Join our family

We provide support, social and educational services through many benefits and programs.

Benefits:

	Free quarterly newsletter with important information on aniridia, treatments, events, research, conference details and deadlines and regular columns like Meet Our Members, Parents Pride, Ask the Doctor.
	Online private area to share information, read the latest medical articles affecting those with aniridia, meet others, develop friendships and support networks.
	Discounted rates for medical conferences that put you there with the best physicians and researchers in aniridia and socials where you can meet others.
	Contacts for the doctors with aniridia experience.
	Helpful suggestions from our Medical Advisory Board, Scientific Board or our Low Vision Teachers / Specialists
	Getting involved with others willing to "make a difference" in the lives of those affected through volunteering, fundraisers, and our committees.
	Speaking with others who have experienced what you are going through and helping you with it.

We believe coming together as a group will not only help us deal with sometimes difficult situations, but provide useful information to those who have dealt with and conquered those problems. It will also show the research community that many low vision and blind people with aniridia exist and need treatments, and research. After all, there is strength in numbers!

JOIN TODAY

Click here to fill out the electronic form or
Download the form in Adobe Acrobat document (pdf) format.
Download the Spanish language form in Adobe Acrobat document (pdf) format.

We understand not all people have time to volunteer. However, with a couple hours a week, it can really help. If you find that you can not volunteer your time, there are other ways to help like making a yearly or monthly donation (by check, credit card or monthly debit by clicking HERE ) OR providing a personal contact name of your friend, colleague or family member's business or foundation to contact for support, OR hosting a fundraising event (dinner party, cocktail, garage sale, ideas are endless)

WELCOME TO ANIRIDIA FOUNDATION INTERNATIONAL

Once your application is processed, you will receive a welcome packet with information, our brochures, your User ID and password for the online area, and the International Aniridia Medical Registry questionnaire. This registry questionnaire is very important to gaining data so that we can have researchers have something to study. Only this way we will move towards a cure. Please participate in this Phase I project. For more information, see your newsletter or the website (www.aniridia.net).