The Dunning Story

Bella was born profoundly deaf, which was an extremely difficult experience. We were fortunate to have access to some of the best and most caring professionals in the world in the Boston area.  Bella began signing at 8 months of age, earlier than most children speak, and after receiving cochlear implants, slowly transitioned to spoken English.  She was soon in a mainstream school maintaining grades on a par with her peers and a reputation as one of the more popular kids in class.

But my wife and I sensed that something else was wrong. Bella had severe balance problems. Even at seven years of age she still couldn’t negotiate a balance beam while her four year old brother could do so with ease. She tripped over things all the time, obvious things, like our poor yellow labrador retriever. One weekend we went camping and Bella was terrified to walk to the outhouse in the dark, even with the aid of a flashlight. She clung to me like plastic wrap as we wound our way down the path.

A few months later it all made sense. Bella had Usher syndrome. Usher was the cause of her deafness and her balance problems. It was also threatening to take her vision. At eight years old, Bella was effectively night blind, requiring 100x more light to see an object than the rest of her family. My wife and I were devastated.

But the truth is that it has only gotten better from there. Bella continues to thrive in school. She rides horses and dances and next year she plans on joining the school chorus. Not bad for a deaf kid with poor balance. Two years since diagnosis her vision has shown no further deterioration, though we fully expect that it will change for the worse over time.

Bella needs supports to succeed. The school provides an aid in the classroom. The aid is there mainly for Bella but helps all the kids in class. Bella uses an FM to assist her in the classroom. Without it, she struggles to hear. She has physical therapy a couple of times a week to improve her strength and offset her balance issues. Her vision is not yet a problem in class, but the school is making arrangements to help her mobility, such as adding bright tape to the edges of stairs to help them stand out. We encourage Bella to carry a small flashlight with her and she has a good friend in class that walks with her during firedrills since in a real fire her lack of night vision might be problematic. In the evenings we often have to hold Bella’s hand in parking lots or when we first enter the house to guide her past obstacles.

This might sound overwhelming and complicated, but it was all done incrementally. We adjusted as problems arose, adding a new procedure or intervention when it became necessary, one at a time. For Bella, it’s just her way of life. She finds none of it odd and few of the other children in school do either.  In fact, Usher syndrome has made her more of a celebrity than an oddity. Perhaps it is just her personality, but Bella seems to see her physical problems as a challenge rather than an inconvenience. Arriving earlier, asking more questions, and working harder is simply the way she lives. She knows nothing else. In short, Bella leads a happy life with few limitations at the moment, so that’s where we focus. Tomorrow is always uncertain, especially with Usher syndrome, but for today life is good.

The McKittrick Story

When Conner was 10 months old we found out he was profoundly deaf. At 13 months of age, he received a cochlear implant and because of this, he was able to attend a mainstream school and lives a life with little impairment. His speech and language is still delayed but within normal limits. As his eyesight degenerates, he has trouble with dark areas, but his sense of humor and supportive family help him to overcome the challenges he meets each day. Now, with the birth of our fourth son Dalton who was born with profound deafness, we are undergoing the process for cochlear implants once again. We work harder than ever to support research to find a cure for our sons and all of those with hearing and vision related disorders.

The Rush Story

Hello. It was nice coming upon your web site. I myself have Ushers and so does my sister. I was born with hearing loss. I remember being fitted with hearing aids. I used to say to myself that I am blessed to have my eyes. Little did I know why I was going to Children’s Hospital of Boston. I never could understand why they were looking at my eyes also. I would say, “I am hear for my ears.” (lol.) By age 6, I started having trouble seeing at nighttime. By the time I was in my late 20’s to early 30’s, I started to lose some of my field vision. I could no longer play sports. I couldn’t see up close. I was using my central vision and peripheral. I had to move my eyes back and forth, sort of like scanning, and then used my thought process to fill in the missing blind spots. Of course, this is very stressful and takes a lot of energy from me. I am constantly bumping into co workers all the time. They now stop walking completely when I am approaching nearby. They get my attention by saying “Hi Mark” so I am able to spot their location and slowly maneuver around them.

I am 49 years young and I have been waiting all my life to be helped or cured. I tell people that I am not handicapped, I am challenged. My beautiful wife and I just had a baby girl 13 months ago. I WANT TO SEE and HEAR HER GROW UP. I hope my story helps others realize how hard it is for people like us with Usher syndrome and that my message reaches others who can help our cause. I don’t want to give up hope.

Sincerely,
Mark Rush

2008/2009 Grants Funded

Vestibular Testing $40,000
Development of Cell-Based Therapies for Usher syndrome $52,000
Building a Foundation for Clinical Trials in Usher syndrome $60,000
Visual Field Modeling, Analysis, and Development of
Outcome Measures for Treatment Trials in Usher syndrome
$50,000

Development of Improved Visual Field Testing

Development of Improved Visual Field Testing as an Outcome Measure for Treatment Trials in Usher Syndrome (funded January 2007)

Grant Summary
Usher syndrome is a genetic condition causing both hearing loss and vision loss, and is the most common cause of deafblindness in the Western world.  Some individuals with Usher syndrome have moderate hearing loss, where others are born totally deaf.  With the advent and increasing availability of the cochlear implant, the hearing loss in Usher syndrome can be managed and even, in many cases, cured.  The vision loss in Usher syndrome, however, results from retinitis pigmentosa (RP), a progressive disorder of the retina for which there is no known cure or effective treatment.  The progressive vision loss resulting from RP is therefore the most disabling aspect of this condition.  Finding and delivering effective treatment for RP is the urgent mission of our research.

Accurate monitoring of retinal function in retinitis pigmentosa requires the use of several test methods, including assessment of the visual field and the electroretinogram (ERG).  The visual field test quantifies visual field loss, while the ERG measures the electrical impulses of the retina to quantify retinal cell function.  Over the last 30 years, the Oregon Retinal Degeneration Center (ORDC), under the direction of Dr. Richard Weleber, has become one of the premier centers in the world for the measurement and standardization of retinal function in RP.  As a direct result of Dr. Weleber’s passion and expertise, the ERG has evolved into a highly accurate, sensitive, and reproducible test method.  The visual field, however, while extremely informative, has a high degree of test-retest variability.  This variability decreases the utility of the visual field test in clinical treatment trials, where accurate, sensitive, and reproducible test measures are vital for monitoring treatment effectiveness.  In fact, the lack of acceptable visual field testing for retinal dysfunction is now a limiting factor in initiating clinical trials for RP and Usher syndrome.  Dr. Weleber has joined with Dr. Chris Johnson, an internationally known visual field expert with over 20 years of experience in glaucoma research and test development, to refine and develop visual field testing techniques specific to field loss in RP.

This study will assess and optimize computerized visual field test methods for patients with RP by addressing the following three specific aims: to ascertain the test-retest variability of visual field measurements in RP, to spatially characterize visual field losses specific to particular subtypes of RP (including Usher syndrome), and to develop novel testing algorithms that will enable us to move forward with clinical treatment trials.  At the conclusion of this study, we will publish our results and make recommendations to the scientific community regarding the best test strategy to use in multi-center clinical treatment trials.

mckittrick family

Development of Methods of Usher Syndrome Gene Therapy

Development of Methods of Usher Syndrome Gene Therapy (funded January 2007)

Grant Summary
Usher syndrome is the commonest inherited cause of combined blindness and deafness.  The progressive vision loss is currently untreatable, although some hearing may be restored with cochlear implants.  Several gene mutations have been identified as causes of the disease, including mutations in the usherin, harmonin and myosin VIIa genes.  Gene therapy is a promising experimental treatment that has the potential to prevent the loss of hearing and sight in this devastating condition, but it needs to be developed and tested before it can be attempted in human patients.

The purpose of this application is to develop safe and effective gene therapy methods for Usher syndrome.  The long-term goal of this project is to facilitate human clinical trials of this therapy.  In this proposal, we have brought together a team of clinical and basic science researchers to accomplish the following goals:

(1) To design and produce a delivery system, using a harmless virus, to deliver the normal usherin, harmonin and myosin VIIa genes to the eye and the inner ear.

(2) To determine the best surgical techniques for safe and efficient delivery of this gene therapy vector to the eye and inner ear.  These studies will use a nonhuman primate, the rhesus monkey, because the structure of its eyes and ears are most similar to humans, and different in critical ways from other animals such as rodents.

(3) To test the safety of this gene therapy in monkeys by examining them for any possible side effects of the treatment.

There are no animal models that have Usher syndrome, and therefore it is not possible to test the ability of gene therapy to treat or prevent the disease.  However, these studies will be able to test the safety of this treatment in healthy animals.  Given the very serious nature of the disease and the potential benefit, clear evidence of safety would make it ethically acceptable to conduct a clinical study in human patients.
Through this project, we aim to provide the foundation for use of gene therapy for Usher syndrome.
We plan that this project will lead to the next steps required to initiate a gene therapy clinical trial:  manufacture of a safe vector suitable for a human patients, and, based on demonstration of the treatment’s safety, submission of the necessary regulatory documents to the FDA and other federal agencies.  With the experience and information derived from the proposed project, our team at the Casey Eye Institute can then build on its extensive patient base and experience with human clinical trials to bring this new therapy to patients with Usher Syndrome.

Population Genetic Studies of Usher Syndrome

Pilot Project of Population Genetic Studies of Usher Syndrome (funded January 2006)

Grant Summary:
The research is being conducted at the Oregon School of the Deaf in Salem, Oregon by Dr. William Kimberling from Boystown University. The goal of this study is to determine the frequencies of known Usher syndrome subtypes and their mutations in a deaf school population and in students with varied hearing losses in special education classes. This project is nearing completion and we received a synopsis of the study from the researchers at the First Annual Usher Syndrome Symposium in Omaha, Nebraska in October 2006.Ultimately, this information is important for many reasons, including increasing awareness of Usher syndrome, improving genetic testing strategies, providing earlier diagnosis, and identifying individuals as potential treatment candidates for future clinical trials. There is an opportunity that if the pilot project is successful, the National Institute of Health will award a 2.5 million dollar grant for the full screening project. This type of research gives us great hope for a cure.

More Hope than Ever!

Breaking research news – Gene Therapy provides vision to nearly blind young adults” Three young adults with virtually no vision can now read several lines on an eye chart and see better in dimly lit settings thanks to an innovative gene therapy aiming to reverse blindness in a severe form of retinitis pigmentosa known as Leber congenital amaurosis or LCA. One person was even able to better navigate an obstacle course several weeks after receiving the therapy.

The three individuals are participating in a Phase I clinical trial at The Children’s Hospital of Philadelphia.

This is an incredible milestone in curing blindness, and this advancement will help pave the way for the development of gene therapies to treat and cure a variety of retinal diseases including Usher syndrome.

Doctors working on Usher syndrome research are working to extend this incredible breakthrough to Usher syndrome. There is great hope that clinical trials for similar gene therapy for Usher syndrome is right around the corner. Future funding is needed for this important research to continue.

Hear See Hope Foundation

[youtube]http://www.youtube.com/watch?v=tei05U_lWUw&feature=plcp[/youtube]

The idea to start the Hear See Hope foundation started in August 2004 when our oldest son, Conner (then 5) was diagnosed with Usher syndrome Type 1. We immediately began doing research on Usher syndrome and all eye degenerative diseases. In this we found great hope that we could make a difference and that with funds there will be a cure for Usher syndrome in Conner’s lifetime. We discovered many very helpful and knowledgeable doctors and researchers that are doing all they can to find a cure for Usher syndrome.

We are a 501(c)3 not for profit organization in search of funds to sustain the fight against Usher syndrome. Please help us make a difference by supporting us in our fundraising efforts for preventing, treating and curing Usher syndrome.

Thank you,
Todd and Lane McKittrick
Founders

There Will Be A Day


There have been significant breakthroughs in Usher syndrome research in the last few years and there is more hope than ever that a cure is in sight.We are a 501(c)3 not for profit organization in search of funds to sustain the fight against Usher syndrome. Please help us make a difference by supporting us in our fundraising efforts for preventing, treating and curing Usher syndrome.