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Solgar Magnesium Citrate
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Magnesium and aspirin
Hi I have been thinking about supplementing magnesium but I have read about it interacting with aspirin which I take on a night, I also take 25mg isosorbide mononitrate and 10mgs atorvastatin any thoughts on this.
Hi I have been thinking about supplementing magnesium but I have read about it interacting with aspirin which I take on a night, I also take 25mg isosorbide mononitrate and 10mgs atorvastatin any thoughts on this.
Radars
in
British Heart Foundation
3 years ago
Cold Laser and EMDR!
On November 3rd 2021 I started seeing a new chiropractor who uses cold laser treatments. It’s like red light therapy on steroids. Look it up! My smell that was diminished is now almost normal. Gait and stiffness improved greatly. Little tremor I had is gone. Can Type 75% better! He does a laser treatment
On November 3rd 2021 I started seeing a new chiropractor who uses cold laser treatments. It’s like red light therapy on steroids. Look it up! My smell that was diminished is now almost normal. Gait and stiffness improved greatly. Little tremor I had is gone. Can Type 75% better! He does a laser treatment
38yroldmale
in
Cure Parkinson's
3 years ago
The Afib Project channel on YouTube
Interesting new video channel recently started over on YouTube: https://www.youtube.com/channel/UCZjkFR0A-gQ6NXgV5pqrAjA/videos So far looked at cardiorespiratory fitness, Covid & AF, ideal waist size and is currently looking at magnesium supplementation. From his bio: "I'm David, an atrial fibrillation
Interesting new video channel recently started over on YouTube: https://www.youtube.com/channel/UCZjkFR0A-gQ6NXgV5pqrAjA/videos So far looked at cardiorespiratory fitness, Covid & AF, ideal waist size and is currently looking at magnesium supplementation. From his bio: "I'm David, an atrial fibrillation
Barny12
in
AF Association
3 years ago
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Palpitations and Magnesium
I've read that magnesium can help with palpitations. Has anyone already on heart meds (I'm on atorvastatin, aspirin, ramipril and amlodipine) tried taking it for that purpose? I've suffered from them for many years, starting long before my HA but they have gotten a lot worse recently. I'd like to do
I've read that magnesium can help with palpitations. Has anyone already on heart meds (I'm on atorvastatin, aspirin, ramipril and amlodipine) tried taking it for that purpose? I've suffered from them for many years, starting long before my HA but they have gotten a lot worse recently. I'd like to do
LesleyJ59
in
British Heart Foundation
3 years ago
Trapped finale (hopefully)
Well guys my update ! I contacted PALS of the hospital 8am no answer obviously to early so dropped them email of my predicament, at 10 30 am sister of ward woke me , as I was totally knackered due to that episode , she told me PALS had been in touch with her and were sorting it and the team who
Well guys my update ! I contacted PALS of the hospital 8am no answer obviously to early so dropped them email of my predicament, at 10 30 am sister of ward woke me , as I was totally knackered due to that episode , she told me PALS had been in touch with her and were sorting it and the team who
Smurff
in
Restless Legs Syndrome
3 years ago
T3 advice
Started taking T3 and worked it up slowly to one full 25mcg tablet per day.Done this for a couple of days then split the 25mcg half in morning and half mid afternoon.Whilst at the same time I reduced my Levo to 50mcg taken in the morning with half the T3 tablet Problem is I’m still feeling terrible fatigue
Started taking T3 and worked it up slowly to one full 25mcg tablet per day.Done this for a couple of days then split the 25mcg half in morning and half mid afternoon.Whilst at the same time I reduced my Levo to 50mcg taken in the morning with half the T3 tablet Problem is I’m still feeling terrible fatigue
jacobite33
in
Thyroid UK
3 years ago
Delaying cognitive decline
I had a BT partially removed in 2009 followed by 30 rounds of RT in 2010. Tumour has been stable since but I have experienced side effects (fatigue, tinnitus, confusion, cognitive decline, etc). Today I had a radio oncologist review and I explained this. He told me that because of dose of the radiation
I had a BT partially removed in 2009 followed by 30 rounds of RT in 2010. Tumour has been stable since but I have experienced side effects (fatigue, tinnitus, confusion, cognitive decline, etc). Today I had a radio oncologist review and I explained this. He told me that because of dose of the radiation
EireAtaxic
in
Headway
3 years ago
Burning legs
I want to appeal to all the knowledgeable RLS sufferers to see if they can help my dear husband who has been suffering from burning feet and legs. It has been diagnosed as a nerve trapped in lower spine which has been troublesome for years and is pretty wonky. He has had cortisone injections in the past
I want to appeal to all the knowledgeable RLS sufferers to see if they can help my dear husband who has been suffering from burning feet and legs. It has been diagnosed as a nerve trapped in lower spine which has been troublesome for years and is pretty wonky. He has had cortisone injections in the past
Daisy2408
in
Restless Legs Syndrome
3 years ago
New Medicines Atorvastatin and Propranaolol Bone Worries
I have had a barrage of blood tests done recently due to Osteoporosis, no blood test was left out, except for Magnesium that I am being tested for in the next lot of blood tests in January. My blood tests show high cholesterol so the doctor prescribed Atorvastatin 20mg. He also prescribed Propranaolol
I have had a barrage of blood tests done recently due to Osteoporosis, no blood test was left out, except for Magnesium that I am being tested for in the next lot of blood tests in January. My blood tests show high cholesterol so the doctor prescribed Atorvastatin 20mg. He also prescribed Propranaolol
Daisi124
in
Osteoporosis Support
3 years ago
I am taking a break from Magnesium. You are welcome to change my mind.
I have not been diagnosed with PD. I have REM Sleep Behavior Disorder. I just have too many supplements on my list and feel I need to cut a player: http://pdprotocols.atwebpages.com/daily_protocols.html The evidence I see for Magnesium seems thin and not specific to PD. I have a high school degree and
I have not been diagnosed with PD. I have REM Sleep Behavior Disorder. I just have too many supplements on my list and feel I need to cut a player: http://pdprotocols.atwebpages.com/daily_protocols.html The evidence I see for Magnesium seems thin and not specific to PD. I have a high school degree and
Bolt_Upright
in
Cure Parkinson's
3 years ago
When to take B complex?
My recent blood tests here. I am currently taking daily: 7.00am 30mg ERFA and 50mcg Levothyroxine 2.30pm 30mg ERFA 6.30pm 2,000iu Vit D3 with K2 -Mk7 10.00pm Magnesium 300mg Where is it best to fit in B Complex? How far apart does it need to be from the ERFA? Any thoughts on the amount I am supplementing
My recent blood tests here. I am currently taking daily: 7.00am 30mg ERFA and 50mcg Levothyroxine 2.30pm 30mg ERFA 6.30pm 2,000iu Vit D3 with K2 -Mk7 10.00pm Magnesium 300mg Where is it best to fit in B Complex? How far apart does it need to be from the ERFA? Any thoughts on the amount I am supplementing
SmPea
in
Thyroid UK
3 years ago
Can a burning pain in the buttocks be part of RLS symptoms ?
Has anyone experienced pain in the buttocks that was related to RLS? I have had RLS for a few years, have on the whole been able to manage the pain in the legs without medication by walking around at night, massages, arnica or magnesium spray; and taking iron supplements. In May I underwent tests confirming
Has anyone experienced pain in the buttocks that was related to RLS? I have had RLS for a few years, have on the whole been able to manage the pain in the legs without medication by walking around at night, massages, arnica or magnesium spray; and taking iron supplements. In May I underwent tests confirming
s_gc
in
Restless Legs Syndrome
3 years ago
Appointment with an electrophysiologist
Hi there, would like to share my experience after my yesterday’s private appointment with one of the leading electrophysiologists (uk, London). Summary: nearly 20 years with PAF, mainly 1-2 episodes a year, last three years 3 episodes up to 36 hours without medication and up to 4 hours with flecainide
Hi there, would like to share my experience after my yesterday’s private appointment with one of the leading electrophysiologists (uk, London). Summary: nearly 20 years with PAF, mainly 1-2 episodes a year, last three years 3 episodes up to 36 hours without medication and up to 4 hours with flecainide
Kittyca
in
AF Association
3 years ago
Side effects of flecainide and coming off it .
Hi all been on flecainide 100mg a day for couple of months , but it has not helped my AF episodes ( twice a week lasting 24 hours ) but has given me side effects of insomnia, constipation , feeling in a fog , and now recently my whole mood has changed and depression has set in , I have decided to come
Hi all been on flecainide 100mg a day for couple of months , but it has not helped my AF episodes ( twice a week lasting 24 hours ) but has given me side effects of insomnia, constipation , feeling in a fog , and now recently my whole mood has changed and depression has set in , I have decided to come
123hi
in
AF Association
3 years ago
New to this group and looking to learn
I was diagnosed with osteoporosis this summer (-2.5), and I was disappointed to see that number. It was my third DEXA scan over the last 10 years following removal of my thyroid for thyroid cancer and subsequent thyroid replacement therapy, and I've watched a continuing decrease in bone density in spite
I was diagnosed with osteoporosis this summer (-2.5), and I was disappointed to see that number. It was my third DEXA scan over the last 10 years following removal of my thyroid for thyroid cancer and subsequent thyroid replacement therapy, and I've watched a continuing decrease in bone density in spite
ksblack519
in
Osteoporosis Support
2 years ago
Is there anyone that can further educate me on the combination of POTS, FND, and other medical issues one of my best friends is facing?
One of my best friends is struggling with many medical conditions and has been diagnosed with having POTS, a FND, has what we call “episodes” in the middle of classes and at times will run out of rooms to avoid being made a spectacle of in front of others. They shortest amount of time they usually last
One of my best friends is struggling with many medical conditions and has been diagnosed with having POTS, a FND, has what we call “episodes” in the middle of classes and at times will run out of rooms to avoid being made a spectacle of in front of others. They shortest amount of time they usually last
ShallowWater
in
Functional Neurological Disorder - FND Hope
3 years ago
Magnesium
I need some information on magnesium. My labs show I'm low but still within the normal range and the doctor advised to take the supplement daily. Ive been taking 500mg of plain magnesium and started to develop severe insomnia and a lot of intense, crazy dreaming. I cut back to 250 mg a day but frankly
I need some information on magnesium. My labs show I'm low but still within the normal range and the doctor advised to take the supplement daily. Ive been taking 500mg of plain magnesium and started to develop severe insomnia and a lot of intense, crazy dreaming. I cut back to 250 mg a day but frankly
drmind
in
Kidney Disease
3 years ago
Help with blood results please
Hi everyone, I started treatment with Levothyroxine in January and reached a dose of 100mcg about 6 months ago. I tested at the end of May and had a suppressed TSH (0.05) range 0.55-0.78 and T3 was 4.9 (range 3.5-6.5) . I have been getting increasing attacks of fatigue recently and discovered that my
Hi everyone, I started treatment with Levothyroxine in January and reached a dose of 100mcg about 6 months ago. I tested at the end of May and had a suppressed TSH (0.05) range 0.55-0.78 and T3 was 4.9 (range 3.5-6.5) . I have been getting increasing attacks of fatigue recently and discovered that my
RobinC21
in
Thyroid UK
3 years ago
Want to stop Prolia
I have been on Prolia for 3 years and want to stop. Rheumatologist only says « you should stay on it » blah blah blah. I know that there’s risks of spontaneous fracture but the side effects and long term effects of Prolia are frightening. Anyone know of any natural remedies ( I am in my 60s). I take
I have been on Prolia for 3 years and want to stop. Rheumatologist only says « you should stay on it » blah blah blah. I know that there’s risks of spontaneous fracture but the side effects and long term effects of Prolia are frightening. Anyone know of any natural remedies ( I am in my 60s). I take
VieuxQuebec
in
Osteoporosis Support
3 years ago
Life with Ectopics - 20 years old
Hi, my name is Abbie McDonald, and I am currently 20 years old. I have had heart issues, specifically ectopics, for over 6 years now. My story is quite long but I will do my best to summarise it all. It all started after my HPV vaccine at school in Year 10. Following the jab, I came down with cold
Hi, my name is Abbie McDonald, and I am currently 20 years old. I have had heart issues, specifically ectopics, for over 6 years now. My story is quite long but I will do my best to summarise it all. It all started after my HPV vaccine at school in Year 10. Following the jab, I came down with cold
AMcDonald
in
Arrhythmia Alliance
3 years ago
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