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ICAN a voluntary not for profit organization, is a group of families and professionals dedicated to lending support to individuals who want to learn more about microphthalmia and anopthalmia and associated genetic counseling.
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Philadelphia, PA 19104 USA
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anophthalmia.org
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💖 So excited for the upcoming ican Conference in Philadelphia! Can't wait to connect with other families and learn from such inspiring speakers. Let's create a supportive community together! 🌟 #icanConference #HopeForAll
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🙌 Huge shoutout to the Planning Committee for all the hard work they're putting into making this conference happen! If you can’t attend, consider supporting this incredible cause. Every little bit helps! 💪 #SupportChildren #AnophthalmiaAwareness
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Poslední diskuze

1. What strategies can we implement to raise awareness about anophthalmia and microphthalmia in our communities, and how can we encourage more families to share their stories?
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2. How can advancements in genetic research improve the support and resources available for families affected by anophthalmia, and what role should NGOs play in facilitating access to these developments?
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ican the International Children039s Anophthalmia Network Menu Home Dear ican Families and Friends The Planning Committee of the ican Conference invites you to the 2022 International Childrens Anophthalmia Network conference in Philadelphia PA. As you read through this registration packet know that the Planning Committee is working hard on your behalf to make this an informative and rewarding conference. You will hear excellent speakers and attend workshops in which participants share experiences and learn not only from the experts leading the sessions but also from one another. If you are unable to participate but would like to help out in other ways or if you know of anyone who may be willing to donate to this worthy cause please email us at icananophthalmia.

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