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Magnesium sulphate
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Bloodwork results-what do you think?
I followed testing guidelines (testing before 9 am no levothyroxine for 24 hours). I asked to have my ferritin tested, but the nurse told me they would only test that if my magnesium blood test came back abnormal. I was previously on 25 mcg of levothyroxine and they bumped me up to 50 mcg. They wanted
I followed testing guidelines (testing before 9 am no levothyroxine for 24 hours). I asked to have my ferritin tested, but the nurse told me they would only test that if my magnesium blood test came back abnormal. I was previously on 25 mcg of levothyroxine and they bumped me up to 50 mcg. They wanted
spookyscaryskeletons
in
Thyroid UK
3 years ago
Private GP? Can they help?
Hi all, I have ordered a private blood tests this morning thanks to this group. Long story short I’m on 75mg of LEVO and have been for 6 years. I have been working with a PT on a calorie controlled gluten free diet for over 6 weeks with little results. The PT suggested I looked into T3 conversation
Hi all, I have ordered a private blood tests this morning thanks to this group. Long story short I’m on 75mg of LEVO and have been for 6 years. I have been working with a PT on a calorie controlled gluten free diet for over 6 weeks with little results. The PT suggested I looked into T3 conversation
Staceoglasgow
in
Thyroid UK
3 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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Supplement timing
Hey just wanted to check in on timing the following supplements and if you would add any others in or increase the amount. I take 150mg of Levothyroxine in the morning an hour before anything but water. I eat a gluten free diet and am careful about cross contamination. Sadly disnt get tested before
Hey just wanted to check in on timing the following supplements and if you would add any others in or increase the amount. I take 150mg of Levothyroxine in the morning an hour before anything but water. I eat a gluten free diet and am careful about cross contamination. Sadly disnt get tested before
Flowerpot108
in
Thyroid UK
3 years ago
Advice re inconsistent and above range FT4 please.
Apologies in advance for long post. GP made me have annual review blood test 21/12/21. Test was done at 8.20am, 24 hours after last dose of levo (150 mcg) and fasting apart from water. Please note, my TSH always appears suppressed because I take Metformin. TSH 0.01mu/L (0.35 - 4.94)
Apologies in advance for long post. GP made me have annual review blood test 21/12/21. Test was done at 8.20am, 24 hours after last dose of levo (150 mcg) and fasting apart from water. Please note, my TSH always appears suppressed because I take Metformin. TSH 0.01mu/L (0.35 - 4.94)
grumpyold
in
Thyroid UK
3 years ago
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
3 years ago
I Can't Keep Up This Stack :(
Update 6/29/22: Berberine may be neurotoxic. It is off of my stack: https://healthunlocked.com/cure-parkinsons/posts/148177820/finding-some-negatives-on-berberine-i-will-keep-digging ========= You all are so much stronger than I am. Or maybe you are living your lives instead of obsessing over things
Update 6/29/22: Berberine may be neurotoxic. It is off of my stack: https://healthunlocked.com/cure-parkinsons/posts/148177820/finding-some-negatives-on-berberine-i-will-keep-digging ========= You all are so much stronger than I am. Or maybe you are living your lives instead of obsessing over things
Bolt_Upright
in
Cure Parkinson's
3 years ago
CSR episode update.
I finally was able to see my retina specialist to ask him questions about my reoccurring CSR. He was able to look at all of my previous scans. When I was able to see him my bleed had gone down it had been close to about 3 1/2 weeks almost a month. It has since then almost completely flattened. That’
I finally was able to see my retina specialist to ask him questions about my reoccurring CSR. He was able to look at all of my previous scans. When I was able to see him my bleed had gone down it had been close to about 3 1/2 weeks almost a month. It has since then almost completely flattened. That’
T109
in
Macular Society
3 years ago
How to Increase BDNF
So somebody over on FB posted they were taking BDNF for PD anxiety (or maybe just for anxiety) so I Googled and found BDNF = Brain-Derived Neurotrophic Factor and BDNF supplements do not contain Brain-Derived Neurotrophic Factor. But I did find this article on strongcoffee.com. https://strongcoffeecompany.com
So somebody over on FB posted they were taking BDNF for PD anxiety (or maybe just for anxiety) so I Googled and found BDNF = Brain-Derived Neurotrophic Factor and BDNF supplements do not contain Brain-Derived Neurotrophic Factor. But I did find this article on strongcoffee.com. https://strongcoffeecompany.com
Bolt_Upright
in
Cure Parkinson's
3 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
3 years ago
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
3 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
3 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
3 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
3 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
3 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
3 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
3 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
3 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
3 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
3 years ago
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