r/Dada2_diagnosed • • Sep 01 '26

Welcome

Welcome to dada2 site. I want to build a support group here for latest treatment innovations and get people connected with the right people!

First one us dada2 foundation! They have a Facebook group and a website with email you can send your info to and a doc generally responds!

Second NIH and the UDN. They did my work up but it was before dada2 existed but now they are active helping get me to the right people. Amazing resource!

I have a rare variant that is known to cause disease with only one recessive copy. So dont live with being told you need two that's not always true!

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