Dancing in the rain
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* Myeloma
- Myeloma Beacon : Independent, up-to-date news and information about myeloma, from the USA
- Myeloma blogs : A place to find other myeloma blogs, or even add your own
- Myeloma UK : Supporting people with myeloma and related disorders
- Myeloma XI trial : Information about the clinical trial I was on at the beginning of treatment
- Wendy : Living with Myeloma in remission, in Manchester, UK
Cancer
- Macmillan Cancer Support : Providing practical, medical and financial support and push for better cancer care
Donating
- Anthony Nolan : A UK charity that registers and matches potential stem cell donors for people with a blood cancer
- Be the Match : National Marrow Donor Programme, in the USA
- Give Blood : If you’re generally healthy and aged 17 or over, do something amazing!
- Nottingham Marrow : A student group recruiting people to the Anthony Nolan stem cell register
- Organ donation : A place to register as a donor – even as a living donor
- Register & Be a Lifesaver : A UK educational programme to raise awareness of blood, stem cell and organ donation
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Tag Archives: blood count
Blame it on the Dex… and other effects
The joys of Dex! I’m now off all medication – not even taking any vitamins or supplements – I just wanted a break before the next round of treatment and medication starts. I started writing this quite a few weeks ago … Continue reading
Glimmers of hope
Another consultant appointment on Monday, this one with Dr Cathy Williams, just because I can choose and I haven’t seen her for a while. It’s nice that we can choose who we see – a bit of patient control. In … Continue reading
Blood results graphs
When I went to clinic on 5 September, they gave me a copy of these graphs which show my blood results over the past six months. The green band is the normal range in each graph. If you click on … Continue reading
Posted in * Myeloma
Tagged blood count, blood test, chemotherapy, fatigue, immune system, stem cell transplant
3 Comments
Sat-Mon SCT Days 9-11
I feel limp and miserable. My nights are punctuated by trips to the toilet, more often than not leaking en route. I don’t have any control and often don’t even feel it happening. It just seems to pour out of … Continue reading
Thu & Fri SCT Days 7 & 8
Thu: Despite my mouth feeling so awful and how hard it is for me to swallow, I’m not feeling as bad today as I did yesterday. Not feeling very lively though. Got my blood results Thu afternoon. I’ve updated the results … Continue reading
Wed SCT Day 6
I’m feeling really low today. Diarrhoeia every time I move and my throat feels almost closed, mouth is sore and coated. I don’t feel like writing or talking. They’re giving me lots of pills and potions to help, but it’s … Continue reading
Tue SCT Day 5
I slept through the whole night, which feels good. My mouth feels horrid – dry, coated, hard to swallow, gums and tongue a bit sore now. This is all to be expected, but doesn’t make me feel like eating the … Continue reading
Mon SCT Day 4
I slept well last night, with only one wake-up wee. Very kindly, the nurses left me to last to wake up this morning for the first set of obs and blood test. No results yet, but they’ll let me have … Continue reading
SCT figures…
I’ve just been given a chart showing my blood test results for the days I’ve been in here and those to come – still blank obviously. I thought I’d record them here for anyone who’s interested in the more technical … Continue reading