Experiences with

Anaemia

I’m new here and was wondering if anyone had the same experience as me. When I was sick with flu like symptoms I had my bloodwork done. It came back with elevated liver enzymes. Then about 3 mos later another test done by my GI dr and still elevated. I have no symptoms and am in good health; just

My health centre is the same one that my parents used and took me and my siblings to. I am 76 years old. The building and street locations have changed and of course the doctors too but we in our town have always considered the present building to be our local, first port of call when we or our own

Recently had bood and iron transfused due to severe Anaemia. HG 72 They also did blood and urine tests and told me I had CKD Stage 3 which was a complete shock, and has left me scared and confused.

Hi, a friend has been supporting me in getting a Pernicious Anaemia diagnosis, as she also has it.

In the context; of these conditions, or anaemia being present, suggest transferrin; saturation to further investigate.

Have not had any sleep again......my leg so painful and jerking non stop.....took 5mgs Targin that I had in cupboard, didn't even calm it down....this is the third night now I have had less than 2 hours sleep......nauseated and beaten. I have a box of Buprenorphine in pantry , the dr has stopped me on

Hi, So a few years ago I had a b12/folate deficiency. I had easy bruising, unexplained weight loss, funny sensations just to make a few. In the end I was really unwell and had Macrocytosis so I was started on loading doses of b12 (followed by injections every 3 months and folic acid. My levels went

I’m going to ask for blood and stool tests, to look for Pernicious Anaemia, antibodies and possible bacteria in my stomach, as follows: Blood: Antibodies to Intrinsic Factor CBC ESR CRP Vitamin B12 Iron Folate Ferritin Vitamin C?

I am on a hormone group someone has shared this I’ve been using milk thistle organic oil orally with vitamin e it doesn’t seem to have had any negative effects on myself thankyou in advance

Hello everyone! Previously, I have performed IM self injections. This has largely been fine and unproblematic, but a painful incident on the most recent attempt made me want to seek alternatives. I'm sure SC injections might be nicer for me as the needle is smaller and a lot of people on this forum

There are four forms of cobalamin commercially available for injection. Cynocabalamin which in tests of a non cobalamin deficient human has been tested for retention times. There is no comparative testing of the efficacy of Cynocabalamin versus other forms including no test of the effect on symptoms

So, as wondered if either PMR or pred could be slowing the healing, I looked on line and came across an article that I found really sensible - follows so much of the guidance offered on this forum. https://bpac.org.nz/bpj/2013 Polymyalgia rheumaticIt also mentioned that PMR can cause mild anaemia which

I have been exercising the same as always and eating clean, but have recently suffered from a cellulite appearance in my legs (when pressing on the skin or walking you can see it only). I am wondering if it is in fact celulite or water refention, and whether it is related to my Hashimoto’s disease.

episodes (feels like a big adrenaline surge) shakiness, pounding heart * ‘Sweet” tasting saliva *Tiredness but feeling hyper, so ends up even more shattered *Thrush that re occurs *Blurred vision (he’s visually impaired BUT has complained of vision being even more blurry this last 6 months) *Anaemia

Hi everyone Just got these results back today A few elevated levels..one below Also elevated APTT 38.5 (26.9-34.5) below range GFR 74 (90-200) Any idea please ..feeling pretty rough x

Diagnosis Pernicious Anaemia in 2010. I recieved no advice about how to resume the thyroxine, ie slowly or all at once. I felt ill resuming it immediately and the pharmacist suggested splitting the dose, which I did. Roughly 8 weeks later I am still not back to where I was.

Hi, I was recently diagnosed with pernicious anaemia. Initially put on 3-monthly injections. Changed to 2-monthly by GP because of recurrence of neurological symptoms (including frequent scintillating scotomas, migraine and balance issues).

I’ve managed to remember to do the anaemia bit of the MMH test. The results are in. Last tested February. Ferritin was 129 (?15-450) Active B12 104 (?37-210) Folate 13.3 (?

I’ll try the Pernicious Anaemia forum too though I get the feeling this isn’t really their area.

My pharmacist requested that I get my prescription altered to state Vencamil now that Aristo has been dropped by Alliance to stave of future confusion ( it currently mentions both)... I did say that I had tried in the past to get it named but they say that they can't... So I spoke with the Surgery and