There are so many ways to join the fight against DCO and Telomere Biology Disorders. Your financial support and personal involvement helps families and provides the medical community with the funds needed to research finding causes, effective treatments and to educate other medical providers.
Your help makes it possible to meet patients’ needs, hold impactful conferences, develop fresh education programs and fund research for the cures, along with improved treatments until cures are discovered.
There are so many ways to join the fight against DC and Telomere Biology disorders. Your financial support and personal involvement helps families and provides the medical community with the funds needed to research finding causes, effective treatments and to educate other medical providers. Team Telomere is a US registered 501(c)(3) corporation, your contributions may be tax deductible. Our tax ID is 26-3776187.
Team Telomere Inc.’s mission is to provide information and support services to families worldwide affected by
Dyskeratosis Congenita and Telomere Biology Disorders. Financial and other information about our charity’s purpose,
programs and activities can be obtained by contacting Katie Stevens, Executive Director, 1562 First Avenue #205-4093,
New York, NY 10028, 208-215-1347. If you are a resident of any of the following states, please review the relevant
NEW YORK: Upon request, a copy of the latest financial report filed with the Attorney General as well as a full description of
the programs and activities supported by contributions can be obtained by contacting Team Telomere Inc. at 1562 First
Avenue #205-4093, New York, NY 10028. Financial reports can also be obtained from the charities registry on the Attorney
General’s website or by writing the Charities Bureau at 28 Liberty Street, New York, NY 10005. For more information about
charities, visit the Charities Bureau online at www.charitiesnys.com or call 212-416-8401.
PENNSYLVANIA: The official registration and financial information of Team Telomere, Inc. may be obtained from the
Pennsylvania Department of State by calling toll-free, within Pennsylvania, 1-800-732-0999. Registration does not imply
CONTRIBUTIONS ARE DEDUCTIBLE FOR FEDERAL INCOME TAX PURPOSES IN ACCORDANCE WITH
APPLICABLE LAW. REGISTRATION IN A STATE DOES NOT IMPLY ENDORSEMENT, APPROVAL, OR
RECOMMENDATION OF TEAM TELOMERE, INC. BY THE STATE.
By joining #teamtelomere and pledge to raise a minimum of $200 for Team Telomere, we’ll hook you up with a great race shirt and reimburse your race fee up to $75. If you raise $1,000 or more, we will cover the entire race fee! Just hang on to your race entry confirmation, raise some money, and we’ll virtual high five you at the finish line.
10,000 Steps for a Cure
November 2021, we pledge to walk 10,000 steps daily to demonstrate our commitment in continuing along the journey towards a CURE for Dyskeratosis Congenita by fundraising for Team Telomere. To register, send an email and we will help you get your Crowdrise set up! #10kSTEPSforaCURE
Team Telomere Turkey Trot
Each November we ask you to join us in a local Turkey Day race in your area. Simply print out the bib and snap a picture of yourself and your friends and family, be sure to use #TTTT2021 on social media! To fundraise for your trot, send us an email to firstname.lastname@example.org and we set you up with your Crowdrise page! Get your wobble on before or after you get your gobble on!
TeamTelomere depends on the commitment, creativity, talent, and energy of its volunteers. They are our local ambassadors, and we rely on their event organizing skills to support patients, family, and friends in their community. Their work also contributes our mission to provide information and support services to families worldwide affected by Dyskeratosis Congenita and Telomere Biology Disorders.
- Learn about Dyskeratosis Congenita and Telomere Biology Disorders
- Make an impact by raising public awareness and funds
- See how programs grow with their support
- Make new friends