Experiences with

Factor Xa inhibitor

I have 1+ proteinurea since last two months nothing is working for me i am much depressed 😔 don't know what i can do for proteinurea, i am on statins and ace inhibitors for proteinurea but still nothing has worked for me

Has anyone ever gone through any type of ACE withdrawal? If so, what were the symptoms and their duration?

Good morning. I am getting pretty debilitating muscle pain in my core - around my groin and up above. I think maybe these are my rectus abdominis muscles. It’s strange because it has happened before and I don’t’ recall doing anything to cause it. It’s very painful, has lasted days and doesn’t seem to

Hello, My husband (age 46) had a heart attack in December and had a stent fitted in his LAD artery. The surgery went well, all other arteries were clear, he attended the rehab programme and was coping well and was discharged. He’s on quite a lot of medication - aspirin, beta blockers, statins and ACE

After a seemingly endless rainy season (never really cold and never really warm) summer seemed to arrive in mid-summer's day. This morning my flat is already 28C with no heating of any kind and no sunny windows. In hot weather your blood vessels dilate and particularly if you are on beta blockers, ACE

76 years old, no heart problems as far as I knew, just had one of my better games of golf for a couple of years and started to get an ache in my chest in the evening. So phoned the Healthline (I live in NZ) and they had a 30 minute wait, so tried the ambulance service, who operate a triage service.

Hi Everyone, My husband had a major STEMI in March 2023 with a full blockage of his circumflex artery. He was 44 years old and playing 5-a-side football in a local sports centre when he collapsed without warning. Thank goodness it happened there of all places however, as the swift actions of his team

I have had restless leg for a good couple of years. Is anyone aware of examples of ACE inhibitors (blood pressure medication) such as ramipiril causing or exacerbating restless leg? Thanks

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