag
in
MPN Voice
2 years ago
How are you sleeping?
Literally… how on earth are you sleeping, because I can’t sleep. I have PBC/PSC overlap and am in early cirrhosis. I take Urso, Ocaliva, Prednisone, Salagen and thyroid meds by prescription. I was taking Benadryl a couple days and it was perfect, out like a light. I read Benadryl may not be safe for
Literally… how on earth are you sleeping, because I can’t sleep. I have PBC/PSC overlap and am in early cirrhosis. I take Urso, Ocaliva, Prednisone, Salagen and thyroid meds by prescription. I was taking Benadryl a couple days and it was perfect, out like a light. I read Benadryl may not be safe for
IAmTheGlue
in
PBC Foundation
2 years ago
sleeping pills and severe cognition
hi everyone im abit confused and hope someone can advice me my husband had a hypoxic brain injury 18months ago he was very aggressive and would not sleep for 3to 4nights non stop in rehab but since his come home he sleeps quite well we do have a few nights where he jus wonst sleep but its probliy once
hi everyone im abit confused and hope someone can advice me my husband had a hypoxic brain injury 18months ago he was very aggressive and would not sleep for 3to 4nights non stop in rehab but since his come home he sleeps quite well we do have a few nights where he jus wonst sleep but its probliy once
fity123r
in
Headway
2 years ago
Mannitol and sense of Taste/Smell
Mannitol was once quite a popular great white hope against PD, but only ever really seemed to benefit perhaps 1 in 5 at best. It did really seem to benefit me though. Given how cheap it is it is always worth a punt (I know big pharma study found no benefit, but we will agree to differ on how believable
Mannitol was once quite a popular great white hope against PD, but only ever really seemed to benefit perhaps 1 in 5 at best. It did really seem to benefit me though. Given how cheap it is it is always worth a punt (I know big pharma study found no benefit, but we will agree to differ on how believable
alexask
in
Cure Parkinson's
2 years ago
Pregabalin and Tramadol
Hello. I have RLS as well as REM Sleep Disorder. For the RSD I am taking 20 mg of Melatonin and for the RLS I am taking 100 mg of Tramadol and 100 mg of Pregabalin. I had trouble with augmentation on just 75 mg of Tramadol so my Sleep Doctor upped the dose to 100 and added the Pregabalin. So far,
Hello. I have RLS as well as REM Sleep Disorder. For the RSD I am taking 20 mg of Melatonin and for the RLS I am taking 100 mg of Tramadol and 100 mg of Pregabalin. I had trouble with augmentation on just 75 mg of Tramadol so my Sleep Doctor upped the dose to 100 and added the Pregabalin. So far,
chihuahualuver
in
Restless Legs Syndrome
2 years ago
"This fruit could treat Parkinson's... even though it causes Parkinson's symptoms."
Soursop, also known as guanabana and other names. The fruit can cause Parkinson's-like symptoms but also contains chemicals that are potentially beneficial. "The chemicals are called tryptamine-derived alkaloids. They're similar in structure to melatonin, a hormone involved in sleep regulation that can
Soursop, also known as guanabana and other names. The fruit can cause Parkinson's-like symptoms but also contains chemicals that are potentially beneficial. "The chemicals are called tryptamine-derived alkaloids. They're similar in structure to melatonin, a hormone involved in sleep regulation that can
Zardoz
in
Cure Parkinson's
2 years ago
Panic Attacks
For about two years, I've experienced panic attacks several times a week. The first time that I had one I went to the ER, because I thought I was having a heart attack. The main symptoms are a shortness of breath, a feeling of tightening in the chest, and an overall sense of weakness. I've had problems
For about two years, I've experienced panic attacks several times a week. The first time that I had one I went to the ER, because I thought I was having a heart attack. The main symptoms are a shortness of breath, a feeling of tightening in the chest, and an overall sense of weakness. I've had problems
Alock2020
in
Cure Parkinson's
2 years ago
HASHI'S, HISTAMINE SENSITIVITY, THYROID
Hashi's, just learning about histamine sensitivity foods and drugs, I am gearing up to go on a histamine free food and drug diet, but have more questions than answers. I can give up the foods, but some of my meds are definitely on the histamine list. Background, born with pituitary tumor, I was always
Hashi's, just learning about histamine sensitivity foods and drugs, I am gearing up to go on a histamine free food and drug diet, but have more questions than answers. I can give up the foods, but some of my meds are definitely on the histamine list. Background, born with pituitary tumor, I was always
kaylee4848
in
Thyroid UK
2 years ago
Melatonin for Tinnitus
Hi, has anyone tried Melatonin for Tinnitus? Just having a spike now for 2 weeks.
Hi, has anyone tried Melatonin for Tinnitus? Just having a spike now for 2 weeks.
chris-104
in
British Tinnitus Association
2 years ago
Melatonin & Balance, MS Study
https://pubmed.ncbi.nlm.nih.gov/35708140/
https://pubmed.ncbi.nlm.nih.gov/35708140/
House2
in
Cure Parkinson's
2 years ago
Why Is Melatonin Worthy Of Consideration by PwP , Diabetics, People With Covid-19 and Everyone Else ?
In the following study it is suggested that nearly two thirds of PwP are insulin resistant : https://www.parkinson.org/blog/science-news/science-article/Parkinsons-Disease-Insulin-Resistance-HOMA#:~:text=This%20study%20suggests%20that%20nearly,some%20cases%2C%20despite%20being%20lean. Here are some very
In the following study it is suggested that nearly two thirds of PwP are insulin resistant : https://www.parkinson.org/blog/science-news/science-article/Parkinsons-Disease-Insulin-Resistance-HOMA#:~:text=This%20study%20suggests%20that%20nearly,some%20cases%2C%20despite%20being%20lean. Here are some very
chartist
in
Cure Parkinson's
2 years ago
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