Someone sent me a letter saying that their family absolutely will not support them in their battle with NeuroLyme. The family will not even ask them how they are or acknowledged that they have the disease. I think its very sad but also a very common experience for people with Lyme. We have only 3 members of our entire family that support us in our battle with this disease. Makes me realize how important sites like Facebook are for people struggling under the weight of chronic illness. Sometimes it is the online "friends" that end up being a life line for those that are struggling with illness and pain everyday.
On a lighter note