One year on

*All posts about Felix were written with express permission from his mother*

A smidgen over a year ago I wrote this post about my lovely friend Jayne and her equally lovely family, her son Felix and his treatment for Acute Lymphoblastic Leukemia. I went on to shave my long hair off and raise £1200 for CLIC Sargent. And I have you lot to thank for it, because it certainly didn’t all come out of my pocket.

So, how’s about an update? Jayne has been doing a 100 day countdown and we’re down to 3! Each day has had a photo, and I’ve got a few to show you. Over the last week or so Felix has been having some finals.

First, his final IV dose of Chemo:

last IV chemo

Then all at once, his final lumbar puncture, spinal Chemo, and the removal of his portacath.

port out

Here’s the port:


This allowed IV access for treatment and to take bloods without having to put a new cannula in every time. Understandably he was VERY happy to have it out! And I can’t think of anyone more deserving of this big bunch of balloons!

portoutop Here is Felix’s medicine shelf on Sunday. As of friday, it will be almost completely empty. Hey, everyone needs calpol.shelf

Thank you so much to everyone who donated or otherwise helped me on my tiny insignificant endeavor last June to help wonderful children like Felix to receive help in the future from CLIC Sargent.

One last one, of Rudy and Felix. just over 3 years, and he’s almost done. He’s been so amazing and brave, I’m proud of you little dude, Nothing can stop you!

rudy felix


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