Community impact newspaper

Grateful to see stories like this shared so openly. Miranda Hart speaking honestly about years of unexplained symptoms, the relief of finally having answers, and the reality of living with an invisible illness will resonate with so many in this community. Lyme disease doesn’t always look the way people expect. And for many, the hardest part is being believed. Thank you to @mheff_official for highlighting this moment and helping bring visibility to lived experiences that too often go unseen… ***