Experiences with

Vitamin B1

Has anyone experienced shaking and anxiety and low appetite from low folate .I inject weekly but am afraid to Inject in case it lowers my folate more

Hi, I was diagnosed about thee months ago and I'm on B12 injections and feeling much better. However, diagnosis remains very uncleal. Very low B12, below limits of the test, but no antigens to intrinsic factor and negative on caeleac disease. Cant fault the GP but feels very limited what they will

I am really struggling.i usually self inject every week and have tried to keep that up but had two bad infections with antibiotics .my thyroid levels were off and I discovered my folate was low at 5 .due to all this my anxiety got bad and doctor prescribed diazepam .I have lost my way re my b12 injections

Hello all, I've been posting on this board for the last week or so fairly regularly to get some support/help from the all of you great people here...for this i am eternally grateful as i self medicate and really have no Dr to turn to. I'm at a point where i need to make a decision now and seeking some

Hi all I take my T4 and T3 first thing in the morning. I also take Omega, Magnesium, Vit C, Vit D and K2, Vit B12. I am trying to find out the times required between supplements or if they can be taken close to each other. Thanks

I was diagnosed as hypothyroid at the end of last year. My GP started me on 50mcg levothyroxine. She increased this to 75mcg in March, then to 100mcg (at my request) in July. I've now been on that dose for 7 weeks and just took a private test (following the standard protocol) with MMH so that I know

I wont but vitamins Bit D antibodies here (as apart from folate) cannot produce methyl folate, B12, Vit D all midrange big (ferritin is always high so might get tested for iron overload), never ever any thyroid antibodies. I will just post the thyroid today, before covid on 3 grains NDT and 2 Grains

Hi, I have experienced this for a few days and have been to Doctors. They said its involuntary nerve misfire. Low in vitamin D can cause it! Hope that helps.

I have long covid, and everyday the neuro symptoms and mechanisms seem to approach Parkinson's disease. So, given the lack of treatments on long covid, I was thinking on trying the options for Parkinson's, and this is what I found: I recently found this link: B1Parkinsons.org where they recommend

Hi everyone, I would like to have some info or personal recommendations of some endocrinologists please. I know this is done through private messaging so I would be very grateful if someone can shed some light and share their experiences with me. I am also trying to source some tests done on Vitamins

I was put on 2 grains of armour by a private thyroid doc, at that point I was feeling ok-ish on 50 Levo and 6 t3. I took 2 grains for 3.5 weeks and started to decrease as I was feeling rapidly and increasingly unwell. I also have a low cortisol output all day and this may have contributed to feeling

My issues with B12 only came to light after booking an iron infusion with Dr. Klein earlier this year. He asked me to stop taking any b vits for a month prior to my blood test. After 3 weeks of not taking B12 and other b complex supplements my health rapidly deteriorated. I became weaker by the day

Hi everyone, just wondering if anyone else had experienced the same thing ? I guess it is down to some issue in my thyroid - but there are no visual lumps externally, just this weird sensation on swallowing. It started in March . Three weeks ago I have had annual bloods by GP and as my TSH is suppressed

Hi. Need help with my latest results please. Thank you. Not on thyroid meds. Was on 25mg Levothyroxine, but was taken off them because GP only tested TSH and thought it was okay. I had stopped them for 5 weeks at least before taking this test. I supplement Heme Iron. What baffles me, as a side note,

I usually self injevt every week but due to going through settling thyroid levels I dint know when I should inject .is anyone else in same position

After about a year and eight months since my diagnosis, which was about two weeks before my 50th birthday, I've tried it all; you name it. The reading up on ADHD, exercising, nutritional biochemistry with supplementation and vitamins, meditation, journaling, etc. The lot. I just came across TWO gamechangers

hi please can someone tell me if I can take my vitamin b complex while currently taking biotin and vitamin d for my hair it went so thin and I’m at my wits end thanks

I found Arty-fact's post on hyperparathyroidism enlightening, as I'd never heard of a connection between HPT and PD. Looking for studies on the subject, I was surprised to learn of a possible connection with restless leg syndrome too, and thought those with this affliction might want to read this paper

I am 33F. 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 it has increasingly become unbearable. I have it deep in my hips, up

Anyone else experienced this? there is research showing statins reduce PAF burden.Used to have episode every 3-6 months, very upsetting! Also take iron, b12 and magnesium supplements. Afib free for a year now. Tempting fate of course....🫣.also enjoying a couple of pints now and then which is nice.