Carson Family
Carson Family
Dear Luke,
We had a wonderful time when we came to stay with you, we seemed to fit so much in to our holiday!
The boys really enjoyed our visit to Kents Cavern and were made really welcome. As Matthew is learning about Victorians at school we then had a visit to Bygones Museum and again we were made to feel very welcome. After that it was time to go to Angels Tea Rooms for a lovely cream tea that everyone thoroughly enjoyed!! Then in the evening the boy's loved the "Laughter Show" at Babbacombe Theatre.
We had a fantastic day at Woodlands theme park and we had great fun at Paignton Zoo, another lovely day was spent at Crealy Adventure park and the boys really enjoyed the bowling.
The meals at the hotel were delicious, the staff very friendly and the company was lovely!!
To top the holiday off the boys even found Whally at the babbacombe Model Village.
It was lovely to see the boys having such a lovely time and it was so relaxing for all the family.
It is difficult to put into words what the children have to endure and for the families to have to watch them struggle on through the treatment is almost unbearable.
Our nightmare started six years ago when our son was diagnosed with neuroblastoma. This had crushed his spinal cord and spread to his tummy. He had to not only endure the pain from an agonising illness, but also agonising surgeries (three in total, adding up to 24 hours) and then complications with his central lines, where a total of five were inserted through his treatment and several cycles of intensive chemotherapy.
Then came his agonising rehabilitation where he amazed us by learning to walk again and his nervous system re-wired itself to allow this!!!
I think it is fair to say that these children are an inspiration!!
The THHN allows the families to escape for a little while and it gives the families something to look forward to. It is fantastic what you are doing and the amount of work you are putting into this project is a credit to you, your colleagues, family and friends.
Once again thank you for your kindness and it was lovely to meet you.
Jane & Rob Carson.

| Published on 11/01/2010 We just found out that we were going on holiday in Devon. We were so exited it will be lots of fun meeting new people and spending time with my family it will be a very enjoyable week. We are staying in a hotel called the Carlton Hotel which has a swimming pool in it, will be in it the whole time. I just can`t wait. We go on the 4th of January. Read whole article |
| Published on 06/01/2010 Omar was diagnosed with Leukaemia in June 2006 when he was just 6 years old. When being told you child has a life threatening illness it is terrible for the whole family. With Leukaemia it is 3 years treatment for boys, first off they have to have their immune system wiped out and then the first 18 months have intense chemo therapy. The following 18 month stage is maintenance stages which is mainly on a monthly basis. Read whole article |
| Published on 28/10/2009 Two years ago, Lottie, our daughter who is now 10 years, was a normal girl doing really well at everything, the ideal child and pupil, top in her class into her sports, like swimming and running, an all round top kid, chosen by a talent scout to take part in a government run dancing school. Then in the October 2007 half term break all of a sudden she started to walk funny and started falling over, chipping her front tooth, she also started having terrible mood swings ,being a secondary teacher I knew it was probably too early for the dreaded hormones and I just knew something was not right, so we took her to our doctor... Read whole article |
| Published on 28/09/2009 Jack Daly our son was diagnosed with a medulloblastoma brain tumour on the 27th of May 2009 after eight previous weeks of being told by GP's there was nothing wrong with him. On the same day of being diagnosed this traumatic news, our 7 year old son was blue lighted from Reading's Royal Berkshire hospital to the John Radcliffe hospital in Oxford to undergo 2 operations. Read whole article |
| Published on 07/09/2009 Well, we dont know where to start!, we want to say a huge THANK YOU for all what you have done for us both and our son, Westley. we felt very welcome from the moment we stepped foot in the door at the Marina Hotel. All of the staff were lovely and friendly and nothing was too much trouble. The Hotel was run in a professional manner yet the staff were easy to talk to and nice people.. Read whole article |
| Published on 25/08/2009 Gemma is aged 10 and can be described as a very active, out going happy child. Back in April we were told she had Acute Lymphoblastic Leukaemia (A L L) the good news, she probably will not need a bone marrow transplant or radiotherapy. The treatment programme however is 2yrs 3 months, throughout which she will need to take daily tablets which range from 4 to 16 per day and every week she must have a blood test. We have just finished the first five months and this is what she has had done so far: 9 operations 41 nights in hospital 153 injections and 11 transfusions. Read whole article |
| Published on 19/08/2009 Our Daughter Hannah is just sixteen and for the last year she has been battling against a cancerous brain tumour, she has had three lots of surgery, radiotherapy and many cycles of chemotherapy- she is still on chemotherapy and has had a stroke but she does not let that stop her from doing almost anything. We were not going to have a summer holiday this year as I had just returned to work after being off for almost a year to look after Hannah. Read whole article |







