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Im am on myofort 760 mg twice a day.I been tested for c diff and negative.plus after complaining about the diarrhea finally they ordered stool tests plus others and all negative. I went and researched magnesium and started a product called mag glycinate as it is gentle on gi system and since starting
Im am on myofort 760 mg twice a day.I been tested for c diff and negative.plus after complaining about the diarrhea finally they ordered stool tests plus others and all negative. I went and researched magnesium and started a product called mag glycinate as it is gentle on gi system and since starting
Parkerbarker
in
Kidney Transplant
2 years ago
vitamins with ranges as l could not work out how to edit posted again sorry đ hope it makes sense now âșïž
serum iron 19.6 umol/l (5.8-34.5 iron binding 63 umol/lu Unbound iron binding 43 umol/l (24.2-70.1) percentage iron saturation 31% (15.0-40.0) alkaline phosphatease level92u/l(35.0-104.0) lplasma alanine aminotransferase level ? 18 u/l (0.0-35.0) Serum total bilirubin level 6 umolL (0.0-35.0
serum iron 19.6 umol/l (5.8-34.5 iron binding 63 umol/lu Unbound iron binding 43 umol/l (24.2-70.1) percentage iron saturation 31% (15.0-40.0) alkaline phosphatease level92u/l(35.0-104.0) lplasma alanine aminotransferase level ? 18 u/l (0.0-35.0) Serum total bilirubin level 6 umolL (0.0-35.0
Hidden
in
Thyroid UK
2 years ago
bloods vit count they claim normal ?
serum iron 19.6 umol/l iron binding 63 umol/l unbound iron binding 43 umol/l percentage iron saturation 31%alkaline phosphatease level 92 u/l plasma alanine aminotransferase level ? 18 u/l serum total bilirubin level 6 umol/l serum total protein level 69 g/l plasma globulin level 33 g/l serum
serum iron 19.6 umol/l iron binding 63 umol/l unbound iron binding 43 umol/l percentage iron saturation 31%alkaline phosphatease level 92 u/l plasma alanine aminotransferase level ? 18 u/l serum total bilirubin level 6 umol/l serum total protein level 69 g/l plasma globulin level 33 g/l serum
Hidden
in
Thyroid UK
2 years ago
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Advice needed
I had kidney transplant 3 months ago and it has been a living hell.I have ibs to begin with and for three months my intestines have been getting destroyed from meds.I have chronic watery diarrhea to the point that i cant leave my home for more then 2 hours and if i do i need to have a bathroom close
I had kidney transplant 3 months ago and it has been a living hell.I have ibs to begin with and for three months my intestines have been getting destroyed from meds.I have chronic watery diarrhea to the point that i cant leave my home for more then 2 hours and if i do i need to have a bathroom close
Parkerbarker
in
Kidney Transplant
2 years ago
Iron, Magnesium & Red light Therapy.
Hi I'm a 62 year old who has had mild to moderate RLS for about 3 decades. It took me some time to realize that it was restless leg syndrome that was causing my insomnia. After just putting up with it for years I finally set about researching the condition and trying to find some solutions. I have tried
Hi I'm a 62 year old who has had mild to moderate RLS for about 3 decades. It took me some time to realize that it was restless leg syndrome that was causing my insomnia. After just putting up with it for years I finally set about researching the condition and trying to find some solutions. I have tried
Rested
in
Restless Legs Syndrome
2 years ago
Looking for Ideas please
Hi there, I have had RLS since my early 20s and am now 56. My symptoms have got worse over the years and I have been managing them with stretching, holding legs in the air, kicking legs out, compressing blood supply to offending leg for short periods, plus various supplements, mainly magnesium. Symptoms
Hi there, I have had RLS since my early 20s and am now 56. My symptoms have got worse over the years and I have been managing them with stretching, holding legs in the air, kicking legs out, compressing blood supply to offending leg for short periods, plus various supplements, mainly magnesium. Symptoms
Bramblespaniel
in
Restless Legs Syndrome
2 years ago
A vagal manoeuvre to tryâŠ
Hello All, I wanted to share with you something that worked for me a couple of weeks ago for my paroxysmal Afib. We had friends over and I took a risk, of not only a very spicy Indian takeaway meal, but it arrived very late and I went to bed just over two hours after eating it đł so a double risky combination
Hello All, I wanted to share with you something that worked for me a couple of weeks ago for my paroxysmal Afib. We had friends over and I took a risk, of not only a very spicy Indian takeaway meal, but it arrived very late and I went to bed just over two hours after eating it đł so a double risky combination
Teresa156
in
Atrial Fibrillation Support
2 years ago
Compression boots w/heat
Hello, So far the only the only things I have found to help my severe RLS is 15 mgs of methodone w/400 mgs of magnesium (long term fix about 24 hrs), hot baths with epsom salt (short term fix, maybe 30 mins.) Being how I do NOT want to be on methodone for ever. I am looking for other solutions.
Hello, So far the only the only things I have found to help my severe RLS is 15 mgs of methodone w/400 mgs of magnesium (long term fix about 24 hrs), hot baths with epsom salt (short term fix, maybe 30 mins.) Being how I do NOT want to be on methodone for ever. I am looking for other solutions.
Anguished
in
Restless Legs Syndrome
2 years ago
Advice on tablets if liquid thyroxine is still unavailable.
Hi all Having seen my GP today to discuss the lack of liquid thyroxine, she tells me that they cannot just discontinue providing it on the NHS as there are several patients that can't take thyroxine in any other form. It seems it is all cost related and pharmacies don't want to order it and be out
Hi all Having seen my GP today to discuss the lack of liquid thyroxine, she tells me that they cannot just discontinue providing it on the NHS as there are several patients that can't take thyroxine in any other form. It seems it is all cost related and pharmacies don't want to order it and be out
Tintin0202
in
Thyroid UK
2 years ago
Any help?
I am pretty much at my wits end with insomnia. My Father recently passed away, and I have struggled with Ă nxiety for many years. I actually live in Thailand, and have been seeing a psychiatrist for years, and I have been prescribed 0.5 MG clonazepam 2 times a day, and 2mg clonazepam at night, but
I am pretty much at my wits end with insomnia. My Father recently passed away, and I have struggled with Ă nxiety for many years. I actually live in Thailand, and have been seeing a psychiatrist for years, and I have been prescribed 0.5 MG clonazepam 2 times a day, and 2mg clonazepam at night, but
patez
in
Mental Health Support
2 years ago
Help &advice, next steps with endo
Recently found this wonderful site and this is my first time posting after lurking for a few weeks gaining knowledge. I'm worried my endo will discharge me at my appointment next month as im "in range" even though I still dont feel right, so looking for advice. I was diagnosed Hyper/Graves June 2021
Recently found this wonderful site and this is my first time posting after lurking for a few weeks gaining knowledge. I'm worried my endo will discharge me at my appointment next month as im "in range" even though I still dont feel right, so looking for advice. I was diagnosed Hyper/Graves June 2021
JUUJOO
in
Thyroid UK
2 years ago
YoYo TSH, any advice appreciated
I didnât want to hijack Rollercoasterâs post as Iâve been on a bit of a rollercoaster myself, so starting a new topic, thanks everyone for all input and advice - this is an amazing group for support and information I was diagnosed with Hashis in Dec 21 by my 1st endo with:
TSH 4.97 (Range 0.35
I didnât want to hijack Rollercoasterâs post as Iâve been on a bit of a rollercoaster myself, so starting a new topic, thanks everyone for all input and advice - this is an amazing group for support and information I was diagnosed with Hashis in Dec 21 by my 1st endo with:
TSH 4.97 (Range 0.35
Kriticat
in
Thyroid UK
2 years ago
Liothyronine and metavive dosage advice
was on Armour in first half of year 1.5 grain tsh around 2.4 Then in summer July swapped to Metatvive bovine 80mg am 40mg pm to try save money but only just had bloods so been about 12 weeks and tsh 5.23! Also fought to get liothyronine again so asked for 15 mcg 3 x 5mg pills On the conversion
was on Armour in first half of year 1.5 grain tsh around 2.4 Then in summer July swapped to Metatvive bovine 80mg am 40mg pm to try save money but only just had bloods so been about 12 weeks and tsh 5.23! Also fought to get liothyronine again so asked for 15 mcg 3 x 5mg pills On the conversion
Merlio18
in
Thyroid UK
2 years ago
Help with blood test results please?
My hair has been falling out lately so I'm just back from doc's where she pronounced everything as "normal" but said my Thyroid and Calcium were both low. She didn't even test T3 so God only knows how she decided my Thyroid was low! The rest of the results were: Iron 116
My hair has been falling out lately so I'm just back from doc's where she pronounced everything as "normal" but said my Thyroid and Calcium were both low. She didn't even test T3 so God only knows how she decided my Thyroid was low! The rest of the results were: Iron 116
infomaniac
in
Thyroid UK
2 years ago
Advice required
My visit to the Endo was again very painful and unhelpful. It is supposed to be one of the best hospitals in the country but yet again failed to be very helpful. Not only that, the dr. got wrong the info re my current medication twice so the level of listening and engagement was not 100%, obviously.
My visit to the Endo was again very painful and unhelpful. It is supposed to be one of the best hospitals in the country but yet again failed to be very helpful. Not only that, the dr. got wrong the info re my current medication twice so the level of listening and engagement was not 100%, obviously.
Carlax
in
Thyroid UK
2 years ago
Gentle Iron
The Gentle Iron I ordered came in today. I read all your advice about taking it and thought the advice was to take it at night. To my surprise, it has B12 in it.! B12 is my energy supplement- I canât take it at night! So, do I take it morning or noon? These supplements and meds are getting very confusing
The Gentle Iron I ordered came in today. I read all your advice about taking it and thought the advice was to take it at night. To my surprise, it has B12 in it.! B12 is my energy supplement- I canât take it at night! So, do I take it morning or noon? These supplements and meds are getting very confusing
agapepilgrim
in
My MSAA Community
2 years ago
fragile spine and multiple fractures
I am a just turned 70 year old woman who has developed IBD in the last few years and have been hospitalised three times in the last year or so with it. Each time I have received IV corticosteroids followed by 8 weeks of Prednisolone orally. Each of the two previous occasions was followed by terrible
I am a just turned 70 year old woman who has developed IBD in the last few years and have been hospitalised three times in the last year or so with it. Each time I have received IV corticosteroids followed by 8 weeks of Prednisolone orally. Each of the two previous occasions was followed by terrible
Valerie0106
in
Bone Health and Osteoporosis UK
2 years ago
Self Care Time
What are you doing for self care? I am thinking we can collect a bunch of ideas on here to potentially try. I am needing self care but having trouble thinking of something that sounds good to me right now⊠- Light candles - meditate - eat extra healthy - take magnesium - calming tea - facial
What are you doing for self care? I am thinking we can collect a bunch of ideas on here to potentially try. I am needing self care but having trouble thinking of something that sounds good to me right now⊠- Light candles - meditate - eat extra healthy - take magnesium - calming tea - facial
Starrlight
in
Anxiety and Depression Support
2 years ago
Can oral B12 supplements help in a functional B12 deficiency and more q's
As a follow on from my first post here: https://healthunlocked.com/pasoc/posts/148543562/help-with-diagnosis-gp-and-anyone-sought-help-from-private-healthcare , I visited Dr K at Nuffield on Friday at Cambridge and he strongly suspects I have non-autoimmune functional B12 deficiency and based on history
As a follow on from my first post here: https://healthunlocked.com/pasoc/posts/148543562/help-with-diagnosis-gp-and-anyone-sought-help-from-private-healthcare , I visited Dr K at Nuffield on Friday at Cambridge and he strongly suspects I have non-autoimmune functional B12 deficiency and based on history
Beccy_123
in
Pernicious Anaemia Society
2 years ago
B12 loading doses
Hey guys, I have recently received 4/6 of my loadind doses of b12. When I reached the 3rd injection, the day after, I started to twitch a lot mostly in my arms and legs but also the odd twitch in my back or neck (doesnt occur very often). I have read about nerves "waking up" so to speak, but the injections
Hey guys, I have recently received 4/6 of my loadind doses of b12. When I reached the 3rd injection, the day after, I started to twitch a lot mostly in my arms and legs but also the odd twitch in my back or neck (doesnt occur very often). I have read about nerves "waking up" so to speak, but the injections
Hidden
in
Pernicious Anaemia Society
2 years ago
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