Experiences with

Vitamin K1

I'm aware that historically Warfarin has a question mark over vitamin K1 for various reasons Some people seem to monitor using inr testing but my question is that more modern anti coagulants use a different mechanism of action.

Metabolic Panel (14); Thyroxine (T4) Free, Direct; TSH; Vitamin D, 25-Hydroxy; Vitamin K1; Triiodothyronine (T3); Triiodothyronine (T3), Free; Ambig Abbrev CMP14 Default (I had my bloodwork done around 8 a.m. after fasting for 12 hours and 24 hours after my last dose of 75 mcg levothyroxine).

I want to add K to my D and don’t know the specifics or dosing. I have a stockpile of about 6-12 months of D3 due to an auto-Amazon order and previously sharing the D with family. I take one a day - D3 at 2500 iu (62.5 mcgs). What specifically can I add to get the right k? K, k1, k2, what about mk7

It’s hard to reconcile that this may be the end. The facts, I’m 42 with low amh (3.0 when tested over a year ago). Partner had cancer so sperm was frozen 20+ years ago meaning fertility help was our only route. Tried 3x IUI and 2x IVF. Due to age this is all self funded. First round I got only 1 egg

I am asking for a friend who lives part of the year in Turkey. Here are her last three test results, although she was not aware of the pre-testing protocol. She is not on any replacement. The following tests were done in the UK. Nobody reported back with any comments. 17/01/24 TSH. 4.7 m/ul (0.27

I've been trawling over my posts/diaries/test results trying to establish a pattern where I feel good. Obviously there can be many co-contributing factors, and I'm not as far as I'm aware a classic hashi as I've always had negative antibodies. I suspect I might be central hypo but no-one has ever confirmed

Hi, I've been on combined T4/T3 medication since December 2023 as T4 alone didn't work for me. I don't have Hashimoto's and an ultrasound of my thyroid was unremarkable. Vitamins and minerals are all optimal. My starting results prior to T3 were:TSH 0.03 (0.3-4.2) FT4 22.2 (12-22) FT3 3.9 (3.1-6.8) I

Hi all - I wasn’t sure if I could post links, so I have pasted the entire article. There is a lot of misinformation and confusion about BBs and I thought this would help, especially the bit about being ‘beta blocked’. I am a male, 55 with history of SVT and palpitations. I take Dronedarone and 2.5mg

Results from october for thyroid and vitamins. Taking levo 100mcg and 5mcg twice a day but still feel tired late afternoon! Could i take anymore t3 at all? Many thanks...

I have PA atrophic gastritis an under active thyroid following RAI a long time ago and Addisons ..wondering what supplements people take I had an iron infusion a year ago that I expect to get again in next three months due to absorption issues .

Hi All, First, thanks to RedApple for posting a link to a study on LS a few months ago. Don't know if this link will show up or not - https://healthunlocked.com/thyroiduk/posts/150659252/lichen-sclerosus-the-silent-genital-health-concern-often-missed (Also good information from a link from @humanbean

I am suffering from a lot of colds - 3 in the last 4 weeks - they seem to wipe me out completely. I often end up in bed for a couple of days, mainly sleeping. I don't know how to stop this, I eat healthy, take exercise (yoga mainly) take vitamins and medication (Levothyroxine) Does anyone else suffer

I am always so tired. I feel like I have a week where Im okay and then boom, exhaustion. I have no energy, I dont want to do anything. I feel like I cant sleep enough. I bought multis but my anxiety is so high Im scared to take them. They also are a VERY high amount of vitamins, they say like 200% of

Hi all, lots of supplements are recommended on this forum for thyroid health. Can this be taken as a multi vitamin or are individual vitamins better? many thanks

sorry i forgot to mention my vitamin levels were ok.👍

I’ve not been fine for a good few months. I’ve got other conditions but I’ve been progressively getting worse and have maintained I think it’s my thyroid. I’ve got hashimotos and have been off levo since 2022. My endo sucks, he falsified to my GP when they requested guidance (after he discharged me

Following on from my previous posts much to my surprise I met with the Endo today who had analysed all my previous results and has offered me a trial of T3 combi action therapy with close monitoring. He has proposed I reduce my levo from 150 to 75 & add 2 x 5 T3 . Having read posts on here I asked

Hi, Lasy year was my worse ever for Chest Infection started Sept&still ongoing although calmed a little since August. Bronchiatitis, Asthma diagnosed after Pneumonia (poss COPD). Prescribed above for Winter months x3 a week. However, I get stomach pains changing to back pains later in the day. I only

Ok dear ones...gotten to the point of researching CBD and looks like many kinds no regulation..where do i start? Im in the states...fall winter pain so much worse and Ive been thru most things...avid on vitamins...so any opinion if that is allowed? pros cons..

Previously I discussed the use of the trio, magnesium, zinc and melatonin as a useful sleep aid in the following link : https://healthunlocked.com/cure-parkinsons/posts/144067482/in-pursuit-of-restful-sleep-and-help-for-nocturia More recently I have been testing Apigenin as a potential sleep