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magnesium
what is the maximum dose of magnesium do people take for AF? I’ve seen on here that you need to take a high dose but Google says too much is not good for you
what is the maximum dose of magnesium do people take for AF? I’ve seen on here that you need to take a high dose but Google says too much is not good for you
babs1234
in
Atrial Fibrillation Support
22 hours ago
long read: asking for community help deciding next steps -- worsening RLS/PLMD, medications, Neurologist, no sleep, HRT
Hi everyone, I haven’t been around in a long while because I’ve been unwell and dealing with family matters. I always feel guilty popping back in after a long while but I’ve not been able to maintain any sort of consistency the last several months. Up until I started HRT I was alright with what I
Hi everyone, I haven’t been around in a long while because I’ve been unwell and dealing with family matters. I always feel guilty popping back in after a long while but I’ve not been able to maintain any sort of consistency the last several months. Up until I started HRT I was alright with what I
HappyGreenBean
in
Restless Legs Syndrome
2 days ago
Constant visual disturbances for 9 weeks
Hi all, I've been having chronic migraines since catching COVID in 2022. I had a bad run of 7 migraines over a week, 9 and a half weeks ago. Which led to the room shaking constantly, whether my eyes are open or closed. The room shaking is one of my signs a migraine is coming on for me, and this time
Hi all, I've been having chronic migraines since catching COVID in 2022. I had a bad run of 7 migraines over a week, 9 and a half weeks ago. Which led to the room shaking constantly, whether my eyes are open or closed. The room shaking is one of my signs a migraine is coming on for me, and this time
Bluemoon37
in
Migraine Support
2 days ago
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I'm RLS free now and want to share how
Hi! As a person more or less RLS free I want to share something. I had to abondone Emoxypine (you can find my original post here) after the initial 7 days course. An elevated level of dopamine caused indigestion in my guts. After some time it became obvious. Now I'm more or less RLS free, since it was
Hi! As a person more or less RLS free I want to share something. I had to abondone Emoxypine (you can find my original post here) after the initial 7 days course. An elevated level of dopamine caused indigestion in my guts. After some time it became obvious. Now I'm more or less RLS free, since it was
Alex2308
in
Restless Legs Syndrome
2 days ago
drop in medication from November
My GP did an annual review in November last year . Since then they have dropped my medication twice so now I’m on 75 Levothyroxine. I haven’t been feeling very well since and slowly going down hill . TSH. T4. T3 3/11/23.
My GP did an annual review in November last year . Since then they have dropped my medication twice so now I’m on 75 Levothyroxine. I haven’t been feeling very well since and slowly going down hill . TSH. T4. T3 3/11/23.
andepande
in
Thyroid UK
3 days ago
Fibre supplements safe & dairy free diets?
Hi I developed C in February, though i think it could be just when i eat fodmaps but im not sure yet. And also due to being on dairy free diet now (anyone else cut out dairy and then struggled with C? and how did you cope? Consultant told me to take Fybrogel but it has sweeteners in it (bad for gut
Hi I developed C in February, though i think it could be just when i eat fodmaps but im not sure yet. And also due to being on dairy free diet now (anyone else cut out dairy and then struggled with C? and how did you cope? Consultant told me to take Fybrogel but it has sweeteners in it (bad for gut
LFHell
in
IBS Network
5 days ago
Positive Update
I previously asked on this forum for advice for my husband in relation to a rls specialist in Ireland. This led to loads of great advice and knowledge in relation to the management of his severe rls as per Mayo Clinic Algorithm. He started taking magnesium glycinate 400 mg, Vitamin B12 and Vitamin D3
I previously asked on this forum for advice for my husband in relation to a rls specialist in Ireland. This led to loads of great advice and knowledge in relation to the management of his severe rls as per Mayo Clinic Algorithm. He started taking magnesium glycinate 400 mg, Vitamin B12 and Vitamin D3
Minijackrussell
in
Restless Legs Syndrome
5 days ago
T3/t4 and supplement spacing
I take t4/t3 in morning 6am and t3 afternoon 12noon and tea time 5pm.I also supplement vit d3 with magnesium glycinate at bedtime 11pm I'm going to start high strength vit c with zinc but am unsure spacing between t3, does anyone know how long after taking t3 I can take vit c/zinc?
I take t4/t3 in morning 6am and t3 afternoon 12noon and tea time 5pm.I also supplement vit d3 with magnesium glycinate at bedtime 11pm I'm going to start high strength vit c with zinc but am unsure spacing between t3, does anyone know how long after taking t3 I can take vit c/zinc?
Geegee777
in
Thyroid UK
5 days ago
Advice on latest test results please
Hello All I'd really appreciate some advice on my latest test results below. Since my last post a few months back I've started taking Metavive II - one in the morning and one at lunchtime. I've been on a pretty strict PK diet, B12 by SI, magnesium by SI, eating liver min once a week, quit working for
Hello All I'd really appreciate some advice on my latest test results below. Since my last post a few months back I've started taking Metavive II - one in the morning and one at lunchtime. I've been on a pretty strict PK diet, B12 by SI, magnesium by SI, eating liver min once a week, quit working for
feistyone
in
Thyroid UK
6 days ago
Vestibular Migraine/ PPPD Or Something Else
I'm at my wits end really. I'm a mid 50's female, my balance issue started very abruptly in April 2022. I have had very sporadic, classic migraine with aura since my teens but could go for years between attacks. I was diagnosed with hypothyroid in 2020 and around that time I noticed my migraines got
I'm at my wits end really. I'm a mid 50's female, my balance issue started very abruptly in April 2022. I have had very sporadic, classic migraine with aura since my teens but could go for years between attacks. I was diagnosed with hypothyroid in 2020 and around that time I noticed my migraines got
Sparklingsunshine
in
National Migraine Centre
6 days ago
Reducing to 25mcg Levo only
Hi all. Just wondered if anyone has ended up on 25 mcg Levo only (no T3 or NDT) as an ongoing, not starter dose? Just had my bloods back (below) and my TSH remains low and T3 high despite dropping from 75 to 50 Levo 3 months ago. TSH .01 ( .3 - 4.2 ) T4 15 ( 9 - 19 ) T3 5.9 ( 3 - 5.4 ) GP
Hi all. Just wondered if anyone has ended up on 25 mcg Levo only (no T3 or NDT) as an ongoing, not starter dose? Just had my bloods back (below) and my TSH remains low and T3 high despite dropping from 75 to 50 Levo 3 months ago. TSH .01 ( .3 - 4.2 ) T4 15 ( 9 - 19 ) T3 5.9 ( 3 - 5.4 ) GP
Amber-sky
in
Thyroid UK
7 days ago
Undiagnosed Hypothyroidism
I've been experiencing hypothyroid symptoms for a couple of years now. My TSH has been steadily creeping up, but so far has remained in the "normal" range when checked in my local surgery, around 3.4. I had some private tests done and my TSH was shown as 4.4 (June) and 5.9 (August). My second test
I've been experiencing hypothyroid symptoms for a couple of years now. My TSH has been steadily creeping up, but so far has remained in the "normal" range when checked in my local surgery, around 3.4. I had some private tests done and my TSH was shown as 4.4 (June) and 5.9 (August). My second test
gelatin
in
Thyroid UK
7 days ago
What on earth is going on with my T4?
I've just got my latest test results back. I am currently on100mcg levothyroxine which was raised from 75 in June. However my T4 levels have significantly decreased since June despite the rise in levo. My TSH results have also decreased. Can anyone explain what is likely to be going on? I've also had
I've just got my latest test results back. I am currently on100mcg levothyroxine which was raised from 75 in June. However my T4 levels have significantly decreased since June despite the rise in levo. My TSH results have also decreased. Can anyone explain what is likely to be going on? I've also had
TheSnufkin
in
Thyroid UK
8 days ago
Any help welcomed with my bloods. I'm so confused.
Hi All these were my blood test results 3 months ago. Ferritin 13 Serum iron 17 range 10-30 Serum transferrin 3 range 2.0-4.0 Transferrin saturation 22.6% range 20-50. Serum cortisol 500 nmol Serum selenium 1.01 0.75-1.46 TSH 3.9 RANGE 0.55-4.78 Free T3 4.4 3.5-6.5 T4 11.2 range 11.5-22.0 Antibodies
Hi All these were my blood test results 3 months ago. Ferritin 13 Serum iron 17 range 10-30 Serum transferrin 3 range 2.0-4.0 Transferrin saturation 22.6% range 20-50. Serum cortisol 500 nmol Serum selenium 1.01 0.75-1.46 TSH 3.9 RANGE 0.55-4.78 Free T3 4.4 3.5-6.5 T4 11.2 range 11.5-22.0 Antibodies
Tinkerbell_84
in
Thyroid UK
8 days ago
Supplements
Does magnesium threonate have a negative effect on your thyroid medication? Are there any other supplements that affect thyroid meds. Thanks in advance.
Does magnesium threonate have a negative effect on your thyroid medication? Are there any other supplements that affect thyroid meds. Thanks in advance.
Puddingym
in
Thyroid UK
9 days ago
digoxin
Hi everyone, went into AF and landed up in A/E last Thursday, have been on 10mg bisoprolol daily for a while. I was given magnesium and metoprolol through a drip. I was told that if that doesn’t work they would start me on Digoxin. My question!! Is digoxin a safe drug and if anyone else is on it, did
Hi everyone, went into AF and landed up in A/E last Thursday, have been on 10mg bisoprolol daily for a while. I was given magnesium and metoprolol through a drip. I was told that if that doesn’t work they would start me on Digoxin. My question!! Is digoxin a safe drug and if anyone else is on it, did
Blueflags
in
Atrial Fibrillation Support
11 days ago
Supplement absorption
I posted the other day about being newly diagnosed and I received loads of brilliant support and advice from people on here about supplements and lifestyle changes that can help with PD progression. I haven’t yet managed to do all the recommended reading but I’m working on it. I’m still looking into
I posted the other day about being newly diagnosed and I received loads of brilliant support and advice from people on here about supplements and lifestyle changes that can help with PD progression. I haven’t yet managed to do all the recommended reading but I’m working on it. I’m still looking into
SallyBeeBobs
in
Cure Parkinson's
12 days ago
RR chart questions KardiaMobile Card
Kardia question Background: I am 78 years old and live in the US. I have had some A-fib for brief times, but not recently. I have had all sorts of tests, including a bike stress test at the Cardio doctor over the years, and I have no physical issues with my heart. In A-fib, my HR has never been above
Kardia question Background: I am 78 years old and live in the US. I have had some A-fib for brief times, but not recently. I have had all sorts of tests, including a bike stress test at the Cardio doctor over the years, and I have no physical issues with my heart. In A-fib, my HR has never been above
davephx
in
Atrial Fibrillation Support
12 days ago
Magnesium?
I’ve been trying to boost my vitamins and built in magnesium. I’ve also been reading the recent research that this could be a real wonder supplement across a range of issues? So it’s attractive! But that aside, I don’t think it’s agreeing with me. I’m (or was) taking a capsule a day, 80mg magnesium from
I’ve been trying to boost my vitamins and built in magnesium. I’ve also been reading the recent research that this could be a real wonder supplement across a range of issues? So it’s attractive! But that aside, I don’t think it’s agreeing with me. I’m (or was) taking a capsule a day, 80mg magnesium from
Calceolaria
in
Thyroid UK
12 days ago
Very belated intro
I've had rls since I was in my teens. I'm now 66 years old. About 6-7 years ago, I was finally diagnosed with RLS, and given a medication that I can't recall the exact name of, but it was something like lebadopa carbadopa?? Anyway, that worked very well for me at first, but after a few months it would
I've had rls since I was in my teens. I'm now 66 years old. About 6-7 years ago, I was finally diagnosed with RLS, and given a medication that I can't recall the exact name of, but it was something like lebadopa carbadopa?? Anyway, that worked very well for me at first, but after a few months it would
GrandmaKarey
in
Restless Legs Syndrome
14 days ago
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