Experiences with

Magnesium aspartate

Hi I am new here. I am a clinical immunologist MD with a history of AF. I have accomplished conversion of my AF to SR with a protocol that will likely be dismissed because the general attitude towards magnesium is we heard it all before. If you take a few minutes I would like you to read my bio which

Good evening all. Is there anyone in this group who takes Magnesium Taurate? If you do can you please tell me where you get it from please? I am looking to buy these but can't find it on any of the reputable sites. I can't trust the others that come up using a search engine. Thanks very much.

Having been on ropinarole for years I had reached maximum dose 4mg pd and symptoms worsening. Via this group I learnt about augmentation and realised that I need to come off it. My GP prescribed Gabapentin 2 x100mg pd. but that made no difference. I realise, via this group, that I need to increase Gabapentin

hi I just want to know if anyone eles takes magnesium why on bisoplorol as I don't know if you can

Hi Folks. What do people think regarding how necessary it is to take these supplements for hypo and hashi's? I keep reading that it is important to take selenium, magnesium and potassium to help with low thyroid function. I was surprised about potassium. Apparently, vitamin D in excess causes low potassium

I am 34F. I had RLS (in my shins) as a teen-early 20s, but it was usually a sign of being tired and going to bed was enough. Eventually it got worse, moved up to my thighs and would not always go away with sleep. The last 3 years became unbearable. I would have it deep in my hips, up my spine and in

I have been looking for Magnesium drops that you can just drop under the tongue. Does anyone have any information on a good general one (not Chloride) that will not upset stomach. Would prefer drops, but will go back to Ancient Minerals Spray if I have to. Also, if anyone has any information on how

I have just had my 3 monthly blood test. I take 1.5 grains of armour thyroid and 15 mcg of Liothyronine daily. I feel great BUT my results don’t reflect that. I’m not sure how to go about obtaining optimal levels. Advice please. I am very nutrition conscious and take supplements as follows. Multi guard

Hi there, I’ve posted previously about my husbands severe rls and most recently advised that he started taking pregabalin, this caused low mood and weight gain but did settle his rls a good bit. Since then he has dropped the dose from 175mg to 150 mg of pregabalin but it’s not holding his rls as well

I check in weekly and have learned so much from everyone. I live in the US still we have a lot in common. I waited months to see an endo. The point of the appt was to review my labs and make any suggestions on meds and see if my GP was on the right track. She is concerned as my weight is the same although

Hiya. I personally have found almost all of my medications like pregabalin given for GAD, sertraline for bipolar and many others increased my symptoms of RLS. I had my 4th breakdown in Nov 24 through severe stress and over the last 2 years I have been weaning myself off from all medications because

How strange my doctors have put me on HRT to help with my server RLS, I've had it for 4 years which is when I was in peri I'm now post, my rls is so bad I'm on ropinirole and it can start from mid day, I actually do sleep as the med knock me out it's the day time I struggle. Cannot sit it's horrendous

This is my existing schedule 7am T3 8am vit D3/k spray, B12 spray 2pm T3 6pm/dinner Provera progesterone tablet (12 days a month) 7pm / magnesium complex daily (and folate if I remember) 11pm T4 I don't eat between 7pm-and 11. 30am. Or an hour or so minimum either side of my T3 where possible. Do

Was initially diagnosed hypothryoid October last year; TSH was 115 (range 0.55-4.78), and T4 <3.9 (range 11.5-22.7). As you can imagine, I felt very rough at that point! Started on 50mg Levothyroxine early October, increased to 100mg late November (due to thyroid inflammation), and have been on that

20/1/25 TSH 0.023 mIU/L (0.27 - 42) -0.6% Free T4 (fT4) 16.80 pmol/L (12 - 22) 48.0% Free T3 (fT3) 5.2 pmol/L (3.1 - 6.8) 56.8% T4:T3 Ratio 3.231  Thyroglobulin Antibodies (TgAb) 17.9 IU/mL (≤ 115) Thyroid Peroxidase Antibodies (TPO) 13 IU/mL (≤ 34) C-Reactive Protein (CRP) 1.7 mg/L (0 - 3) 56.7% Vitamin

Hello, my son is 10 and has been taking Guanfacine 1mg for a few months now. At first it was great, he was paying attention in school, not defiant, not argumentative, HAPPY. Then a couple months ago, he started getting really sad, upset and angry really quick. He is constantly cussing and we are trying

Hi, I have just moved to a new B12 practice, lovely GP but they are a bit wobbly on frequncy of b12. Im taking methy foliate, B2, iron, magnesium, D and potassium daily plus injecting hydroxycobalamine 1mg every week. I feek OK on that. perhaps not perfect but no neurologicalsymptoms, I can work and

Hi, should this help with sleep and RLS or does it make RLS worse? Appreciate any thoughts. Thank you

This forum is, obviously, primarily for thyroid issues. But, as most know, the parathyroid glands are physically adjacent to thyroid tissue. And it is well-known that some thyroid treatments (thyroidectomy and radio-active iodine for two) can result in damage to the parathyroids. We usually have four

I had 2 cryio ablations in 2019 and largely successful for 2 years. AF returned so back on Flecainide but NSR would not return without cardioversion. Flecainide upped and all well until radio frequency ablation was offered after a years wait. Decided to go for it in August 24….was told successful and