Experiences with

Vitamin K

I started on armour 7 weeks ago and have steady increase in weight since ( my diet has not changed, all bloods B12, Folate, etc in range. ). Have autoimmune hypothyroid and had left untreated for years as didnt feel any particular symptoms. My TSH was 4.3 when starting it , Free T4 12.3; Free T3

I've just got my latest test results back. I am currently on100mcg levothyroxine which was raised from 75 in June. However my T4 levels have significantly decreased since June despite the rise in levo. My TSH results have also decreased. Can anyone explain what is likely to be going on? I've also had

Hypothyroid with T3 consistently below range - several years on levothyroxine. Recently started on T3 Most recent doses: Levothyroxine: 70mcg daily Liothyronine: 7mcg daily (split over 3 doses) Results from blood tests on Monday 9th September: TSH: 0.2 (0.27 - 4.2) FT4: 18.2 (12 - 22) FT3: 3.8

Hi Everyone, I'm about to be started on Methotrexate for Psoriatic Arthritis. I'm hypothyroid and currently take 125ug Levo daily. My question is does anyone have any experience of these two things in combination? I know about taking Folate with Methotrexate but not sure about what it might do to my

With my understanding of the medicial field including research I decided to study antibiotics as being appropriate for healing from B12 associated issues and found it unlikely it would have been considered by experts. I came across this and other references: https://pubmed.ncbi.nlm.nih.gov/10809040

I had some Lola blood tests 37 tests. 26 normal 11 abnormal as follows Haemocrit 0.526 L/L 0350-0470 Above normal Mchc 279 g/L 300-350 Below normal Mch 24.8pg 27.0 - 33.0

Hi All these were my blood test results 3 months ago. Ferritin 13 Serum iron 17 range 10-30 Serum transferrin 3 range 2.0-4.0 Transferrin saturation 22.6% range 20-50. Serum cortisol 500 nmol Serum selenium 1.01 0.75-1.46 TSH 3.9 RANGE 0.55-4.78 Free T3 4.4 3.5-6.5 T4 11.2 range 11.5-22.0 Antibodies

HI all I was b 12 deficient and started supplementing. Recently I am feeling tired and experiencing burning eyes. I checked my b12 it is over 2000. The last time I checked my serum folate it was 7.6 in the month of july. Are my symptoms related to low folic acid ?I guess 7.6 is good isn’t? From past

Started b12 injections 1st loading dose and have to say I feel awful headaches on and off through out the day couldn't sleep hot & cold Does it wear off 🤔

I have been living with hypo type symptoms for decades but have been very unwell for the last 10 years. I have long suspected thyroid issues being a part of it. I had a diagnosis of M.E. in 2021 but likely would have had one earlier if I had gone to GP's. I am mostly home bound often bed/sofa bound.

Hello Folks I often find myself thanking many lovely peeps in here for their "shares" and useful information sources and guidance. It's really quite a wonderful thing...what the Internet should be about I feel. By way of small return, I am posting a picture that I have found helpful in "seeing

After thirteen months, my NAGALASE count .95 is in the high normal range and my final weekly Vit C/ hydrogen peroxide infusion was yesterday. I'll continue the Clioquinol +50mg zinc, 1000mg myomin, 5mg copper, 500mg quercetin 7/7 and 20mg Ivermectin 5/7 until Nag count gets to .5. NAGALASE is an enzyme

I just wondered if anyone else experienced this. I used to get a B12 jab every 3 months but this was changed due to the fact that in the run up to my next jab I get neuro symptoms, twitching legs, muscle twitches, and the pins and needles in my hands and feet which are always present, get worse. So now

I am currently using NDT, and I have been taking Thyroid S for several years with varying batch success. I have just started a new batch 23T01008. I have also been trialling Roseway Labs Compounded NDT on and off due to the fewer ingredients to see if it suited me better as I have not been feeling optimum

Hi, I was wondering if I could have some advice on sublingual B12. I know that most say injections are the only option for absorption issues but I really don't want another injection after a bad reaction. I know people say to get through the reversing out symptoms but I never had low B12 symptoms

has anyone else had problem with nurse saying are you sure you’re taking your thyroid tablets I’ve been asked twice this week . It’s really upset me. Apparently the lab said non compliant or dose needs adjusted. why would anyone not take tablets I don’t want to feel this way. They said but you

Hi, Do I take them with food? In the morning/evening? Thanks

Hi, I’m wondering if any of you lovely lot have had a similar experience please? I got very ill in January , extreme tiredness, stumbling, having visions, breathlessness , poor memory and pain and parathesia down right side of body . Long story short I was diagnosed with pernicious anaemia in February

Could someone take a look at this link for me before I order as I don't want to make a mistake... I'd be grateful of all advice.Thanks in advance Allywales https://www.arzneiprivat.de/product/vitamin-b12-depot-hevert-ampullen.245042.html

Hi,I'm hoping to get insights into my latest test results and symptoms I continue to have. I had my thyroid out in 2012 (Graves), I'm located in Australia and currently taking 100mcg of Eltroxin and 16mcg of slow release (compounded) t3 daily. Around 2yrs ago I got quite sick, I had extremely heavy fatigue