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Jill Nerby and Aniridia Foundation International
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Jill Nerby was the first to welcome me to Aniridia Foundation International (AFI) when I joined. Shortly after beginning to volunteer for AFI’s members’ newsletter, I approached Jill about doing this book. Instantly she approved of my idea and told me if I needed anything to let her know. She has been instrumental in shaping the book’s content and eliciting the participation of all the doctors and professionals. Her support and wisdom have helped create this informative book for you, and they have meant a great deal to me. She is caring and friendly to all. Jill inspires us to strive towards goals for AFI and in our own lives. Here is her inspiring personal life story and the tale of how she began Aniridia Foundation International (formally the USA Aniridia Network). Jill Ann Nerby was born in Milwaukee, Wisconsin, in 1961 to her parents, Dennis and Sullen Nerby. She was officially diagnosed with aniridia when she went for her three-week check-up. Jill’s parents were told that she was only the second person in the state of Wisconsin to be diagnosed with aniridia. Dr. George Worm realized something was wrong with her eyes and sent her to a well-known ophthalmologist in Chicago, Illinois, with experience in aniridia. This doctor tested Jill for glaucoma and found that she had been born with it. She was then put on eye drops, since the doctor felt Jill was too young to have surgery. Jill’s parents were devastated, since she was their first child and the family’s first grandchild. They did not even know if she could see and thought she might be blind already. They asked many people and sisters at the Catholic convent to pray for Jill. Today Jill has a younger sister, Marybeth, and a younger brother, Jeff; they do not have aniridia. Jill says growing up was challenging at times. Kids would sometimes tease her, leave her out, or pick her last.
Title: Jill Nerby and Aniridia Foundation International
Description:
Jill Nerby was the first to welcome me to Aniridia Foundation International (AFI) when I joined.
Shortly after beginning to volunteer for AFI’s members’ newsletter, I approached Jill about doing this book.
Instantly she approved of my idea and told me if I needed anything to let her know.
She has been instrumental in shaping the book’s content and eliciting the participation of all the doctors and professionals.
Her support and wisdom have helped create this informative book for you, and they have meant a great deal to me.
She is caring and friendly to all.
Jill inspires us to strive towards goals for AFI and in our own lives.
Here is her inspiring personal life story and the tale of how she began Aniridia Foundation International (formally the USA Aniridia Network).
Jill Ann Nerby was born in Milwaukee, Wisconsin, in 1961 to her parents, Dennis and Sullen Nerby.
She was officially diagnosed with aniridia when she went for her three-week check-up.
Jill’s parents were told that she was only the second person in the state of Wisconsin to be diagnosed with aniridia.
Dr.
George Worm realized something was wrong with her eyes and sent her to a well-known ophthalmologist in Chicago, Illinois, with experience in aniridia.
This doctor tested Jill for glaucoma and found that she had been born with it.
She was then put on eye drops, since the doctor felt Jill was too young to have surgery.
Jill’s parents were devastated, since she was their first child and the family’s first grandchild.
They did not even know if she could see and thought she might be blind already.
They asked many people and sisters at the Catholic convent to pray for Jill.
Today Jill has a younger sister, Marybeth, and a younger brother, Jeff; they do not have aniridia.
Jill says growing up was challenging at times.
Kids would sometimes tease her, leave her out, or pick her last.
Related Results
Meibomian gland dysfunction and keratopathy are associated with dry eye disease in aniridia
Meibomian gland dysfunction and keratopathy are associated with dry eye disease in aniridia
AimsTo investigate the aetiology and characteristics of dry eye disease (DED) in a Nordic cohort of patients with congenital aniridia.MethodsThirty-four Norwegian and one Danish su...
Glaucoma and Frequency of Ocular and General Diseases in 30 Patients with Aniridia: A Clinical Study
Glaucoma and Frequency of Ocular and General Diseases in 30 Patients with Aniridia: A Clinical Study
Purpose
To evaluate the following in patients with aniridia: age at first examination at the University Eye Hospital and age at diagnosis of glaucoma; visual ac...
A rare missense PAX6 mutation causes atypical aniridia in a three-generation Chinese family
A rare missense PAX6 mutation causes atypical aniridia in a three-generation Chinese family
AIM: To investigate the molecular diagnosis of a three-generation Chinese family affected with aniridia, and further to identify clinically a PAX6 missense mutation in members with...
Congenital aniridia: an epidemiological approach on 105 patients
Congenital aniridia: an epidemiological approach on 105 patients
PurposeAniridia is a rare ocular disorder affecting beside iris, cornea, angle structures, lens and fovea, and possibly associated with other anomalies. This study aims at understa...
Ahmed valve surgery for secondary post-traumatic glaucoma in aniridia patients
Ahmed valve surgery for secondary post-traumatic glaucoma in aniridia patients
Relevance. Secondary post-traumatic glaucoma (PTG) in patients with
aniridia presents a complex clinical challenge due to severe anatomical
changes in the eye’s drainage system. St...
Structural brain abnormalities in 12 persons with aniridia
Structural brain abnormalities in 12 persons with aniridia
Background:
Aniridia is a disorder predominately caused by heterozygous loss-of-function mutations of the
PAX6
gene, whi...
Structural brain abnormalities in 12 persons with aniridia
Structural brain abnormalities in 12 persons with aniridia
Background:
Aniridia is a disorder predominately caused by heterozygous loss-of-function mutations of the
PAX6
gene, whi...
PAX6 disease models for aniridia
PAX6 disease models for aniridia
Aniridia is a pan-ocular genetic developmental eye disorder characterized by complete or partial iris and foveal hypoplasia, for which there is no treatment currently. Progressive ...

