Showing posts with label leukaemia. Show all posts
Showing posts with label leukaemia. Show all posts
The Big Questions
Labels:
acute lymphoblastic leukaemia,
bone marrow,
chemotherapy,
chemotherapy side effects,
leukaemia,
lymphoid cells,
port-a-cath,
relapse,
remission,
white blood cells
·
Posted by
Lisa Griffiths
at
14:41
After three years of treatment, I suspect many people are a bit lost with Hugo's illness and treatment. Here are some of the questions I have been asked and a few others that I thought people might want answers to.
Day in the Life - Medication
Labels:
chemotherapy,
chemotherapy side effects,
childhood cancer,
childhood leukaemia,
cytoxic drugs,
dexamethasone,
gabapentin,
leukaemia,
maintenance phase,
mercaptopurine,
methotrexate,
septrin,
sytron,
Vincristine
·
Posted by
Lisa Griffiths
at
09:32
I often get asked if Hugo is still on chemotherapy. Has he finished, or is he due another cycle? Treatment for blood cancers can differ from other cancer treatment plans. It is often long, in some cases life long, and I think this can be difficult to comprehend - I know it was for us when we were told his treatment would last for over 3 years. Hopefully this explains a little more about the medication, chemo and otherwise, that Hugo takes for his type of leukaemia (acute lymphoblastic leukaemia).
Day in the Life - Bloods
Labels:
acute lymphoblastic leukaemia,
bloods,
central line,
chemotherapy,
childhood cancer,
childhood leukaemia,
community nurses,
ferritin,
leukaemia,
liver function,
port-a-cath,
relapse,
vitamin D
·
Posted by
Lisa Griffiths
at
20:34
Once a week a community nurse comes to our house to take some blood from Hugo via his bumpy. This blood is then sent to the lab and later that day, or the following day, we get a phone call with the results, which I write in our blue folder.
Day in the Life - Steroids
Labels:
acute lymphoblastic leukaemia,
ALL,
childhood cancer,
leukaemia,
steroid side effects,
steroids
·
Posted by
Lisa Griffiths
at
16:13
Hugo encounters many different side effects from both the leukaemia and the medication he takes for it, but on a day to day basis, steroids are definitely the cause of the most challenging (which is why they get a blog all to themselves!). He takes a 5 day course every 4 weeks, alongside the IV chemotherapy (together they are referred to as 'pulses'). The effects differ slightly each time and we never know quite what we are going to get from month to month. Some months they seem to hit harder and others we feel we have gotten off lightly.
My Other Child
Labels:
acute lymphoblastic leukaemia,
cancer,
childhood cancer,
childhood leukaemia,
leukaemia,
siblings
·
Posted by
Lisa Griffiths
at
14:01
A few months ago I posted a photo of Henry on Facebook. We were on a day out, just me and him. A treat day to spoil him a little, because it's tough when you're the sibling of a child with cancer.
What Would Hugo Say?
Labels:
Blood Cancer Awareness Month,
Bloodwise,
charity,
childhood cancer,
fundraising,
leukaemia,
social media
·
Posted by
Lisa Griffiths
at
13:20
A few weeks ago the charity Bloodwise asked if Hugo and I would be the face of their Blood Cancer Awareness Month campaign. My first thought was to immediately say yes. To be able to share our story and raise awareness for a subject that has become so close to our hearts seemed like an amazing opportunity. But it also brought to mind a question that I have been pondering for a while now. What would Hugo say?
Subscribe to:
Posts (Atom)