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Solgar Magnesium Citrate
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Starting to feel bad again
Hello everyone! (sorry for the long post) I posted here about a year ago in regards to my test results and my GP's certainty that my labs were normal. I was trying to find that past post so I could remember all the details, but I dont know if it's been deleted since? Or if I'm being technologically
Hello everyone! (sorry for the long post) I posted here about a year ago in regards to my test results and my GP's certainty that my labs were normal. I was trying to find that past post so I could remember all the details, but I dont know if it's been deleted since? Or if I'm being technologically
Starling87
in
Thyroid UK
2 years ago
Massive Headaches During Dialysis
I really need some help if there's anyone who can help. I am a "complex patient" who has Crohn's disease, bowel resections as well as ESRD. Chronic anemia too. Unlike most dialysis patients I have low magnesium, low potassium, low sodium. The headaches I have are excruciating. I take 4x 500mg
I really need some help if there's anyone who can help. I am a "complex patient" who has Crohn's disease, bowel resections as well as ESRD. Chronic anemia too. Unlike most dialysis patients I have low magnesium, low potassium, low sodium. The headaches I have are excruciating. I take 4x 500mg
sbrenn01
in
Kidney Disease
2 years ago
Stomach issues
Hello everyone, I'm almost 2 years in now with PA diagnosis. I get b12 injection once every 4 weeks. Things have gotten better but I still suffer from gastric problems. I've tried gluten free and other diets but I can't seem to pin down what type of food cause this low level pain in gut sometimes
Hello everyone, I'm almost 2 years in now with PA diagnosis. I get b12 injection once every 4 weeks. Things have gotten better but I still suffer from gastric problems. I've tried gluten free and other diets but I can't seem to pin down what type of food cause this low level pain in gut sometimes
25092
in
Pernicious Anaemia Society
2 years ago
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Vitamins?
I've been struggling with asthma which comes and goes - when it goes I am fine - this might last for month. I have restrictive lung disease - where a person of my height should be able to breath in 400 I can only breath in 200 at best, sometimes only 75. I've been researching all of this a lot for
I've been struggling with asthma which comes and goes - when it goes I am fine - this might last for month. I have restrictive lung disease - where a person of my height should be able to breath in 400 I can only breath in 200 at best, sometimes only 75. I've been researching all of this a lot for
amberbrown
in
Asthma Community Forum
2 years ago
Low eGFR
I volunteered for a PD-related research study but was excluded because of a low eGFR (58 and then 43). I’ve never had this before (it was 68 five months ago), but I wondered if it was possibly related to the Magnesium L-Threonate I take? I take two in the morning and two at night. Anyone have experience
I volunteered for a PD-related research study but was excluded because of a low eGFR (58 and then 43). I’ve never had this before (it was 68 five months ago), but I wondered if it was possibly related to the Magnesium L-Threonate I take? I take two in the morning and two at night. Anyone have experience
jocelyng
in
Cure Parkinson's
2 years ago
still here and still clear
Hi all Just to let you know I still keep an eye out for your posts, It's been 4years now since my RF ablation and I am very pleased to report that I am still AF free apart from a few ectopic's which I treat with magnesium turate I am in great shape. if anyone is in doubt about having an ablation
Hi all Just to let you know I still keep an eye out for your posts, It's been 4years now since my RF ablation and I am very pleased to report that I am still AF free apart from a few ectopic's which I treat with magnesium turate I am in great shape. if anyone is in doubt about having an ablation
Brizzy50000
in
AF Association
2 years ago
Cystitis looming
I think I’m about to suffer from cystitis shortly if not already started. All the classic symptoms are beginning. I want to nip it in the bud. . Given it is nearly 5 pm onFriday, can anyone advise if it’s ok to take Cystocalm a Sodium citrate otc powder sachets whilst on Levo?... thanks
I think I’m about to suffer from cystitis shortly if not already started. All the classic symptoms are beginning. I want to nip it in the bud. . Given it is nearly 5 pm onFriday, can anyone advise if it’s ok to take Cystocalm a Sodium citrate otc powder sachets whilst on Levo?... thanks
App1
in
Thyroid UK
2 years ago
further thyroid Blood results
hoping someone can help, as utterly feel a shaking mess, ive been having ongoing panic attacks , jitters etc, several visits to a&e and blood panels done. Supplementing vits magnesium , Vit D and selenium. As mentioned on a previous thread ive a goiter and hashi’s and its swelling alot most nights
hoping someone can help, as utterly feel a shaking mess, ive been having ongoing panic attacks , jitters etc, several visits to a&e and blood panels done. Supplementing vits magnesium , Vit D and selenium. As mentioned on a previous thread ive a goiter and hashi’s and its swelling alot most nights
Void1234
in
Thyroid UK
2 years ago
Hmmmm..... results in - should I be pleased or not ??
Hello wonderful people, Following a thyroid and vitamin blood test with Medichecks in May this year, my GP increased my Levo from 75mcg to 100mcg (yaay). I have recently had an NHS blood test and was tested for TSH...... T4 AND T3 .... (another yay). Not sure how to interpret the results and was hoping
Hello wonderful people, Following a thyroid and vitamin blood test with Medichecks in May this year, my GP increased my Levo from 75mcg to 100mcg (yaay). I have recently had an NHS blood test and was tested for TSH...... T4 AND T3 .... (another yay). Not sure how to interpret the results and was hoping
goingholiday
in
Thyroid UK
2 years ago
allergic to benralizumab today started on mepolizumab feeling rough
hey so after 2 stat doses of first biologics I had to go back to mdt to be discussed as was reacting within minutes each time and requiring close monitoring for 4hrs both times. So today started mepo within 5 mins same but not quite so severe I feel rubbish. They've now added benralizumab to my list
hey so after 2 stat doses of first biologics I had to go back to mdt to be discussed as was reacting within minutes each time and requiring close monitoring for 4hrs both times. So today started mepo within 5 mins same but not quite so severe I feel rubbish. They've now added benralizumab to my list
mylungshateme
in
Asthma Community Forum
2 years ago
Hi hope everyone is well. Went to my dr to check thyroid bloods. I was on 112 T4 and 25 mcg of T3. My dr. Raised my T3 meds from 25-50.
Is that too large an increase all at once. I’ll give results below thanks. Total T4-5.1. Range 0.27-4.20. Free T4 1.3 Range 0.9-1.8. Free T3-2.44. Range1.80-4.60. T-3 71. Range 80-200. This was red flagged and caused dr. To raise my T3 meds. TSH is 0.01. It’s always that low as I have secondary
Is that too large an increase all at once. I’ll give results below thanks. Total T4-5.1. Range 0.27-4.20. Free T4 1.3 Range 0.9-1.8. Free T3-2.44. Range1.80-4.60. T-3 71. Range 80-200. This was red flagged and caused dr. To raise my T3 meds. TSH is 0.01. It’s always that low as I have secondary
Nanny23
in
Thyroid UK
2 years ago
Need someone Knowledgeable in adhd medications
Hi, I'm here for my 10yr old grandson. He was 48" tall and 48 lbs almost 2 years ago. He Looks more like 7 yrs old. He has been taking concerta for the last 3 years until about 2 months ago. It's good for him, but he will not grow and will not eat. Plus, it makes him have horrible constipation
Hi, I'm here for my 10yr old grandson. He was 48" tall and 48 lbs almost 2 years ago. He Looks more like 7 yrs old. He has been taking concerta for the last 3 years until about 2 months ago. It's good for him, but he will not grow and will not eat. Plus, it makes him have horrible constipation
sisymay
in
CHADD's ADHD Parents Together
2 years ago
advice on oestrogen and magnesium welcomed. ..lingering fatigue
hi all I would welcome some advice on lingering fatigue. I am on a trial of t3 with nhs endo. Currently on 75mcg t4 and 15 t3. I am fairly well on this. Given that endo is highly unlikely to change this as he wants my tsh higher, I am thinking this is me now. However t3 allows me to exercise and
hi all I would welcome some advice on lingering fatigue. I am on a trial of t3 with nhs endo. Currently on 75mcg t4 and 15 t3. I am fairly well on this. Given that endo is highly unlikely to change this as he wants my tsh higher, I am thinking this is me now. However t3 allows me to exercise and
BiscuitBaby
in
Thyroid UK
2 years ago
Rectocele Cystocele Prolapse.
i have been reading posts on this site. most of them over 5yrs old. I have been diagnosed by :Gynecologist: cholorectal: Urology, Gastroenterology. Tests : Endoscopy : Gastroscopy : Colonoscopy : Defacating Proctogram . : Colonic Transit
i have been reading posts on this site. most of them over 5yrs old. I have been diagnosed by :Gynecologist: cholorectal: Urology, Gastroenterology. Tests : Endoscopy : Gastroscopy : Colonoscopy : Defacating Proctogram . : Colonic Transit
Coolbug2591
in
Pelvic Pain Support Network
2 years ago
’not significant autoimmune involvement’? Help! NHS rheumatologist now wants to discharge me? Positive ANA
hi, I finally thought I’d get some answers & more importantly help! private rheumy was pretty sure it ‘all pointed towards lupus’ Could only afford initial consultation, GP referred me on nhs due to ongoing symptoms. I currently have: fatigue. Muscle spasms & aches, rash on face that comes & goes
hi, I finally thought I’d get some answers & more importantly help! private rheumy was pretty sure it ‘all pointed towards lupus’ Could only afford initial consultation, GP referred me on nhs due to ongoing symptoms. I currently have: fatigue. Muscle spasms & aches, rash on face that comes & goes
Frenchfancy
in
LUPUS UK
2 years ago
Feeling low
Hi hope everyone’s ok? Since being diagnosed a few months ago I’ve had quite a few flare ups, I take medication from the doctor, plus vit d, magnesium citrate, cbd, use Epsom salts to soak my feet in, have tried a flotation tank, go to a fibromyalgia support group but had to stop as can’t go at the
Hi hope everyone’s ok? Since being diagnosed a few months ago I’ve had quite a few flare ups, I take medication from the doctor, plus vit d, magnesium citrate, cbd, use Epsom salts to soak my feet in, have tried a flotation tank, go to a fibromyalgia support group but had to stop as can’t go at the
Fibro_fairy
in
Fibromyalgia Action UK
2 years ago
Seeing endo on Monday – question about low TSH/hypothyroidism
Hi all, I’m still working to get an official diagnosis for the complicated mess of adrenal/thyroid/pituitary conditions I’ve been experiencing for the past few years and have a much-awaited appt with my endo on Monday. I get super nervous before any appts for fear of not communicating clearly enough
Hi all, I’m still working to get an official diagnosis for the complicated mess of adrenal/thyroid/pituitary conditions I’ve been experiencing for the past few years and have a much-awaited appt with my endo on Monday. I get super nervous before any appts for fear of not communicating clearly enough
slowtraveller
in
Thyroid UK
2 years ago
Magnesium and other Supplements
Anyone taking Magnesium for their arrhythmia's or otherwise? If so, what kind -- citrate, succinate, taurate, etc? -- and what dose of mg are you taking a day? Brand names welcome. And what has been your experience? Also, besides good for your heart rhythm, one of the benefits I've read is blood pressure
Anyone taking Magnesium for their arrhythmia's or otherwise? If so, what kind -- citrate, succinate, taurate, etc? -- and what dose of mg are you taking a day? Brand names welcome. And what has been your experience? Also, besides good for your heart rhythm, one of the benefits I've read is blood pressure
mjames1
in
Atrial Fibrillation Support
2 years ago
Magnesium L Threonate
has anyone had good results using magnesium L Threonate tablets, or any other suggestions to help with brain fog in PD please?
has anyone had good results using magnesium L Threonate tablets, or any other suggestions to help with brain fog in PD please?
Cherub-
in
Cure Parkinson's
2 years ago
Man Lost Ability to Walk After Taking Too Many Vitamin B6 Supplements
A man in Australia lost his ability to walk after consuming 70 times the recommended daily dose of vitamin B6, ABC Radio Melbourne reported. But 50 milligrams is much higher than the standard dose recommendation in both Australia and the US, which is 1.7 milligrams of vitamin B6 per day for men over
A man in Australia lost his ability to walk after consuming 70 times the recommended daily dose of vitamin B6, ABC Radio Melbourne reported. But 50 milligrams is much higher than the standard dose recommendation in both Australia and the US, which is 1.7 milligrams of vitamin B6 per day for men over
Hidden
in
Cure Parkinson's
2 years ago
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