About Melissa Tumblin

Helping Malosi hear his best thanks to Ear Community and Oticon Medical

Malosi hearing sound better for the first time with a donated Oticon Medical Ponto 3 SuperPower sound processor on May 19th, 2017.

Ear Community is excited to share this sweet story about a little boy named Malosi Sualua who was born with Left Microtia and Atresia.  Malosi is 4 and lives in Laguna Beach, CA with his two older sisters and parents, Heidi and Leie.  Malosi means “strength” in Samoan and his mother, Heidi, says that the name really suits him.  “He is tough, he is sweet, and he is smart.”  When Malosi was born, his parents were given conflicting information about what the next steps would be.  They were told things like “he only needs one good ear” and “you must get a BAHA on him or he will lose speech and development”.  During the early days when Malosi was just an infant, Heidi and Leie couldn’t just enjoy their precious little boy, they had to face their new reality and try to go from there.

In February, this year, Heidi reached out to Ear Community.  She needed someone to talk to who understood what she was going through with her adorable little boy.  After exchanging e-mails and a phone call, we knew that Ear Community needed to help.  Through the https://www.oticonmedical.usincredible connections with Oticon Medical, Ear Community was able to secure a Ponto 3 Super Power on a soft band head band for Malosi.  On May 19th, 2017, Malosi went to his audiologist, Dr. Maria Abramson at the Hear Now Abramson Audiology in Laguna Beach and received a brand new Oticon Ponto 3 Super Power device and soft band.  When Malosi first had his Ponto on, Dr. Abramson whispered, “Malosi, I love you” into his left side.  He whipped his head around and said, “What’s that?!” Malosi and his family were also able to be introduced to the Oticon Medical Rep, Megan Everson, who gave him his very own Oticon Monkey (complete with a Ponto on, just like Malosi) and played with Malosi while Dr. Abramson went over the details with his mom, Heidi.  Each day he is wearing it longer and longer, and discovering more sounds as he goes.  Heidi said that he likes to put his hand over the Ponto and say, “it’s working!” – he is clearly excited to experience ‘surround sound’ finally.

Ear Community would like to thank Jared Schnackenberg, President of Oticon Medical US, and Alan Raffauf, Vice President of Marketing for Oticon Medical US, for giving our organization the opportunity to help Malosi hear better.  A very special thank you to Beverly Ostrowski of Oticon Medical for helping work with us to improve lives with better hearing.  We would also like to extend a warm thank you to Malosi’s Audiologist, Maria Abramson, AuD at Hear Now Abramson Audiology in Laguna Beach for working with Ear Community to help Malosi.  Thank you to Ear Community’s donors and to the friends and relatives to the late Curt Gorman (past President of Oticon Medical US) who have also helped make it possible for hearing device recipients, like little Malosi, receive the gift of hearing.

As Malosi continues to grow and go to school, his Ponto 3 Super Power is going to give him equal access to the sound he needs to succeed throughout his education and life.  Ear Community has been honored to work with the Sualua family and be able to help Malosi hear better.  Heidi said that she couldn’t tell us what a huge weight was lifted off her shoulders.  That the entire experience, from the first phone call to receiving Malosi’s Ponto 3 Super Power has just filled her heart with so much gratitude.  We are so happy for Malosi and his entire family, and can’t wait to see how he grows.  Good luck, Malosi, may all your dreams come true and may you enjoy all the beautiful sounds this world has to offer!

Karen Smith, Executive Director of the Broomfield Community Foundation retires – Mentor to Melissa Tumblin of the Ear Community Organzation

Broomfield Community Foundation’s Karen Smith talks with Tom Currigan Senior Director with Kaiser Permanente, who has been a sponsor of Heart of Broomfield for more than 10 years, during the annual Heart of Broomfield Awards banquet on Monday at the Omni Interlocken Resort in Broomfield. (Jeremy Papasso / Staff Photographer)

Karen Smith, Executive Director of the Broomfield Community Foundation, is retiring this fall.  Karen was my mentor who guided me and taught me how to run a nonprofit organization, how to run our Ear Community Organization. I will never forget the day when I met with her to tell her about my passion for wanting to start a nonprofit organization (in 2011) and about the cause that I wanted to support for children and adults who have Microtia and Atresia. Karen loved what I was trying to do and agreed to run it past the Broomfield Community Foundation’s board of directors to see if the Foundation would be interested in awarding a fiscal sponsorship.  The board and Karen then invited me to present to the board of BCF and they loved what I was trying to do and all agreed to give me a chance at being their very first fiscal sponsor where Ear Community would be taken under their wing and guided as a nonprofit organization, being offered 501c3 status.  After helping carry the Ear Community Organization under your wing Karen, for four years until my organization became it’s own 501c3, thank you for all that you did to help me with Ear Community, for understanding my passion for wanting to help people, and for believing in me and my organization’s cause! I would not have been able to do this without your help and to have gotten Ear Community to where it is today.

Article follows:

“After 14 years at the helm, Karen Smith is stepping down as executive director of the Broomfield Community Foundation.”She’s a remarkable person and I don’t think we’ll replace her,” Foundation Board of Directors President Bruce Erley said. “I think we’ll find someone to fill the position, but she can’t be replaced.”

The Foundation was established in 1993.

Smith is incredibly tuned in to the community needs, he said.

“She’s so integrated into the community in every way,” Erley said, “and wears the Foundation on her sleeve.”

Erley announced the retirement at Monday night’s Heart of Broomfield Awards ceremony.

A search team to look for a new director began last fall, he said, and the group hopes to have the job description completed this month. The team, made up of past and present board members, will interview candidates in June and July.

Smith will help the new director for a month or so to transition into the position, and will be on-call the rest of the year.

Janell Daly, the Foundation’s administrative assistant, will remain on staff.

Smith and Erley called Daly a valuable asset to the Foundation.

Losing someone like Smith means losing a tremendous amount of cultural history, Erley said, and Daly carries a lot of that institutional knowledge..

Smith, who has been asked for years when she’ll participate, will compete in this September’s Dancing with the Broomfield Stars as a send-off. A few weeks after that performance will be her last day as director.

Carina Martin, founder and CEO of A Precious Child, remembers when the Foundation awarded the nonprofit its first grant.

“On the day of the reception, I walked up sobbing,” Martin said. “I thought ‘someone believes in me and my organization and the work we’re going to do.’ I just lost it.”

Smith, she said, has been a longtime friend and someone who cares deeply about children.

“She’s always there for you,” Martin said. “She’s one of the kindest people I know.”

Smith will spend her retirement working with her husband in his part-time handyman business and will have time to volunteer around Broomfield.

She said it has been her pleasure to work with the various board and committee members, and witness their dedication to the Foundation and to Broomfield.

The rebranding process the Foundation rolled out last year was an “excellent continuation of the board’s strategic planning process that resulted in a message for the Foundation that we can be united in telling,” she said.

“Our tagline, ‘One Community. Many Hearts. Unlimited Impact,’ says it very well,” she said. “We are a leading voice of philanthropy for Broomfield.”

She is proud that three years ago the Foundation moved to a complete online grant application process that makes it easier for non-profits to plan and more efficient for the grant committee to review applications and see final reports.

The Foundation reached $1 million in its Legacy Partners endowment fund in 2013. Their next goal is to raise $2 million by 2020.

“I so appreciate the donors to the Foundation and hope they continue with their support and that we continue to get our message to the community to expand our donor base and build our Legacy endowment fund,” she said.”

Jennifer Rios: 303-473-1361, riosj@broomfieldenterprise.com or Twitter.com/Jennifer_Rios

 
You will be missed Karen, but I will never forget your help, kindness, knowledge, and generosity.  Thank you for helping me with Ear Community and for understanding my need to help children and adults who have Microtia and Atresia all over the world.
– Melissa Tumblin
Founder and Executive Director of Ear Community
(a Broomfield, Colorado headquartered 501c3 charity organization)

Helping Joan hear better thanks to Oticon Medical and the Ear Community Organization

Joan Yirenkyi of Greensboro, North Carolina receives a newly donated Oticon Medical Ponto 3 through the Ear Community Organization on April 3rd, 2017.

Ear Community is thrilled to introduce you to Joan Yirenkyi.  Joan is a beauty at 27 years old and lives in Greensboro, North Carolina with her family.  She was born with Treacher Collins Syndrome along with Microtia and Atresia of her left ear and other birth defects.  Being born with craniofacial abnormalities such as Treacher Collins Syndrome can create an extremely difficult path through life.  She has had to undergo several surgeries, including several on her teeth and face.

Joan did not give up; she is a fighter!  She worked hard through school, despite massive obstacles both through her peers and not receiving equal access to all the information.  She has met with countless specialists during her young life to gain better access to sound.  In January of this year, Joan reached out to the Ear Community Organization to see if we could help.

With the help of Oticon Medical, the Ear Community Organization was given the opportunity to donate a new Ponto 3 sound processor to Joan so that she can have access to sound!  On April 3, 2017, Joan was finally able to get her Ponto 3 and gain sound while wearing the soft band head band.  When she tried on her new Ponto 3, Joan said, “I am so happy for this!  Thank you SO much!” Someone with as much spirit and perseverance as Joan definitely needs to have hear voice heard and we know that by giving her the gift of hearing, she is going to do great things!

Ear Community wishes to thank Jared Schnackenberg, President of Oticon Medical US, and Alan Raffauf, Vice President of Marketing for Oticon Medical US, for giving our organization the opportunity to help Joan hear better.  A very special thank you to Beverly Ostrowski of Oticon Medical for helping work with us to improve lives with better hearing.  We also would like to extend a warm thank you to Joan’s audiologist, Dr. Shannon Frymark, AuD at Aim Hearing and Audiology in Greensboro for donating her time and services to fit and program Joan’s new hearing device!  Thank you to Ear Community’s donors and to the friends and relatives to the late Curt Gorman (past President of Oticon Medical US) who have also helped make it possible for hearing device recipients, like Joan, receive the gift of hearing.

Sometimes it takes a village, and we are all happy to be a part of Joan’s incredible journey.  We are so proud of the things Joan has accomplished and faced so far in her life, and we can’t wait to see how far she’ll go.  You are an incredible woman Joan, and you now have the access to sound that you fought for.  Good luck, Joan, show the world how bright you shine!

We’re so proud of you Joan!
Ear Community
www.EarCommunity.org

Giving back: how one communtiy member helps a child hear better through the Ear Community Organization

Daniel Alejandro (2.5 years old) of Mexico receives a gently used donated Cochlear Americas Baha 4 hearing device from Samantha Pillion of the United States on April 1st, 2017.

Please meet one of our cutest Ear Community members, Daniel Alejandro, from Mexico.  Daniel was born on July 14th 2014 to his wonderful parents Patricia and Daniel.  From the first moment of his precious life, he was admitted into the neonatal intensive care unit and stayed there for an agonizing two months.  During that time, he showed determination and toughness that proved he was ready to fight for his life!  Daniel’s parents didn’t have any answers on his condition, even when they were released from the hospital.  Finally, they met with a geneticist who explained some test results to them.  Daniel was born with a rare genetic disorder that caused him to have Bilateral Microtia and Atresia as well as low muscular tone, strabismus (misalignment of the eyes), and a high degree of hypermetropy which also makes it difficult to see.  Daniel had a long, hard road ahead of him but his parents fought to give him everything he needed.  They made sure he received physical, feeding, and sensory therapy.  Finally, when Daniel was almost a year and a half old, he started to crawl and pull himself up to a standing position!

Patricia and her husband, Daniel, reached out to the Ear Community Organization to add another fitting piece to little Daniel’s puzzle.  They wanted to help him hear.  For hearing parents, it can be so daunting to have a baby who is born without hearing in either ear.  When that is compounded with countless other conditions and hours of therapy, it can become exhausting.  Ear Community was happy to help, and were able to find a generous donor to give Daniel the chance at sound.

Samantha Pillion

Samantha Pillion, a student at American University had a very gently used Cochlear Americas Baha 4, which she had never quite warmed up to.  She is in the MPA program and set to graduate this year.  Samantha contacted Ear Community, wanting to share this generous gift with someone who needed a device, and we knew exactly who to send it to!  Along with the Baha 4 that Samantha donated, she included lots of goodies for the lucky recipient such as:  Hal-Hen Mini Super Dri-Aid in its original box, 28 batteries with the magnetic tool, listening tool so others to experience listening through the Baha 4, an abutment cleaning brush, sound processor cleaning wipes, sterile wipes, digital battery tester, Bluetooth microphone accessory, cords/clips/wires, a spare back for the sound processor, user manual, and warranty card.

On April 1st, 2017, Daniel traveled with his family from Monterrey Mexico to the United States to pick up his new Baha 4.  The difference in Daniel was almost immediate says his mother, Patricia, “…his face lit up when he heard our voices and we could tell it was a once-in-a- lifetime moment.”  Daniel’s parents were just thrilled for their precious little boy and now can’t wait to see how the world opens up for him now that he has access to sound.

Ear Community would like to extend our warmest gratitude to Samantha Pillion, who thought to share this device with someone who could use it.  She is little Daniel’s hero for hearing.  A special thank you to Luis, a close family relative, who lives in San Juan, Texas who was able to hold onto Daniel’s Baha 4 and keep it for him until his family could pick it up.

Daniel, there is so much good in the world, and our organization is so happy that you can now hear countless joyful things throughout your life!  We wish you all the very best, and are excited to watch you grow and learn.

Here’s to happy hearing, Daniel!
Ear Community
www.EarCommunity.org

Ear Community Timeline – How Ear Community began (2010 to Present)…


Ear Community
Organization
 Timeline

Some may wonder how does a nonprofit get started.  Here is the timeline story of how the Ear Community Organization became a nonprofit organization after beginning as an online support group.

September 2009, Melissa Tumblin’s daughter was born and she couldn’t find the answers she was looking for about why her child was born with Microtia and Atresia.

May 20, 2010
, Melissa Tumblin started the
“Microtia and Atresia Support Group” on Facebook to help connect families and to help others in the same situation.  She and her daughter also didn’t want to be alone with Microtia and Atresia.  This support group quickly became a global support group within the first year.

June 2010, Melissa attends a training course in IEP and 504 Plans to her learn how to help children and their families advocate better who have hearing loss in the school classroom.

June 11, 2011, Melissa Tumblin and her family host the first “Microtia and Atresia Support Group” family picnic for Microtia and Atresia families in Denver, Colorado.  After driving around to 13 grocery stores asking for gift cards to be donated to help provide food for this event, Cochlear Americas and Oticon Medical offer to help with this picnic after discovering the help that Melissa and her family were offering to the community.

October 11, 2012, Melissa Tumblin begins working on creating the Ear Community website that would be used as a portal of information to help medical professionals and families with loved ones who have Microtia and Atresia all over the world.

February 12, 2012, the Ear Community website is launched and a press release goes out announcing that the website is the “First to offer support and resources to individuals and families around the world living with Microtia and Atresia and associated syndromes including Hemifacial Microsomia.

During February of 2012, Melissa Tumblin was encouraged by many to start a nonprofit organization for the Microtia and Atresia community.

February 2012 – As a stay at home parent, concerned about the amount of work that may be involved with running a nonprofit organization, Melissa Tumblin reached out to a couple of local 501c3 nonprofit organizations for guidance, in which one offered to take her under their wing and mentor her.  This nonprofit organization was called the Broomfield Community Foundation, the city’s community organization in which Melissa lives in in Colorado (Broomfield).

On August 16, 2012, after applying, interviewing, and presenting to the Broomfield Community Foundation, the Foundation agreed to take Melissa and the Ear Community Organization under their wing and grant her 501c3 status through their organization as a fiscal sponsor recipient.  Till this day, the Broomfield Community Foundation remains impressed with Melissa’s drive to help Microtia and Atresia families find answers and support about Microtia and Atresia.

During the summer of 2012, Ear Community hosted (7) picnics across the United States, including (2) in Canada.

During the year of 2013, the Ear Community Organization is given the opportunity, through industry relationships that Melissa developed, including Microtia and Atresia donor families, to begin helping children in need of hearing devices obtain donated hearing devices thanks to Cochlear Americas and Oticon Medical believing in Ear Community.  The organization was also able to begin accepting donations with 501c3 status, allowing the organization to award college scholarships and begin to provide for operational costs of the organization.

April 2013, Ear Community is given the opportunity to help further education about Microtia and Atresia with the help of Oticon Medical proudly sponsoring the accredited webinar about Microtia and Atresia through AudiologyOnline, on a Parent’s Perspective about Microtia and Atresia.  This course continues to remain a helpful educational resource for medical professionals and families of loved ones with Microtia and Atresia.

July 2013, Ear Community is invited to present about Microtia and Atresia  at the EAA (Educational Audiology Association) conference.

2014 till present, Ear Community continues to give back to the Microtia and Atresia community, globally, by hosting (6-7) picnic events each summer that bring families together in the same situation.  Some abroad Ear Community picnic locations include Denmark, South Africa, Australia, the UK, Spain, and Canada.  Ear Community continues donating hearing devices (over 60 hearing devices donated since 2016), awarding college scholarships, and helping with financial assistance toward surgical travel cost reimbursement when funds are available.

April 2015, Melissa Tumblin is asked to sit on the advisory board for :Project MyEar” in hopes of helping with the development of stem cell research for bioengineering ear cartilage.

June 29, 2016, Melissa Tumblin finally believes that she is ready to apply for 501c3 status for Ear Community to become its own entity.  Ear Community, Inc. was proudly awarded 501c3 status by the IRS just two months later (August), after applying.

September 2016, Melissa Tumblin presents another webinar that is proudly sponsored by Oticon Medical and offered through AudiologyOnline, helping discuss the struggles about unilateral hearing loss for children, after advocating for her daughter for the past 7 years.  This webinar continues to be viewed and was organized in hopes of promoting educational awareness about how hearing loss can affect individuals differently, even if they still have one working ear.

November 9, 2016, in an effort to help promote educational awareness and to help raise public awareness, including stopping the bullying, Melissa Tumblin applies for a National Awareness Day for Microtia and Atresia families.  On November 9, 2016, the Ear Community Organization hosts it’s very first National Microtia Awareness Day where families all over the United States, including other countries as well, celebrated our first National Awareness Day together, for Microtia individuals, everywhere.

January 2017
, Melissa Tumblin begins working closely with Vanderbilt University Medical Center on the launch one of the first all options Microtia and Atresia clinic.

Here are also a few helpful articles and resources that may be helpful to families who have loved ones born with Microtia and Atresia:
Our Story article
– Mixed Feelings article
First National Microtia Awareness Day
– Microtia and Atresia webinar through AudiologyOnline (sponsored by Oticon Medical)
How to overcome the struggles of pediatric hearing loss through AudiologyOnline (sponsored by Oticon Medical)

The Ear Community Organization is a 501c3 nonprofit organization.
Federal Tax ID#46-0923897
www.EarCommunity.org

Ear Community Announces 2017 Summer Picnics for Families of Children with Microtia and Atresia

AudiologyOnline News Release


The mission of AudiologyOnline is to enhance the quality of life for the patients and clients in the care of the professionals we serve.

We support this mission by:

  • Providing the most relevant, convenient, and economical continuing education opportunities presented and authored by the leading experts in their respective professions to enhance clinical knowledge and skills.
  • Connecting quality professionals to the right job to better serve clients and patients.
  • Enhancing students’ clinical knowledge and skills to become meaningful contributors to the profession.

 

February 27, 2017

_______________________________________________________________________________________

February 20, 2017.  Ear Community, a 501(c)(3) nonprofit organization and global support network for individuals born with microtia and/or atresia, is excited to announce its 2017 schedule of free family picnics.

Since 2011, Ear Community has hosted picnics to bring together families who have children with microtia and atresia. This year’s picnics will take place in the United States in Annapolis, Maryland; Austin, Texas; Broomfield, Colorado; Nashville, Tennessee; Ardsley, New York; and Fort Pierce, Florida. Ear Community’s picnics offer families the opportunity to come together, share experiences, and make new friends. The picnics offer a delicious lunch, as well as plenty of games and activities such as balloon artists and magicians to ensure children have fun.  Parents and caregivers can also meet world-renowned professionals including microtia and atresia repair surgeons, anaplastologists, ENTs, and audiologists, and learn about all the latest hearing and medical devices from representatives of leading device manufacturers. Ear Community thanks the 2017 summer picnic sponsors: Cochlear Americas (Platinum), Oticon Medical (Gold), and Medtronic (Silver), as well as Stryker for providing information about Medpor.

Ear Community believes that education is empowerment, and looks forward to hosting more welcoming and informational experiences for families via this year’s summer picnics. More information including contact information for RSVPs can be found at http://earcommunity.org/6823-2/6823/

For more information about AudiologyOnline, click here.
We look forward to seeing everyone this summer at our organization’s family events!
Ear Community

Mazie receives the gift of hearing thanks to Cochlear Americas and the Ear Community Organization

Mazie Herzing of Richmond, Virginia receives a newly donated Cochlear Americas Baha 5 through the Ear Community Organization on February 16, 2017.

Ear Community is proud to introduce Mazie Herzing, our newest Baha recipient!  She was born last July and diagnosed with Microtia and Atresia of her right ear and Hemifacial Microsomia.  She lives with her big sister, twin brother, and parents Carly and Shelley in Richmond, Virginia, USA.  When Mazie was first diagnosed, her parents were told that she would never have hearing on her right side.  Carly and Shelley went for a second opinion and that was when they were informed about a Baha as a possible way to help little Mazie hear “surround sound.”  Like most parents, Mazie’s moms had worried about the inability for Mazie to access to auditory information.  With Microtia and Atresia being so rare, getting all of the correct information can be hard to come by, so three cheers for Mazie’s parents for looking deeper for solutions that taught them more than they would ever imagine!  While Mazie’s parents were doing their research, Carly’s sister, Amanda Bray (Mazie’s Aunt), was also learning more about Microtia and Atresia and thankfully found the Ear Community Organization.

On February 16th, 2017, the Ear Community Organization was given the opportunity to donate a brand new Cochlear Americas Baha 5 to little Mazie to help her hear better!  When Mazie’s moms anticipated the day of the fitting, the happiness and excitement built even more.  And when Mazie turned her head to Shelley that first time, when listening through her Baha, their hearts exploded with a million and one emotions they could never even explain.”  Mazie’s moms said, “Thank you for helping us give hearing to our littlest one” when they were leaving the audiologists office, Shelley was talking on Mazie’s Microtia side, and she turned her head and smiled which was the first time she had done that!  Mazie is a “brave, tenacious, and stubborn little girl” and Ear Community is thrilled to give her the opportunity to hear through both ears!  Mazie’s big sister said to her, “You can hear out of your baby ear!  You make me so happy!”  This is a great thing for their whole family!

Carly’s sister, Amanda Bray, said, “I truly do not think we can put into words how much this has meant to us. When my sister and Shelley found out about the approval for Mazie to obtain a Baha through Ear Community, I truly do not think they have experienced a happier moment in their entire lives.  Amanda said “I would like to personally thank Ear Community for “hearing” my sister’s story and considering our family for this incredible gift. Your clear commitment to helping the “community” find answers to some of parents and families most difficult questions about these beautiful little miracles is nothing short of amazing.  I hope you know how much you have touched our lives, and I am certain the lives of many, many others. What you have built is incredible on so many levels.

Ear Community would like to say thank you to Meredith Heiner, Au.D., CCC-A at the VCU Health Systems Audiology Department for donating her time to fit and program Mazie’s Baha 5.  Ear Community would like to express a special thank you to Nancy Klein of Cochlear Americas for releasing Mazie’s donated Baha 5 and making sure it made it’s way to Dr. Heiner’s office for Mazie’s fitting.  Mazie would not be able to hear better today if it were not for wonderful corporations like Cochlear Americas who make amazing hearing technology.   From all of us, thank you for helping Mazie hear better!  “Cochlear is the global leader in implantable hearing solutions. It has a dedicated global team of more than 2,500 people who deliver the gift of sound to those with hearing loss in over 100 countries. Its vision is to connect people, young and old, to a world of sound by offering life enhancing hearing solutions. In 2013, Cochlear celebrates 100,000 Baha System users – all with unique stories of how being able to hear again has impacted their lives. The Cochlear promise of “Hear Now. And Always” embodies the company’s commitment to providing its recipients with the best possible hearing performance today and for the rest of their lives.”

We are all so happy that Mazie can hear so much better now and for knowing how bright her future will be from here on out.  We’re also very proud of Mazie’s family for doing their research and finding help through the Ear Community Organization for Mazie and for themselves, as a family.

Mazie, we wish you the best of everything that this world has to offer, and look forward to watching the great impact you’ll have!

Ear Community Organization
www.EarCommunity.org

2017 Ear Community Microtia and Atresia Summer Family Picnics

2017 Ear Community Microtia and Atresia Summer Family Picnics

Ear Community hosts picnics every year around the world helping bring Microtia and Atresia families together.  This year’s picnics will take place in the United States in Annapolis, Maryland/ Austin, Texas/ Broomfield, Colorado/ Nashville, Tennessee/ Ardsley, New York/ and Fort Pierce, Florida!  It is very exciting for many families! Everyone enjoys attending our picnics and our Ear Community picnics always offer such a wonderful opportunity for Microtia and Atresia families to come together, share experiences with each other, and maybe even make a new friend.  Medical professionals such as world renown Microtia and Atresia repair surgeons, anaplastologists, ENTs, audiologists, and therapists along with the world’s leading hearing device and medical device companies all come together to mingle with us at our picnics, helping educate us on all of our options including hearing loss.

We look forward to seeing you at our Ear Community picnics this year!

Melissa Tumblin,
Founder and Executive Director of Ear Community
Founder of the Microtia and Atresia Support Group on Facebook

2017 Ear Community Picnics

Maryland Ear Community Picnic
Annapolis, Maryland
Date:  Saturday June 10th, 2017
Time:  11AM to 3PM
RSVP to Heidi at:  AnnapolisEarCommunityPicnic@gmail.com

Texas Ear Community Picnic
Austin, Texas

Date:  Saturday, June 10th, 2017
Time:  11AM to 3PM
RSVP to Heidi at:  AustinEarCommunityPicnic@gmail.com

Colorado Ear Community Picnic
Broomfield, Colorado
Date:  Saturday June 24th, 2017
Time:  11AM to 3PM
RSVP to Melissa at:  ColoradoMicrotia@hotmail.com

New York Ear Community Picnic
Ardsley, New York
Date:  Saturday, July 22nd, 2017
Time:  11AM to 3PM
RSVP to Heidi at:  ArdsleyEarCommunityPicnic@gmail.com

Florida Ear Community Picnic
Fort Pierce, Florida
Date:  Saturday, July 22nd, 2017
Time:  11AM to 3PM
RSVP to Heidi at:  FortPierceEarCommunityPicnic@gmail.com

Tennessee Ear Community Picnic
Nashville, Tennessee
Date:  Saturday, July 22nd, 2017
Time:  1PM to 5PM
RSVP to Melissa at:  TennesseeEarCommunityPicnic@gmail.com

Vanderbilt University and Children's Hospital

Vanderbilt University and Children’s Hospital

*  This Ear Community picnic will be in collaboration with a FREE surgeon conference that will take place at Vanderbilt University Medical Center.  This conference is a wonderful opportunity to learn about all of your options for Microtia and Atresia and again…it is FREE to Microtia and Atresia families as Vanderbilt University and Children’s Hospital is a nonprofit organization.
Our collaborative event will begin at 8:30AM – 5:00PM with educational presentations by:

– Ron Eavey MD SM Director, Professor and Chair for Research and Causes of Congenital Ear Malformation, Vanderbilt
– Scott Stephan MD Facial Plastic Reconstructive Surgery Medpor, Vanderbilt
– Sivakumar Chinnadurai MD MPH Pediatric Otolaryngology Rig Graft, Vanderbilt
– Alejandro Rivas MD Neuro-otology Hearing Restoration in Aural Atresia, Vanderbilt
– Margaret McRedmond Au.D. CCC-A Audiology, Vanderbilt
– Scott Fiscus B.C.O.,  Anaplastology Ear Prosthesis, Nashville, TN
– Parent Panel
*  A delicious lunch will be provided as we kick off our Ear Community picnic along with a face painter, balloon artist, and magician.  We look forward to seeing everyone at our event.  A special thank you to Vanderbilt Medical Center and Dr. Ron Eavey for making this event possible with Ear Community.  Please join us for an amazing day!

National Microtia Awareness Day Ribbon for Ear Community Organization – November 9th, 2017.

Annual National Microtia Awareness Day
Throughout the United States and anywhere wishing to celebrate with all of us!
November 9th, 2017
To hear all about our amazing first National Microtia Awareness Day, please click here
Click here for our press release…
Click here for an interview with AudiologyOnline about National Microtia Awareness Day…
Click here for our radio commercial for raising awareness about Microtia and Atresia…
Coming soon….click (here) anytime during the year to order official National Microtia Awareness t-shirts…
THANK YOU TO EVERYONE WHO CELEBRATED OUR FIRST NATIONAL MICROTIA AWARENESS DAY ON NOVEMBER 9TH, 2016, WITH ALL OF US HERE AT THE EAR COMMUNITY ORGANIZATION IN THE UNITED STATES, INCLUDING ALL WHO ALSO CELEBRATED WITH US IN OTHER COUNTRIES ALL OVER THE WORLD!!!  This day was SO amazing and so very special to so many of us, everywhere!

 

How one father was willing to travel to another country to help his daughter hear better with the help of Oticon Medical and Ear Community

Raheeg Abdelrahman of Sudan, 4 years old, January 2017 recipient of (2) Oticon Medical Ponto Plus’.

We are excited to introduce you to Raheeg Abdelrahman, a lovely four-year-old girl who lives in Sudan with her younger twin siblings, her mother, and her father Eltahir.  She was born with bilateral Microtia and Atresia, her father said that they couldn’t find a hearing device in Sudan so they traveled two days to Egypt in order to meet with an audiologist who could help them find something to help Raheeg hear.  Sadly, due to no insurance and financial difficulty, the family had to return home without a sound processor.

Through Ear Community’s amazing partnership with Oticon Medical, our organization was able to donate two Ponto Plus hearing devices on January 11, 2017 to Raheeg.  Because Raheeg’s family had to travel two days each way from Sudan to Egypt, it was a very exciting trip for her.  Eltahir said, “Please convey my deepest heartfelt thanks and appreciation to all of Oticon Medical staff for the help and support they provide to everybody in our Ear Community, and special thanks for Mr. Alan Raffauf, Tove Rosenbom, and Claus Frees Horneman…THANKS to YOU dear friends for giving me hope that my daughter can go to school, hearing sounds and practice her life like other kids.  Thank you for making my impossible dream become real!”

When Raheeg was finally fitted for her Ponto Plus devices, she absolutely loved them and showed very good responses.  Her father said, “She can answer our call easily and surely this will help her to receive her lessons like other kids…it is difficult to get words to express my thanks but I say God bless you!”

Ear Community would like to offer special thanks to the entire team that made it possible for Raheeg to hear.  Thank you to Oticon Medical for donating the Ponto Plus devices and for helping make it possible for Raheeg to receive her new hearing devices.  Thank you to Sr. Director for Clinical Research and Training for BAHS, Dr. Tove Rosenbom, for programming Raheeg’s Pontos and for making sure she had everything she needed with them, including extra batteries.  Thank you to Claus Frees Horneman, the Oticon Medical rep who made sure Raheeg’s devices made it to Egypt by hand delivering them!  We would like to thank the donors to the Ear Community Organization who also helped make it possible for Raheeg to receive her hearing devices, including donors who are friends and relatives to the late Curt Gorman and Gabe Murphy who wanted to help a child hear better.

A very special thank you to Alan Raffauf, Vice President of Marketing for Oticon Medical US, for choosing to donate two new Oticon Medical Ponto Plus hearing devices to Ear Community so they could be donated to Raheeg to help her hear better during her early years.   As a tribute to Curt Gorman, Oticon Medical’s past president, who passed away in August of 2015, may Raheeg thrive in the hearing world with her new hearing devices and never miss a beat as she continues to grow.  Curt Gorman had a passion for helping children hear better as he was a pioneer in the hearing device industry, especially for bone anchored hearing devices.   Many who loved and knew Curt have made donations to also help children hear better through the Ear Community Organization.  Thank you for everyone’s support and for helping Ear Community continue with its mission of helping individuals with Microtia and Atresia. Oticon Medical believes in helping individuals with hearing loss so that they can live a better quality of life. Oticon Medical is a well-respected international hearing device manufacturer that is a part of the “William Demant Group [which has] 100-plus years of experience in audiology and sound processing and established manufacturing and logistics infrastructure.”

Raheeg, we are so proud of you and we hope that you have the very best life possible!  We hope that you flourish and grow, especially now that you have access to the sounds you have craved for so long!  We hope to hear how your life continues to improve and progress, congratulations on hearing your best Raheeg!  Here are some adorable pictures of Raheeg with her brand new Ponto Plus’.

Melissa Tumblin
Founder and Executive Director
and Ear Community Board Members
Ear Community Organization
www.EarCommunity.org

First Annual National Microtia Awareness Day with the Ear Community Organization – November 9th, 2016

National Microtia Awareness Day Ribbon for Ear Community Organization - November 9th, 2016.

National Microtia Awareness Day Ribbon for the Ear Community Organization – November 9th, 2016.

On Wednesday, November 9th, 2016, the Ear Community Organization launched and celebrated the very first National Microtia Awareness Day that took place throughout the United States.  Families from all over were truly excited to finally have a national day to celebrate, helping promoting awareness and education about Microtia and Atresia.  In fact, many amazing moments took place on this special day for families and individuals with Microtia and Atresia everywhere!  Hundreds of children and adults, with their families, submitted pictures online in their National Microtia Awareness Day t-shirts and/or wearing blue and black, celebrating and helping promote awareness.  Many changed their online profile pictures to our awareness ribbon and blogged on Instagram, Twitter, and Facebook.  Not only did we have families celebrate from many countries all over world….Israel, Indonesia, Malaysia, Denmark, Mexico, Poland, Ireland, China, Australia, New Zealand, Canada, and the UK just to name a few, but many children shared a newfound confidence where they got up in front of their classrooms and talked about their ears and their hearing loss (while wearing their Microtia Awareness Day t-shirts) and explained why having an awareness day was so important to them.  Parents brought in treats to their children’s schools such as blue awareness cupcakes and frosted cookies.  Some families with newborns affected by Microtia and Atresia found hope and a sense of belongingness that helped them finally feel comfortable enough to tell their families and friends about their child having Microtia and Atresia without worry or concern.  There were also a series of group gatherings that took place with Microtia and Atresia families coming together to celebrate on our special day.  Many hearing device companies such as Cochlear Americas, Medtronic – Sophono, and Oticon Medical, socially blogged about National Microtia Awareness Day, celebrating in their offices and educating employees more about hearing loss and Microtia.  Medical device companies such as Stryker CMF, and medical facilities such as Johns Hopkins University, ReconstratA, and Vanderbilt University, also celebrated National Microtia Awareness Day by either dedicating a webpage about Microtia on their websites or tweeting about this special day.  Many plastic surgeons helped promote awareness and education about Microtia and Atresia by posting educational information about surgical options on their websites as well.

Celebrate with us on National Microtia Awareness Day on November 9th, 2016.

Celebrate with us on National Microtia Awareness Day on November 9th, 2016.

In a press release by National Day Calendar, Melissa Tumblin, Founder of the Ear Community Organization, explains that “Approximately one child in every 9,000 (in the United States) is born with Microtia (when the ear(s) do not fully develop during the 1st trimester of pregnancy).  Often affecting one ear or both ears, Microtia is diagnosed at birth, but there is no understanding as to why Microtia occurs. Facial challenges, hearing loss and the longing for social acceptance are some of the daily concerns for those who are born with Microtia.  “Children are born into this world not knowing they are any different from anyone else. Many with Microtia share similar stories of curious stares, bullying, or awkwardness.  Individual personalities, social conditioning, available treatments and bullying all impact how every child develops and copes as an adult.  By removing unnecessary boundaries and replacing them with resources, tools, and support, we can eliminate bullying and clear the way for an even more successful future.”

November 9th is dedicated to spreading hope and knowledge concerning a congenital birth defect, which derives its name from the Latin terms for little ears.  Mark the calendar for Microtia Awareness Day for November 9th and think of the number 9 as the shape of an ear.  In an interview with AudiologyOnline, Tumblin was asked “Why was it so important to have a national awareness day created?  Tumblin stated, “It is the intention of Microtia Awareness Day to help promote public awareness.  As the mother of a child who has microtia, and the founder of Ear Community, my hope is that families who have new babies born with microtia will leave the hospital armed with more answers than questions, and their dreams for their children intact.  I think that if more people learn about microtia and atresia, that they will be kinder and more accepting.  It is also my intention for anyone who is born without an ear(s) to realize that they are not alone.  Through this national day, they can find out about organizations and resources for information and support.”  Since 2010, the Ear Community Organization has brought over 6,500 people together from around the world at the organization’s events making it possible to share experiences and resources. The community is made up of not only children and adults with Microtia and their families, but teachers, advocates, and medical professionals from around the world who foster awareness and assistance for this amazing group of people. Board members for Ear Community either have the condition themselves or a family member who does, so they have close personal experience with the obstacles from a myriad of perspectives.

Celebrating the first National Microtia Awareness Day at an elementary school in Colorado with teachers and principals and students who have Microtia and Atresia.

Celebrating National Microtia Awareness Day at Ally’s elementary school in Broomfield, Colorado where teachers, principals, families, and students came together to support those classmates who have Microtia and Atresia, November 9th, 2016.  The Broomfield Chamber of Commerce helped make this day special with a ribbon cutting ceremony.

Many people came together to help make our National Microtia Awareness Day possible.  Not only did we have three short weeks to organize a celebration after receiving news of obtaining our national awareness day, but there was a tremendous amount of passion and support from others that helped make our celebratory day even more special.  Three graphic designers donated their time to help bring our cause and our Microtia Awareness ribbon to life!  Thank you to Michelle Cowan of Colorado for helping design one of our “celebrate with us” ad logos for our special day!  Thank you to Del Rocha of MaxMediaDenver for designing our new website banner for our Ear Community website!  We love it!  Thank you!  A very special thank you to Mark Johnson of Florida who helped design our official Microtia Awareness ribbon and the layout for our awareness t-shirts!  Mark’s daughter, Eva, has Microtia and Atresia and it was very important to the Tumblin Family and the Ear Community Organization to have a true passion behind the meaning of our awareness ribbon, especially being designed by a loving Microtia family.  Thank you Mark!  A very special thank you to Jeff Norman of MaxMediaDenver who not only donated his time and services for graphic design with Del Rocha, but Jeff’s media office also created and made a national commercial about Microtia and Atresia for the Ear Community Organization that went out over various radio stations in cities throughout the United States during the two week span leading up to our National Microtia Awareness Day on the 9th of November.  Thank you so very much for your support Jeff and MaxMediaDenver and for helping us promote awareness about Microtia and Atresia!  Thank you to Robert Valdez, one of Ear Community’s Board of Director Members, for putting Ear Community in touch with Jeff Norman of MaxMediaDenver!  Thank you to Cindy Bader of “Sweet Cakes” bakery for making our day even sweeter with awareness cupcakes on our special day for Ally and Hailey’s classrooms.  A very special thank you to Dr. Arturo Bonilla, who not only is one of the most skilled Rib Graft outer ear reconstructive surgeons in the United States for Microtia repair, but Dr. Bonilla is also the owner of www.CausaTees.com, the t-shirt store that Ear Community’s National Awareness Microtia t-shirts were printed by and shipped from to everyone!  Dr. Bonilla started CausaTees for his niece, Naty, who has Lupus.  Naty wanted to have a business where she could be able to give back.  At CausaTees, for every t-shirt ordered, $2 gets donated back to either Lupus or Cancer foundations.  With the $2 from every t-shirt, Naty is able to purchase blankets that she enjoys bringing to children at Children’s Hospitals who get cold when their temperature drops during chemotherapy treatment or when having a blood transfusion.  Ear Community was happy to help Naty give back and to also give back and be able to support two other great causes!  Ear Community is also very happy to have Dr. Bonilla be a part of making our Ear Community Microtia awareness t-shirts!  A very special thank you to all of Ear Community’s sponsors (Cochlear Americas, Medtronic-Sophono, Oticon Medical, and Stryker CMF) for not only being a part of Ear Community’s passion for helping individuals with Microtia and Atresia, but thank you once again for being so happy for our organization on our special day and for supporting all of the children and adults who have Microtia and Atresia and for celebrating with us on our annual awareness day!  Thank you so much for your support!

Melissa Tumblin of Ear Community stated that “The celebration of the first National Microtia Awareness Day was more than I could have ever imagined or wished for and it was absolutely an amazing day for so many!  I am humbled and yet overwhelmed with the excitement and joy from so many families and organizations that participated on National Microtia Awareness Day!  Thank you!

Click here for Press Release…

Click here for interview with AudiologyOnline about National Microtia Awareness Day…

Click here for radio commercial…

Click here to order official National Microtia Awareness Day t-shirts…

Here are just a few of some of our wonderful memories from National Microtia Awareness Day that took place on November, 9th, 2016:

Thank you for celebrating with all of us in 2016!

Melissa Tumblin
Founder and Executive Director
and
Ear Community Board Members
The Ear Community Organization
www.EarCommunity.org

Translate »