Super Seraph vs. Neuroblastoma

https://solvingkidscancer.org.uk/campaigns/seraph/

Please now go to the above link to support Seraph. Gofundme can no longer collect donations for us.

We have moved to become part of a registered charity, and continue to raise funds for Seraph's treatment.

Thank you so much for your support and love. We so appreciate it. We hope you will continue to follow us on Facebook, Twitter, and Instagram, and share our story, in order that Seraph may get the vaccine in the US, and remain the happy, well, boy he currently is.  Love, Cass, Liam, Logan, and Seraph. xxx***************************************************************************************************************
We have moved to become part of a registered charity, and continue to raise funds for Seraph's vaccine treatment here

@ https://solvingkidscancer.org.uk/campaigns/seraph/

Thank you so much for your support and love. We so appreciate it. We hope you will continue to follow us, and share our story, in order that Seraph may get the vaccine in the US, and remain the happy, well, boy he currently is.  Love, Cass, Liam, Logan, and Seraph. xxx

***************************************************************************************************************

Meet Seraph. 

Seraph is a very cheeky little monkey- As many four year olds are. He likes dinosaurs, Lego, Minecraft, and giggling like an idiot. Most of all though, he loves his big brother, Logan. 

Seraph also has High Risk Neuroblastoma; an aggressive form of paediatric cancer, with only a 40% chance of surviving the next 5 years.

In 2017, he was a just normal 3 year old; finding his feet at nursery, making new friends, climbing on everything!  One night, just before Christmas, he fell out of his cot and broke his arm. Just our luck, we thought. Not knowing what was to come. Over Christmas, he still seemed in a lot of pain, so we returned to A+E. An exploratory ultrasound revealed a tumour in his abdomen. Further investigation showed the cancer was in his skeleton and bone marrow. The broken arm had very much been 'a lucky break.' Without it, our first trip may well have been to PICU.

Seraph has been through so much; surgery, chemotherapy so strong it has damaged his hearing,  a stem cell transplant (which had him in isolation for a month, and in hospital for 2).  He was the first patient at Addenbrookes to undergo 5 weeks of radiotherapy for this disease, and he did each day without general anaesthetic (unusual for a child so young). Finally, we hope he'll finish Immunotherapy in June 2019. 

Although this is one of the most intensive protocols for any paediatric cancer (and all the NHS can currently offer) still about half of the children who make it through, relapse. Therefore we are fundraising for future treatment. Current possibilities cost in the hundreds of thousands of pounds, and are (just now) only offered abroad.

'Logan is our moon. Seraph is our sun. I honestly don't know what we'd do without him. Every child deserves a full and happy life, and we need both our children to shine.'

Please share and donate to allow Seraph access to potentially life-saving treatment.

Follow Seraph @

https://www.facebook.com/TeamSuperSeraph/ 



*Should money raised not be needed by Seraph, this would be put towards helping other Neuroblastoma families, or for Neuroblastoma research.