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Trialling Levo only after an issue with NDT, severe headache subsided to a point, BUT now feeling brain fog, fatigue and very bloated belly.
On first diagnosis, I was prescribed Levothyroxine and reached 100mg until I became pregnant with twins 13 years ago and had to increase it to 300mg, put on tons of weight, and it wouldn't shift after the birth. Fatigue also plagued me. After no support from the NHS, I decided to try NDT, being Thyroid
On first diagnosis, I was prescribed Levothyroxine and reached 100mg until I became pregnant with twins 13 years ago and had to increase it to 300mg, put on tons of weight, and it wouldn't shift after the birth. Fatigue also plagued me. After no support from the NHS, I decided to try NDT, being Thyroid
Hidden
in
Thyroid UK
2 years ago
Before thyroid blood test…
hello, reaching out to you wonderful wise people again for some advice please- I’m seeing the endo in December for a follow up after increasing my meds to 100mcg levothyroxine for two months, for hashimotos. Sadly I feel worse, zero energy! Anyway, think I read here to not take levothyroxine morning
hello, reaching out to you wonderful wise people again for some advice please- I’m seeing the endo in December for a follow up after increasing my meds to 100mcg levothyroxine for two months, for hashimotos. Sadly I feel worse, zero energy! Anyway, think I read here to not take levothyroxine morning
Hopetoheal22
in
Thyroid UK
2 years ago
Magnesium D3
Daily dose for Hypothyroidism please?Magnesium type & amount? ( to help sleep & joint/muscle pain) D3 & K2 amount? Thank you
Daily dose for Hypothyroidism please?Magnesium type & amount? ( to help sleep & joint/muscle pain) D3 & K2 amount? Thank you
Topaz21
in
Thyroid UK
2 years ago
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Endo asking for calcium and magnesium blood tests
Hi, my private Endo is considering prescribing t3 and has asked for a whole range of tests before our next appointment. These include calcium and magnesium blood tests. I have read here that the magnesium test is not very accurate but leaving that aside I'm wondering: (a) what the tests might mean
Hi, my private Endo is considering prescribing t3 and has asked for a whole range of tests before our next appointment. These include calcium and magnesium blood tests. I have read here that the magnesium test is not very accurate but leaving that aside I'm wondering: (a) what the tests might mean
Pearlteapot
in
Thyroid UK
2 years ago
Lost, confused, worried - trying to conceive and thyroid/lining/progesterone issues
Looking for some help/guidance/support. Apologies in advance for the long post. My husband and I, both 31 and healthy, have been trying to conceive for a year now with no success. We've both had a number of tests and through my own reading and persistent private re-testing have identified my thyroid
Looking for some help/guidance/support. Apologies in advance for the long post. My husband and I, both 31 and healthy, have been trying to conceive for a year now with no success. We've both had a number of tests and through my own reading and persistent private re-testing have identified my thyroid
er2012
in
Fertility Network UK
2 years ago
Lost/confused/worried - trying to conceive and thyroid function
Looking for some help/guidance/support. Apologies in advance for the long post. My husband and I, both 31 and healthy, have been trying to conceive for a year now with no success. We've both had a number of tests and through my own reading and persistent private re-testing have identified my thyroid
Looking for some help/guidance/support. Apologies in advance for the long post. My husband and I, both 31 and healthy, have been trying to conceive for a year now with no success. We've both had a number of tests and through my own reading and persistent private re-testing have identified my thyroid
er2012
in
Thyroid UK
2 years ago
RLS and Medication
Madlegs, Sue Johnson, Joolsg,Ladies, first I wish to thank you for all the help you give us. You are heaven sent angels I have been having RLS every night. I have to keep walking all night. It lasts till 7 AM. It was recommended that I discuss my medications with you ladies. The following are all
Madlegs, Sue Johnson, Joolsg,Ladies, first I wish to thank you for all the help you give us. You are heaven sent angels I have been having RLS every night. I have to keep walking all night. It lasts till 7 AM. It was recommended that I discuss my medications with you ladies. The following are all
Josana13
in
Restless Legs Syndrome
2 years ago
Any hope?
hey I’m 25 currently still waiting for a diagnosis. In absolute agony in my fingers and wrists, hips occasionally hurt and arm muscles feel weak and it all started with my back which is the main area of pain for me. (Entire back and spine hurts) just seems to be getting worse looking for some hope,
hey I’m 25 currently still waiting for a diagnosis. In absolute agony in my fingers and wrists, hips occasionally hurt and arm muscles feel weak and it all started with my back which is the main area of pain for me. (Entire back and spine hurts) just seems to be getting worse looking for some hope,
Amywoodx
in
NRAS
2 years ago
Celadrin, magnesium, vit d? Help
hey I’m currently still waiting for a diagnosis. In absolute agony in my fingers and wrists, hips occasionally hurt and arm muscles feel weak and it all started with my back which is the main area of pain for me. (Entire back and spine hurts) looking for some hope, has anyone tried Celadrin capsules
hey I’m currently still waiting for a diagnosis. In absolute agony in my fingers and wrists, hips occasionally hurt and arm muscles feel weak and it all started with my back which is the main area of pain for me. (Entire back and spine hurts) looking for some hope, has anyone tried Celadrin capsules
Amywoodx
in
Pain Concern
2 years ago
RLS newbie
Hi all, I was hoping you could give me some advice about where to begin, as I'm finding reading through the posts, although very helpful, also overwhelming! I have self diagnosed as having RLS for about 20 years. It has been relatively ignorable until the last few years. Now it is affecting my sleep
Hi all, I was hoping you could give me some advice about where to begin, as I'm finding reading through the posts, although very helpful, also overwhelming! I have self diagnosed as having RLS for about 20 years. It has been relatively ignorable until the last few years. Now it is affecting my sleep
Awakeat3am
in
Restless Legs Syndrome
2 years ago
Another way to view and treat Parkinson's?
Transformative information: a chart from a study by Patrick Holford on depression. Providing nutrients to increase dopamine in a natural way instead of giving Levodopa?Almost the entire population is deficient in magnesium, zinc, all the vitamins of the B group, etc. Even more so in Parkinson's patients
Transformative information: a chart from a study by Patrick Holford on depression. Providing nutrients to increase dopamine in a natural way instead of giving Levodopa?Almost the entire population is deficient in magnesium, zinc, all the vitamins of the B group, etc. Even more so in Parkinson's patients
parkinsonshereandnow
in
Cure Parkinson's
2 years ago
Not everyone believes in zinc and vitamin D
I seem to end up following the wisdom of my elderly mum over diet and supplements as we seem to have rather similar health patterns. So like many on this board are fully signed up to adding vit D, zinc and magnesium. I read an article today from a group who call themselves the root cause protocol
I seem to end up following the wisdom of my elderly mum over diet and supplements as we seem to have rather similar health patterns. So like many on this board are fully signed up to adding vit D, zinc and magnesium. I read an article today from a group who call themselves the root cause protocol
Danielj1
in
Thyroid UK
2 years ago
Arythmia
Some thoughts. I had pretty bad arythmia and ended up in ICU twice in 2021 for a total of 14 days. Now its totally under control and here is what I did: 1) Eat very well, reducing carbs, sugar and eliminate Caffeine 2) Reduce alcohol consumption to a minimum 3) Increase Omega 3 and fibre intake to
Some thoughts. I had pretty bad arythmia and ended up in ICU twice in 2021 for a total of 14 days. Now its totally under control and here is what I did: 1) Eat very well, reducing carbs, sugar and eliminate Caffeine 2) Reduce alcohol consumption to a minimum 3) Increase Omega 3 and fibre intake to
Seiznem
in
Arrhythmia Alliance
2 years ago
Anyone clued up on bone health please?
I recently had a bone scan and was very concerned to learn that there had been severe degenerative changes to both my spine and hips which weren't expected as my scan 3 years ago wasn't bad. They did take me off Alendronic Acid 18 months ago at which time I also went gluten and dairy free (found out
I recently had a bone scan and was very concerned to learn that there had been severe degenerative changes to both my spine and hips which weren't expected as my scan 3 years ago wasn't bad. They did take me off Alendronic Acid 18 months ago at which time I also went gluten and dairy free (found out
Delgor
in
Thyroid UK
2 years ago
Thyroid and vitamin d possible side effects
Hi everyone. Quick question I've just lowered my thyroxine from 150/125 mg alternative to just 125mg everyday. I was getting weird anxiety and just mentally feeling unwell. Especially around 4-6pm. Now I'm little better after 3 months but occasionally I seem to be feeling mentally not right. I need
Hi everyone. Quick question I've just lowered my thyroxine from 150/125 mg alternative to just 125mg everyday. I was getting weird anxiety and just mentally feeling unwell. Especially around 4-6pm. Now I'm little better after 3 months but occasionally I seem to be feeling mentally not right. I need
MrTHG
in
Thyroid UK
2 years ago
Osteoporosis/alendronic acid
I have had a reasonably uneventful PMR journey so far 🤞. Diagnosed April 2020 slow pred reduction from 15mg now reducing 5.5mg/5m. I also take lansoprazole15mg/ vitamin D 800iu as prescribed by my GP since first diagnosis ( she said my diet was high enough in calcium) and following advice on this invaluable
I have had a reasonably uneventful PMR journey so far 🤞. Diagnosed April 2020 slow pred reduction from 15mg now reducing 5.5mg/5m. I also take lansoprazole15mg/ vitamin D 800iu as prescribed by my GP since first diagnosis ( she said my diet was high enough in calcium) and following advice on this invaluable
Clarbeston
in
PMRGCAuk
2 years ago
Vitamin confusion - advice please!
Hello, I have posted a few times previously and the advice given has always been so helpful, I'm hoping for the same again please! So, I'm trying to sort out my vitamin levels. I have taken supplements but then when I've run out I haven't been very good at buying again and then I go for weeks/ months
Hello, I have posted a few times previously and the advice given has always been so helpful, I'm hoping for the same again please! So, I'm trying to sort out my vitamin levels. I have taken supplements but then when I've run out I haven't been very good at buying again and then I go for weeks/ months
ElephantShoes
in
Thyroid UK
2 years ago
Been very hard to find a suitable multi-vit
I have been here long enough now to realise that I need only very select vits/mins in high quality and the right doses and absolutely do not need a ton of stuff that ordinarily gets put into the std packages eg iodine / iron/E/A/boron /B plus the rest etc etc But as I try to save packaging and costs
I have been here long enough now to realise that I need only very select vits/mins in high quality and the right doses and absolutely do not need a ton of stuff that ordinarily gets put into the std packages eg iodine / iron/E/A/boron /B plus the rest etc etc But as I try to save packaging and costs
Danielj1
in
Thyroid UK
2 years ago
magnesium spray Liothyronine
I take my second dose of Liothyronine at about 7.30 pm and use magnesium spray at about 10.30 pm. Should so leave more time in between? Also is there any risk of overdose and effects if used regularly? Thank you.
I take my second dose of Liothyronine at about 7.30 pm and use magnesium spray at about 10.30 pm. Should so leave more time in between? Also is there any risk of overdose and effects if used regularly? Thank you.
Flecmac
in
Thyroid UK
2 years ago
magnesium and heart benefits
Hi everyone I’ve been reading about magnesium citrate and it’s health benefits. Does anyone use this for heart health? Thanks
Hi everyone I’ve been reading about magnesium citrate and it’s health benefits. Does anyone use this for heart health? Thanks
Worvera
in
British Heart Foundation
2 years ago
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