Children with FND

[ValueFamily]

Im just wondering and at my wits end with FND. Is there any support groups or other mums here with children with FND. My daughter is 14 x

Fingers and toes crossed that the consultant is right and that the medication works. I was so struck by Suzanne O’Sullivan’s book in which she said that in many ways epilepsy is an easier diagnosis than functional seizures because we do have meds for them.

On money saving - my son’s successful (tho still ongoing) treatment for FND has been more expensive than anyone can imagine - I thank all my stars that it’s the NHS that pays. Pills would have been incomparably cheaper!