We still Hope
Brief introduction and background. My name is Bukky and I am 20 year old college student.
In 5 days I will be leaving the United States to study abroad in Marseille, France for 5months. I have done all the logistics to take care of myself while away (filled prescriptions, informed doctors etc.)
However, I was wondering if anyone on the site has had experience with Sickle Cell Anemia with abroad and more specifically in France (even more specifically in Marseille).
I have not had a crisis in a year so I do not anticipate falling sick while away but I would like to hear of personal experiences of dealing with Sickle Cell outside of the US.
Living in the nation's capital I often take for granted the accessibility of sickle cell treatment.
I look forward to hearing about your experiences ...
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Hi Gregory,
Thank you so much for your feedback. That's good to hear!
Definitely helpful to know the french name for SCD.
I actually havent seen very many hospitals here but I heard France has one of best health systems in the world sooo (in the unlikely chance) that something happens I feel a lil safer.
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