Experiences with

Cyanovit-B12

Hello, I am newly being treated for a B12 deficiency. High MCV, high MCH, low red blood cells, low B12. I have RA and have had nuero issues in legs for many years, tingling, heavy breathing etc... classic symptoms, but was told for 15 years to take supplements. I am wondeeing what is the typical course

Hi everyone 1. Do I need to stop taking B12 supplements before taking blood for an iron panel test? 2. I am considering trying 100mcg and 50mcg on alternate days rather than cutting tablets in half to facilitate 75mcg per day because the half tablets get messy and it's a faff, but do not want to create

Just had bloods back was wondering if anyone who self inject b12 .have had their glucose levels come back inconclusive ..is their a link and if so ...why rest of bloods are fine got to have glucose done againMany thanks

I think I’m very lucky so far with my ET Journey, no real side effects except itching and tiredness. However, Just a couple of moans from me today I’m afraid. I’m not overweight, I eat a lot of fruit and vegetables, olive oil. I weigh around 12 stone (that’s around 168 pounds ) and am 5’11” tall (180

i’ve started having awful panic attacks again. they are debilitating! i got put on fluoxetine which only made things worse! i then had a blood test and my folate is at 2! in 2021 i was found to have a b12 deficiency. i also had panic attacks when my b12 was low. i’ve since been having injections every

I've been injecting subcutaneously for 3 months. Today, I forgot to push the air out of the syringe first. I injected into my thigh with a 2ml needle and 1ml of B12. There was a small amount of air at the top next to the needle. Hopefully, I didn't hit a blood vessel but I can't be sure. Should I be

Evening all - please could I have some advice on my latest results? All of a sudden my Frees have leapt up and TSH has dropped right down. I think I need to reduce my Levo a bit and would be grateful for some advice on how to do so - e.g. how much/how quickly to reduce? Any and all advice always welcome

Hi, I'm sorry this is very long, I've put all my bloods at the bottom, for the past year or so in order of most recent ones in the hope it helps explain my complex situation! It's alot, so I apologise but if anyone could help at all I'd be so so grateful please, I'm feeling quite scared eight now to

Due to covid when an endo was not available on the NHS I was forced to go down the private route. Due to cost pressures I have been trying for several months to revert to the NHS to get an endo appointment but without any success. Each time my GP'S have asked our NHS hospital for an appointment

I have received my results from Medichecks and would like your opinion on them. Unfortunately I left 24 hours between taking my pills and doing the test so my t3 will appear low. I take 81 mcg t4 and 10 mcg t3 in the morning after rising. Here are my results. Ferritin. 258ug/L. (30-332)

Back end of last year i had an endoscopy to check up on my Coeliac disease. There was some biopsies taken and initially it appeared to be atrophic gastritis which led me to looking into PA. I ordered some private tests and found some historical tests from my GP. All are below. From the tests it does

I have been self injecting for several years as I was taken off B12 injections and told I didn’t need them, however my symptoms came back and the only thing that makes me feel better is B12. It took a while to work out what frequency works for me, and over the last couple of years I have found once a

I was diagnosed with Hasimoto about two years ago. (I have a major health issue which is well controlled with strong medication that effects absorption of things like vitamins). I am on 75mcg Levothyroxine (accord brand). Had a resent blood test at GP's and he said my vit D was low (so prescribed vit

So I.had low folate and was given folic acid had bloods again two months later as I was feeling dreadful even after the two months of folic acid my b12 was 258 I was blaming that but that has also gone up to 366...I'm still having chronic fatigue eye disturbances lightheaded it's given me health anxiety

Hi All I'll try and keep this brief! Last year I experienced a severe dperessive episode. This has been treated with antidepressants and generally is much improved. However, since then I also delveloped a whole host of other symptoms and have honestly felt more unwell than I have ever done in my life

I have been buying b12 from Germany for many years, please can anyone advise me if I should be taking a b12 complex every day to help with the other b vitamins?

This is my first post here and am looking for help with support with test result before I see my GP. I am a long term user of Levo (2004) and as per my bio increased to 125 of accord by 2020. During covid I changed my diet and miraculously lost 35lbs however this resulted in hospital trip due to tachycardia

How often do you take Vitamin B12? I feel like I've been taking it too often. 3X a day! Thanks. Leslie

Hi everyone! I know that we have one of these posts every week but I want to share my latest communication with Endo. I had my first appointment with him end of last year and he was very sceptical about the use of T3 - it will cause osteoporosis BUT he was willing to prescribe and test with his ultimate

Wasn’t sure whether to start new post as this is a follow on from my post about chronic pain & using finger prick tests? I have been diagnosed with Hashimoto’s & UA. I only have left side of thyroid which is very inflamed (thyroid inferno) & been referred from ENT to Endocrinology. My first 2 months