Showing posts with label relapse. Show all posts
Showing posts with label relapse. 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.
What happens next?
Labels:
acute lymphoblastic leukaemia,
ALL,
chemotherapy side effects,
childhood cancer,
childhood immunisations,
childhood leukaemia,
end of treatment,
end of treatment bell,
GOSH,
port-a-cath,
relapse
·
Posted by
Lisa Griffiths
at
11:44
During our last appointment at GOSH, our oncology nurse specialist answered the all important question - 'what happens when treatment ends?' I've asked many questions relating to this along the way. Always hesitantly, not wanting to look too far ahead, not wanting to assume we will make it that far. One day at a time, that was always the way to deal with this, but sometimes the practical side of me would come out and I needed to know, I needed a glimpse into the next stage of our lives. Now we are here, now it was time to get the full story.
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.
A Mini Holiday
Labels:
acute lymphoblastic leukaemia,
Calcot Manor,
childhood cancer,
Cotswold Farm Park,
Cotswolds,
maintenance,
relapse,
transient synovitis,
Vincristine
·
Posted by
Lisa Griffiths
at
20:06
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