Written by Dena, Carys' Mum
Carys is 12 years old and is the only one in our family to have NF2.
At 9 years of age she was diagnosed with a brain tumour after having multiple seizures. She was lucky that the surgeon quickly operated and was able to remove it all. The recovery from this surgery was very slow. It took her a full year to be able to have enough energy to attend school full time.
The following year she was genetically tested for NF2 after discovering a second tumour growing off her spine. At this stage we really had no idea what NF2 was as we had never heard of anyone ever having it, nor was it in our family. When the tests came back positive we were absolutely devastated, our world felt like it had turned upside down. We could not believe this was happening to our beautiful girl.
We kept saying to ourselves why is our sweet little Carys being burdened with this awful genetic disease? Why her? What has she ever done to deserve this? All of these questions just kept going around in our heads. We came to the realisation there is no answer to these questions and we just must be loving, supportive and strong for her."
When she asks similar questions, we tell her she is the extra special one and only children brave and strong like her can deal with this. She loves knowing she is an NF hero.
After every MRI scan (where she must stay completely still for up to 90 minutes, which is traumatic in itself) we hold our breath that nothing new has appeared.
Her most recent scan has shown the potential starting of two more tumours off her spine. The doctors say all we can do now is keep scanning and watch them and hope they don’t cause pain.
Carys is currently doing amazingly well. She loves dancing and netball so we keep her as active as she can be. It is important that she enjoys this time as we just don’t know what the future holds for her.