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Donate by Check or Donate Online or PRINT Donation Form for Offline Donations

Make your check payable to the "Turner Syndrome Foundation, Inc." and mail it to:
Turner Syndrome Foundation, Inc., PO Box 726, Holmdel, NJ 07733

Pay by credit card online or call to process over the telephone by calling 1-800-594-4585.
Your gift is 100% tax deductible. 



"First a baby, soon a growing child, and finally a woman, our efforts must transcend the Turner syndrome life span". 


Thank you for your generosity!

 Turner Syndrome Foundation, Inc. is a registered 501(c) 3 nonprofit organization


A Gift of Support

The Turner Syndrome Foundation is dedicated to the life and future of all girls that are affected by this complex disorder. As we know there is no certainty on the viability of a fetus with Turner Syndrome and we realize there is a great need for answers. Why did this happen to my baby? Will this happen again in future pregnancies? How could this mutation have been prevented? What will come of her future? There are many unknowns, and we are dedicated to tackling these difficult questions to search for answers and to provide education, information, and support through our programs areas of Awareness, Advocacy, Education, and Research.

Over the past years, we have spent much time and energy engaging with professional organizations delving into a higher level of understanding and information sharing about Turner Syndrome. The foundation holds a rigorous exhibition schedule at major national conferences where information is disseminated and collaborations incited. We have produced a number of education videos and have jointly sponsored the first web based education program for pediatric care providers. We enlist the volunteerism efforts of good people and companies who can help once or help often on one of our committees. A National Council of State Leaders has been formed to arm the United States with a coordinated advocacy effort to raise awareness, increase education opportunities regionally, and support research. We rely on charitable contributions to achieve much of this work, and our tireless energy and your support truly make a difference. 

Your support helps us to continue these programs that have proven successful to improve the lives of babies, caregivers, and their community. There is so much more that needs to be accomplished, and we hope that we can count on you for your generous support.

There are many reason one may choose to make a gift to the Turner Syndrome Foundation. 

A Gift of Celebration
Happy is the Day...
A new baby, birthday, anniversary, new job, driver's license, marriage, graduation, retirement, get well, good luck, or best wishes. 
These are some of the celebrations that can be honored with a gift to the foundation.

Send a sentiment along with a gift card honoring a special occasion.
Send a Celebration Greeting card 

A Memorial Gift
Losing a loved one is painful, and your kind gesture in sending a memorial card may bring comfort to those who are left behind.
A memorial gift card in lieu of flowers is a lasting gift to honor a treasured friend or loved one who has passed or is remembered.

Send your sentiment in a memorial card

Tribute donations can be made online or by contacting us for person to person service.
 

Investing In Their Future 
How will my donation be used?

Learn How You Can Help

Donor Bill of Rights

Legacy Society

Commercial Sponsorships

Corporate Giving / Online Shopping

TD Bank Affinity Program

Workplace Donations

Employee Matching Program

Personal Fundraising

Host a Special Event

Vehicle Donations



































































How will my donation be used?



Your contribution is an investment in the lives of babies born affected by Turner Syndrome. Our mission to raise awareness to reduce the age of diagnosis does not end there. Our vision is to bring hope and promise for improved outcomes and healthier futures for all babies born with this disorder.

These funds help support our programs for awareness, advocacy, education, research and support to achieve the following:

  • Decrease the current age of diagnosis through a strategic awareness campaign that has successfully been active in Arizona, Florida, New York, New Jersey, Washington, Tennessee, and Texas... and we are just getting started!
  • Improve quality of life issues and care outcomes by providing online resources, webinars, workshops, and more to increase knowledge and advocacy efforts
  • Inspire professionals to understand the prevalence of Turner Syndrome and to know the indications
  • Inform the general public and physicians to take a closer look at short girls
  • Raise awareness about the realities and social norms of this female condition 
  • Increase scientific advancements to find answers to questions
  • To ensure there is dignity in care to every child who survives with this lifelong disorder
  • To promise patients and caregivers support closer to home
Stay connected, and watch us grow. Join our efforts. Support our movement. 
Register today to receive our monthly e-Newsletter

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Donor Bill of Rights


                                                                    



To assure that philanthropy merits the respect and trust of the general public, Turner Syndrome Foundation supports the Association of Fundraising Professionals and other fundraising organizations in a declaration that all donors have the following rights.
Philanthropy is based on voluntary action for the common good. It is a tradition of giving and sharing that is primary to the quality of life. To assure that philanthropy merits the respect and trust of the general public, and that donors and prospective donors can have full confidence in the non-profit organizations and causes they are asked to support, we declare that all donors have these rights:

Read the statement in both Spanish and English

English  Spanish 








 


 
























































 

 

Make A Difference

Legacy Society

Leaving A Legacy


Planning now for their future. 


Providing for the future of others is admirable and significant. When you designate a gift in your will or estate plan to the Turner Syndrome Foundation, Inc. you are leaving an enduring gift that promises a better future for babies born with Turner Syndrome.

A thoughtful way to ensure that your support continues after you are gone is by taking a few simple steps when preparing your estate plan. You can maximize the amount that will go to charity and minimize the amount paid for taxes while knowing that you have earned thanks of those who will be helped by your caring generosity.  A gift in your will, called a bequest, could be the right option for you.  Bequests allow you to have an impact on the future without parting with your assets today.  And, your generosity will continue long after you are gone.  

We provide an opportunity for people of all financial means to contribute in a meaningful way. Depending on your philanthropic priorities and your financial situation, you can talk with your attorney or financial advisor to determine which strategy and type of gift best suit your charitable goals. Give to a cause you care about most while gaining maximum tax benefits under state and federal law. Schedule a time to discuss ways you can maximize your gift. 

You have flexibility.  A bequest lets you balance your philanthropic goals with your concerns about the future.  Because you are not actually parting with assets today, you don't need to worry that you might later need those assets to live on.  Plus you can change your mind at any time.

You can be sensible in your commitment.  Your gift can be made as a percentage of your estate, allow you to benefit Turner Syndrome Foundation and loved ones in relative proportion.

Contact your lawyer to add a charitable gift in your will.  Decide what amount or percentage you want to give.  Work with your lawyer to update your existing will with a simple codicil or to begin developing your estate plan.  Notify us of your intention so we can thank you for your future gift, recognize you (we will honor your preferences regarding anonymity) and keep you informed of our ongoing activities.

Specific Language For Your Bequest

Outright Bequest

"I give, devise, and bequeath to Turner Syndrome Foundation, Inc., PO Box 726, Holmdel, NJ 07733, $______ or ____% of my estate to be used for (general purposes OR write your specific purpose here.)"

Residual Bequest

"I give, devise, and bequeath to the Turner Syndrome Foundation, Inc., PO Box 726, Holmdel, NJ 07733, ____% of the residual of my estate to be used for (general purposes OR write your specific purpose here.)"

Contingent Bequest

"In the even that ___________ predeceases me, I give, devise, and bequeath his/her share of my estate to the Turner Syndrome Foundation, Inc., PO Box 726, Holmdel, NJ 07733, $______ or ____% of my estate to be used for (general purposes OR write your specific purpose here.)"

Join the Legacy Society of the Turner Syndrome Foundation. Legacy Society form

Should you have questions, please contact 800-594-4585 for more information.

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Corporate Giving


A new way corporations are giving back is to support their customers and giving back to the Turner Syndrome Foundation at no additional cost to you. 
AmazonSmile - shop online
Ebay Giving Works
GoodSearch.com
OneCause.com
TSF Program - Travel for TS:  travel@tsfusa.org
Vehicle Donation - Free Towing!


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TD Affinity Program




Our friends at TD Bank will support our charity, but we need your help.

TD Bank Affinity Member Program
Call 1-888-751-9000 or 732-264-5702 and tell TD Bank you want your balances to benefit an enrolled affinity membership organization.
Designate Turner Syndrome Foundation as your membership organization, Affinity Code #A3538

TD Bank will make an annual contribution based on the average balance in all members’ accounts. Checking, Savings, Money Market, CD and IRA accounts are all included in the program.

Contributions are calculated at 1/2% on checking balances and 1/4% on savings, CDs, Money Markets, and IRA balances. Members’ accounts are not affected in any way by this contribution. Your account balances are used to determine the level of contribution and are kept confidential. 



If you are already a TD Bank Customer, visit any TD Bank location and ask to have your balances included as part of your organization’s Affinity Membership Program.

View the TD Bank Affinity Program Flyer 



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Commercial Sponsorships
  



uprinting
Printing Services by UPrinting.com






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Workplace Giving

Workplace Donations

Workplace donations are a simple way to donate to the Foundation through payroll deduction plans. You may designate your gift to the Turner Syndrome Foundation through the Combined Federal Campaign (forthcoming), United Way or other employee giving programs. For more information, please contact your Human Resources or Charitable Giving Department to learn more about your company’s campaign.




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Employer Matching Gift Program

Gifts can be doubled through Matching Gift Programs. Many companies match employee and/or retiree charitable contributions annually, dollar-for-dollar up to a given amount per company policy through a company Matching Gift program.

If you or your spouse work for, or are retired from, a company that matches employee gifts, please contact them directly to obtain a matching gift form from the Human Resource Office. Please send it to us with your donation, and we will complete the form for your company’s matching gift.


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Personal Fundraising

Through the generosity of charitable donations, the Turner Syndrome Foundation has been able to expand our reach to familes affected by Turner Syndrome, produce and distribute more educational materials to doctors and educators, host seminars about TS at local universities for educators to earn continuing education credits, advocate for our girls’ rights in Washington, DC and much, much, more.

This process can be accelerated by your contribution to fundraising activities such as individual donations, grassroots fundraisers and corporate partnership and sponsorship.

Download an application

Read more about personal fundraising


CHILDREN'S BOOK
Katie Volz, illustrator of children's book, Tiggy Finds a Home, was diagnosed with Turner Syndrome 11 years ago. Now 20, Kate attends college, works part-time and is the illustrator of her mom, Carole Volz' book.  This is the beginning of a small series of Tiggy books...so Kate's not finished illustrating.   
Tiggy would like you to please contact Carole for a hard cover copy because proceeds of the sale of her book will be donated to the Turner Syndrome Foundation.  




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Host a Special Event

Lend your time and talent, especially your passion, to make a difference to host a special event in support of the Foundation.
Read the guidelines
Fundraising Ideas
Special Event Form
Let us know how you would like to help. We ask you write a cover letter and send it along with the Special Event Form.

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Vehicle Donations


Donate just about any vehicle, motorcycle, van, motor home, boat, jetski, etc., and get a tax credit letter, plus free towing. You must have the registration title for the vehicle, provide your information, and the vehicle will be picked up from anywhere in the US and Canada.  Donating is easy! Call or click: 1-855-TSF-4CAR



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Contact Us

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