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We recently conducted a survey to research the gaps in knowledge and care for (MS). We then teamed up with Robin Arzon, Vice President of Fitness Programming and Head Instructor at Peloton, to moderate a panel discussion sharing the survey highlights along with several women from the MS community. Together, they exchanged stories of resilience while addressing the common challenges many MS patients face.
After the discussion, we partnered with the Little Words Project to craft bracelets as tangible reminders of inner strength and positivity for these women as they navigate their health journeys. Check out some highlights.
Lamar experienced cycles of remission and recurrence when he was first diagnosed with Hodgkin’s lymphoma at the age of 25. He underwent treatment with different types of therapies until he eventually went into long term remission. It wasn’t until several years later that he was diagnosed with a completely different type of known as diffuse large B-cell lymphoma (DLBCL). Learn more about Lamar’s inspiring story of resilience, and how clinical trials offered him renewed hope. http://spr.ly/6189mRlQN
As comes to a close, hear from James Ian, a contributor to our SMA My Way program. James helped write and perform on the hit song SPACES, participated in the Double Take fashion show, and took to the stage at the musical comedy, “Most Likely Not To…”. Hear from him how he believes these initiatives are shaping industry standards in film, music, fashion, and beyond in the video below: https://www.gene.com/topics/spinal-muscular-atrophy
We recently conducted a survey to research the gaps in knowledge and care for (MS). We then teamed up with Robin Arzon, Vice President of Fitness Programming and Head Instructor at Peloton, to moderate a panel discussion sharing the survey highlights along with several women from the MS community. Together, they exchanged stories of resilience while addressing the common challenges many MS patients face.
After the discussion, we partnered with Little Words Project to craft bracelets as tangible reminders of inner strength and positivity for these women as they navigate their health journeys. Check out some highlights below.
Every year, an estimated 3,300 adults in Washington, D.C. are diagnosed with diabetes. Yet less than 36% of these individuals receive an annual eye exam, when studies have shown they can help significantly prevent vision loss. Due to deep-rooted inequities, Black and Hispanic/Latino people are at higher risk of losing their sight from diabetic eye disease. To address this, we’ve teamed up with the American Diabetes Association (ADA) to launch an initiative in underserved communities across D.C. to remove barriers to quality eye care. Learn more about this important work from Danielle Haney, PhD, Director of Patient Advocacy Relations at Genentech.
Navigating a chronic condition like multiple sclerosis (MS) can be overwhelming. Connecting with a doctor about treatment options shouldn’t be. Hear how Victoria, Brittany and Azure built trust with their care teams so they could get personalized care sooner. http://spr.ly/6189Y4txH
For many patients with cancer, biomarker testing may help identify treatment options best suited to combat their specific disease. For Mike, getting his biomarker results was the “first injection of hope” after his lung cancer diagnosis. Listen to his story about learning his biomarker type and learn why it's important to discuss biomarker testing with a healthcare provider. Learn more and Ask About ALK. http://spr.ly/6186c4XXK
Biomarker testing is a critical step to receiving a complete lung cancer diagnosis and may help guide treatment decisions. However, a significant number of people with lung cancer aren’t aware of biomarker testing and don’t know to ask for it. When Nikki received her lung cancer diagnosis, her doctor suggested they test her right away for certain biomarkers such as ALK. Listen to Nikki’s story and learn about the importance of talking to a healthcare provider about biomarker testing. Learn more and Ask About ALK: http://spr.ly/6188chUH0
Many diagnosed with cancer have never heard of biomarkers, let alone know to ask their doctors to test for them. For Matt and Stephanie, biomarker testing helped them better understand their path forward after Matt’s diagnosis of ALK+ lung cancer. While waiting for results can be overwhelming, the information gained can lead to a more personalized treatment approach. Talk to a healthcare provider about biomarker testing and Ask About ALK: gene.com/AskAboutALK
A lung cancer diagnosis can be overwhelming, often leaving patients with unanswered questions. One important question is if the lung cancer has a specific genetic driver, or ‘biomarker,’ such as ALK. Knowing about these biomarkers can lead to a more personalized treatment plan. Talk to a healthcare provider about biomarker testing and Ask About ALK. Learn More: http://spr.ly/6182i9Ynu
ALK is a biomarker that impacts some people with non-small cell lung cancer (NSCLC). As part of a complete diagnosis, every person with lung cancer should be tested early for biomarkers when there is greater opportunity to treat cancer before it spreads. Learning if your cancer is ALK-positive - or if you have any other biomarkers - provides crucial information to inform your treatment plan. Learn more about the biomarker testing process: http://spr.ly/61895qoJJ
Testing a patient’s lung cancer for biomarkers allows doctors to give a complete diagnosis and helps patients start a personalized treatment specific to their type of cancer. ALK is one of these biomarkers seen in non-small cell lung cancer (NSCLC). Patients with ALK-positive NSCLC are typically diagnosed at a younger age than other types of NSCLC. Learn more about biomarker testing: http://spr.ly/61835qoGW
Giving back is an important way that we deliver on Our Promise to serve society. Earlier this month, we held our 15th annual Genentech Gives Back where thousands of our employees came together for a full week of volunteering and giving in South San Francisco and our other Site communities. See below for some of our favorite moments from this meaningful week, and learn more about how we give back locally here: http://spr.ly/618657IPA
When it comes to stroke, time is everything. It can happen to anyone, regardless of age, ethnicity or occupation. In the U.S., about 800K people experience stroke each year, and one in five of those people are under the age of 55. That’s why it’s important for everyone to be aware of their risk factors and learn to recognize the signs. One way to do this is by memorizing, BE FAST which highlights the signs and symptoms to ensure immediate medical care. Read stories from survivors who have experienced a stroke here: http://spr.ly/6184d1guo
Brett’s son, Ben, was diagnosed with multiple food allergies at 11 months old. His allergic reactions have caused several hospital visits and continues to impact his relationship to food. Today, Brett is a vocal advocate as the Leader of the Northern Virginia Food Allergy Group, an initiative dedicated to helping families feel more confident about handling food allergies. This , learn more about food allergies and how they impact 17 million children and adults in the US: https://www.gene.com/stories/living-with-food-allergies.
Victoria and Brittany learned early on in their journey about the importance of self-advocacy. Learn what empowered them both to take on the challenge. . http://spr.ly/6184d13hu
Not all lung cancers are the same. Some tumors have specific genetic “drivers” called biomarkers that cause cancer to grow and spread. Biomarker testing identifies these drivers and may unlock information about specific types of cancer, including in the lungs. Learn more about biomarker testing here: http://spr.ly/6180jxLqq
Pictured below are Cathy, Jasmine, Christine, and Sue. Each are navigating life with various chronic conditions and face unique challenges every day. Although their journeys may not look the same, they share a common thread - advocating for their well-being, and seeking support to pursue their passions. Whether it’s running a business, being a mother, or empowering others who may be on a similar path as them. This , honor the strength and vulnerability of these women, as well as others who inspire you.
Last week our Gene Academy students, teachers, and mentors got a surprise visit from South San Francisco Assemblymember Diane Papan and South San Francisco Unified School District Superintendent Dr. Shawnterra Moore. During their visit, Assemblywoman Papan and Superintendent Moore observed South City students in the 3rd through 5th grades build compasses and electromagnets in a fun science experiment. At our company, we believe that human connection through mentoring builds confidence in young students and ensures that the future of the healthcare and scientific workforce reflects the diverse communities in which we live. Our Gene Academy is just one of the ways we're doing this. Learn more about the program here: http://spr.ly/6183jH8UW
When Brandon and Amber’s son was diagnosed with A at birth, they were afraid about how it would affect his life. However, support groups and resources gave them comfort and allowed them to meet others in the same position.
“Hemophilia resources helped us realize that our son can live a happy, fulfilling life like any other kid. We hope that future generations continue to create a community for themselves and continue to support each other.”
Learn more about hemophilia A this
https://www.gene.com/topics/hemophilia
For Brandon and Amber, learning to manage their son’s A was a challenge. Thanks to medical advances, they feel more comfortable with him just being a kid. Learn more about how the hemophilia A landscape has been changing. http://spr.ly/6188kfcsp
Every woman has a story. As members of the Roche group, we're working to make healthcare more equitable and accessible so that all people, including women across the globe, can attain their full health potential. Listening to and amplifying women's voices is one step on our journey. Read more below:
What better way to wrap up National than with a dance party? In January, mentors and mentees from across our mentoring programs, including our Gene Academy science education initiative supporting South San Francisco Unified School District elementary students, came together to celebrate the importance of mentorship in their lives – and have a blast on the dance floor! Mentorship is a powerful tool that can open new career possibilities and help build the next generation of innovators, doctors and STEM leaders, and we’re grateful for all of our employees who mentor fellow colleagues and students in our local communities. Check out the video below to see highlights from the event, and learn more about our Gene Academy mentoring program here: http://spr.ly/6189XdMLx
Today on Rare Disease Day, tune in to watch “Most Likely Not To…” a musical comedy livestream written and performed by the spinal muscular atrophy (SMA) community.
This first-of-its-kind event will highlight the astonishing situations people living with disabilities have found themselves in, due to both ableist notions and inaccessibility.
Support for “Most Likely Not To…” is provided by our SMA My Way program. Watch the livestream starting at 3 pm PT/ 6 pm ET here: https://www.smamyway.com/the-musical/
Announcing a first-of-its-kind musical comedy written and performed by the spinal muscular atrophy (SMA) community this Rare Disease Day! The musical event titled “Most Likely Not To…” will showcase romance, feuds, commentary on ableism, and show-stopping songs that share an eye opening look into life with a disability.
This event was created in partnership with the community and support from our SMA My Way program. Watch the livestream on Feb 29 at 3pm PT / 6pm ET here: MostLikelyNotTo.com
is often linked to social isolation. But despite being diagnosed with , Barbara leads a very active social life, thanks to regular treatment. She’s now living life to the fullest thanks to regular eye treatments and a tenacious attitude. Eye exams are especially important for people over 50. Schedule yours today.
is an opportunity to celebrate a vibrant and diverse community, and to acknowledge the legacy of systemic inequities that continue to impact the wellbeing of Black people across the U.S. For example, Black women continue to be disproportionately affected by breast cancer but remain underrepresented in clinical research. With support from our Health Equity Innovation Fund, Touch, The Black Breast Cancer Alliance is activating a joyful, energized community of Black women with breast cancer to advocate for themselves and each other to increase access and participation in clinical research. Learn how their groundbreaking initiative, When We Tri(al), is helping more Black women enroll in clinical cancer research: http://spr.ly/6187nXahf
can take a toll on your mental health. For Gary, a diagnosis in 2002 left him feeling distraught. But thanks to regular treatment, he is still able to serve in his community, teach courses to students, and volunteer.
“Early detection is most important,” Gary states. He hopes his story will encourage others to get their eyes checked regularly.
When John went in for his eye exam in 2014, he didn’t expect to be diagnosed with . And thanks to treatment that stabilized his eyesight, John can still enjoy cooking and traveling with his wife, Connie. John hopes his experience will inspire others to get their eyes checked regularly. Schedule your next eye exam today.
Yan Wu, Senior Fellow and Vice President of Antibody Engineering, credits early mentors at Genentech for seeing her potential and trusting her to take on new responsibilities that expanded her skillset and eventually enabled her to rise to the leadership level. She has paid forward that investment in her career by mentoring young talent who bring new ideas to help fuel innovation at our company. In honor of Day, we recognize and thank Yan and all of the mentors who support our employees to flourish in their professional journeys!
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