Donate

The XLH Network needs your support to continue to achieve our goal to discover better treatment and ultimately a cure for this rare and neglected heritable bone disease affecting 1 in 20,000 babies and adults worldwide. To date there is no cure for XLH and the current treatment is not always successful, and if not carefully monitored it can be damaging to organs. Your contribution helps our organization continue the support and fund ongoing research and bring awareness to pediatricians so our babies can be diagnosed at an early stage improving the future for every child and adult affected with XLH. We cannot exist without your donations every donation regardless of the amount can make the difference in achieving our Mission. It is the spirit of giving that really counts. The XLH Network is currently funded entirely by donations from those people whose hearts we've touched, and we are very grateful to those individuals.

There are many ways to help us:

 You can contribute worldwide via PayPal or Credit Card:  

                                             DonateNow

  ~ OR ~


Checks (USA banks only) may be mailed to: 

The XLH Network, Inc.
911 Central Ave., #161
Albany, NY 12206
USA


Other ways to help: 
 

  • Employer Matching Gift
    Many employers have programs to match donations made by their employees.  Check with your employer to see how to add The XLH Network, Inc. to their employer matching gift program.
  • Planned Giving
    Ask your financial and legal advisors about including The XLH Network, Inc. as a beneficiary in your will or whether there may be ways to help us that would also benefit you financially while you're still alive.  
  • Shop and search online to support The XLH Network, Inc. at:

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  • Donate a vehicle to support The XLH Network, Inc. at:           

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  • Fundraising Ideas

The XLH Network, Inc. is a not-for-profit corporation and is recognized in the USA as a tax-exempt 501(c)(3) publicly supported charitable organization.   

The XLH Network needs your support to continue to achieve our goal to discover better treatment and ultimately a cure for this rare and neglected heritable bone disease affecting 1 in 20,000 children and adults worldwide. To date there is no cure for XLH, and the current treatment is not always successful and often includes damaging side effects.

The XLH Network contributes to research efforts geared toward finding a cure for XLH in an attempt to improve the future for every child and adult affected with this disease. Your donations help our organization continue to raise awareness among medical and patient communities in invaluable ways.

The XLH Network is currently funded entirely by donations from those people whose families and friends are afflicted with XLH. Please consider making a donation to help ensure better lives for those living with XLH.

© 2011, The XLH Network Inc.
The authors of this web site are not medical professionals, and this information does not substitute for medical care. Information on these pages is based on biomedical research, published in peer-reviewed journals, and international research conferences. Additionally, in some cases anecdotal information is provided by subscribers of the F-HYPDRR group, a mailing list for The XLH Network Inc. A listing of XLH research is available. Please read our full disclaimer 

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Last modified Dec 10, 2013


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