IT’S RARE DISEASE DAY!💛🦠💊
Our founder, Faye, shares her experience of living with a rare disease. It can be a constant battle, one that makes you feel alone as you constantly have to prove that your life is worth it.
Although, one of the positives of the Rare Community is the love and support everyone has for each other.
The same love and support that Leigh Network has created over the years 🤝💛🦋
If you are struggling with loneliness and need some love and support, please reach out to us.
Watch Faye’s video on the Leigh Network Instagram
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#RareDiseaseDay2022 #raredisease #leighsdisease #mito #mitochondrialdiseases #charitysupport