Respiratory good news

I met with Mr Hussain at the hospital today and the results from the bronchoscopy showed that I have an infection causing the pneumonia. This is good news because I have now been given the specific antibiotic that will clear it up! He thinks that they will work in 2-3 days, but it's possible that the cough won't disappear completely as my lungs are so inflamed from the infection. I may need some steroid treatment in a few weeks time. In the meantime, I'm looking forwards to a quiet house with no coughing, sleeping all night, eating, getting some energy back and being pain free!  

Lumpy

I was booked in for a general anaesthetic to remove the lump on my back today, but after discussing my pneumonia, it was decided to do the procedure by local. Not for the faint-hearted!  I did get to see the inside of the operating theatre, all the many staff and scary looking machines. I could also hear the surgeon talking through the procedure with the students. That's when I heard him confirm that the lump was in fact, just a fatty lump and not a swollen lymph. It will still be sent to the lab for analysis, but good news all round, and the wound is not too sore at the moment either!

The marvellous NHS

My hematologist, Mr Stewart,  phoned me at home last night to check what had happened at the respiratory clinic. I was really reassured and touched by his concern, especially as he told me that the CT scan from last week had showed no sign of the lymphoma. I am booked in tomorrow for the biopsy on the lump on my back, and Monday for a broncoscopy to test my lung to see what exactly is causing the pneumonia. The  respiratory consultant thinks it will be one of two things - an infection that can be treated with antibiotics, or an 'organising' pneumonia - an autoimmune problem that can be treated with steroids (my old friend prednisolone).
My treatment under the NHS at the UHNS has been exceptional and I'm very grateful. But to be called at home to update me on results and check on progress is above the call of duty.

No more Rituximab

Keith came with me to the clinic today as there were a few things we've both been worried about. I've still got the cough but now started with night sweats and found a strange lump on my back, so they are sending me for another CT scan that will check what's happening with my chest and cough, the lump, and  to see if any of the internal lymph are swollen. I've also got some new cough medicine! Just looking back at the history, I can see that the cough has had a serious impact on my year - so many days where I was tired from lack of sleep, feverish, or got painful pulled muscles in my ribs. It's been gradually getting worse over the months, so I'm glad there is to be more investigation.

I was worried that the last two doses of Rituximab would give me an extra 4 months guaranteed remission, but apparently, the 12 doses over 2 years is an arbitrary figure, not evidence-based. So now I'm officially in remission which means that the lymphoma is not active, and hopefully it will stay that way for a very long time! I was in remission for 25 years last time, so I plan for at least the same. Although there is no clear evidence for what causes lymphoma, it is on the increase in developed countries and there is some evidence that suggests that farm pesticides and hair dye may be connected so over the last few months I've been adjusting my lifestyle to minimise the things that may be associated with lymphoma or cancer generally, and to maximise the things that are known to increase well-being. I've stopped eating beef and processed pork as well as increasing my fruit and veg intake. My hair is coloured with henna, but I'm gradually growing that out. I exercise everyday by cycling and/or dancing, and I make time for friends and family.