By Sueli Silva Barros
I have had UCE for nine years, and I only discovered the diagnosis of this disease in 2017.
For me, the hardest thing was dealing with the fact that people didn't know about the disease, so I think the 3000 days blog is important. No 3000 dias foi que eu tomei conhecimento melhor sobre UCE, o que me ajudou a encontrar uma médica que realmente me deu o diagnóstico correto, e olha que eu já tinha peregrinado por vários médicos…
The disease still limits me a lot. But the important thing is to live one day at a time!
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