Experiences with

Vitamin B

I just had my thyroid labs done and just want some input …. Im on 100mcg T4 and 10mcg T3 …. 2 weeks ago I had Iron infusion almost 4 weeks on 50,000 Iu of Vitamin D once a week. FT3: 3.0 (2.0-4.4) THIS NEVER CHANGES FT4: 1.40 (0.82-1.77) this jumped up too T3: 130 (71-180) this jumped up TSH: 0.503

Hi everyone. I am in my 2nd round of PMR and have been on Pred since last July. Doc has got me reducing by 1mg a month and now down to 2mg. The trouble is, I have got exhaustion so extreme I am struggling to copeI have numerous Health Problems including Kyphoscoliosis, Afib and very severe Lymphodema

I appreciate that self injection is the most sensible route but haven’t made that decision for myself. Where do you buy the sublingual b12 as I can only see tablets? Can you give me the name of the product and site for buying. Thanks.

List of my meds.Methylated Vit B Selenium Zinc Vit D Levothyroxine Vit c with Rosehip Magnesium What order should I take these in, I'm wondering if some are counteracting others. I usually take B, Zinc & Selenium in a morning on am empty stomach. 8am Then around 10 take levo Lunchtime vit d an

Hi everyone 😊, Me again! My investigations continue and this is my most recent test to try to piece together what's going on. Any input most welcome please 🙏 Backstory since joining HU last November - Iron deficiency anaemia now corrected and ferritin getting close to optimal. All other vitamins

Hi .. as per previous posts my rls is extremely bad a few times a week , my ferritin levels were 41 before but have gone up to 74 today after more blood tests last week . ( I’ve been taking iron ) However , they said I’m deficient in vitamin D so I had a look online and they say studies have been linked

I never got the hang of knowing when I used up my B12 as some experience. Likely as I was also B1 deficient. The only way to determine if you are B1 deficient is to do a trial. The blood test is useless. Functional Deficiency of a Vitamin may be nothing more than a work around for not understanding

HiI am being treated for PC. After diagnose I was put on ADT treatment. This stops testosterone production. Had a bone scan and found I have osteopenia. I am taking a calcium citrate with vitamin D. Also once per week Alendronate 70mg. Has anyone else been in the same boat? Thanks

Hi 👋 Please can anyone tell me if they see anything 'abnormal' or concerning about my below latest Blood results from 01/05/24? My GP Surgery says that apart from my TSH result, they're all 'normal'. Background: I am Hypo (Hashimotos) for 13 years. Late diagnosis & undertreated the entire time - and

Hi I posted about a sudden deterioration in my health after 4 years of successful self-injection eod, daily or twice a week (depending on how I was doing). My last post questioned whether it was due to a bad batch of B12 depot - unfortunately, using newly ordered B12 doesn't seem to be making an improvement

I’m currently on 125mcg of levothyroxine. Overall I’m feeling much better with most bothersome results now being constipation and intense itching which comes and goes. My doctors seem very reluctant to increase my levo and I’ve had to push for each increase so far. These are my recent results.

I recently was able to see my moms records. She has been told she has mds too. Also there is a problem with her blood levels. The doctors cant seem to get her blood levels to go up. She is taking a needle injection every other day. Last night i stayed up with her again cause it was so severe. Sometimes

I had my B12 jab last week, I get these every 2 months and am grateful to have them. I've suffered B12 issues since childhood, have dim memories of blood tests and B12 jabs back in the day. I changed surgeries in the early 90's due to moving and have been with this practice ever since. So I'm not sure

recently diagnosed - switched from 20mg x2 daily Ritalin to 30mg Vyvanse. I have noticed every afternoon at the same time I get a red face, red ears, red neck. I also have anxiety so my mind untimely goes to worse case scenario, something very wrong. I also struggle taking new meds (part of my anxiety

I was diagnosed a year ago with pernicious anemia. I find that literally half an hour after my injection I'm back to being exhausted again. I do also have RA so do get a lot of tiredness from that and the bucket load of medication I take. I did mention it to the nurse when I had my last injection

Hi All I am posting on behalf of a member who is very poorly and who lives in Hebden Bridge, HX7. She needs help with her B12 injections as she is too weak to be able to do them effectively as she is so unwell. Please contact me via Chat if you think you could help and I shall put you in touch with

gp switched me fro omeprazole to lanzoprazole a few weeks ago . I seem to have developed very loose bowels every morning . I have recently been prescribed folic acid for low folate ? Has anyone had this side effect to either of these 2 meds please ?

Hi, I posted a little while ago with recent Thyroid results. SlowDragonsuggested I come back with some other results once I had them. I'm not diagnosed with a Thyroid issue as of yet. These results are following an appointment with an NHS Endocrinologist. I didn't think about him taking bloods at

, vitamin D + B12, magnesium, selenium, etc.

Hi…I’ve recently read an article, but can’t find it at mo! that low SigA levels along with high gastrin levels can indicate b12 deficiency. It caught my attention as on 2 previous tests, a stool and a saliva test, the SigA was included and very low both times which says can give rise to infections,allergies