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Solgar Magnesium Citrate
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Entire body/nervous system sensitivities with Afib?
Hi, I’m curious to find if anyone else has had similar changes in their body or nervous systems as I think I have had during recent extreme episodes of Afib. I found that when my heart rate was very high and erratic and my blood pressure was extremely high. (I was taken by ambulance to hospital resulting
Hi, I’m curious to find if anyone else has had similar changes in their body or nervous systems as I think I have had during recent extreme episodes of Afib. I found that when my heart rate was very high and erratic and my blood pressure was extremely high. (I was taken by ambulance to hospital resulting
IsobelBrown54
in
Atrial Fibrillation Support
3 years ago
Low potassium and magnesium
I’m halfway through a Pace and Ablate procedure, Pacemaker placed on June 30th. My recovery was going well until yesterday when I got a phone call from my GP to say that my routine blood test showed low Potassium and Magnesium and to go straight to A&E. Went and spent 12 hrs there several in Resus, I
I’m halfway through a Pace and Ablate procedure, Pacemaker placed on June 30th. My recovery was going well until yesterday when I got a phone call from my GP to say that my routine blood test showed low Potassium and Magnesium and to go straight to A&E. Went and spent 12 hrs there several in Resus, I
ETFCfan
in
AF Association
3 years ago
osteoarthritis and hot weather then rain on the way!
I have osteoarthritis [genetic] after all this hot weather, the cirrus clouds, weather forecast, rain coming, but the pain in my knees have really flared up, sitting here with my legs up, any idea of pain relief, usually I use a magnesium spray around the knee caps, but I need something a bit more drastic
I have osteoarthritis [genetic] after all this hot weather, the cirrus clouds, weather forecast, rain coming, but the pain in my knees have really flared up, sitting here with my legs up, any idea of pain relief, usually I use a magnesium spray around the knee caps, but I need something a bit more drastic
Adlon57
in
Healthy Evidence
3 years ago
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Problem with magnesium?
Hi, been taking magnesium citrate for a few weeks, about 200 mg a day, upped it to 300 mg the last couple of days. Couldn’t sleep last night as every time I was just about to drop off , I got the sensation of falling( best way I can describe it) and I was jolted awake again. Vaguely remember someone
Hi, been taking magnesium citrate for a few weeks, about 200 mg a day, upped it to 300 mg the last couple of days. Couldn’t sleep last night as every time I was just about to drop off , I got the sensation of falling( best way I can describe it) and I was jolted awake again. Vaguely remember someone
kizzie105
in
British Heart Foundation
3 years ago
More Levo has raised my TSH! Please help.
Hello to all, My TSH has gone way up even though I’ve been increasing the dose, and I feel worse than ever. I’ve posted results from Nov. to May. See below. In Nov, I was on 88 Levo four times a week and 75 for the rest. My TSH was 1.32.( Range: 0.20 – 5.00) FT3 and FT4 haven’t changed as much.
Hello to all, My TSH has gone way up even though I’ve been increasing the dose, and I feel worse than ever. I’ve posted results from Nov. to May. See below. In Nov, I was on 88 Levo four times a week and 75 for the rest. My TSH was 1.32.( Range: 0.20 – 5.00) FT3 and FT4 haven’t changed as much.
Koola
in
Thyroid UK
3 years ago
My New Supplement List (I cut a bunch of players)
I just cut out a bunch of supplements. These are what I removed (I may add things back. I was taking too many): 1 -Idebenone (is being trialed to slow progression of REMSBD to PD/LBD). Thanks gginto and Ponieboy! Lion's Mane is back on the stack! 3 - NAC. 4 - Glycine. 5 - Magnesium L-Threonate. 6 -
I just cut out a bunch of supplements. These are what I removed (I may add things back. I was taking too many): 1 -Idebenone (is being trialed to slow progression of REMSBD to PD/LBD). Thanks gginto and Ponieboy! Lion's Mane is back on the stack! 3 - NAC. 4 - Glycine. 5 - Magnesium L-Threonate. 6 -
Bolt_Upright
in
Cure Parkinson's
3 years ago
Newly ectopic
Hi, I have been lurking here a few weeks. I was glad to find this community. 3.5 weeks ago woke at 4am feeling horrendous with my heart thudding in my chest. Ended up going to GP and to hospital, told by both that I had an ectopic beat. I felt like death warmed up - had no energy for two weeks. Gradually
Hi, I have been lurking here a few weeks. I was glad to find this community. 3.5 weeks ago woke at 4am feeling horrendous with my heart thudding in my chest. Ended up going to GP and to hospital, told by both that I had an ectopic beat. I felt like death warmed up - had no energy for two weeks. Gradually
CurlyPretzel
in
Arrhythmia Alliance
3 years ago
Hot Flashes
Third night with no hot flashes, even reduced during day. Just from 450 MG of magnesium clycinate an hour or two before bedtime. Whoever recommended it, thank 😊
Third night with no hot flashes, even reduced during day. Just from 450 MG of magnesium clycinate an hour or two before bedtime. Whoever recommended it, thank 😊
spencoid2
in
Advanced Prostate Cancer
3 years ago
Brain Fog
I almost have night hot flashes solved. They are very minor now using magnesium. I have accepted my sporadic muscle weakness cramping etc. I still need to learn to not do stupid things. Yesterday I rescued an old blind dog who got stuck in the creek near our house. I fell into a patch of poison oak but
I almost have night hot flashes solved. They are very minor now using magnesium. I have accepted my sporadic muscle weakness cramping etc. I still need to learn to not do stupid things. Yesterday I rescued an old blind dog who got stuck in the creek near our house. I fell into a patch of poison oak but
spencoid2
in
Advanced Prostate Cancer
3 years ago
Whats going on with me (long)
I don’t even know where to start with my issue because its so bazaar and annoying. Two months ago I went to see a neurologist about a weird burning skin sensation that I have had for a year and only effects the tops of my feet and hands and occasionally my entire body (sunburn sensation) without the
I don’t even know where to start with my issue because its so bazaar and annoying. Two months ago I went to see a neurologist about a weird burning skin sensation that I have had for a year and only effects the tops of my feet and hands and occasionally my entire body (sunburn sensation) without the
Batty1
in
Thyroid UK
3 years ago
Please help with my results
Hello All. I live in The US and was hoping for some help on my blood work. I am seeing a functional practitioner for my Hashimoto but had to find another practitioner because I moved. She changed my medication to 25 mcg of Cytomel and 60 mcg NP thyroid. I am taking 10,000 IU D3, 450 mg Magnesium, 1000
Hello All. I live in The US and was hoping for some help on my blood work. I am seeing a functional practitioner for my Hashimoto but had to find another practitioner because I moved. She changed my medication to 25 mcg of Cytomel and 60 mcg NP thyroid. I am taking 10,000 IU D3, 450 mg Magnesium, 1000
TXFiona
in
Thyroid UK
3 years ago
Magnesium Supplements
I'm taking 350mg soluble magnesium carbonate every other day, as suggested by my GP before I was diagnosed. However, I have read that Magnesium Glycinate is specifically recommended for absorption and also as a sleep aid of sorts. Would welcome any feedback - i.e. what dose should be taken daily
I'm taking 350mg soluble magnesium carbonate every other day, as suggested by my GP before I was diagnosed. However, I have read that Magnesium Glycinate is specifically recommended for absorption and also as a sleep aid of sorts. Would welcome any feedback - i.e. what dose should be taken daily
Pr0jection
in
PMRGCAuk
3 years ago
latest blood results
Hi everyone last year just at the beginning of covid i had an accident and smashed my shoulder it's still not right at first didn't feel too bad but over the last 5 months i have felt rotten no energy, hair falling out, weight gain, got no eyebrows now,dry skin swollen with water retention and worst
Hi everyone last year just at the beginning of covid i had an accident and smashed my shoulder it's still not right at first didn't feel too bad but over the last 5 months i have felt rotten no energy, hair falling out, weight gain, got no eyebrows now,dry skin swollen with water retention and worst
foxyeyes
in
Thyroid UK
3 years ago
magnesium glycinate
I finally got my magnseium glycinate which is supposed to help with sleep? I can not find the post where it was recommended and need to know a suitable dose. I bought powder so I can make any dose I need. I also learned that prednesone might be keeping me awake so I am taking it at noon.
I finally got my magnseium glycinate which is supposed to help with sleep? I can not find the post where it was recommended and need to know a suitable dose. I bought powder so I can make any dose I need. I also learned that prednesone might be keeping me awake so I am taking it at noon.
spencoid2
in
Advanced Prostate Cancer
3 years ago
Nutrients to help repair your blood-brain barrier
Nicely put together page of useful information on things that (may?) help the blood brain barrier: Resveratrol Curcumin Sulforaphane: If you take sulforaphane in supplement form, make sure it contains the co-factor myrosinase. Vitamin D B vitamins. Several B vitamins support the health of the blood-brain
Nicely put together page of useful information on things that (may?) help the blood brain barrier: Resveratrol Curcumin Sulforaphane: If you take sulforaphane in supplement form, make sure it contains the co-factor myrosinase. Vitamin D B vitamins. Several B vitamins support the health of the blood-brain
Bolt_Upright
in
Cure Parkinson's
3 years ago
Low Oxalate Diet, an explanation for why it works
More than six years ago I found that I could turn my RLS discomforts on and off by controlling the amount of oxalate in my diet. My original breakthrough in understanding came after about 5 years of closely monitoring my diet and my daily discomfort level. Many people who conscientiously follow a
More than six years ago I found that I could turn my RLS discomforts on and off by controlling the amount of oxalate in my diet. My original breakthrough in understanding came after about 5 years of closely monitoring my diet and my daily discomfort level. Many people who conscientiously follow a
notnowdad
in
Restless Legs Syndrome
3 years ago
Probiotics
Hello I am waiting to do my next fet. I’m taking vitamin d, folic acid and magnesium. I’ve heard of people taking probiotics can I ask what this is for and what kind you take? Thank you
Hello I am waiting to do my next fet. I’m taking vitamin d, folic acid and magnesium. I’ve heard of people taking probiotics can I ask what this is for and what kind you take? Thank you
Boo718
in
Fertility Network UK
3 years ago
A&E Experience
So on Friday night, I went to be with AF, I took a Flecainide and tried to sleep. I work up in the night very hot and sweaty. After finally getting some sleep I work up still experiencing AF. Doing some regular checks on my Apple Watch my heart rate was fluctuating between 70 - 202 for no reason.
So on Friday night, I went to be with AF, I took a Flecainide and tried to sleep. I work up in the night very hot and sweaty. After finally getting some sleep I work up still experiencing AF. Doing some regular checks on my Apple Watch my heart rate was fluctuating between 70 - 202 for no reason.
Hidden
in
AF Association
3 years ago
Too much B12
I think I’ve overdone it on the B12....!!! 😩 I had annual leave last week so I decided to SI daily hydroxocobalamin alongside taking a sublingual Cyano, 400mcg folic acid, magnesium, calcium, B Complex and an electrolyte drink (9 days in a row) and then after 2 days break I SI Cyano for the first time
I think I’ve overdone it on the B12....!!! 😩 I had annual leave last week so I decided to SI daily hydroxocobalamin alongside taking a sublingual Cyano, 400mcg folic acid, magnesium, calcium, B Complex and an electrolyte drink (9 days in a row) and then after 2 days break I SI Cyano for the first time
User2020-1
in
Pernicious Anaemia Society
3 years ago
Nowhere left to go, all out of options now
I wrote here 4 months ago that I would have to stop both Tiromel & Metavive as my BP went haywire. I tried to stop metavive (having stopped T3) however I became too ill to last more than about 3 days without. My TSH feedback look is crippled, & cortisol in the gutter + I cannot produce any T4 - for
I wrote here 4 months ago that I would have to stop both Tiromel & Metavive as my BP went haywire. I tried to stop metavive (having stopped T3) however I became too ill to last more than about 3 days without. My TSH feedback look is crippled, & cortisol in the gutter + I cannot produce any T4 - for
Jenny583
in
Thyroid UK
3 years ago
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