Friday, March 13, 2015

Join us on Saturday May 16th at the La Jolla Library!






SAN DIEGO, CALIFORNIA
LOCAL SUPPORT GROUP MEETING INVITATION
Please plan to join us at the next meeting of your local Acoustic Neuroma Support Group.
We welcome you to learn about the latest treatment options, to network with other acoustic neuroma patients and find encouragement and support.

DATE/TIME:
Saturday, May 16, 2015
1:00 - 4:00 p.m.

PLEASE NOTE NEW MEETING LOCATION:
San Diego Public Library - La Jolla-Riford Branch
7555 Draper Avenue at Pearl Street
La Jolla, CA 92037
MAP/DIRECTIONS:  See back of invitation.

TOPICS:  ● Making the Most of your Health Care Visits
● Strategies for Selecting a Medical Professional
● Questions to Ask Before, During and After Treatment
When initially diagnosed, few patients have a clear idea of where to turn in their selection of a qualified medical professional for treatment of their tumor or the questions to ask.  Please join us for a group discussion to help prepare you for your acoustic neuroma journey and feel more confident in the treatment you choose, as well as specialists that can provide post-treatment therapies and rehabilitation.  We will also discuss tips to help you make the most of your doctor appointments, so you can be actively engaged and communicate effectively with your health care team. 
● Caring and Sharing

TO RSVP, PLEASE CONTACT YOUR LOCAL SUPPORT GROUP LEADERS:
Wanda Crook, Local Support Group Leader/Facilitator
Phone 760-315-2599 or Email:  movementlearningcenter@att.net
Helen McHargue, Local Support Group Leader/Facilitator 
Phone 760-728-0309 or Email:  foodsmarts@gmail.com
Wanda Crook, PT, and Helen McHargue, an acoustic neuroma post-treatment patient, will facilitate meeting.

●NOTE Social Media Sites
Facebook - Acoustic Neuroma Association San Diego Support Group (ANASDSG)
ANA San Diego Support Group Blog - www.anasandiegosupport.blogspot.com
Who should attend?  Family members, caregivers, friends and interested persons are encouraged to attend.
Benefits of attending a local support group include communicating in a nurturing, non-judgmental environment with others who have shared a common acoustic neuroma experience; sharing information on dealing with specific problems, educational opportunities about the latest acoustic neuroma topics of interest; and providing emotional support to all patients, both pre- and post-treatment. This helps in reducing the isolation and loneliness that many acoustic neuroma patients feel.




Directions

Take the La Jolla Parkway Exit from the I5 freeway.
Follow the road which turns into Torrey Pines Rd. 
Go 1.5 miles and turn left onto Girard Ave. 
Take 1st right onto Pearl Street for .2 miles. 
Turn right onto Draper Avenue. 
Library is on the right. 






USC Surgery on Litlle Leaguer

http://news.usc.edu/77196/thanks-to-usc-neurosurgeons-little-leaguer-is-back-in-the-game/

Sunday, February 8, 2015

Meeting Saturday, February 21st, 2015


ACOUSTIC NEUROMA ASSOCIATION



SAN DIEGO, CALIFORNIA
LOCAL SUPPORT GROUP MEETING INVITATION
Please plan to join us at the next meeting of your local Acoustic Neuroma Support Group.
We welcome you to learn about the latest treatment options, to network with other acoustic neuroma patients and find encouragement and support.

DATE/TIME:
Saturday, February 21, 2015
1:00 - 3:00 p.m.
NOTE:  PLEASE PLAN TO ARRIVE PROMPTLY AT 12:45 PM AND MEET AT THE SECURITY DESK, THE CONFERENCE ROOM IS NOT ACCESSIBLE WITHOUT A SECURITY ESCORT.

PLEASE NOTE NEW MEETING LOCATION:
Scripps Proton Therapy Center Main Conference Room
9730 Summers Ridge Road
San Diego, CA 92121
PARKING/DIRECTIONS:  See attachment.

TOPICS:
● Overview of Proton Therapy and Radiation Treatment Options for Acoustic Neuroma
Presented by Ryan Grover, MD, Radiation Oncologist
● Tour of Proton Therapy Center

PLEASE RSVP WITH YOUR LOCAL SUPPORT GROUP LEADERS:
NOTE:  An RSVP is appreciated and is extremely helpful in planning successful meetings!
Wanda Crook, Local Support Group Leader/Facilitator
Phone 760-315-2599 or Email:  movementlearningcenter@att.net
Helen McHargue, Local Support Group Leader/Facilitator
Phone 760-728-0309 or Email:  foodsmarts@gmail.com
Wanda Crook, PT, and Helen McHargue, an acoustic neuroma post-treatment patient, will facilitate meeting.

●NOTE Social Media Sites
Facebook - Acoustic Neuroma Association San Diego Support Group (ANASDSG)
ANA San Diego Support Group Blog - www.anasandiegosupport.blogspot.com
Who should attend?  Family members, caregivers, friends and interested persons are encouraged to attend.
Benefits of attending a local support group include communicating in a nurturing, non-judgmental environment with others who have shared a common acoustic neuroma experience; sharing information on dealing with specific problems, educational opportunities about the latest acoustic neuroma topics of interest; and providing emotional support to all patients, both pre- and post-treatment. This helps in reducing the isolation and loneliness that many acoustic neuroma patients feel.

Thursday, October 16, 2014

Vestibular Rehabilitation Presentation



!!!!!!DIZZY!!!!!
Mark your calendar for our next meeting: Saturday, Nov. 15th, 2014 from 1:00 - 4:00 p.m. at Sharp Grossmont Rehabilitation Center, Conference Room.

Topic: Vestibular and Balance Rehabilitation
The presentation, including demos on the Balance Master, will be about 1 hour in length, followed by time for questions and for meeting, greeting and sharing information. 

Recently I spent some time "surfing" through the Vestibular Disorders Association (VEDA) website and found plenty of useful information. Much of it is simple validation of the symptoms/problems I personally experience with my AN and perhaps you do too. It's amazing how much our balance or lack of it affects our lives! This article is available on the web site in a PDF format if you wish to print it out. 



How I feel sometimes. How about you?


Tuesday, July 29, 2014

NEXT MEETING: SUNDAY, AUGUST 10th

The lovely meeting room at the La Jolla Public Library

Next meeting: Sunday, August 10th at the La Jolla Public Library, 7555 Draper Avenue at Pearl Street, La Jolla, CA  

Time 1:00 - 4:00

Our speaker will be Marilyn Weinhouse.


"Marilyn Weinhouse is the owner of Hear Gear, a company which sells Assisted Listening Devices. Marilyn herself is afflicted with moderate hearing loss and wears two hearing aids. After retiring from her career as a teacher, she decided to start a business selling assisted listening devices and teaching others about the latest technology to improve hearing. 

Marilyn's presentation will cover the subjects of home hearing loops, personal amplifiers/listeners, TV listening systems, bluetooth products and MFI's- the "made for iphone" trend. 

On her website,(click here or go to www.heargear.net) you can read more about Marilyn's interesting background and how she was inspired to help the hearing impaired understand the technology which can make our lives (and those of our loved ones) better. For a real treat and lots of great information, check out her interesting and entertaining blog by clicking here or at www.heargear.wordpress.com." 

After Marilyn's presentation and a question and answer period, we will have plenty of time for an informal "meet and greet" where we can hear each other's stories and exchange information. La Jolla is beautiful all year long but particularly lovely during the hot summer months. Why not make a day out of this meeting; come early for brunch or stay after the meeting for a late lunch or early dinner at one of the many great restaurants. There are so many good options in the town.

If you plan on coming, please let us know by calling Helen McHargue (760) 728-0309 or email: foodsmarts@gmail.com OR Wanda Crook at (760) 315-2599 or email: movementlearningcenter@att.net

SEE YOU THERE!!!!!





Thursday, June 5, 2014

Meeting June 7th

There will be a meeting of the San Diego Support Group on Saturday, June 7th at 1:00 - 4:00 p.m.
Location: Tri City Medical Center - Meeting Room 5, 4002 Vista Way, Oceanside, CA 920056.

Primary Topic: The Yale University Acoustic Neuroma Study which is the first causation study to determine whether are are possible genetic risk factors that cause AN. The meeting will provide the opportunity for the group to work together to take the survey and sample collection. We need everyone to participate in the first study of its kind.

We will have a general support meeting after the Yale study. If you do not wish to participate in this portion of the meeting, you may stop by for the Yale study only.

Please come and participate. For statistical power and validity, the study requires 1000 AN patients. To date we have collected only 400 samples. Because there are so few us your sample submission REALLY COUNTS!!!!!

Sunday, February 23, 2014

Sleep Like the Dead


overdriveonline.com


If you suffer from tinnitus like many acoustic neuroma sufferers and have a hard time sleeping, you might benefit from some of the tips offered on the "Sleep Like the Dead" website. The site creator was an insomniac for many years and sleep research became his passion. He rates by surveying hundreds of users, sound masking machines, ear plugs and even sleeping pills. It's worth a look. 


Sleep Like the Dead



Tuesday, January 21, 2014

Leah Keith Story

Leah Keith produced the Mark Ruffalo interview which can be viewed on the ANA web site. 

Here's an article she wrote about her AN experience. It appeared in the New York Times, Modern Love section, April 11th 2013. 

Despite the Losses, So Much Gained


Brian Rea
By LEAH KEITH

Dude was a doctor who wanted to leave medicine. We met almost 20 years ago, when he applied to a writing fellowship program at the movie studio where I was an executive.

When I called him with the good news, he jumped up and down and screamed into the phone. Then he told me he didn’t hear anything after the word “accepted.” “To me,” he said, “you just sound like an angel.”

No one had ever called me an angel before.

Months later, Dude moved to Los Angeles. In the beginning of our professional relationship, I would give him notes on his screenplays.

Our personal relationship happened later. I was a 26-year-old black woman from Georgia, and he was a New York Italian 13 years older. I don’t remember when or why he became Dude, but after the naming, he anointed me Lilly, short for Li’l Dude. From then on, we were those people to each other.

Dude loved biking, hiking and anything I cooked. I loved Pilates, arctic martinis and anything he wrote. We sang. We danced. We watched movies and debated their merits. We read to each other before falling asleep.

Our relationship was not an obvious one, but neither of us liked the obvious. Dude smelled like freshly folded laundry, baked chicken, red wine and loaves of bread as they rose in the oven. He said my smile lit up a room.

Waiting for success was not easy for Dude. Achieving a No. 1 ranking in his Ivy League graduating class had been effortless compared with selling a screenplay. I tried to explain that in Hollywood, success equaled talent plus luck, but he didn’t understand, and I couldn’t understand why he didn’t understand. We argued. It felt like the beginning of the end of us.

Dude broke up with me before leaving for the airport to bury his father. The phone call was as sudden to me as his ailing father’s death had been to him. I told myself I had pushed him too hard. I told myself I wasn’t “this” or “that” enough. I told myself he just didn’t love me as much as I loved him.

Eventually, time brought on the occasional check-in phone call. I learned that to make ends meet, Dude took an administrative-assistant job at a Hollywood studio. “It’s better than staring into a microscope for hours,” he said.

Hollywood, for him, had lost its luster. He was no longer writing, but he also had no interest in returning to medicine. I knew that I, as his marginally successful producer former girlfriend, had become a reminder of the only defeat he had ever known. I feigned excitement about his new job.

I didn’t want to know much about his dating life, and he didn’t seem curious about mine. Calls became less frequent, and dinners happened only at birthdays. But when we were together, we laughed, ate, drank and sang as we always did. Then we returned to our separate lives.

Everything changed two years ago, when my ear began to ring. I was awaiting a “green light” on an animated film. The ringing was loud and constant. I called Dude.
After a hearing test, CT scan and M.R.I., my life turned into someone else’s movie. Dude said he would come with me to get the results. I didn’t stop him.

I was found to have a 2.5-centimeter acoustic neuroma, a benign tumor of the nerve connecting the ear to the brain; it occurs in about 2 of every 100,000 people. Unbeknown to me, I had already experienced 50 percent hearing loss in my right ear, and my facial nerve had been engulfed by the tumor. Removing it would be difficult. Half of my face could become paralyzed.

This was highly specialized surgery, and my doctor said I was blessed because the best surgeon was only 15 minutes away; he was the Michael Jordan of neurotology.I could feel Dude trying to contain his excitement about meeting His Airness of the ear and brain. I gave him permission to geek out. I figured someone should be happy about something.After the appointment with M. J., Dude and I walked silently. Once we arrived at my car, I broke down. Dude held me. 

I was scheduled for a translabyrinthine craniotomy, the most conservative approach. I would be deaf in one ear, but if M. J. was as good as everyone said, I would still have the smile Dude had once loved.
The movie I was producing was going into storyboards. During that time, Dude and I talked on the phone every night until I fell asleep. In my doubting moments, when I asked if we were doing the right thing, Dude would say: “We have the best surgeon. We chose the right surgery. We will be fine.”
I liked that he used the word “We.”

In my darkest moments, when I asked if he would still love me if I lost half my face, he said: “Hell, no. Deformed people make me nervous. So if Lilly’s face gets busted, Dude out.”
We laughed, and then the man whose constant reply to my “I love you, Dude” had always been “Ugh” said: “I will always love you. No matter what happens.”

“Here is your medical directive,” said the hush-toned woman on the other side of the table.
Dude had joined me at 8:30 a.m. at the hospital, where I signed enough paperwork to buy a house. My mother and sister had flown in and waited outside the door while Dude and I handled the grimmest of business. Dude wouldn’t allow me to read the medical directive. He turned it over to the signing page and placed his hand over the words.
“Sign!” he said.
I did as told, but not before I turned to him and said: “Don’t pull the plug too soon. I’d like to become a Lifetime movie.”
He smiled and nodded. That was all we said about the fact that I could die that day.

My mother called Dude her “son,” and my sister referred to him as her “brother from another mother.” We had become an unconventional family.
“Who ordered a pizza pie?” were the first words I heard from Dude as he entered my hospital room the next day carrying my dinner over his head. I smiled broadly. He smiled back even broader. I knew that he smiled because I could smile.

The next days were filled with wobbly steps, tightly held hands and many firsts. After I got home, Dude and I continued our pre-op ritual with almost nightly phone calls.
Thirteen months after my diagnosis, on an ordinary Tuesday in November, we talked for hours. He spoke of his love of James Brown and his longing for forbidden foods like bacon and foie gras. He made me ask Siri on my new iPhone to do pornographic things to him. We laughed until I fell asleep.
The next day, Dude’s worried assistant (he was running the department now) called to say he hadn’t shown up for work. When I arrived at his apartment, the paramedics were leaving.
Dude had died.

He had not been ill. He had not had an accident. His heart was just done with its work.
I held on to a railing, and the paramedic sat with me until my world stopped spinning. I knew once I entered the apartment, life would be forever divided. “Before Dude” and “After Dude” would preface everything.

The police arrived. There were interviews, phone calls and a three-hour wait for the coroner. During it all, I stood behind the kitchen counter staring at the back of Dude’s always pristinely blow-dried head. Soon I would have to call his friends and family and divide their lives, too.

Now Dude lives in photographs, one voice mail, one piece of video, one pair of hiking boots, his favorite jacket, a few worn sweatshirts, his watch, his cat, his screenplays, his copper pots and pans, his surgical instruments that he used to fry chicken, and the recesses of my memory.

I will never again hear him explain that Miller Genuine Draft 64 only has 64 calories as justification for why it’s O.K. to drink a six-pack in one sitting. I will never hear him explain every stage of the Tour de France in a way that makes me wish I could ride a bike. I will never know that he is hanging on to my every word when I tell him some ridiculous story about my day, and I will never again hear him laugh at that story.

When my rare tumor was found, I thought it was the worst thing that could ever happen to me. Now I know I was the luckiest woman in the world. For 13 lucky months, I got to stare into the abyss and feel safe jumping into it because a man who loved me promised to hold my hand all the way down.
If I had known that I would be the one who had to let go, would I have done anything differently? No.

Leah Keith is an independent live-action and animation film producer in Los Angeles.

Monday, September 23, 2013

Diagnosis in a Dream

Mark Ruffalo is among those of us afflicted with an acoustic neuroma.

Here's an interview with him about his unusual experience.  He dreamed he had a brain tumor and it turned out he did! Read about it here:

Interview with Mark

Bionic Ear


Caption: Scientists This "bionic ear" is capable of receiving radio signals. Photo by Frank Wojciechowski
This “bionic ear” invented in a lab at Princeton University is capable of receiving radio signals.                                                            Frank Wojciechowski photo 

PRINCETON, NJ—Blending electronics and biology, scientists at Princeton University have used readily available 3D printing tools to create a functioning “bionic ear” that can detect radio frequencies far beyond the range of normal human capability.
In a May 1 news release, John Sullivan of the Office of Engineering Communication at Princeton reported that the primary purpose of the researchers was to develop an effective means of merging electronics with biological tissue. The scientists used 3D printing of cells and nanoparticles followed by cell culture to combine a small coil antenna with cartilage, creating what they termed a bionic ear.
The lead researcher is Michael McAlpine, an assistant professor of mechanical and aerospace engineering at Princeton. He told Sullivan, “There are mechanical and thermal challenges with interfacing electronic materials with biological materials. However, our work suggests a new approach–to build and grow the biology up with the electronics synergistically and in a 3D interwoven format.”
The Princeton team has been doing research in cybernetics for several years. This promising field seeks to design bionic organs and devices to enhance human abilities. The bionic ear project was the first effort by McAlpine and colleagues to create a fully functional organ: one that replicates a human ability and then uses embedded electronics to extend it.
Writing in the journal Nano Letters, the scientists said that cybernetics, “has the potential to generate customized replacement parts for the human body, or even create organs containing capabilities beyond what human biology ordinarily provides.”
In order to replicate complex three-dimensional biological structures, the researchers turned to 3D printing. A 3D printer uses computer-assisted design to conceive of objects as arrays of thin slices. It then deposits layers of materials to build up a finished product.
One example of this approach is CAMISHA (computer-aided-manufacturing-for-individual-shells-for-hearing-aids), which was invented by Soren Westermann at Widex, and is now used to build 95% of custom hearing aids.
According to Princeton, the bionic ear project marked the first time that researchers have demonstrated that 3D printing is a convenient strategy to interweave tissue with electronics. The researchers used an ordinary 3D printer to combine a matrix of hydrogel and calf cells with silver nanoparticles that form an antenna. The calf cells later develop into cartilage.
The initial device developed by McAlpine and colleagues detects radio waves, but the team plans to incorporate other materials that would enable it to hear acoustic sounds. While it will take much more work to develop a bionic ear that could restore or enhance human hearing, McAlpine said that in principle it should be possible to do so.
The team that developed the bionic ear consists of six Princeton faculty members, two graduate students from Princeton and Johns Hopkins University, and Ziwen Jiang, a high school student at the Peddie School in Hightstown, NJ. McAlpine said of the precocious teenager, “We would not have been able to complete this project without him, particularly in his skill at mastering CAD designs of the bionic ears.”

Saturday, August 17, 2013

Founding of the Acoustic Neuroma Association

If you haven't seen or heard Ginnie Fickel Ehr talk about her experience and how she founded the Acoustic Neuroma Association, you should watch this 8 minute video.

Ginnie was at the recent symposium in Los Angeles and celebrated her 84th birthday with the group.
What a woman!

Founder of the Acoustic Neuroma Association

Wednesday, August 7, 2013

Acoustic Neuroma Patient's Memoirs

Following are the titles and Amazon summaries of three memoirs written by Acoustic Neuroma patients. The fourth, "A Whole New Normal..." is not on Amazon but available on-line from Village Books in Seattle. 

Diagnosis: Brain  Tumor: My Acoustic Neuroma Story by C Micheal Miller:

Since I wasn’t allowed to move my head or upper body at all, I was watching my toes wiggle a little dance in my sneakers while I sang, in my head, the song that the Typewriter Guy used to sing on Sesame Street. Nooooney, Noooney, Nooney, Noo... T. Toes. I chuckled a little. I was in the middle of getting a cranial MRI scan and was watching my toes do their little dance in my sneakers in the angled mirror that I think was supposed to make me feel less claustrophobic. I just thought it was handy for keeping an eye on my toes while they wiggled and danced to the song I sang in my head. I’m guessing that’s not what the company who designed the MRI machine really had in mind, but I wasn’t worried about it. A sudden movement in the smoked glass window beyond my feet caught my eye. The silhouette in the control room was pointing and gesturing at something. There were quickly other shadows that came over to gather around and see what had attracted the first silhouette’s attention. My song faded off into nothing and my toes stopped dancing as the profile of a man wearing a tie came into view and started pointing and gesturing as well. This can’t be good, I thought. Pointing and gesturing during medical tests like an MRI is generally bad, even if it’s just pointing done by silhouettes and shadows. Little did I know what the future held in store for me.

An Acoustic What?One Patient's Acoustic Neuroma Journey by Yvonne Tommis

Just how did an uncontroversial and mild mannered piano teacher become the first UK patient to cross the Atlantic to be treated by Dr Gil Lederman using Fractionated Stereotactic Radiosurgery? The journey began in 1995 when I was diagnosed with a benign brain tumour; an acoustic neuroma. At the time I was advised to have it removed surgically; a long and complicated procedure with serious side effects. So I searched for a less intrusive treatment. It was a very lonely and difficult journey as friends and family wanted me to follow medical advice and have surgery. It took two years to find the treatment, during which time I was denied information, given misleading information and given false information. This book tells the medical and personal story. I hope it will help those who are facing difficult medical decisions, and their friends and family.

A Whole New Normal..an acoustic  neuroma journey by Marla Bronstein



When I was first diagnosed with an Acoustic Neuroma, I went straight to the internet. I found out what it was, treatment options, and read personal stories of resulting complications from long, frightening surgery. I wanted a map to help guide me through the months ahead of surgery that might show me a light at the end of the tunnel with a happy ending. I don't think anyone will read this and come away with “the answer” to all of the questions that arise when deciding how to treat an acoustic neuroma. I hope my story will help people find their own path in dealing with any life-threatening/changing situation.

About the Author


Marla makes her home in the Pacific Northwest. She lives in Bellingham, Washington with her husband Ken. Her favorite children are Zoe and Caleb. She is still trying to figure out what she wants to do when she grows up.


Hell in the Head: My War with a Brain Tumor and Other Evil Things 
 by David Douglas Shannon

He got sucker-punched, blindsided with something that only happens to other people. Actor David Shannon had a brain tumor. It was called an Acoustic Neuroma. In late 2007, he had surgery to have it removed. All should have gone well. It didn't. Gradually over the next two years, Shannon made one disturbing discovery after another that left his acting career and his former life in ruin. Hell in the Head is his story. With a knack for story-telling, Shannon takes us along on his medical misadventure with irreverent wit. As he weaves his way through his newly found post-surgery world, he shares heart-rending losses and his dashed hopes for recovery as well as stories of achievement and inspiration. From learning the bitter truth to running a half marathon to meeting Crooked smile and others facing the same ordeal, Shannon tells the good and the ugly with the same wry humor that will have you laughing and crying at the same time. In the end, after a three-year-ride on a roller coaster of emotional chaos, he presents an advocacy for improved care and counseling for Acoustic Neuroma patients. Hell in the Head is a story of wit and inspiration for all readers and a must read for Acoustic Neuroma patients and "posties."

Friday, August 2, 2013

 
 
News DeskFriday, August 02, 2013
From Print Edition
 
 

 
Straining to catch the gist of conversations is frustrating enough, but a new study shows that seniors with hearing loss are also at increased risk for hospitalization, illness, injury and depression.

Researchers analyzed data from more than 1,100 American men and women aged 70 and older with hearing loss, and found that over a four-year period they were 32 percent more likely to have been admitted to the hospital than more than 500 adults with normal hearing. Hearing-impaired seniors were also 36 percent more likely to have prolonged stretches (more than 10 days) of illness or injury and 57 percent more likely to have extended episodes (more than 10 days) of stress, depression or bad mood, according to the study, published online June 11 in the Journal of the American Medical Association.

“Hearing loss may have a profoundly detrimental effect on older people’s physical and mental well-being, and even health care resources,” said study senior investigator Dr. Frank Lin, an otologist and assistant professor at the Johns Hopkins University School of Medicine and Hopkins’ Bloomberg School of Public Health. “Our results underscore why hearing loss should not be considered an inconsequential part of aging, but an important issue for public health,” Lin said in a Hopkins news release.

Hearing deficits can lead to social isolation, which in turn contribute to physical and mental declines, Lin said. Hearing loss affects as many as 27 million Americans over age 50, including two-thirds of men and women aged 70 years and older, according to Lin. The study doesn’t prove that being hard of hearing directly leads to other health problems, but it does show an association between the two. And health policymakers need to consider the broader health impact of hearing loss when making decisions for older people, study lead investigator Dr. Dane Genther, a resident in otolaryngology/head and neck surgery, said in the news release. Genther’s recommendations: expanded Medicare and Medicaid reimbursement for hearing-related health care services, wider installation of hearing loops in various facilities, and more accessible and affordable approaches for treating hearing loss.

From the News International: 


 

Tuesday, July 30, 2013

Cyclist Rides to Advance Acoustic Neuroma Research

Endurance Cyclist Prepares to Ride 466 Miles to Advance Neural Tumor Research

Released: 7/22/2013 6:00 AM EDT
Source Newsroom: House Research Institute
Newswise — Los Angeles, Calif. – July 19, 2013 – Steve Meichtry is one of the rare breeds of extreme athletes who enjoys testing the outer limits of distance endurance. When he discovered that he had an acoustic neuroma - a tumor on his left balance nerve that leads to the brain- he thought his cycling days were over.
What – After Steve Meichtry was successfully treated for his acoustic neuroma by Neurotologist Derald E. Brackmann, M.D., of the House Clinic and House Research Institute, Steve wanted to help others with acoustic neuromas by raising support for neural tumor research at the non-profit House Research Institute in Los Angeles, CA. To accomplish his goals, he is taking on his toughest endurance ride yet by entering the Inyo Ultra 466, a new 466-mile ultra endurance bike race in the High Sierra.
When – Right away, people can follow and support Steve as he trains for the
August 14th Inyo Ultra 466 race athttp://www.gofundme.com/466steve#.
His training blog can be found athttp://www.whiteowlscyclingblog.blogspot.com/
Where –The Inyo Ultra 466 Race is a mind- and muscle-bending 466-mile course through the steep Eastern Sierra mountains northwest of Bishop, CA!
Race route info. is at http://ridewithgps.com/routes/2272565.
Steve resides and trains in So. California’s San Fernando Valley.
About House Research Institute –
House Research Institute is a non-profit 501(c)(3) organization dedicated to improving the quality of life for people with hearing loss and related disorders through scientific research, patient care and the sharing of knowledge. For more information about the House Research Institute, please call (800) 388-8612 or (213) 483-4431, e-mailinfo@houseresearch.org or visitwww.houseresearchinstitute.org.
# # #

Friday, July 26, 2013

Symposium

We are getting ready for the big ANA symposium being held August 9 - 11th, almost in our own back yard this year. The program is excellent and the event is a must attend for anyone with an acoustic neuroma.

Find out more here:
Acoustic Neuroma Association Symposium

Test Post


San Diego Support Group

This is a test post for the blog. We have plans to post stories of individual's experiences during their AN diagnoses, treatments and recoveries. If you read this, please post in the appropriate spot at the bottom of the blog so we know you have visited.

Thank you.