We cannot Thank everyone enough for their support and donations towards Nathan’s treatment in Texas.
The update we have now for everyone is after a long battle with the hospitals, we have a date – HOORAY!!!
We will be flying out on the 7th July, he will have tests carried out for the first 2 weeks with surgery scheduled on the 21st July, then all being well we fly home on the 30th July.
But due to circumstances, we are asking once again for your help to cover the final costs for his treatment.
We managed to raise the cost for his operation, this was from all your generosity, but to our surprise the final total came in a lot higher than we first expected. (I will upload this for everyone to see so you are aware of the final total too). This final amount will help cover the final part of the costs and any additional we may have to pay while he’s out there.
Since the page closed we still received donations from everyone, which we would like to thank too but we are still a bit short.
Also Justgiving take their 5% plus card processing fees from the final total.

Thank you for taking the time to help and support Nathan once again and we look forward to updating you all very soon.
Follow his updates on Facebook – www.facebook.com/SmileforNathan

Just a little about Nathan and his condition -
Our son Nathan who is 7 is a very happy, cheeky little boy who lives with a rare condition - Hypothalamic Hamartoma which was diagnosed in October 2014. He suffers every day with different types of epileptic seizures, gelastics, complex-partial seizures, drop attacks, tonic-clonic seizures, any combination will happen everyday resulting in him having anywhere between 15-25 seizures.
He has also been diagnosed with Autism, ADHD and ODD which are all linked to the condition.
We have been fighting for his treatment which will have a very high chance of curability, this is only available in Texas, USA.
We discovered the NHS will not fund his treatment.

Thank You! xx