Update 05/08/2015: Sophie continues to do great and never ceases to amaze us every day as she grows up way too quickly! She’s now finished year R at school and had a great holiday in France last week where she discovered pony riding!
Update 22/02/2015: We received some fantastic news mid-January, Sophie has now officially been in remission for two years! Sophie had a 75% chance of relapse so this is an amazing milestone to reach and we are, of course, ecstatic and incredibly proud of our little lady.
We are feeling very thankful and incredibly lucky! Thank you once again to everyone who helped this become a reality.
Update 22/05/2014: Sophie’s running a mile in Westminster this weekend raising money for Frimley Park hospital! If you’d like to sponsor here you can read more about the run here.
Update 04/04/2014: Two years ago Sophie relapsed but the amazing support she received from everyone, coupled with her incredible strength, means she’s now a very fit and well little princess! And, thanks to the very kind generosity of the Rays of Sunshine charity she’s just been on a magical holiday to meet the other princesses at Disneyland in Paris. Hope you like the photos!
Update 10/07/2013: Sophie is doing great! She’s so full of life and energy, so healthy and active, that it’s easy to forget how different things were a year ago. Her AFP is still consistently under 2 and she’s just returned back from her first holiday abroad where she had an amazing time with her younger brother James and Grandma and Grandpa (or Grampa-Grampa to her).
Update 12/05/2013: This time last year we were told Sophie had relapsed and were asked if we wanted to put her in palliative care. After that devastating day it’s been an incredible journey and with so much amazing support from you all she’s now 3 months in remission, back at nursery and due to have her Hickman Line removed on Tuesday so she can go swimming again. Thank you so much.
Update 29/01/2013: Great News! After 18 months of treatment comprising of 18 rounds of chemotherapy and 3 major operations Sophie is now stopping treatment. Thanks so much everyone for what you did, you can read more here.
Check out the amazing charity single and video here!
Update 07/10/12: Read all about how Sophie’s been doing in the 6 weeks since she returned from New York here.
Update 21/08/12: Thanks to your amazing generosity Sophie has now had the operations in New York on her left and right lungs that, combined with further chemotherapy in the UK, will give her the best chance at survival. We will keep you up to date with her progress both here and once she’s back in the UK. Thanks again Xx.
Update 18/07/12: We’re extremely disappointed to say Sophie’s surgery is being re-planned, with potential cost implications, and has been delayed until August 9th. In light of this we’ve raised the fundraising target to £350,000 to try to cater for the worst case that the re-planned surgery will now cost more and that she would need an air ambulance home. You can read the full details of what’s happened over the last few days here.
Please watch this wonderful video which tells Sophie’s story. By Kate Tweed, Andy Humphreys and Tracey-Ann Obermann courtesy of AMV BBDO.
Our amazing friends at ACM released a charity single for Sophie, ‘Shout it from the Rooftops’, which you can purchase here http://sophierobertsstory.bandcamp.com/.
They’ve also produced a fantastic video to accompany the song:
Update 29/06/2012: The support we have received to raise money for Sophie’s treatment has been truly overwhelming.
We are so happy to say that he have hit our target on the team page www.justgiving.com/teams/sophierobertsstory after an incredible 6,000 donations from around the world, with even a dedicated fundraising site in France. That means we can go ahead and get Sophie the surgery that she needs to give her the best chance. We’re looking forward to later in the year when hopefully our beautiful girl will be in remission again!
If you are moved by Sophie’s story and still want to donate this would be fantastic as any excess money raised will be managed by the charity we have been working with, Kids ‘n’ Cancer, to help other children who are in situations like Sophie get a head start in getting the critical treatment they need. Some funds may be retained for Sophie by Kids ‘n’ Cancer, in case she requires treatment again. Should there come a time, for whatever reason, that Sophie no longer requires treatment, those funds would be made available for other children.
We’ll continue to update this blog and the various social media services we’ve been using (such as Twitter and Facebook) to let you know how Sophie’s getting on, and to let you know about fundraising events we’re running. Friends and family will continue to work hard for her cause over the coming weeks and months and anything we raise will be managed by Kids ‘n’ Cancer to help her and other children.
Our gorgeous daughter Sophie was diagnosed with liver cancer, which had spread to the lungs, in June 2011. This is a cancer that affects only a few children each year. The prognosis for children with this type of cancer when first diagnosed is extremely poor at just 30%. Sophie bravely endured 3 rounds of traumatic chemotherapy before having liver surgery on 16th November 2011 when 25% of her liver and the entire primary tumour was removed. She then started a further 4 rounds of chemotherapy to clear the remaining tumours in her lungs and went into remission in March 2012. By this happy time she’d spent over 50 nights in hospital and a ¼ of her life suffering from a life threatening illness.
Unfortunately, our happiness and joy was short lived as the cancer returned aggressively throughout her lungs in early May. Treatment options for this kind of relapse are very limited, and she is currently being treated with new chemotherapy to control the disease. Her condition is so rare that the doctors cannot give us a prognosis. We are documenting our brave girl’s ongoing fight and treatment, to raise £230,000 to help to pay for surgery and to raise awareness of this awful rare disease. The best treatment option for Sophie is surgery; two UK surgery teams have refused to operate but luckily a team at Sloan-Kettering in New York has agreed to offer her life saving surgery. This surgery has to be privately funded by Sophie’s family, so we are asking for help with raising this money.
We have already lost several very close family and friends to cancer over the years and will do whatever it takes to ensure we do not lose anymore. Please donate through the JustGiving link on the right and you’ll keep us fighting and hoping.