| |  | FEATURED IN SEPTEMBER 2026 |
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| - 2026 Symposium videos and photos now available
- Meet our Ambassadors - Pat Camalliere
- Good News
- News & Shorts - articles, podcasts, and more
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| SYMPOSIUM 2026 VIDEOS NOW AVAILABLE |
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| Thank you to everyone who joined us in Boston for the 2026 Head & Neck Cancer Survivorship Symposium! We hope you left the event with helpful information, new connections, and a renewed sense of community. SYMPOSIUM SESSION VIDEOS Symposium videos are now available on YouTube. Each session has been posted individually, and you can find them all together in our 2026 Survivorship Symposium playlist. Whether you missed a session, attended virtually, or want to revisit a presentation, we hope these recordings remain a useful resource. LOOKING AHEAD - SURVIVORSHIP SYMPOSIUM 2027 We’re already looking ahead to next year. The 2027 Head and Neck Cancer Survivorship Symposium is tentatively planned for late October in Atlanta. Please note that the timing is preliminary and may change. We’ll share confirmed dates and additional details as plans are finalized. Thank you again for being part of the 2026 Symposium and the Head & Neck Cancer Alliance community. |
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| | | | | SYMPOSIUM PHOTOGRAPHS All photos taken during the Symposium are also available to view and download at no cost. You may download, share, and use the photos for personal purposes without attribution. If you use a photo in a professional or commercial capacity, such as in a presentation, publication, professional website or promotional materials, please credit the photo to Head & Neck Cancer Alliance. |
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| | | | Pat Camalliere Retired Health Care Professional Survivor of HPV-attributed Tongue Cancer |
| | After more than 40 years working in health care, much of it alongside physicians treating people with cancer, Pat Camalliere never expected to become a patient herself. After retiring, she began a second career as a historical mystery novelist. Then, in 2017 at age 75, a tender lump under her jaw led to an unexpected diagnosis of HPV-related squamous cell cancer. Pat underwent 35 radiation treatments and eight chemotherapy infusions, experiencing firsthand many of the challenges she had witnessed throughout her career. During treatment, Pat began writing a weekly blog about her experience, hoping that sharing what she was learning could help others facing cancer. Treatment brought significant challenges, including pain from radiation and difficulty eating, and taught her how different the experience of cancer can be when you are the patient rather than the health care professional. Eight years later, Pat is cancer-free, although she continues to manage late effects including lymphedema, neuropathy, coughing, and difficulty swallowing. She has returned to many of the things she loves, including writing, spending time with family, and speaking publicly. Through sharing her experience, Pat hopes to help others with head and neck cancer and their loved ones feel more prepared and less alone. |
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| | | SHARE YOUR GOOD NEWS! We want to celebrate the wins in our community, big or small. Finished treatment, joined an awareness event, welcomed a grandchild, or reached a personal milestone? We’d love to share your good news. This is open to patients, survivors, caregivers, and medical professionals. Email your story and a photo, and tell us what you’re celebrating. By submitting, you give us permission to share it in our newsletter or on social media. We can’t publish every submission. Send your good news to [email protected]. |
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| | | Head and Neck Cancer Alliance Ambassador Richard Page recently participated in Project Lab Coat, a unique initiative that brings together fashion, medicine, advocacy, and personal storytelling. Presented during New York Fashion Week, Project Lab Coat reimagines the traditional lab coat as a symbol of resilience, science, and hope. Through its runway presentations, Project Lab Coat shines a spotlight on important health causes and the people whose lives have been impacted by them. Richard’s participation provided an opportunity to bring greater visibility to the head and neck cancer community and share the perspective of survivorship through a creative platform. |
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| TONGUE CANCER SURVIVORS - The Icahn School of Medicine at Mount Sinai is conducting a study to better understand the survivorship experiences and quality of life of people diagnosed with tongue cancer at a young age. - If you are between 18 and 50 years old and have a history of tongue cancer, you may be eligible to take part.
- Participation involves completing a one-time online survey (about 10 minutes).
- Participation is voluntary and anonymous.
Survey link: http://bit.ly/48q3qWo |
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| JOIN IMERMAN ANGELS FOR NAVIGATING RELATIONSHIPS AFTER CANCER - FREE WEBINAR September 29 - 7 PM ET Not only does a cancer diagnosis upend your life — it can significantly impact your relationships. Join us for an honest and compassionate conversation about the realities of navigating relationships after cancer. Through personal stories and expert insights, we’ll explore the highs and lows of how cancer can affect relationships with parents, siblings, children, partners, friends, and more. Designed for cancer fighters, survivors, previvors, caregivers, family members, and friends, this session will highlight common relationship challenges after a diagnosis and provide validation and practical guidance for understanding and strengthening connections after cancer. REGISTER HERE |
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| | THANK YOU SPONSORS! Corporate sponsors play a crucial role in the mission of the Alliance. Their support not only provides vital funding for our programs and services but also amplifies awareness of head and neck cancers. Together, we create hope, spread knowledge, and save lives. |
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| MONTHLY GIVING - DONATE TODAY Start the year with hope. Monthly giving provides steady, year-round support for people affected by head and neck cancer. Your monthly recurring gift helps sustain - education
- survivorship resources
- patient support every month
With your support, we can continue to help individuals and families find help when they need it. Join our Monthly Giving Community today! |
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| | REVIEW US ON GOOGLE! If our programs and materials have made a difference to you, please consider reviewing us on Google. Your review will help make us more visible so other patients, survivors, and caregivers can easily find us while searching online! To write a review, you'll need to sign up for a free Gmail account. |
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| | PICTURE THIS! We're looking for pictures of real people to use on our website, brochures, and social media. We don't want to use boring stock photos! Your photos could provide hope and inspiration to others going through head and neck cancer! |
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| DO YOU FOLLOW? Are you following us on social media? It's just one more way to keep up to date with what is going on with us as well as other head and neck cancer related news and opportunities. So pick your favorite platform and give us a follow! Facebook | Twitter* | LinkedIn | Instagram *also known as X |
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| | | *Statement on Sponsor Content and Corporate Support: The information published on this website and in our materials is intended to educate you about Head and Neck Cancer. The content is not intended to take the place of a discussion with a qualified physician who is familiar with your medical situation. It is important to remember that each individual is different, and the reasons for—and outcomes of—any treatment plan depends on the patient's individual condition. If you have questions or concerns after reading any information on this website or in our materials, you should discuss them openly and honestly with your physician. Any products and manufacturers included on this site are presented for informational purposes only and do not constitute product approval or endorsement by HNCA. The content provided by HNCA is in no way intended to be a substitute for medical consultation with a qualified professional. HNCA encourages those using its resources to be careful when evaluating medical information or products. If you are unsure about your medical condition, consult a physician. Funding from our corporate partners supports HNCA’s programs and educational initiatives, and HNCA maintains independence in its design of programs, content, and initiatives. |
| | Be sure to add our email address to your address book or safe senders list so our emails get to your inbox. Having trouble viewing this email? View it in your web browser |
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| Head & Neck Cancer Alliance PO BOX 21688 | Charleston, South Carolina 29413 866-792-4622 | [email protected] |
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