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Never accept “I don’t know” when looking for answers!
Hey all!
Hope your week is going well so far!
I know some of you are familiar with The Mighty community, but for those who aren’t, it’s a great resource and community for other rare disease patients! The do have a section for LEMS patients along with many other diseases.
I was interviewed along with two other LEMS patients to share our “misdiagnosis stories” along with some of the frustrations that come with having LEMS.
I wanted to share the article with you!
“LEMS Advocates: Never Accept ‘I don’t know’ When Looking for Answers”
Let me know what you guys think!
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