Cystic fibrosis is supposed to cost up to a quarter of a million dollars per year for medical care per patient. Two members of my household have it. I've supported us all on well under $20k annually for at least eight years and we were homeless for nearly six years.

I often have insufficient money for food. Yet, we are still alive.

I respect your genuine and valid concerns about giving advice in situations where you don't know what you are talking about. Trying to give me advice to do things like volunteer in a hospital or donate money I don't have falls in that category.

Maybe take a few minutes to at least look up cystic fibrosis before commenting further about what you think I should be doing.