Showing posts with label chemotherapy. Show all posts
Showing posts with label chemotherapy. Show all posts
End of Treatment Bubble
Labels:
acute lymphoblastic leukaemia,
ALL,
chemotherapy,
chemotherapy side effects,
childhood cancer,
childhood leukaemia,
end of treatment,
physio,
steroids,
Thomasland
·
Posted by
Lisa Griffiths
at
11:59
It has now been three weeks since Hugo took his last dose of chemotherapy. So what does life on the other side look like?
In many ways it doesn't look very different to life on treatment. There has been medication every day, (although not the yucky chemotherapy or steroid type), the nurse has been twice and the physio has visited Hugo at school. We have all had colds and the worry that Hugo's will develop into something more serious has been there, just like it has been for over 3 years.
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.
Leaving Normality
Labels:
acute lymphoblastic leukaemia,
ALL,
chemotherapy,
childhood cancer,
childhood leukaemia,
port-a-cath
·
Posted by
Lisa Griffiths
at
13:44
A couple of months ago, on the way back from a hospital appointment, Hugo asked me what it felt like when I had my bumpy taken out. Bumpy is our name for Hugo's port-a-cath/central line. The little device that sits just under the skin to the side of his chest. It will be removed a few weeks after treatment finishes. I explained that I'd never had one and we chatted for a while about why he does. He seemed content with this, but a couple of days later he asked big brother Henry what it felt like when his bumpy came out. It made me wonder how much Hugo understands of his illness and what 'end of treatment' actually means to him.
Day in the Life - Side Effects
Labels:
anaemia,
chemotherapy,
chemotherapy side effects,
childhood cancer,
immunocompromised,
muscle weakness,
neutropenia,
neutrophils,
night sweats,
peripheral neuropathy,
steroids
·
Posted by
Lisa Griffiths
at
10:45
During the early phases of treatment Hugo suffered with many of the side effects synonymous with cancer. His hair fell out, he was sick, tired and pale. He lost weight, his light dimmed and he looked ill. Now, in this final maintenance phase, the side effects are often less obvious, but very much still there.
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.
The Long Version
Labels:
acute liver failure,
bumpy,
chemotherapy,
childhood cancer,
childhood leukaemia,
low platelets,
pneumonia,
port-a-cath,
relapse,
social media,
temperature,
wiggly
·
Posted by
Lisa Griffiths
at
13:36
Over the last few weeks we have had a couple of little blips. Small bumps along the road of our new normal.
We have these every so often. I don't tend to write about them, because everything turns out to be ok. There's nothing to worry about and it just doesn't seem newsworthy in the bigger picture, once the moment has passed. But I should. Because these bumps are so much a part of our cancer journey. They are the reason why our life is so far from normal, they are the story behind the chemotherapy and the more familiar aspects of a cancer experience.
Bring it on 2018!
Labels:
acute lymphoblastic leukaemia,
chemotherapy,
chemotherapy side effects,
childhood cancer,
childhood leukaemia,
relapse,
steroids
·
Posted by
Lisa Griffiths
at
12:39
So, we have reached 2018, the year Hugo will finish treatment. It feels significant. The countdown can well and truly begin.
I remember, just after Hugo was diagnosed, reading that treatment for his type of leukaemia would last just over 3 years. I thought it must be a mistake, a bizarre typo. How could life continue with any semblance of normality for that period of time. How could anyone manage 3 years of chemotherapy, let alone a child, my child.
Things I Have Learnt
Labels:
acute lymphoblastic leukaemia,
ALL,
chemotherapy,
chemotherapy side effects,
childhood cancer,
childhood leukaemia
·
Posted by
Lisa Griffiths
at
21:45
It has now been 2 years since Hugo was diagnosed with acute lymphoblastic leukaemia. 24 months of our strange, new, cancer filled life. The learning curve has been steep and I'm pretty sure it's not done yet. Here are a few of the things I have learnt.
Screw you Cancer
Labels:
acute lymphoblastic leukaemia,
cancer,
chemotherapy,
childhood cancer,
childhood leukaemia,
steroids
·
Posted by
Lisa Griffiths
at
19:46
What is maintenance all about?
Labels:
acute lymphoblastic leukaemia,
bone marrow,
chemotherapy,
childhood cancer,
GOSH,
maintenance,
mercaptopurine,
methotrexate,
neutrophils,
septrin,
steroids,
Vincristine,
white blood cells
·
Posted by
Lisa Griffiths
at
21:33
Consolidation
Labels:
acute lymphoblastic leukaemia,
chemotherapy,
childhood cancer,
co-trimoxozole,
methotrexate,
steroids
·
Posted by
Lisa Griffiths
at
13:34
Flying High
Labels:
acute lymphoblastic leukaemia,
chemotherapy,
childhood cancer,
childhood leukaemia,
consolidation,
GOSH,
Great Ormond Street Hospital,
lumber puncture
·
Posted by
Lisa Griffiths
at
21:14
Minimal Residual Disease
Labels:
acute lymphoblastic leukaemia,
bone marrow aspirate,
chemotherapy,
childhood cancer,
GOSH,
Great Ormond Street Hospital,
induction,
minimal residual disease,
remission,
Vincristine
·
Posted by
Lisa Griffiths
at
13:39
Teardrops
Labels:
acute lymphoblastic leukaemia,
ALL,
chemotherapy,
Port,
Vincristine
·
Posted by
Lisa Griffiths
at
22:30
Phase 1 - Induction
Labels:
acute lymphoblastic leukaemia,
ALL,
bone marrow aspirate,
chemotherapy,
dexamethasone,
GOSH,
Great Ormond Street Hospital,
induction,
lumber puncture,
methotrexate,
UKALL 2011
·
Posted by
Lisa Griffiths
at
20:08
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