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Magnesium sulphate
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Advice needed - before I lose the plot!
Evening all, looking for a little bit of advice. A few months ago my TSH which had been under control with levo had pretty much doubled within a couple of weeks, the Dr increased my meds from 100mcg to 125mcg. I left it 3 months before Re-testing through medichecks as I was unable to get a drs appointment
Evening all, looking for a little bit of advice. A few months ago my TSH which had been under control with levo had pretty much doubled within a couple of weeks, the Dr increased my meds from 100mcg to 125mcg. I left it 3 months before Re-testing through medichecks as I was unable to get a drs appointment
Henson1980
in
Thyroid UK
3 years ago
Help for a friend with corticobasal degeneration.
Dear forum friends: I have a friend who has been diagnosed with corticobasal degeneration. I can't find much specific information about this atypical parkinsonism. Except for Dr. Costantini's reference in the famous interview (number 30) or the comments on medical cannabis oil, I can't find any information
Dear forum friends: I have a friend who has been diagnosed with corticobasal degeneration. I can't find much specific information about this atypical parkinsonism. Except for Dr. Costantini's reference in the famous interview (number 30) or the comments on medical cannabis oil, I can't find any information
parkinsonshereandnow
in
Cure Parkinson's
3 years ago
Will coming off fluoxetine stop RLS?
I’ve been on fluoxetine for 9 yrs and had RLS for the past 3. Sometimes it seems to effect arm and side of face as well as legs, either down one side or another. Usually starts around 9pm. I sit in cold bath 2-3 x nightly to numb legs enough to get some sleep. It often wakes me up and I have to sit
I’ve been on fluoxetine for 9 yrs and had RLS for the past 3. Sometimes it seems to effect arm and side of face as well as legs, either down one side or another. Usually starts around 9pm. I sit in cold bath 2-3 x nightly to numb legs enough to get some sleep. It often wakes me up and I have to sit
Tesslegs
in
Restless Legs Syndrome
3 years ago
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Vitamin E for Restless Legs
Vitamin E for Restless Legs Please poke around on the Internet; i.e. do your own research. Good search term is perhaps: Vitamin E Restless legs Have been taking a number of Quality Supplements for years for good health. I take Vitamin E 800ug daily (2 ea Nature's Way 400ug Occasionally do NOT take
Vitamin E for Restless Legs Please poke around on the Internet; i.e. do your own research. Good search term is perhaps: Vitamin E Restless legs Have been taking a number of Quality Supplements for years for good health. I take Vitamin E 800ug daily (2 ea Nature's Way 400ug Occasionally do NOT take
johnnorthwest
in
Restless Legs Syndrome
3 years ago
Sifrol withdrawal, need Help Please.
Hello all together, I took my last Sifrol 66 days ago. I didn't go the cold turkey way, I started in November 2020 tapering to dosage of 0.03 Mg. (I started with 0.09mg 3 years ago) I don't have restlesslegs anymore. Since I quit i think I do have DAWS. Not all symptoms but extremely anxiety, panic
Hello all together, I took my last Sifrol 66 days ago. I didn't go the cold turkey way, I started in November 2020 tapering to dosage of 0.03 Mg. (I started with 0.09mg 3 years ago) I don't have restlesslegs anymore. Since I quit i think I do have DAWS. Not all symptoms but extremely anxiety, panic
Dina1234
in
Restless Legs Syndrome
3 years ago
Started Levo and wondering when I might start to feel better - any supplements I need to add?
I finally managed to get the GP to try me on 25mcg Levothyroxine, which I have been taking for just under a month now. My results before starting were TSH - 5.91 (0.34-5.60mu/l) Serum free T4 - 10.2 (7.9-20pmol/l) Serum T3 - 6.2 (4.00 - 6.60pmol/L) I have also stopped eating gluten, and am also taking
I finally managed to get the GP to try me on 25mcg Levothyroxine, which I have been taking for just under a month now. My results before starting were TSH - 5.91 (0.34-5.60mu/l) Serum free T4 - 10.2 (7.9-20pmol/l) Serum T3 - 6.2 (4.00 - 6.60pmol/L) I have also stopped eating gluten, and am also taking
Sleepybunny21
in
Thyroid UK
3 years ago
Does Magnesium really help
Magnesium is it worth the outlay
Magnesium is it worth the outlay
ford08
in
Mental Health Support
3 years ago
3 months on- Feeling better than I was
As in the title, after following advice given to me on here, by Seaside Susie and Slow Dragon….i feel much better. Not 100% but getting there I hope! I managed to get an appointment with a new doctor who agreed to raising the dose of my Levo by 25mcg which is what I had been trying for with no luck…
As in the title, after following advice given to me on here, by Seaside Susie and Slow Dragon….i feel much better. Not 100% but getting there I hope! I managed to get an appointment with a new doctor who agreed to raising the dose of my Levo by 25mcg which is what I had been trying for with no luck…
Hashibegone
in
Thyroid UK
3 years ago
Afib
At last, after 4 years my partner managed to get a trace of his palpitations on a heart monitor and he has been diagnosed with Afib. His consultant has told him to take a magnesium tablet daily to see if this helps. He has also mentioned an operation for Afib, has anyone had this operation and if so
At last, after 4 years my partner managed to get a trace of his palpitations on a heart monitor and he has been diagnosed with Afib. His consultant has told him to take a magnesium tablet daily to see if this helps. He has also mentioned an operation for Afib, has anyone had this operation and if so
kipper1958
in
IBS Network
3 years ago
Want to mange this thing!
I had catheter ablation for supraventricular Tachycardia in March and second one in June. Was told 2nd ablation would fix me, as the Electrophysiologist now knew what to do/where to ablate and would use special mapping equipment and higher powered catheters. He ablated SVT site and found a Flutter site
I had catheter ablation for supraventricular Tachycardia in March and second one in June. Was told 2nd ablation would fix me, as the Electrophysiologist now knew what to do/where to ablate and would use special mapping equipment and higher powered catheters. He ablated SVT site and found a Flutter site
Fabfibber
in
AF Association
3 years ago
Cramp!
Think I may have asked about this before but does anyone have a “ Go to” remedy for night cramps? These are really vicious in my calves & feet, have tried quinine (on the loo pretty much all day) drinking more, bananas, tonic water, magnesium tablets. After yet another bad night I’m really desperate!
Think I may have asked about this before but does anyone have a “ Go to” remedy for night cramps? These are really vicious in my calves & feet, have tried quinine (on the loo pretty much all day) drinking more, bananas, tonic water, magnesium tablets. After yet another bad night I’m really desperate!
gilox
in
NRAS
3 years ago
Are you worried about purity of supplements
Here is an article from Hardys on their testing. If you are taking many of the ingredients individually why not try switching to Hardys with extra vitamers at least for a trial to see if it makes a difference to you. https://www.hardynutritionals.com/blog/2021/09/purity-and-testing-we-only-source-the-best
Here is an article from Hardys on their testing. If you are taking many of the ingredients individually why not try switching to Hardys with extra vitamers at least for a trial to see if it makes a difference to you. https://www.hardynutritionals.com/blog/2021/09/purity-and-testing-we-only-source-the-best
LAJ12345
in
Cure Parkinson's
3 years ago
Trial on ERFA/Levo raised heart rate consultant suggest Liothyronine/Levo instead - any thoughts experience on this very welcome.
I started trial on NDT (ERFA) in February 2021 with private consultant. I have Hashimoto’s and for years been on 100mg Levo. My FT3 always in lower range and still had many symptoms of hypothyroidism. So took the plunge to trial adding FT3. The consultant took me straight off Levo one day and on to ERFA
I started trial on NDT (ERFA) in February 2021 with private consultant. I have Hashimoto’s and for years been on 100mg Levo. My FT3 always in lower range and still had many symptoms of hypothyroidism. So took the plunge to trial adding FT3. The consultant took me straight off Levo one day and on to ERFA
SmPea
in
Thyroid UK
3 years ago
Help please
Hi. I recently had B12 result of 189 (180-700 range). I have tingly feet and hands, Tiredness, visual disturbance and muscle aches. My father and brother both have pernicious anaemia . Intrinsic factor and parietal were negative and Hb and MCV ok. Saw GP yesterday ( young locum) who did full neuro
Hi. I recently had B12 result of 189 (180-700 range). I have tingly feet and hands, Tiredness, visual disturbance and muscle aches. My father and brother both have pernicious anaemia . Intrinsic factor and parietal were negative and Hb and MCV ok. Saw GP yesterday ( young locum) who did full neuro
Lunadoo
in
Pernicious Anaemia Society
3 years ago
Magnesium
As we know magnesium can become depleted, especially if we take calcium supplements, so some of us supplement our dietary intake of magnesium. Here is an interesting article described ten different kinds. By the way, magnesium is to green plants what iron is to animals, so it is relatively plentiful
As we know magnesium can become depleted, especially if we take calcium supplements, so some of us supplement our dietary intake of magnesium. Here is an interesting article described ten different kinds. By the way, magnesium is to green plants what iron is to animals, so it is relatively plentiful
HeronNS
in
PMRGCAuk
3 years ago
How to work out dosages for supplements?
Are there any hypo sufferers who know how to work out how much selenium,zinc, copper and magnesium you might need after seeing your blood test results? Or any article about dosage (s)? All hints and tips appreciated.
Are there any hypo sufferers who know how to work out how much selenium,zinc, copper and magnesium you might need after seeing your blood test results? Or any article about dosage (s)? All hints and tips appreciated.
Esmielola
in
Thyroid UK
3 years ago
Hot sweats
Good morning fellow sufferers, I have started over the past couple of months getting really bad hot sweats exactly like the ones I used to get on my menopause and they were so bad I looked like I had just stepped out of the shower. I'm 72yrs old and I'm on 125mcg of Levothyroxin, I am well over due for
Good morning fellow sufferers, I have started over the past couple of months getting really bad hot sweats exactly like the ones I used to get on my menopause and they were so bad I looked like I had just stepped out of the shower. I'm 72yrs old and I'm on 125mcg of Levothyroxin, I am well over due for
Loopyloo243
in
Thyroid UK
3 years ago
Is Magnesium glycinate available in smaller caps/tabs?
I bought a bottle called "doctor's best high absorption magnesium 100% chelated" 100mg tablets (ingredient says from magnesium lysinate glycinate chelate) to help with sleep, but the tablets r too huge for me to swallow, n when I tried to crush them n mix with water, the taste was so horrible I vomited
I bought a bottle called "doctor's best high absorption magnesium 100% chelated" 100mg tablets (ingredient says from magnesium lysinate glycinate chelate) to help with sleep, but the tablets r too huge for me to swallow, n when I tried to crush them n mix with water, the taste was so horrible I vomited
ejaji
in
Restless Legs Syndrome
3 years ago
Hashimoto confirmed? Blood test back!
So I’ve just got my Blue Horizon tests back done by finger prick on 20/09/21 at 7-8am, fasted. I’ve also added the tests I’ve just done with the 9th with the GP for comparison. (Done 8.20am on 09/09/21) GP repeated antibodies and FT3 today but don’t have the results of that yet obviously. Also my cortisol
So I’ve just got my Blue Horizon tests back done by finger prick on 20/09/21 at 7-8am, fasted. I’ve also added the tests I’ve just done with the 9th with the GP for comparison. (Done 8.20am on 09/09/21) GP repeated antibodies and FT3 today but don’t have the results of that yet obviously. Also my cortisol
OudMood
in
Thyroid UK
3 years ago
Anyone able to interpret these iron overload studies please. I don’t understand the relationship between them
I have Hashimoto’s and take: Iron B complex Selenium D3 with K2 Zinc (soon to stop) Magnesium (broad spectrum) Beef liver (soon to stop) Metavive and Adrenavive (phasing both out in favour of ones without nucleotides or possibly NDT ) Nov 20 IRON OVERLOAD C reactive protein (0 - 6) <4 Ferritin (10 -
I have Hashimoto’s and take: Iron B complex Selenium D3 with K2 Zinc (soon to stop) Magnesium (broad spectrum) Beef liver (soon to stop) Metavive and Adrenavive (phasing both out in favour of ones without nucleotides or possibly NDT ) Nov 20 IRON OVERLOAD C reactive protein (0 - 6) <4 Ferritin (10 -
Noelnoel
in
Thyroid UK
3 years ago
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