Site © 2017 par Anthony W. Rose (anthony.rose@ctnnb1.org) pour la sensibilisation mondiale au syndrome du CTNNB1. L’information présente sur ce site ne se substitue pas à un conseil médical personnalisé. Veuillez consulter un clinicien qualifié pour toutes questions concernant le diagnostic génétique, la gestion de la maladie et
la santé.

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Do you remember what it was like to get the diagnosis of CTNNB1 Syndrome?  You frantically searched the Internet for some information about CTNNB1 Syndrome, but could only find a few scientific studies.  You wondered how you were going to help your child achieve the life that you had dreamed for him or her.  This was something that each of us at CTNNB1 Syndrome Awareness Worldwide experienced, and it is the driving force behind our creation of ctnnb1.org.

 

We are registered as a charity in Ohio, USA as CTNNB1 Syndrome Awareness Worldwide. As you may have read elsewhere on this site, we are seeking donations to support our filing for non-profit status as a 501(c)(3) organization.   All donations that are given prior to our achieving that status cannot be deducted from your US income tax. However, we desperately need your support right now to help us achieve this designation. Our initial projection for filing fees and non-profit status expenses is around $500 US for the first year.

 

Our goal is to be 100% transparent to our donors about how their money is being spent.  Click here to see a spreadsheet showing donations and expenditures since our founding in 2017.  Our goal is to update this spreadsheet at least once a week.  Until we file for non-profit status, all funds received will go toward filing expenses, unless you designate otherwise.   

WE APPRECIATE YOUR DONATION!

Thanks for all you do to support us!