The Ear Community Organization Welcomes Newest Advisory Board Member – Dr. Ron Eavey

Dr. Eavey holding his Microtia and Atresia Awareness Day coffee mug.

Introducing, Dr. Ron Eavey!
– Ear Community’s newest Advisory Board Member!

The Ear Community Organization is incredibly proud and absolutely honored to introduce and welcome our newest Advisory Board Member – Dr. Roland “Ron” Eavey!

First, I just have to say a little bit about Dr. Ron Eavey “The Legend”, before sharing his bio and welcoming him as our newest Advisory Board Member. Ron is an incredible person who has dedicated decades of his work and care to the microtia and atresia community! He is my friend that I hold near and dear to my heart and someone that I am proud to call my mentor. Our organization is lucky to have him join our Board!

Ron has attended lots of Ear Community picnics over the years, seeing the joy microtia and atresia families find coming together at our events! Our picnics mean so much to Ron that he has brought his beautiful wife, Dr. Sheila Desmond, and his father, with him to our events. Getting to know Ron has been wonderful over the years! He is someone who takes you under his wing and is willing to offer support wherever he can! In 2016, Ron gave me an opportunity to work for him at Vanderbilt, helping launch the first all options microtia and atresia clinic at VUMC, which was an absolute honor! In 2018, Ron was right by my side when our organization presented before the FDA during a listening session about microtia and atresia.

For years, Ron has dedicated much of his work to helping our community. In fact, many of you may recall the research where an ear was grown on the back of a mouse. Well, Dr. Eavey was one of the researchers collaborating with Vacanti Labs on this work, which proved that complex tissues could be engineered in labs, laying the groundwork for modern organ regeneration and reconstructive medicine. AMAZING! Ron has also researched hearing loss and microtia for years with Drs. Jon and Christine Seidman at Harvard! Knowing all of the incredible things that Ron has worked on for our community, imagine my excitement when he asked me what else would I like to work on! Of course, I said I wanted to know why microtia happens! The next day, Ron had a call scheduled for us with Dr. Jon Seidman, which began our collaborative research that has since yielded new findings on microtia genetics due to damaging variants on FOXI3.

Ron Eavey’s bio:
“The pediatric ear has been the major career focus of Dr Roland (Ron) Eavey.

He is trained and double-boarded in both Pediatrics and Otolaryngology (Ear, Nose,Throat). He founded the Pediatric Otolaryngology Service at the Massachusetts Eye and Ear Infirmary and served in that capacity for three decades where he was also a Full Professor at Harvard Meical School. He also has a degree in healthcare management from the Harvard School of Public Health.

Dr Eavey was appointed the position at Vanderbilt University as the Director of the Bill Wilkerson Center for Otolaryngology and Communication Sciences as well as the Chair of the Department of Otolaryngology-Head and Neck Surgery where he held the Guy M. Maness endowed Professorship. The Bill Wilkerson Center consistently has achieved the #1 national rankings for educational and training for Otolaryngology, Audiology, and Speech-Language Pathology, as well as #1 ranking in research funding from the NIH.

Most of Dr Eavey’s research collaborations have been oriented to the pediatric ear such as tissue engineering, – ‘the mouse with the ear on its back’ – in the Vacanti Lab, genes for sensorineural hearing loss and microtia in the Seidman Lab, epidemiology of hearing loss with the Curhan lab, and surveys for perception of hearing loss with MTV courtesy of Ms. Shari Redstone and Viacom. These publications have appeared in medical publications such as the New England Journal of Medicine and the Journal of the American Medical Association of the as well as in media contributions such as Rolling Stone Magazine, CBS News, The BBC, Oprah, and the New York Times.

Internationally, for many years Dr. Eavey served as the US representative to the World Health Organization in Geneva concerning Ear disorders. He has traveled dozens of times globally, educating physicians about ear conditions.

He is a proud father and grandfather.”

Melissa Tumblin and Dr. Ron Eavey at the FDA presenting on microtia and aural atresia during a listening session in 2018.

Thank you for all that you have done for the microtia and atresia community, Ron, and thank you for liking what the Ear Community Organization does to help give back the microtia and atresia community! It is an absolute honor to have you join our organization’s Advisory Board!
Melissa Tumblin
Founder – Executive Director
Ear Community

Zuria Receives the Gift of Sound thanks to Pax’s Ear Fund and Cochlear Americas

Zuria in North Carolina receives the gift of hearing through Ear Community, thanks to Cochlear Americas and Pax's Ear Fund made possible by the Gross Family Foundation.
Today, May 21st, 2026, our Ear Community Organization proudly helped Zuria receive the gift of hearing!Zuria is six years old and was born with microtia and atresia of her right ear. She lives in North Carolina and enjoys school and dancing! Zuria’s hearing loss recently began changing and has impacted her academic progress along with her speech. She has had to repeat a school grade. Also, at Zuria’s last audiology visit, her parents discovered her hearing was changing, realizing she was struggling to hear. Her family noticed she was not responding to instructions on the first attempt lately and they have found themselves explaining things to her multiple times. Zuria’s parents could not afford the cost of a BAHS, but her family found our organization where we could help!

Today, May 21st, Zuria received a NEW Baha 7 Max with a sweet pink headband and was fitted and programmed by her audiologist, Dr. Madeleine Nevin, at UNC Hospitals in Chapel Hill! Thank you also to Ear Community Board Member, Dr. Shannon Culbertson, for helping with this request! Shannon was born with bilateral microtia and atresia and is an incredible audiologist at Chapel Hill!❤️👂

Zuria is also a recipient of receiving help through Ear Community’s Pax’s Ear Fund, helping cover the cost to program and fit her new Baha 7 Max!

Thank you to Dr. Nevin for finding the help Zuria needed and for helping make sure she can hear her best now! A special thank you to Keesha Pfeiffer and Cochlear Americas helping Zuria hear with her NEW Baha 7 Max! We are also grateful for Pax’s Ear Fund and the support of the Gross Family Foundation for making this fund possible to help reimburse audiologists for the fitting/programming service fee when families cannot afford to pay or when insurance denies this service. Pax’s Ear Fund helps audiologists still give the gift of hearing through our organization! Thank you to Pax, a sweet little boy who’s helping kids & adults hear! Together, we can make wonderful things happen for our community!

Thank you to everyone involved with helping Zuria hear better! We are so happy for her and excited for her to do so much better in school and dance! #HearNowAndAlways
Thank you!
Ear Community

Ear Community Turns 16 Years Old Today!


Today, May 20th, is Ear Community’s 16th Birthday!
It’s hard to believe that today marks 16 years of service to the Microtia and Atresia community through the Ear Community Organization! Our daughter, Ally, was only 6 months old when we decided to do something about the lack of information that was out there about this rare cause.

For the past 16 years, the Ear Community Organization has paved the way for microtia and atresia families! Ear Community, along with our online support groups, created a community that was needed, being there for our microtia and atresia families since 2010! Ear Community is proud to promote education and awareness and to give back to our beautiful community in many ways! Most importantly, our organization will always make sure no one ever feels alone with microtia and atresia!

Our family felt lost and alone and struggled to find the answers we were looking for when our daughter, Ally, was born with microtia and atresia. As a result, we wanted to help give back and make things easier for the next family that has a child born with microtia and atresia. Our family wishes we had an Ear Community when our Ally was born! Thankfully, we now have an entire beautiful community, that is like family, to be belong to through Ear Community!

If you enjoy supporting nonprofits and the work they do, consider making a donation to support the Ear Community Organization!
EarCommunity.org/donate
We look forward to seeing everyone this summer at our organization’s events!
– The Tumblin Family

Ear Community visits Seidman Labs at Harvard for Microtia genetics research

Harvard Medical School’s Dr. Jon Seidman and Barbara McDonough with Melissa Tumblin of the Ear Community Organization

Last week on March 25th, 2026, I had the opportunity to meet with our microtia genetics team at Siedman Labs at Harvard Medical School when traveling to Boston! I met with Dr. Jon Seidman and Barbara McDonough, to catch up and discuss our new findings about the increased risk of FOXI3 causing microtia and craniofacial microsomia.

I have known Jon and Barbara for the past 10 years and am incredibly grateful for their passion behind wanting to help find the answers our community is looking for when it comes to what causes Microtia and Craniofacial Microsomia. Visiting them is like visiting with family! Dr. Seidman and Barbara have brilliant minds and are known for their research at Harvard and around the world with Seidman Labs and I am so proud of their passionate work that is at the forefront of genetics research for our microtia community! This is an incredible team we have and I am forever grateful to Dr. Ron Eavey (Vanderbilt) for introducing me to Dr. Seidman! I am also incredibly grateful to Dr. Dan Quiat (Harvard) for his work during our last grant project for microtia and atresia research, including the many researchers who all worked very hard on finding the answers the microtia and atresia community is looking for. While we still have a lot to understand and figure out, the increased risk on FOXI3 is new information and is discussed in our published papers and in the presentation by Dr. Jon Seidman on our website.
Contributing Authors in collaboration with our work include:
Daniel Quiat, Andrew T. Timberlake, Justin J. Curran, Michael L. Cunningham, Barbara McDonough, Maria A. Artunduaga, Steven R. DePalma, Milagros M. Duenas-Roque, Joshua M. Gorham, Jonas A. Gustafson, Usama Hamdan, Anne V. Hing, Paula Hurtado-Villa, Yamileth Nicolau, Gabriel Osorno, Harry Pachajoa, Gloria L. Porras-Hurtado, Lourdes Quintanilla-Dieck, Luis Serrano, Melissa Tumblin, Ignacio Zarante, Daniela V. Luquetti, Roland D. Eavey, Carrie L. Heike, Jonathan G. Seidman and Christine E. Seidman.Genetics research is important to our rare community for so many reasons! As a mother, I can’t tell you how important it is to know about genetic information for our rare cause. This information helps give mothers some peace of mind that they did not do anything during their pregnancy to cause their child’s ear(s) to be missing as well as helping provide some of the missing puzzle pieces when it comes to microtia for our community!

Barbara McDonough – thank you for always taking the time to meet with me and catch up and for always being so welcoming and excited to discuss all things microtia! Thank you for helping change people’s lives with your work and with Drs. Jon and Christine Seidman, everyday!❤👂

More information on genetics research for microtia, along with our published papers, can be found on our Ear Community Organization’s website at:  https://earcommunity.org/genetic-research-on-microtia-and-aural-atresia/

Thank you,
Melissa Tumblin
Ear Community 

 

Ear Community presents at the American Cleft Palate Craniofacial Annual Meeting in Boston

Advocates Melissa Tumblin, Amy Schefer, Dina Zuckerberg, Marly Eugenio and Melissa McGowan present at the Annual ACPA Meeting in Boston during March 2026.

I am grateful for the opportunity to have attended and participated in the American Cleft Palate Craniofacial Association (ACPA) Meeting that was held in Boston last week! Each time I attend this annual meeting, I feel as though it is a second home for me, coming together with existing friends in the craniofacial field and making new friends each time.

While at the ACPA meeting, I had the opportunity to present along side four incredible advocates, sharing about our journey, what we have learned, struggled with and overcome, including the work we are doing to help give back to the community. What an honor it was to present along side these following incredible women advocates: Amy Schefer, Dina Zuckerberg, Marly Eugenio and Melissa McGowen! Each one of us is dedicated to creating change in our communities that will help make things easier for the next family that has a child born with a rare cause. A special thank you to Amy Schefer for submitting our abstract for our panel presenation so each one of our voices could be heard for the communities we serve! Thank you to the ACPA for spotlighting our panel in the captured moments of this year’s meeting and for creating a platform for medical professionals and advocates to share their voices, together! Thank you for everyone’s advocacy!

At ACPA, I embraced connecting with the Vanderbilt team I have worked with over the years with microtia and atresia. I am always happy to see members of our CARE Research team who have worked very hard on collaborative research for our microtia and atresia community over the past five years together. It is always wonderful to see Ear Community friends from Nemours Children’s, Seattle Children’s, Nationwide Kids, and Old Dominion U and of course everyone at the ACPA! THANK YOU to the ACPA for creating a much needed platform and a place for collaboration where medical professionals and advocates can come together to share our voices and work! Thank you for everyone’s advocacy!

It is always wonderful to be brought together throughout the craniofacial world as an advocate! Advocates come in all shapes and sizes and what we offer is often priceless!

I always look forward to seeing the incredible advocates in our community that include patients themselves as well as some pretty incredible organizations that help those in need, creating a home for so many! Whether it is a mother’s love for her child or a child who has overcome struggles along their journey, but is now advocating for others just like them – we all have a common goal of providing help, support, community and compassion that will ultimately lead to helping make someone else’s life easier or sharing the journey of hope and learning from each other.

Here’s to the advocates at ACPA and in the combined communities who make incredible change and provide the hope and help when in need! Advocates also include medical professionals and representatives who help market medical technology that can help make our lives better and along side researchers, writers and volunteers. Thank you for everyone’s advocacy – always! Thank you to the ACPA for always creating such a professional meeting for the craniofacial field and community! Executive Director Adam Levy always does such a great job for the ACPA!

The following are just some of the many friends and faces that I always appreciate seeing at meetings like ACPA! Choose kind! ❤👂

Thank you,
Melissa Tumblin
Founder – Executive Director
Ear Community

Microtia and Atresia picnics offered through the Ear Community Organization for summer of 2026

Ear Community’s picnics are coming up this summer and we look forward to seeing so many of our beautiful microtia and atresia families come together on one of our special days!

Our Ear Community picnics are priceless and FREE! For the past 16 years, our Ear Community Organization has been bringing our microtia and atresia families together so the kids can play and maybe make a new friend, parents can share their journeys and so no one ever feels alone with microtia and atresia!

* Please RSVP to Lauren at LaurenEarCommunity@gmail.com

Summer of 2026 Picnic Line up:
Brookline, MA – Saturday, June 6th
San Diego, CA – Saturday, June 13th
Jeffersonville, IN – Saturday, June 27th
San Antonio, TX – Saturday, July 11th
Broomfield, CO – Saturday, July 25th

Join us for lunch and a day of fun with face painters, balloon artists and magicians! We’ll learn about the latest in bone anchored hearing devices thanks to Cochlear Americas, MED-EL USA and Oticon Medical! We’ll also have our microtia glasses at our picnics thanks to Ear Community’s Pax’s Eyewear Fund and our friend, James Hermsen of SuhHermsen Adaptive Eyewear Solutions who designs these glasses for microtia kids along side Dr. Donny Suh! We’ll have medical professionals joining us so everyone can find the answers they are looking for including Su-Por educating on the porous polyethylene implant used in auricular reconstruction ! We’ll also have some anaplastologists joining us as well to help educate us about prosthetic ears! It will be a wonderful day to come together and learn about your options when it comes to microtia and atresia!

* Our Colorado Ear Community picnic this year is in collaboration with Dr. Sheryl Lewin! Please click on the following link for conference registration details with the Earicle’s Conference!

A HUGE THANK YOU to our Ear Community picnic hosts for bringing their community and our families together at this year’s events!
The Furze Family
The Smyth Family
The McClellan Family
The Quesada Family

The Parcher Family

A special thank you to all of our Ear Community Sponsors for helping make our special days possible for our community and for helping support the good work our Ear Community Organization does for our community!
See everyone soon!
Ear Community 👂❤️

Oticon Medical Undergoes Successful Ownership Transition Following Acquisition by Impilo


Gothenburg
31 March 2026

On Tuesday, March 31st, 2026, Oticon Medical is pleased to share that Demant has successfully finalized the agreement with Impilo, transferring ownership of Oticon Medical to Impilo and marking the beginning of a new strategic chapter for the organization.

The acquisition positions Oticon Medical to further accelerate innovation, strengthen its market presence, and continue delivering life changing bone anchored hearing solutions (BAHS) to patients worldwide.

The agreement includes a long-term collaboration between Oticon Medical, Impilo, and Demant, ensuring continuity and advancing joint development of next generation Ponto and Sentio sound processors, alongside continued manufacturing, and supply partnerships.

For customers, partners, and patients, the transition brings full operational continuity—daily operations, local sales structures, and customer support remain unchanged.

“Impilo shares our values and vision, and as our new owner, brings the investment and strategic focus needed to further strengthen our position in the BAHS market,” says René Govaerts, President & General Manager, Oticon Medical. “We are confident this partnership will help us continue delivering exceptional solutions and support.”

“We are delighted to partner with management on the acquisition of Oticon Medical to accelerate growth, drive innovation, and further improve patient outcomes. The company has established itself as a leading player in the attractive and underpenetrated global BAHS market and has strengthened its position with the recently launched transcutaneous product, Sentio, which has already demonstrated impressive results. We are deeply impressed by the management team’s expertise, their ability to deliver outstanding patient support, and their unwavering commitment to improving patient outcomes. We look forward to our partnership with management and to the journey ahead, advancing the development of cutting-edge BAHS solutions that will further enhance the lives of patients.” says Magnus Edlund, Partner at Impilo.

Oticon Medical remains dedicated to delivering solutions that elevate hearing and enrich lives. With a clear vision ahead and the support of its new owner, the company is poised to advance boldly into the next era of growth and innovation.


 About Oticon Medical

Oticon Medical is a global company in implantable hearing solutions, dedicated to bringing the power of sound to people at every stage of life. For more than a decade, we have made bone anchored hearing systems more accessible by simplifying the treatment for physicians, audiologists, and patients alike.

We believe that patients and hearing care professionals should be able to choose the best possible solution at any time along the patient journey. We call it “Freedom of Choice” and it has always been paramount to Oticon Medical. This is the reason why our solutions are designed to be compatible whenever possible. As a result, an implant from Oticon Medical stands as a true testament to our unwavering lifelong support.

We work collaboratively with professionals to ensure that every solution we create is designed with our users’ needs in mind. We have a strong passion to provide innovative solutions and support that enhance quality of life and help people live life to the fullest – now and in the future.

Because we know how much sound matters.

About Impilo

Impilo is a Nordic investment company focused solely on investments in lower-mid-market Nordic healthcare companies. It seeks majority buyouts of privately held companies across the pharmaceuticals, MedTech, specialist pharma services and other healthcare & related services industries. Target companies must contribute to the positive and sustainable development of the markets in which they operate, as well as have a credible path to becoming a market leader in their respective niche. Impilo has a well-diversified portfolio of healthcare investments and manages approximately €2 billion of capital from leading international investors.

Medical Professionals take to Capitol Hill to advocate for support of Ally’s Act, H.R. 4606 and S. 3400 honoring World Hearing Day

Melissa and Ally Tumblin World Hearing Day ASHAMarch 3rd was World Hearing Day!

This year’s theme for World Hearing Day is “From Communities to Classrooms – Hearing Care for Every Child.”World Hearing Day is an annual day to raise global awareness on preventing deafness and promoting proper ear and hearing care. Organized by the  World Health Organization (WHO), this event highlights ear care as a critical public health issue. The 2026 theme, “From Communities to Classrooms: Hearing Care for All Children,” focuses on early identification and prevention of hearing loss in children.

Over the last two weeks, members of AAO-HNS Government Affairs and American Academy of Otolaryngology—Head and Neck Surgery, advocated on Capitol Hill in Washington DC during Congressional Advocacy Day, advocating for legislation that would help improve hearing healthcare for children, like Ally Tumblin, and for legislation like Ally’s Act, H.R. 4606 and S. 3400 this week in DC!

Standing on the steps of the U.S. Capitol, these physicians represent more than their practices. They represent the patients and families who rely on access to high-quality ENT care every day. By meeting with lawmakers, they are sharing real patient stories and advocating for policies that protect access to care, advance hearing health equity, and strengthen the future of our healthcare system. Thank you to the dedicated members and medical professionals for lending their expertise and their voices on behalf of patients and thank you for advocating for support of Ally’s Act, H.R. 4606 and S. 3400! Your support and advocacy for this bill alone would help give hundreds of thousands of children and adults better quality lives with better access to bone anchored hearing systems and cochlear implants when it comes to private insurance coverage for these hearing devices! Thank you for your advocacy! A special thank you to Dr. Amelia Drake of Chapel Hill (ENT), Dr. Rahul Shah (CEO of the American Academy of Otolaryngology – Head and Neck Surgery (AAOHNS) and Harry DeCabo (Director of Advocacy AAOHNS) for your support of Ally’s Act!

ASHA – the American Speech-Language-Hearing Association also advocated for Ally’s Act on Capitol Hill in support of World Hearing Day! ASHA, along with speech therapists, advocated for how important hearing health care is and how important it is for children and adults to be able to benefit from hearing device technology, newborn hearing screenings and therapy services that help prevent the risk of speech delays and help improve the quality of life for those individuals who have hearing loss. A special thank you to Josh Krantz, Director of Federal Affairs at ASHA and Jerry White, Director of Federal and Political Affairs, for their advocacy in fighting for legislation that is needed, like Ally’s Act, H.R. 4606 and S. 3400. In addition to these congressional advocacy days on The Hill with meetings, many within the community made calls and sent emails to their Congressmen and Senators, asking them to cosponsor Ally’s Act, sharing their stories and explaining why this bill is needed and has been needed for decades. Many requested that their Representatives help with getting a hearing for our bill!
Video of Melissa and Ally Tumblin by ASHA

Passage of Ally’s Act would allow the children and adults within our community to be able to thrive in their communities and live a better quality of life. After all, hearing is essential to everyday life, allowing our loved ones to be able to contribute to society and be able to provide for themselves. Bone Anchored Hearing Device Systems and Cochlear Implants give children and adults their lives back! When these hearing device systems are the only hearing devices that these individuals can benefit from, it is unacceptable for private insurers to determine who gets to hear and who does not when these devices are medically necessary and needed. Ally’s Act would close the loop hole for private insurers to deny coverage for BAHS and CI hearing device implant systems for both children and adults from birth to age 64. These hearing device systems are already covered by Medicaid and Medicare.

Thank you again to everyone who is advocating for Ally’s Act, H.R. 4606 and S. 3400 to pass!
Melissa Tumblin
Ear Community

#entadvocacy #aaohnsadvocacy #patientaccess #otolaryngology #allysact #boneanchoredhearingdevices #cochlearimplant #EarCommunity

Ear Community welcomes new Program Director

Lauren and Paxton Hoyal

Welcome to our newest Ear Community staff member! Meet Lauren Hoyal, Ear Community’s new Program Director!

Lauren is responsible for managing our organization’s events, advocacy outreach for hearing device donations and fundraising. Lauren and her family found Ear Community after her youngest son, Paxton, was born with microtia and atresia. The Hoyal Family has since then been involved with our organization as a picnic host family, advocating for Ally’s Act and have fundraised for our organization.

Lauren earned her Masters in Elementary Education from Valdosta State University where she taught 1st grade for three years before deciding to stay home with her beautiful daughter, Vada. Lauren also serves on the Thomaston Upson Arts Council Board of Directors where she is the Children’s Art Chair. She is also the Director of the Thomaston First Methodist Church Preschool. Lauren’s husband, Perry, is a firefighter and flight paramedic who saves lives everyday!

I am grateful for Lauren and Perry and their beautiful family! Lauren has become an incredible advocate for our community and a wonderful friend to me! Thank you for helping me serve our community through the work of our Ear Community Organization, Lauren!

Welcome aboard! I am lucky to have you!
Melissa Tumblin
Founder – Executive Director
EarCommunity.org

The Ear Community welcomes newest Board Member, Dr. Kripa Raman!

The Ear Community announces it’s newest Board of Directors Member, Dr. Kripa Raman.

“We would like to welcome Dr. Kripa Raman to Ear Community’s Board of Directors, says Melissa Tumblin, Founder and Executive Director of the Ear Community Organization. I have had the honor of knowing Kripa over the past four years. She has already been doing incredible work in our community, helping make connections and advocate for our microtia and atresia families in the Ontario area and all over Canada! I am grateful for her help and her shared passion for helping our children as well as her dedication to our microtia and atresia community!”

Kripa is a mother to two boys in Ontario, Canada. Her oldest son, Jahnu, was born with unilateral microtia and atresia of his left ear. Currently he is unaided and thriving! Kripa has a PhD in Molecular Biology and Genetics from McMaster University. She works in pharmaceuticals leading health economic assessments to secure funding for new therapeutics. Her advanced scientific and healthcare background has been very helpful when navigating the Canadian health care system and advocating for her son. When she is not entertaining the boys, she is planning their next family trip, listening to an audiobook, or trying a new recipe.

Kripa has been the organizer behind the Ontario Ear Community picnic in both 2023 and 2025. For her, these events are all about connection. “Given the rarity of microtia, I felt quite lonely after the initial diagnosis. Balancing new motherhood with those
unknowns was a source of anxiety, but finding the Ear Community online gave me the connection I needed. The picnics are amazing since for many kids, it’s the first time they’ve ever seen little ears like their own. I want my son to know he belongs to a community, and seeing him meet others just like him is so special.”

Board Members for the Ear Community Organization consist of members of the community that include individuals who were born with microtia and aural atresia, family members and medical professionals. “It is important for our community to be informed of all options for microtia and aural atresia, says Melissa Tumblin, Founder of Ear Community. It is also important to hear from parents, like Kripa, and to see how her family journey with microtia and atresia is going. It is incredibly helpful for children and adults and their families to see what others in the community are doing regarding the decisions they make along the way on their journey. This is where advocates can play a big part in helping others understand decisions and choices and also to help give some perspective when talking with others in the same situation”.

“We are looking forward to Kripa joining our board,” said Ear Community Founder, Melissa Tumblin! Our community is made up of amazing advocates and role models and Kripa is already an amazing advocate in our community! We are honored to have her serve on our Board as she continues helping families and community members in Canada who have microtia and aural atresia!”
Melissa Tumblin
Founder – Executive Director
Ear Community

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