[mikehardyParticipant]

Hi. As everyone is different and emotional at this stage, May I recommend that to have a nice chat with one the Myeloma Org nurses. They are so knowledgeable and impartial. It gives you the chance to ask questions as you go along.

My Best Wishes

Mike (Smoulderer)

[mikehardyParticipant]

I just want to introduce myself having just been confirmed as a Smoulderer…………….

I am Mike Hardy (68) living in Banbury and the Churchill Hospital in Oxford are looking after me. I was diagonosed with MGUS some 10 years ago and had 6 monthly blood tests. In Dec 2015, plasma was showing in the results although the other main parameters have remained stable.

I have Ankylosing Spondylitis, an auto-immune disease like RA so I have SI, lower spine and neck pains constantly so being able to identify new bone pains will not be easy. Also, as I self catheterise, I am experienceing regular UTIs. My immunity is under constant attack.

Does anyone have ways and means to boost their immune system?

Bye for now, as I get my head around all this lot!!
Mike

[mikehardyParticipant]

I just want to introduce myself having just been confirmed as a Smoulderer…………….

I am Mike Hardy (68) living in Banbury and the Churchill Hospital in Oxford are looking after me. I was diagonosed with MGUS some 10 years ago and had 6 monthly blood tests. In Dec 2015, plasma was showing in the results although the other main parameters have remained stable.

I have Ankylosing Spondylitis, an auto-immune disease like RA so I have SI, lower spine and neck pains constantly so being able to identify new bone pains will not be easy. Also, as I self catheterise, I am experienceing regular UTIs. My immunity is under constant attack.

Does anyone have ways and means to boost their immune system?

Bye for now, as I get my head around all this lot!!

Mike

[Author]

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