Experiences with

Vitamin and mineral deficiencies

Hi Everyone, Well, that dripping tap must have got me, finally!! No symptoms but a routine Rheumy appt preceded by the usual blood tests revealed that my CRP is over 100 😱 and my ESR is 80 something. But I feel no pain, except for the usual little niggles that I thought came with being nearly 70.

I just recently found out I am in Stage 3b. I am a 71 year old female. If I hadn't pointed out my unusual lab results to my family doctor, I might still not know. I had been told for years that they were "going to keep an eye on it." Yet no one did. I had to request to see a specialist. Now that

Hi everyone, I posted this same message in my previous post but I don't think it has been seen by anyone so creating a new post here... I got my blood test results back this morning. Here they are – TSH mIU/L: <0.005 (range 0.27 - 4.2) FT3 pmol/L: 7.7 (range 3.1 – 6.8) FT4 pmol/L: 18.2 (range 12 –

That’s from an MRI taken six weeks after 10 sessions of IMRT were completed for a surgically inoperable metastasis in my skull. Apparently this means the contrast agent shows increased blood flow or activity in the tumor. Does that sound normal to still have increased blood flow or activity six weeks

Hey everybody happy Sunday 😇I have a biopsy the 26th and I'm deadly afraid doctor said there was skin cancer it's everywhere the lesions are getting worse by the day... The pain of the lesions is getting very bad can't even touch them I was just wondering how are you all handling or do you have pain

This has probably been mentioned before but just thought I'd post it for any forum members from Norway. B12-Foreningen https://www.b12-foreningen.no/ Another link for Norway below. https://www.b12info.com/very-useful-links/ PAS (Pernicious Anaemia Society) accepts members from across the world.

Having been treated for hypothyroidism since 2000 when I had a thyroid nodule, I have struggled with my weight and wellbeing to varying degrees over the years. I'm now 79, but active. I saw an Endo privately in October had a few blood tests which I have posted, (including Medichecks in Feb I think)

Hi all, I’ve been quite stable for a number of years now. I was on NDT and doing ok but not perfect, adding a small amount of Levo to my NDT at the end of 2019 made me feel really well, pulling my FT4 up in the range a bit made a big difference. At the beginning of May this year I thought I caught

My HB and Platelets have been bad for a while. Mainly because I haven' eaten anything. I am now eating again and feel much better (I had other reasons), but she has ordered me back for new blood tests and wants me to change to Xeloda. I want a chance to get my appetite back up and eating normally before

I am 74 (F) and was diagnosed in Nov, 2019 with PV and JAK 2 positive. I have been in clinical remission for 18 months and take Jakafi 10mg 2x daily. I have an allele burden of 15 currently down from 60 at diagnosis. My blood draws have been within limits for 18 months with only a blip in the blood calcium

I have being taking, Liquid Drops 3000 mcg Methylcobalamin + Adenosylcobalamin. From Natures Way. It is in 3000 mcg per dropping under the tongue. I have tried tablet form Methylcobalamin also. There seems no improvement on my, balance, fatigue, feet cramps at night and numbness plus tingling in my right

so, here’s where we are… My Joe has been experiencing increasing pain in his left hip and thigh. Today he said the thigh is numb. PET scan scheduled this coming Tuesday. He thinks it’s a hairline fracture. Is it wrong of me to hope he’s right, vs his cancer having landed there? He’s 4 months post-Pluvicto

Hello, I have been on NDT since June of 2021. I am currently taking 175mg of compounded thyroid. About two hours after taking my thyroid capsule I often feel hot and sometimes a bit anxious ( like being overmedicated) but in the afternoon I am out of gas. My cortisol is high in the early morning, good

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Can anyone direct me to some data/peer review study or such confirming there is no health risk of frequent B12 injections? I saw one GP who confirmed her understanding of the recommendation of 1mg per 3 months and anymore is unsafe...arghh! My current GP is asking for information - thank heavens!!

I'm going to start taking Folate, any recommendations for a brand or strength please? Last folate result was: Serum Folate 19.10 range 8.83-60.8

Two weeks ago I was diagnosed with non small cell lung cancer. I have an appointment with md Anderson in 4 weeks which seems like eternity. I ended up at md Anderson emergency room due to some blood clots. They ran a ct with contrast & this is what report says Bilateral segmental/subsegmental pulmonary

Hi, Can anyone relate to how I am feeling? I was diagnosed back in Feb this year after my Intrinsic Factor blood test came back positive and I was diagnosed with Pernicious anaemia. I went to the drs with symptoms of exhaustion, pins and needles, heart palpitations and nausea as well as brain fog

I little bit of my B12 history: diagnosed 7½ years ago, been self injecting for 7 years, and am currently SI'ing every 3 days. With this protocol I have no symptoms. I can walk for miles every day, I can do weight training at the gym 2 to 3 times a week, I work, I go out, I have a happy, healthy marriage

Hi, I have been asked by the end to start on 75mcg Levothyroxine today. I am gluten free and have reactive hypoglycaemia so avoid sugar/ carbs; is there a particular brand of Levothyroxine that might be good for me? I also take a bunch of supplements; Vit D, B complex, selenium, magnesium, iron;