Register for our cycling event and help raise funds for LMNA research!

Exciting News: Blood Donation Opportunity at the Laminopathies Meeting in Paris

LMNA patients and gene mutation carriers can donate blood during the Laminopathies Meeting in Paris, thanks to our dedicated expert partners.

Details:

  • Donation slots are available during lunch breaks or at the start/end of the day.
  • Small groups will travel by taxi to the hospital for blood donation.
  • At the hospital, you will sign a consent form and undergo a blood draw.
  • A taxi will return you to the meeting venue.

Register now to secure your spot! We’ll also explore options for joining during the meeting, subject to availability.

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Every contribution, regardless of its amount, fuels crucial efforts in research, medical education, patient advocacy, and raising awareness about LMNA cardiac diseases.

You can make a difference in various ways: by committing as a regular monthly donor, offering a single donation, organizing fundraising events both online and in person, contributing to our special tribute funds, or through your unique fundraising initiatives!
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