Our Mission

The Telomere Project funds research toward treatments and cures for telomere-related pulmonary fibrosis.

Inherited mutations that shorten telomeres are the most common known genetic cause of familial pulmonary fibrosis, a progressive, irreversible and ultimately fatal lung disease. We direct our support to leading laboratories working to understand this disease and turn that understanding into therapies.

Funding research toward treatments and cures for telomere-related pulmonary fibrosis by partnering with leading labs at Columbia, Harvard / Boston Children's and Johns Hopkins.

Supporting patients and families affected by telomere-related pulmonary fibrosis, including hosting community events such as Thrive Tribe gatherings.

Our Priorities

Join Us

We are always looking for dedicated people to join our efforts! If you are interested in joining our best-in-class Scientific Advisory Board or are interested in getting involved in another capacity, we would love to hear from you - please contact us.

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