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💙 CMT Awareness Month
Each September, we honor CMT Awareness Month by shining a light on what it means to live with a rare disease — and how stories, support, and science can change the future.
Join us in spreading kindness, embracing differences, and giving hope to those affected by CMT.
Together, we are stronger. Together, we are seen.
Our Affiliate Partner: The Hereditary Neuropathy Foundation (HNF)
Together, we’re raising awareness, sharing stories, and inspiring the next generation to embrace kindness, inclusion, and hope.
HEREDITARY NEUROPATHY
FOUNDATION
We are proud to partner with the Hereditary Neuropathy Foundation (HNF) — a nonprofit organization dedicated to improving the lives of those affected by Charcot-Marie-Tooth disease (CMT) and inherited neuropathies. As an award-winning author living with CMT, this partnership is deeply personal.
HNF is at the forefront of research, advocacy, and community support. Through education, outreach, and innovative programs, they empower individuals and families affected by CMT to thrive. Their efforts are making real change possible — and we’re honored to stand alongside them.
You can learn more about their mission and the important work they do by visiting hnf-cure.org.
📖 You can also read my feature on their website:
