CFS or B12 deficiency? - the journal of my journey (2025)

18/11/2023

Injected today (sub cut in stomach). This is my 3rd time. Mouth ulcers returning for first time in a couple of months.

12/11/2023

Nearly 8 years ago, when I was 33 years old, I was diagnosed with chronic fatigue syndrome (CFS). Now, I think that diagnosis might be incorrect. I think I may actually be deficient in B12 as a result of my long-standing gut issues. These issues are difficult to diagnose and expensive to treat... Perhaps its a coincidence that the NHS would prefer I was diagnosed with CFS - it's a cheap and not very cheerful diagnosis.

On this page, I will share the history of the last eight years along with journaling what's happening as it happens.

You might want to follow this page if you have or think you have B12 deficiency (I've done a lot of research and so you might find helpful info here). You might want to be here if you have (or think you have) CFS. You might want to read this if you believe the NHS E&W and/or NHS Scotland are deliberately ignoring research and/or conditions which don't suit them due to resourcing requirements. You might want to have a look to learn a new perspective. Or you might want to pass on by. Just no haters, please. This page is my honest account of a very difficult and stressful situation, which has immeasurably and negatively affected my life, with my own opinions thrown in for good measure.

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CFS or B12 deficiency? - the journal of my journey

18/11/2023

12/11/2023

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