One thing I hear a lot of people with sickle cell talk about is their struggle with having small veins. I don’t know if this is due to the biology of an individual with sickle cell, or repeated use (IV fluids, transfusions, injections etc), or a mixture of both, but I do know it is a persistent problem within the community.
Do you have any tips that you can share that help with access to your veins?
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