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Magnesium Query
Hi, I am looking to supplement magnesium & after reading some very helpful information on this forum, I think I need magnesium malate to help with muscle & joint pain & fatigue. Could anyone please recommend a brand or dosage as there are so many to choose from online! Thank you lots Xx
Hi, I am looking to supplement magnesium & after reading some very helpful information on this forum, I think I need magnesium malate to help with muscle & joint pain & fatigue. Could anyone please recommend a brand or dosage as there are so many to choose from online! Thank you lots Xx
Liz599
in
Thyroid UK
2 years ago
Timing of Nutrient / Vitamin Regime for Hashimotos
UPDATE Aug 2022 below post. ORIGINAL POST April 2022: Dear all, I don’t post very often as my Hashimotos condition seems to be quite manageable. I feel good, but the only thing I would like to address is my inability to lose weight. I am expecting a full blood result back any day, at which point
UPDATE Aug 2022 below post. ORIGINAL POST April 2022: Dear all, I don’t post very often as my Hashimotos condition seems to be quite manageable. I feel good, but the only thing I would like to address is my inability to lose weight. I am expecting a full blood result back any day, at which point
CBDB
in
Thyroid UK
2 years ago
Foods trigger dystonia?
I'm trying to ween my self of sugar, I'm doing pretty good , but every once in awhile cravings are overwhelming , I made gluten free namasta rice flour pancakes, no sugar except maple syrup, strawberries/blueberries , last week I ate during the day and notice toes curling when waiting for Carbidopa
I'm trying to ween my self of sugar, I'm doing pretty good , but every once in awhile cravings are overwhelming , I made gluten free namasta rice flour pancakes, no sugar except maple syrup, strawberries/blueberries , last week I ate during the day and notice toes curling when waiting for Carbidopa
akgirlsrock
in
Cure Parkinson's
2 years ago
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TUMS as a good source of calcium? No.
As I understand it, there are different types of calcium, and they are not all equally absorbed. I was told that calcium citrate is best if you can’t get sufficient calcium from your diet. I am easily getting 1200 mg by drinking three 8 oz glasses of skim milk daily.
As I understand it, there are different types of calcium, and they are not all equally absorbed. I was told that calcium citrate is best if you can’t get sufficient calcium from your diet. I am easily getting 1200 mg by drinking three 8 oz glasses of skim milk daily.
IndianaLady
in
Osteoporosis Support
2 years ago
Latest results and some advice please.
Hello I posted on here last year for advice on my blood test results and had some very helpful replies. My latest test results from 12/04/22 at 7am. Ft4- 14.6 pmol/L (9.1- 17.6) FT3- 3.9 pmol/L (2.4- 6.0) TSH- 0.04 mu/L (0.35- 4.9) Thyroid peroxidase antibodies 62 iu/m/L (0.0- 6.0) Ferritin 98
Hello I posted on here last year for advice on my blood test results and had some very helpful replies. My latest test results from 12/04/22 at 7am. Ft4- 14.6 pmol/L (9.1- 17.6) FT3- 3.9 pmol/L (2.4- 6.0) TSH- 0.04 mu/L (0.35- 4.9) Thyroid peroxidase antibodies 62 iu/m/L (0.0- 6.0) Ferritin 98
Jphill49
in
Thyroid UK
2 years ago
Taking various medications .Do any contraindication taking Magnesium as a supplement.
I find it virtually impossible to contact my GP to ask the question.13 in queue for triage.E consult gives no simple choices & says I need to contact GP. I take Omeprazol,Adizem.citrizine,bendromethafluizide,Edoxaban, candesartan,Simvistatin. Any help & advice welcome. UPDATE I spoke to Arythmia nurse
I find it virtually impossible to contact my GP to ask the question.13 in queue for triage.E consult gives no simple choices & says I need to contact GP. I take Omeprazol,Adizem.citrizine,bendromethafluizide,Edoxaban, candesartan,Simvistatin. Any help & advice welcome. UPDATE I spoke to Arythmia nurse
kkatz
in
Atrial Fibrillation Support
2 years ago
AF and Cognitive Decline
There has been a lot in the news here in Australia over the past week or so about the link between AF and cognitive decline/dementia. As someone who is caring for a mother with dementia, it is not good news. That said, at least I'm on anti-coagulants and my AF is under control thanks to my ablations,
There has been a lot in the news here in Australia over the past week or so about the link between AF and cognitive decline/dementia. As someone who is caring for a mother with dementia, it is not good news. That said, at least I'm on anti-coagulants and my AF is under control thanks to my ablations,
Kaz747
in
AF Association
2 years ago
Omeprazole
Hope I’m right, yesterday had dreadful cramping both hands lasted nearly 3 hrs So painful. After it subsided I reviewed me medication, starting with Omeprazole Read this
.
**********************
Long-term side effects.
If you take omeprazole for more than 3
Hope I’m right, yesterday had dreadful cramping both hands lasted nearly 3 hrs So painful. After it subsided I reviewed me medication, starting with Omeprazole Read this
.
**********************
Long-term side effects.
If you take omeprazole for more than 3
Ronzy
in
PMRGCAuk
2 years ago
Magnesium Supplements - Fatigue & Migraines
I have suffered with awful migraines since not long after I was diagnosed with APS. I have another auto immune condition, inflammatory arthritis which is bad in my neck causing a lot of my migraines (when my INR is good and in range). Environmental factors also affect them too. In the early days of my
I have suffered with awful migraines since not long after I was diagnosed with APS. I have another auto immune condition, inflammatory arthritis which is bad in my neck causing a lot of my migraines (when my INR is good and in range). Environmental factors also affect them too. In the early days of my
chelb29
in
Hughes Syndrome APS Forum
2 years ago
EOD makes symptoms much worse!
Injectioning EOD, my neurological symptoms seem to get much worse. Is that healing or my body trying to get rid of the b12. If I wait by the 4th day I feel better. I wonder if I could still heal if I took it weekly. If I take massive doses of folate, it seems to help the symptoms. I take Vitamin D, Magnesium
Injectioning EOD, my neurological symptoms seem to get much worse. Is that healing or my body trying to get rid of the b12. If I wait by the 4th day I feel better. I wonder if I could still heal if I took it weekly. If I take massive doses of folate, it seems to help the symptoms. I take Vitamin D, Magnesium
38yroldmale
in
Pernicious Anaemia Society
2 years ago
Heart failure
My husband has been diagnosed with heart failure and want to know if Magnesium Bisglycinate is good for him
My husband has been diagnosed with heart failure and want to know if Magnesium Bisglycinate is good for him
Gabdt
in
British Heart Foundation
2 years ago
Tingling hands and wrists, fatigue, achey but also feelings my system is wound up? Is this a flare up?
I am in a complete dilemma. I am experiencing all the above symptoms and I'm not sure why it is. It could be two things, but whatever the cause, I am feeling pretty yucky, which is really annoying because I was doing quite well apart from menopausal flushing. First possible cause is that I've finished
I am in a complete dilemma. I am experiencing all the above symptoms and I'm not sure why it is. It could be two things, but whatever the cause, I am feeling pretty yucky, which is really annoying because I was doing quite well apart from menopausal flushing. First possible cause is that I've finished
Hidden
in
Thyroid UK
2 years ago
Really lost.
so so fed up and in tears. The self injecting of B12 is going well, not arranged re checking of bloods yet going to ask in a few months. So I am fat, have carried extra fat for a few years, but seems to have got out of hand last couple. Early last year had all sorts of blood done after insisting
so so fed up and in tears. The self injecting of B12 is going well, not arranged re checking of bloods yet going to ask in a few months. So I am fat, have carried extra fat for a few years, but seems to have got out of hand last couple. Early last year had all sorts of blood done after insisting
Polo22
in
Pernicious Anaemia Society
2 years ago
Test results - GP vs Blue Horizon with ranges
Good morning all. I will try to include all the info this time. I am currently taking 50mcg levothyroxine and 20 mcg of liothyronine. If I put BH results first and then GP, the layout might work better BH CRP 0.91 (<5.0) mg/L Ferritin 249 (High) (13 - 150 ) ug/L magnesium 0.98 (0.66 - 0.99) mmol
Good morning all. I will try to include all the info this time. I am currently taking 50mcg levothyroxine and 20 mcg of liothyronine. If I put BH results first and then GP, the layout might work better BH CRP 0.91 (<5.0) mg/L Ferritin 249 (High) (13 - 150 ) ug/L magnesium 0.98 (0.66 - 0.99) mmol
OllyTojo
in
Thyroid UK
2 years ago
Me fighting back
Got my armamentarium today (: starting with B1 n Mucuna first n will see if I need to add s adenosyl methionine. Not taking KCl for now n sticking to magnesium for my RLS
Got my armamentarium today (: starting with B1 n Mucuna first n will see if I need to add s adenosyl methionine. Not taking KCl for now n sticking to magnesium for my RLS
Divii
in
Cure Parkinson's
2 years ago
Can’t sleep
I dunno why I can’t sleep ; took dopamine (I have YOPD), dopamine agonist to take care of RLS, magnesium to calm me down, warm shower , massaged my feet with lukewarm mustard oil, rubbed peppermint oil on pillow, put cucumbers on eyes but still can’t.. been three hours!
I dunno why I can’t sleep ; took dopamine (I have YOPD), dopamine agonist to take care of RLS, magnesium to calm me down, warm shower , massaged my feet with lukewarm mustard oil, rubbed peppermint oil on pillow, put cucumbers on eyes but still can’t.. been three hours!
Divii
in
Sleep Matters
2 years ago
Morley Robbins magnesium man, his theory on degenerative brain/ most diseases, what's your opinion on this theory.
https://www.gotmag.org/1656-2/ Magnesium is a given, it's the iron I'm concerned about.
https://www.gotmag.org/1656-2/ Magnesium is a given, it's the iron I'm concerned about.
akgirlsrock
in
Cure Parkinson's
2 years ago
Recent results
Recent results can someone tell me what this means . I’m on levithyroxine 50/75mcg alternate days.. obviously under medicated as I know tsh should be under 2. But don’t know what ft3 and ft4 mean Ft3 4 (3.1-6.8) Ft4 17.5 (12-22) Tsh 2.44 (0.5-4.2) Ferritin 30 (13-150) Haemoglobin 142 (112-155) Vit d
Recent results can someone tell me what this means . I’m on levithyroxine 50/75mcg alternate days.. obviously under medicated as I know tsh should be under 2. But don’t know what ft3 and ft4 mean Ft3 4 (3.1-6.8) Ft4 17.5 (12-22) Tsh 2.44 (0.5-4.2) Ferritin 30 (13-150) Haemoglobin 142 (112-155) Vit d
Holiday12345
in
Thyroid UK
2 years ago
News that worried us and studies that gave us hope (04/2022).
This is the information that gave us hope while my father was alive and has given hope to many since then (March 2012). 1. News that worried us. In the coming decades the number of Parkinson's disease patients is feared to increase very worryingly, to double by 2030 (Dorsey 2007) and even to triple
This is the information that gave us hope while my father was alive and has given hope to many since then (March 2012). 1. News that worried us. In the coming decades the number of Parkinson's disease patients is feared to increase very worryingly, to double by 2030 (Dorsey 2007) and even to triple
parkinsonshereandnow
in
Cure Parkinson's
2 years ago
Club Bed
Happy New Year Beautiful People! I have been living wirh chronic fatigue since 2013 and still struggling I have been in bed on and off since last year October, more in bed than off. This is terrible, i struggle to make my bed, clean myself, prepare and cook meals, i have an active 15 year old and
Happy New Year Beautiful People! I have been living wirh chronic fatigue since 2013 and still struggling I have been in bed on and off since last year October, more in bed than off. This is terrible, i struggle to make my bed, clean myself, prepare and cook meals, i have an active 15 year old and
PaigeyPaigeForLife
in
Myalgic Encephalomyelitis Community
2 years ago
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