Experiences with

Antihemophilic factor

Hello I'm posting on behalf of my partner, who just had these medichecks done. I'm also hypothyroid, hashi and have P.A and cortisol issues which have all affected my vit/min absorption so I've been worried about him for ages. For the last few years he's become extra tired and achy, he's put on loads

Hi all I discovered in May that I had Intestinal Metaplasia and this was a real shock. I’ve had abdominal pain, stomach cramps, diarrhea, bloating, difficulties with digestion, excess gas (sorry!) for a long time. Also feeling of fatigue and low energy and mood. Then I only had blood test last week

Hi, my GP recently stopped my B12 injections which I have been having every 3 months for the past year as my intrinsic factor test was negative. I had previously asked for a greater frequency I injections because I was feeling like there were some benefits for a short while but these benefits were short

Hi again 👋! I posted about 4 weeks ago with my Blue Horizons test results but, since then, have had a GP appointment (with 2 trainees and GP supervision) and further blood tests, including antibody ones for pernicious anaemia. I never had a call from the GP with the test results, so looked them up

Hi, I was just looking for some B12 ampoules on shop.apotal.de and came across these tablets:- B-COMPLEX w.Methylfolate+Intrinsic Fact.KLEAN LABS I've not come across any tablets that include intrinsic Factor before & was wondering it they would work better for people with PA. Has anyone tried

Mentions the Parietal Cells, Intrinsic Factor and B12. https://m.youtube.com/watch?v=3pYzDqyBZig

I posted this earlier as a part of a reply to another post [i]I saw the doc today as I have been getting extra pain across my right hand, palm and fingers which doesn't respond to pain killers, which really knocks out it being my OA, but may be a sign that it's PMR starting to reappear or even RA or

Hi Guys I need cheering up please. As you know I was dx with PA by my GP in Oct 2022 with a B12 0f 106 ng/L. Vitamin D and folate were also rock bottom. I had lots of symptoms including neurological symptoms such as heart palpitations, pins and needles, visual disturbances, facial neuralgia, extreme

hi all, I have been experiencing a number of health issues recently and have had an Intrinsic factor antibody test. Please see photo for result, is this a positive or negative result? I am so poorly and just looking for answers. Any words of wisdom would be appreciated

I have been told by one Dr that I have Pernicious Anaemia as my B12 was low this year and last year. My ferritin was also low. I had been on a high dose of PPis for 4 years and intermittently for many years before that. Intrinsic factor this year was negative and when I had a gastroscopy last year

Hello, I am new to the group and full of questions. My father had pernicious anemia so when I started feeling off after months of trying to figure out what was wrong...I had my labs drawn. My intrinsic factor was listed at 47.7. I can not find anything to indicate if this is what would be considered

hi everyone, just wanting peoples thoughts or advice on the following: I had a B12 serum test done which showed my B12 was low at 188 on the 28th of august. This was repeated on September the 2nd and came out at 232 without treatment. My intrinsic factor was also negative. I have loads of B12 symptoms

Hello all. I recieved my formal diagnosis of RA last week and trying to learn as much as I can. I often see you all discuss blood results/ CCP levels and wondered if someone coukd give me a beginners guide to understanding how yo interpret and what it all means. My letter says CCP positive 157, Rheumatoid

Long post warning but to summarise I have just been seen by rheumatology after a 6 month wait to be told that I do not have RA because all my blood tests are negative. Serum C reactive protein level 0.8 mg/L [< 5.0] Rheumatoid factor IgM level < 10 IU/mL [< 14.0] Serum anti-cyclic citrullinated

recently had the Intrinsic Factor Antibody test and Paretal antibody test. IF antibody was unequivocal and the Paretal AB test was positive. Ii was immediately diagnosed with Pernicious Anemia. It took 3 years to get diagnosed. In the past 6 years I’ve had numerous trips to specialists and been prescribed

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 have recently had the result of an Intrinsic Factor test. The normal range is listed as between 0 - 6 u/mL Mine was 480 u/mL Is anyone able to advise the relevance of this please as it appears quite extreme. Thanks

Hello everyone, I am a lady of 67. Ive been taking lansoprazole for years. Then I began to feel ill with various symptoms the doctor was not interested in or would virtually say I was a hypocondriac. I nagged and got sent to a consultant who said I had neurological problems caused by fibromylgia and

My Medical No is 112624120. (sequence of factorials). My doctor can ring me on is 0112358132134. (Fibonacci code) I am 48 years old, 169 cm tall, weigh 54 kg, I have 6 children. My vital statistics are………..Sorry, I thought I was Angelina Jolie for a moment. In 2023, The World Health Organisation

I’ve been feeling grotty for a couple of years and have thyroid antibodies. Started on levothyroxine and liothyronine, happy with levels just taken. Symptoms that continue to bother me: Headaches & headpains Sore mouth, tongue swollen Poor balance Back pain Urinary incontinence Loss of sensation