So... Wotsit finally had his lumbar puncture on the 6th
August and we got the good news yesterday that his results were positive.
The likelihood of the leukaemia recurring is now within ‘normal’ limits (v
small). The hospital have also confirmed Wotsit’s course of treatment and
he will be participating in the clinical trial which is what we were hoping
for. This means that over the next 8 weeks, once a fortnight, he will
receive a very high dose of Methotrexate. This is given intravenously
over a 24 hour period. We will be in hospital for c4 days during this
time as he is only discharged once the Methotrexate has cleared his
system. We’re told that children following this protocol don’t seem to
suffer too much. Although of course this varies by individual
child. We’re hoping – given Wotsit’s track record! – that he’ll be in
good spirits throughout. The main side effects are hair loss (he only
last about two thirds of his hair before) and mouth ulcers (so far, he’s not
had any). So, fingers crossed.
This is the third phase of Wotsit’s treatment (Interim
Maintenance) and it’s also when the 3 year countdown begins. I.e. 3 years
from now, his treatment (all going well) should be complete. The fourth
phase also lasts for 8 weeks and is called Delayed Intensification (similar to
the first 2 phases with some steroids thrown in for good measure). Then
we move into the final Maintenance period. As Wotsit is having such a
high dose of Methotrexate during the current phase, he will not require any
chemo via lumbar punctures during the final phase (previously given every 12 weeks).
He will also not be given Vincristine or steroids – we are really pleased about
this.
It’s been a long while waiting for Wotsit to have the lumbar
puncture and to get the results but it has meant that he has been chemo free
for c4 weeks, so he is on top form. Pickle is very happy to have his
playmate completely back and we have had a lovely summer break so far.
The next 8 weeks (starting on the 21st August) will be particularly
tough on Pickle as he will miss his brother (possibly his Mummy) and will be a
bit frustrated, and maybe worried, if Wotsit’s not feeling great.
Hopefully he’ll get through it okay with lots of support from us, school,
grandparents & friends.
We’ve managed to keep Wotsit’s birthday a ‘treatment free’ day so
looking forward to celebrating that on the 27th. He will also
be able to attend his first day of Year 1 (although he will be whisked to
hospital at 3.15pm the same day!).
We’ll keep you posted on how he’s getting along and see some of
you soon.
Lots of love
xx
P.S. Participating in a ‘trial’ seemed quite scary initially when
you’re trying to ensure your child is fully fixed from leukaemia. Rest
assured, they’re not allowed to do anything crazy! The protocol Wotsit
will be following is tried and tested in other countries and is the method the
UK is hoping to adopt as it should give children a much better quality of life
during the treatment.