Volunteering with ANA
We make it easy to get started!
If you are considering volunteering, thank you! We encourage you to read these three steps to help you maximize the experience for both you and ANA.
Our nationwide volunteer network is dedicated to serving the AN community by increasing ANA's outreach and impact in several meaningful ways. If your are interested in joining our volunteer network, you can choose from a variety of programs and activities listed below that match your interests, skills and availability.
Support Group Program
ANA Support Groups are led by volunteers and are people just like you.
ANA Support Group volunteers serve as Leaders or Co-Leaders, scheduling and coordinating Support Group meetings in their local communities. The meetings provide opportunities to learn about acoustic neuroma topics of interest through educational presentations and guest speakers as well as offering supportive time for caring, sharing and networking with attendees.
Volunteer with one of our many existing Support Groups today! Click on our locator map to find a Support Group in your area. If there is not a Support Group in your area, please consider starting one now.
ANetwork, Peer Support Program
ANetwork volunteers are valuable resources that provide a one-on-one personal connection for support and encouragement via phone and email contact.
The ANetwork Program provides access to a variety of acoustic neuroma patients from across the U.S. and covers all treatment types, various tumor sizes as well as caregivers/family members of acoustic neuroma patients.
The participants in the ANetwork Program volunteer their time to share their own personal AN experience in an effort to increase awareness and educate patients about AN diagnosis and treatment, as well as provide encouragement and support. This helps in reducing the isolation and loneliness that many acoustic neuroma patients feel.
Community Connections Program
Community Connections provides informal meeting opportunities with local acoustic neuroma patients in a variety of areas across the U.S. Enjoy casual networking time with other acoustic neuroma patients and find encouragement and support through shared experiences.
There are milestones or anniversaries that people remember as a significant event noting a special achievement during the AN journey from a very personal, individual perspective. For some, a milestone can be making a tough treatment decision after months of information gathering. For others, it may be a treatment anniversary, or perhaps reaching a specific goal after treatment. Whether large or small, milestones and anniversaries are meaningful markers and are as unique as the individual.
We hope that seeing these realistic and personal events, submitted by patients, caregivers or family members, will provide a sense that you are not along and you will find comfort from others that have faced similar circumstances. Together we can make a difference by encouraging others on their AN journey.
At age 33 and mom to two small children, I learned I had a 2.5cm AN. I had successful Translab surgery in May 2017. Unfortunately, I awoke from surgery with facial paralysis and struggled to get back on my feet without help. I wanted to be strong and healthy and get back to what I loved - running. I kept a positive attitude (even though there were plenty of bad days), had an amazing support system and set a goal to run my first race six months post-surgery. I completed a 10K and raised $3,000.00 for ANA!
VIEW MILESTONE GALLERY
Team ANA, Peer-to-Peer Fundraising Program
TEAM ANA members are acoustic neuroma fundraising volunteers raising funds and increasing awareness and education of acoustic neuroma while challenging themselves and encouraging others to set and reach meaningful personal goals.
Do you like to run? Maybe walking is your thing. Do you like to entertain? Consider hosting a house party? The possibilities are limitless. Be a part of TEAM ANA and give your passion a purpose!
Fundraising feels good and it is a great way to give back to those who have helped you. ANA depends on supporters such as you to raise awareness and funds to enhance current educational and support services and to establish future programming for those not yet diagnosed.