Sickle Cell mini interview

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If there is any one who has sickle cell disease and willing to answer a few questions for my pediatric research paper I would greatly appreciate it. I am wanting to get a personal view on this disorder with real and up to date information.

You can message me the answers to the following questions. It will be completely anonymous and I will not use a any names in the paper.

Thank you soooooo much :)

Did your parents have genetic testing to know the chances of having children with sickle cell?

If not, when did they first find out you had acquired sickle cell?

How did you respond the first time you had a sickle cell crisis? (fear, pain, etc.)

How often do you have crises?

What are some things you do to prevent a crisis?

How has this impacted your life socially, psychologically, and physically?

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