Servier shared a post on LinkedIn:
“On Rare Disease Day, we had the pleasure of speaking with Morgan, mother and full-time caregiver to Madilynn, who lives with spinocerebellar ataxia type 5 – one of the rarest forms of ataxia.
Morgan shared her family’s journey through years of uncertainty, the challenges of raising a child with a rare condition, and the strength they found in honesty, resilience, and joy.
Her message to other families facing a rare diagnosis is a powerful reminder: your feelings are valid and your child remains the same child you love.
Watch her inspiring story on our Instagram account.”
Other articles featuring Servier on OncoDaily.