top of page
DONATE
Home
What is Lynch Syndrome
Genetic Testing
Screening
Knowing your Family History
Education & Advocacy
Podcast
Living with Lynch videos
Patient Community Discussions
Downlodable Resources
Social Media Toolkit
Feedback Survey for Podcast
Blog
Resources
Peer to Peer Support with Imerman Angels
How do I know if I have a LS mutation?
Guidelines
MSI-H and mismatch Repair Deficiency
Find a Clinic
Donate
Donate Now!
Lynch Syndrome Research Accelerator
Team AliveAndKickn NYC Marathon
Team AliveAndKickn NYC Half
Headlines
About
More
Use tab to navigate through the menu items.
Blog
Clayton and Kirah
My journey into finding that I have Lynch Syndrome (PMS2) was about the hardest you could fathom, I lost my oldest daughter, Kirah at 19...
bottom of page