Jamie Fergusson

Jamie's chest waxing page!

Fundraising for Solving Kids’ Cancer UK
£203
raised of £150 target
by 16 supporters
Donations cannot currently be made to this page
Event: Vanessa Riddle Campaign, on 31 December 2015
We fund research and support families to access clinical trials for children.

Story

Thanks for taking the time to visit my JustGiving page.( By the way, thats not me in that picture, i'm not that skinny! )

Please note you can now text donate by texting JAMF89 and how much you want to donate £1 - £10 to 70070. Eg JAMF89 £10 to 70070. Thanks :-)

I am trying to raise some money for Vanessa Riddle, Her story below:

 

In Feb 2009 our then 8 year old daughter Vanessa, was diagnosed with Stage 4 (High-Risk) Neuroblastoma, a very rare, aggressive and difficult to treat form of childhood cancer. Fewer than 100 children in the UK are diagnosed with neuroblastoma each year, most of which are below the age of 5 and generally have a better prognosis as the older the child is the worse the prognosis is.

 

Since Feb 09, Vanessa has undergone many different treatments at Yorkhill Hospital in Glasgow, these include; 12 rounds of High Dose Chemotherapy, two 7 hour surgical operations, the removal of one of her kidneys, a stem cell transplant, Radiotherapy, Retinoic Acid treatment and Immunotherapy treatment……all of which was agonising to watch as parents never mind to have to endure as a child!

 

Having undergone all this difficult and often very painful treatment the fact remained that due to a high relapse rate the long term prognosis for Vanessa's survival remained very poor with less than a 40% survival rate. All the same, Vanessa finished her treatment at Yorkhill Hospital in Aug 2010 and was given the all clear.

 

In Dec 2011 after routine scans, Connie and I were given the devastating news that Vanessa had relapsed. She has many hotspots on the skull, neck, spine, leg & knees. The UK doctors have told us that this time round there is very little chance of survival; “much less than 10%” they said, as we do not have any relapse protocols in the UK. This is due to the Government not investing any money into relapse treatments for this disease. This is a very different story to the United States where there are many relapse protocols and taking her there will dramatically increase her chances of long term survival.

 

We now find ourselves in the position of urgently having to take Vanessa to the United States for relapse therapy treatment which the NHS will not fund. The treatment Vanessa requires is likely to involve Antibody Therapy and cost in excess of £500,000. Vanessa’s latest scan results will be used to determine which therapy is best and this is likely to happen at The Children’s Hospital of Philadelphia.

 

Please help us to raise the funds in order to save Vanessa’s life

 

 

A very worthy cause, which I am sure you agree.

I shall be getting my chest waxed on 07/02/12 in the Lonsdale Bar, Troon at 7pm along with a few other people and we are looking for sponsers! So please get in contact and sponser me as much as you possibly can, or if you would like to text donate to Vanessa then you can do so by texting VANY99 and your amount £1 - £10 to 70070.

 

Thank you all for your support, and im sure Vanessa thanks you too!

 

Jamie

 

About the charity

Donations are paid into Solving Kids' Cancer’s general funds for our charitable activities. We help families affected by neuroblastoma through the provision of support and information; as well as investing in research and advocating for access to better treatment

Donation summary

Total raised
£203.00
+ £19.00 Gift Aid
Online donations
£108.00
Offline donations
£95.00

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