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Magnesium oxide
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Magnesium for palpitations
Hi all, Just wondering what type of magnesium you take to improve palpitations. I have been taking magnesium citrate but on reading up I think magnesium taurate may be the current one? I have not had much luck with the citrate. If anyone has had any improvements with magnesium can you share which
Hi all, Just wondering what type of magnesium you take to improve palpitations. I have been taking magnesium citrate but on reading up I think magnesium taurate may be the current one? I have not had much luck with the citrate. If anyone has had any improvements with magnesium can you share which
Compostella1
in
Thyroid UK
2 years ago
Fibromyalgia In PD And Some Potential Relief
Fibromyalgia (FM) is slightly more common in people with PD and FM can cause all over body pain that moves around and can affect tissues, joints and muscles. This group of people with PD and FM are more likely to get dementia and have worse symptoms. FM can cause painful flare-ups at random times, but
Fibromyalgia (FM) is slightly more common in people with PD and FM can cause all over body pain that moves around and can affect tissues, joints and muscles. This group of people with PD and FM are more likely to get dementia and have worse symptoms. FM can cause painful flare-ups at random times, but
chartist
in
Cure Parkinson's
2 years ago
Very dry eyes and constipation linked to dose decrease?
So me going down from 112mcgs to 100mcgs failed after 3 weeks. No blood test to confirm it yet but I'm supposed to get more blood work done at the end of the month. But are dry eyes a hypo symptom? Also started having bad constipation and bloat. Magnesium Citrate 600mgs a day doesn't seem to be working
So me going down from 112mcgs to 100mcgs failed after 3 weeks. No blood test to confirm it yet but I'm supposed to get more blood work done at the end of the month. But are dry eyes a hypo symptom? Also started having bad constipation and bloat. Magnesium Citrate 600mgs a day doesn't seem to be working
T808
in
Thyroid UK
2 years ago
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Test Results
I am having hypothyroid symptoms which are becoming worse. Tinnitus, tendinopathy, loss of muscle/strength, brain fog, weight gain, osteo arthritis, dry brittle hair, loss of body hair, air hunger, tiredness, don't have the energy output to walk fast for long etc. My results in August 2021 are - CRP
I am having hypothyroid symptoms which are becoming worse. Tinnitus, tendinopathy, loss of muscle/strength, brain fog, weight gain, osteo arthritis, dry brittle hair, loss of body hair, air hunger, tiredness, don't have the energy output to walk fast for long etc. My results in August 2021 are - CRP
Dramlouie
in
Thyroid UK
2 years ago
Maybe RS3PE on top of the PMR
Has anyone had RS3PE with pain but no swelling? My hands are not swollen but the backs of them are so sore and painful. I haven’t had this pain in the backs of my hands before in my PMR journey. So sick of this blasted illness and the pain. I am on 5 mg but in so much pain everywhere today and have
Has anyone had RS3PE with pain but no swelling? My hands are not swollen but the backs of them are so sore and painful. I haven’t had this pain in the backs of my hands before in my PMR journey. So sick of this blasted illness and the pain. I am on 5 mg but in so much pain everywhere today and have
SusyTe
in
PMRGCAuk
2 years ago
What does a leg blood clot feel like? Going to docs shortly-
Hi, 33F with very controlled Behcets, never had a DVT- Left calf has been cramped since thursday. Been good about water, magnesium, walking, changing shoes. This morning I woke up with more left leg cramps, a dull but consistent one, and had trouble walking (leg kept giving out on me). I am very physically
Hi, 33F with very controlled Behcets, never had a DVT- Left calf has been cramped since thursday. Been good about water, magnesium, walking, changing shoes. This morning I woke up with more left leg cramps, a dull but consistent one, and had trouble walking (leg kept giving out on me). I am very physically
rooser1
in
Behçet's UK
2 years ago
DEXA scan - help please interpreting my results and help with my suggested regime to improve my bone density
I would be very grateful if somebody could kindly help me to interpret my DEXA bone density results. I am not an expert regarding this but it's clear to me I need to improve my bone density however if somebody could kindly interpret my results in more detail I would be very grateful. I think the
I would be very grateful if somebody could kindly help me to interpret my DEXA bone density results. I am not an expert regarding this but it's clear to me I need to improve my bone density however if somebody could kindly interpret my results in more detail I would be very grateful. I think the
SarahBa
in
Bone Health and Osteoporosis UK
2 years ago
How to get from 1mg to 0 pred
I was diagnosed with PMR in Oct 20 on 15mg and in April 21 told it was highly unlikely I ever had PMR and just needed to now getting off steroids . At that point I was on 9mg and got down to 3 mg pretty easily by Sept ish using DSNS . Below that has been hard but now finally trying to get from 1mg
I was diagnosed with PMR in Oct 20 on 15mg and in April 21 told it was highly unlikely I ever had PMR and just needed to now getting off steroids . At that point I was on 9mg and got down to 3 mg pretty easily by Sept ish using DSNS . Below that has been hard but now finally trying to get from 1mg
Sydney0503
in
PMRGCAuk
2 years ago
Timings for Supplements
Good morning everyone. Now that I'm over a month into my Levo prescription (50mcg trial agreed to by GP with some gentle persuasion from fabulous knowledge from you all ;)) I'm looking to start adding some supplements in gradually to try to get my vitamin levels back on track. My D3 was low so GP has
Good morning everyone. Now that I'm over a month into my Levo prescription (50mcg trial agreed to by GP with some gentle persuasion from fabulous knowledge from you all ;)) I'm looking to start adding some supplements in gradually to try to get my vitamin levels back on track. My D3 was low so GP has
AtemiM
in
Thyroid UK
2 years ago
Is mineral water good or bad?
Unlike a lot of you who are petite, I'm medium frame and slightly overweight. When I was diagnosed with op, I started going overboard on things like almonds and cheese. I now realize I've gained 10 pounds that might cause other health issues if I don't stop it I take a few supplements, (D3 and K2 MK7
Unlike a lot of you who are petite, I'm medium frame and slightly overweight. When I was diagnosed with op, I started going overboard on things like almonds and cheese. I now realize I've gained 10 pounds that might cause other health issues if I don't stop it I take a few supplements, (D3 and K2 MK7
Bubba3xt
in
Osteoporosis Support
2 years ago
Any hints for diet and/or lifestyle living with PMR?
I’ve been living with the condition for approx 18 months now, and from what I read here my experience is pretty standard; in fact, I’m probably getting off lightly compared to some. I almost managed to taper to no pred, but had a (possible) mild flare a couple of months ago which has responded well to
I’ve been living with the condition for approx 18 months now, and from what I read here my experience is pretty standard; in fact, I’m probably getting off lightly compared to some. I almost managed to taper to no pred, but had a (possible) mild flare a couple of months ago which has responded well to
calibriel
in
PMRGCAuk
2 years ago
What vitamin D dose do you take?
Could I ask what vitamin D dose you take please? I could barely walk 4 years ago, and my levels were around 22, and was prescribed the loading dose, and told to take 800iu for a few weeks thereafter. After discovering this forum, I was told to take several thousand iu, I can’t remember the exact dose
Could I ask what vitamin D dose you take please? I could barely walk 4 years ago, and my levels were around 22, and was prescribed the loading dose, and told to take 800iu for a few weeks thereafter. After discovering this forum, I was told to take several thousand iu, I can’t remember the exact dose
CornishChick
in
Thyroid UK
2 years ago
Another disappointing endocrinologist - Cornwall
I know I am unable to discuss individual Doctors here, but thought it might help others to mention what happened at my NHS endo meeting. I saw a female endo via the NHS yesterday, who is based in Truro, Cornwall and off Thyroid UKs list of Endos who (amongst other things) may help with low DHEA (my
I know I am unable to discuss individual Doctors here, but thought it might help others to mention what happened at my NHS endo meeting. I saw a female endo via the NHS yesterday, who is based in Truro, Cornwall and off Thyroid UKs list of Endos who (amongst other things) may help with low DHEA (my
CornishChick
in
Thyroid UK
2 years ago
Medichecks results
Good morning everyone These are my latest results from Medichecks from last week I followed guidance from here with regard to blood being drawn before 9am nothing to eat or drink before hand and last dose of thyroxine 24 hours before test .Also stopped Thorne Basic B complex 7 days before test. I am
Good morning everyone These are my latest results from Medichecks from last week I followed guidance from here with regard to blood being drawn before 9am nothing to eat or drink before hand and last dose of thyroxine 24 hours before test .Also stopped Thorne Basic B complex 7 days before test. I am
Starmen
in
Thyroid UK
2 years ago
16+ years since dx and what we’ve learned
I’ve posted before about our trials with synthetic and natural levadopa but after reading Dr. Jonathan Sackner-Bernstein‘s essay, I wanted to shout a big “hooray”! I’ve long suspected levadopa was doing more harm than good and that the whole idea that PD being all about dopamine deficiency was in some
I’ve posted before about our trials with synthetic and natural levadopa but after reading Dr. Jonathan Sackner-Bernstein‘s essay, I wanted to shout a big “hooray”! I’ve long suspected levadopa was doing more harm than good and that the whole idea that PD being all about dopamine deficiency was in some
Bfp69
in
Cure Parkinson's
2 years ago
BLOOD TEST RESULTS FROM 22/02/2022 taken at 7.45AM
Hi all, once again could you knowledgeable people please pass comment on my most recent results. Unfortunately due to dr requesting follow up test within two months the lab has rejected some of the tests, annoyingly, I wanted to know if my vitamin intake and iron tablets may have improved my ferritin
Hi all, once again could you knowledgeable people please pass comment on my most recent results. Unfortunately due to dr requesting follow up test within two months the lab has rejected some of the tests, annoyingly, I wanted to know if my vitamin intake and iron tablets may have improved my ferritin
DarkHorseJen
in
Thyroid UK
2 years ago
New regime
Hi everyone, well I’ve come a little way since I last posted. I’m now taking: Vitamin D3 5000iu daily Vitamin K2 100 mcg daily Folic acid 5 mg per day Magnesium 200mg two tablets B6 complex 1 tablet a day and a B12 injection once a month (was once a week.) My last tests on Monday came back as: Vitamin
Hi everyone, well I’ve come a little way since I last posted. I’m now taking: Vitamin D3 5000iu daily Vitamin K2 100 mcg daily Folic acid 5 mg per day Magnesium 200mg two tablets B6 complex 1 tablet a day and a B12 injection once a month (was once a week.) My last tests on Monday came back as: Vitamin
Hidden
in
Pernicious Anaemia Society
2 years ago
Lactulose and Bones
I have just been reading that lactulose inhibits bone loss in post menopausal women AND increases absorption of Vit D, calcium and magnesium. Has anybody else come across this?. It seems too good to be true. I was looking at the safety of using it long term as since I have had osteoporosis I have been
I have just been reading that lactulose inhibits bone loss in post menopausal women AND increases absorption of Vit D, calcium and magnesium. Has anybody else come across this?. It seems too good to be true. I was looking at the safety of using it long term as since I have had osteoporosis I have been
Daisi124
in
Osteoporosis Support
2 years ago
Magnesium question - another one!
I used to take Magnesium to try and help the symptoms of my AF. I still have permanent AF but also a Pacemaker, so I stopped taking it. I am wondering what others in this community think.
I used to take Magnesium to try and help the symptoms of my AF. I still have permanent AF but also a Pacemaker, so I stopped taking it. I am wondering what others in this community think.
Barb1
in
AF Association
2 years ago
Feeling more like my 'old self'
I was diagnosed with AFIB in October 2020 at the age of 79. Since then I have been on a learning curve about an ailment of which I had little prior knowledge. Health Unlocked with its daily mail bag of the trials and sufferings of fellow AFibbers has been a valuable source of information. During
I was diagnosed with AFIB in October 2020 at the age of 79. Since then I have been on a learning curve about an ailment of which I had little prior knowledge. Health Unlocked with its daily mail bag of the trials and sufferings of fellow AFibbers has been a valuable source of information. During
Shyman
in
AF Association
2 years ago
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