A Vitiligo interview , Autoimmune Hemolytic Anemia / Cold Agglutinin Disease.

Charlotte's interview


How did all start?

I noticed it in 2007 on holiday in Mexico my fingertips where white it spread from there

Do you already have a diagnosis? How long did it take you to get it?

Doctors just agreed with me when I told them I think I have vitiligo

For what medical specialties have you been treated? What has been the most useful specialty for your?

None it doesn't bother me

What has been the most useful thing for you so far?

I use bath emoilent and cream for the dry skin that's it

What have been your biggest difficulties?

People thinking my skin or face is just dirty

How has your social and family environment reacted? Have your social or family relationships changed?

Family thought I was mad at start now it's more noticeable they comment a lot about it saying every tiny mark they have is vitiligo and how lucky I am that I don't care it would upset them to have it

What things have you stopped doing?

Nothing

What do you think about the future?

I hope it becomes more notiacable on my face so people don't think I just don't wash other than that it does not affect my life

So far, which years have been the best years in your life? What have you done during them?

I was in the army TA 2003 to 2010 was so much fun helped me grow as a person and 2017 I had a baby boy he is my world

What would you like to do if you didn’t have your condition?

I do everything I want nothing stops me

If you had to describe your life in a sentence, what would it be?

There is more to life than what lies on the surface

Finally, what advice would you give to a person in a similar situation?

People who care don't matter and Thoes that matter dont care. Everyone is special in their own way ours is just more noticeable so embrace it.


Jun 22, 2018

By: Charlotte

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