Our Stories

Faces of MAPT FTD: Stories of Courage, Loss, and Hope

Behind every diagnosis is a person. A family. A life forever changed.

Our Stories: Living with MAPT FTD

MAPT FTD doesn't just affect one generation, it ripples through families, touching grandparents, parents, children, and grandchildren. These are the stories of our community: Caregivers watching their loved ones change, gene carriers facing an uncertain future, advocates fighting for treatments that don't yet exist.

These stories are raw, honest, and deeply human. They speak to the isolation, the grief, the small moments of beauty, and the fierce determination to change the future for those who come after us.

Ansel's Story

At 30, Ansel carries the MAPT gene. He traces how FTD took his mother's creativity and made the difficult decision not to have biological children. A meditation on living with genetic risk.

Présymptomatique
Jeune adulte

Catherine's Story

Three generations of FTD. As a child, Catherine saw her grandfather as a "forgetful pirate." After watching her father fade and learning she's a carrier, she turned pain into purpose.

Présymptomatique
Jeune adulte

Erin's Story

Erin's husband went from corporate counsel to needing full-time care. Misdiagnosed as Parkinson's, then FTD. A story of teamwork, disability battles, and choosing love through profound change.

Soignant
Époux

Linde Jacobs présente à l'UCSF une histoire émouvante sur la DFT génétique : se battre pour un avenir

Le 18 novembre, Linde Jacobs, cofondatrice et militante de Cure MAPT FTD, a prononcé une allocution émouvante à l'UCSF devant un groupe de chercheurs sur la DFT génétique. Linde a passé des années à soutenir sa mère, porteuse du gène MAPT FTD. Maintenant qu'elle risque elle-même de développer la DFT, elle est une ardente défenseure du changement au sein de la communauté scientifique.

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Linde's Story

Linde watched FTD take her grandmother, then her mother. Four weeks after her mom's death, she learned she carries the gene. Now she leads research advocacy and fights for her daughters' future.

Présymptomatique
Soignant
Jeune adulte

Marian's Story

Life was perfect until FTD "beamed an alien" into her husband Rob. Over nine years, Marian learned to let go of fixing and focus on loving. Sometimes accepting help is the most loving choice.

Widow
Époux
Soignant

Susan's Story

After generations of FTD in her family, Susan tested positive at 64. The news hit "like a landslide." Now 67 and still asymptomatic, she's grateful for every birthday her mind stays intact.

Présymptomatique

Tanya's Story

Tanya's husband Bob, a beloved teacher, died at 58 from MAPT FTD. A car accident he fled, completely out of character, marked the turning point. Now she fights stigma and advocates for a cure.

Soignant
Époux
Whether you're a caregiver, at-risk family member, positive carrier, or scientist, we want to hear your journey.