I'm wondering if any of you are parents of children with Lyme Disease. My brother and sister in law are in that predicament now with their daughter (my niece) and I'm trying to get them as many resources as possible for them to find out more about others with children diagnosed with Lyme Disease.
Do any of you know of child-specific support groups for parents? I really think it would benefit them and would love to hear if you have personal experience with any groups out there!
Do any of you know of child-specific support groups for parents? I really think it would benefit them and would love to hear if you have personal experience with any groups out there!