I've been contacted by a representative from Nationwide Children's Hospital in Columbus, Ohio about a study they are working for treating Pilonidal with laser hair removal. They are in the funding stage and will be recruiting participants from the local area soon. The PSA has become a stakeholder to assist in their study.
I offered to post their questionnaire here on the forums to gather opinions from people suffering to help their research be as extensive as possible. The questions are below.
If you feel so inclined, please copy/paste the questions and add your answers. I'll forward on to the research team.
Pilonidal disease is a very difficult problem and treatment often takes a long time. Is there anything that you wish you knew at the beginning when you were first diagnosed with pilonidal disease that you know now?
I didn't find the right solution from the Internet.
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