The Scottish Intercollegiate Guidelines Network (SIGN) is due to start developing guidelines on Early Diagnosis and support of Children with FAS and FASD. We are looking for patient/carer representatives living in Scotland to sit on the guidline group with healthcare professionals. If you or someone you know would be interested in helping with this, please get in touch with Karen Graham (karen.graham2@nhs.net). We want to make sure that the patient/carer voice is heard!
FAS/FASD clinical guidelines - patient/carer ... - FASD Support
FAS/FASD clinical guidelines - patient/carer involvement
Written by
patientnetwork2016
To view profiles and participate in discussions please or .
Not what you're looking for?
You may also like...
Hi just wondered if anyone knows of any support groups in the North East England area?? Possible adoption match 3yr old with diagnosis FASD
We know she is diagnosed as being on the spectrum for FASD and have done a lot of research, but...
Finally a EHCP and a Choice of school
Good morning everyone
After nearly three years of...
Sons behaviour worse with me and my husband
My nearly 5 year old adopted son has an FASD diagnosis. He is at reception at school and copes...
No Funding!
Hello all; back in the summer we were referred to the Surrey Clinic for diagnosis and we thought...
Advice please?
Hi all
We have two adopted children , who at present we have documentation to state that...
Coiled spring
Transition to secondary school
Weight gain in FASD
Biological parents of babies and children with FASD
Hi everyone. This is my first post here. My DD, age 7, has recently been diagnosed with FASD. 
