The girl with no hair is her third book for health press. Advice for children and young people with alopecia. In these uniquely challenging and isolating times, we want to assure our support for you and the entire community affected by alopecia areata. Alopecia areata aa is a nonscarring autoimmune disease of the hair follicle that can present at any age.
Parents of a child with alopecia areata say that it can feel just as traumatic for them as it does for their child. Thankfully, there are many positive and productive things that you can do to cope with your child s alopecia areata. Alopecia areata in children national alopecia areata. Murphymelas wrote the book to help children cope with the social and emotional implications of living with alopecia areata. Building selfesteem, providing support and raising awareness. She is the author of a number of special needs books for young readers. Alopecia areata johns hopkins university press books. You can join a support group of parents who also have children with. Alopecia areata and covid19 national alopecia areata. Childrens alopecia project alopecia support and awareness. Current treatment strategies in pediatric alopecia areata. Alopecia areata aa including alopecia totalis at and alopecia universalis au a guide to wigs links to our downloaded pdf wig guide, and information on the nhs england wig report. Alopecia areata in children mostly occurs on the scalp where you will see distinct round patches with no hair on it.