New Routine….Same Wait

Chemo routine subtly changed. Still Tuesdays and  Fridays Still Bloods to be taken Still Valcade to inject Same observations. Same Questions  Numbness? Hearing? Walking? Buttons? Location changed Clinic 7 to Ingham Fast through Clinic 7 Same long wait at Ingham Staff down  Nurses short Pharmacy slow Some things don't change. Waiting.

Be Aware!

Today is the start of Myeloma Awareness Week and I make non bones (pardon the pun) about sharing some of the promotional material released today.  The focus of the campaign this year is Early Diagnosis and since I have crossed one hurdle it is worth emphasise that 1 in 5 people who are diagnosed are [...]

Drugs War

Progress is being made and I continue to remain  healthy and better than I have been for several months in so many ways. The chemotherapy is working but there is a battle going on, inside a drugs war against my very own mutant cells. The bad guys, Myeloma Cells, are being taken out but there [...]

Waiting Times

It's become routine.  Anything up to to four hours at the hospital. Waiting. Waiting in a queue of cars on the bypass. Waiting to find a parking space. Waiting for blood at Clinic 7. Waiting for nurses to do the tests. Waiting for tablets at the pharmacy. Waiting for chemotherapy on Ingham Ward. Waiting.... Waiting.... [...]

Sunday Summary – 28th May (Symptoms)

Three weeks on from my previous Sunday Summary and a chance to take stock of where things are. This is a summary which is a good stopping off point if you are interested but don't want to wade through all my posts. I am now very much out of hospital and undergoing chemotherapy as an outpatient. I [...]

Home

Finally, finally I'm home.  At 6:30pm this evening I was released from Lincoln County Hospital. My potassium levels had continued to yoyo up and down but were settling at a lower level ranging from 4.8 and 5.7 This evenings reading needed to be less than 5.7 to be released and it settled at 5.6. Close [...]