Interesting conversation that I’m not quite sure what to make of it.
Maybe a misunderstanding ?
I’d say probably a generalisation of future intention of the insurance company?
I’ve taken snippets from the thread
Hello everyone,
I have a few questions for you guys:
We are living in Germany and our little girl (4yo) got diagnosed with Rett syndrome in may. She has a mild variant call Zappela (in Germany) or atypical Rett syndrome……
……We just received a letter that our insurance would cover the cost of Daybue which we are thrilled about……
Response to post
- very glad that you insureance will cover Daybue. We are living in the Netherlands and desperately want to try Daybue too for our daughter of 7.
Does the farmacie provide Daybue in Germany, I didn’t know that it iş available in Europe…..
Reply from author
- I still don’t know how to get it but the insurance agreed to cover the cost. As soon as I find out more I will let you know
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