Volume 15 | March 2022


Celebrities with endometriosis sharing stories and spreading awareness

In recognition of Women’s History Month and Endometriosis Awareness Month, we are highlighting well-known women who have the condition.

One in ten women suffers from endometriosis. The condition occurs when tissue, similar to the lining of the uterus, grows outside the uterus in a woman’s abdominal cavity. It causes heavy bleeding, abdominal pain, and can cause infertility. Several prominent women have spoken out about their experiences.

Actress/YouTube Star Tia Mowry-Hardrict, 43, thought she was alone in her suffering because she didn’t know anyone else who had endometriosis. Like many women, she was told that her pain was just severe cramps. After consulting with her doctor, she learned she had endometriosis and that many African American women are misdiagnosed because less research has been done on Black women . After several surgeries, Mowry-Hardrict’s doctor told her she needed to change her diet and focus on health and wellness. A year later, she found out she was pregnant. Her son, Chree, was born in 2011, and she gave birth to her daughter, Cairo, at age 39. She has continued to speak about her experiences and promote a healthy diet.

Actress/Activist Susan Sarandon, 75, was diagnosed at age 36, after years of struggling with fainting and heavy bleeding. Sarandon says she thought her pain was a natural part of being a woman, and that she would need to learn to live with it. Her doctor prescribed birth control pills as well as pain pills. She was also told she would never have children, but went on to become a mother of three. She says in a video made by the Endometriosis Foundation of America, “Early detection and treatment are the best prevention.” She also says, “It’s not okay to miss a part of your life because of pain and excessive bleeding.” She encourages women to listen to their bodies.

Top Chef Television Host Padma Lakshmi, 51, was diagnosed when she was 36. Lakshmi says she felt angry because it took so long for her to be diagnosed and that she had been losing “a week of [her] life every month of every year…” Lakshmi struggled for over 20 years before being officially diagnosed. In 2009, she co-founded the Endometriosis Foundation of America with the doctor who diagnosed her, saying, “I didn’t want the next generation of women to go through what I went through, to feel betrayed by their own bodies or to feel alone.”

If you or someone you know suffers from endometriosis, you are not alone! We hope that these stories will encourage you to reach out here on Inspire (start a discussion in our Endometriosis community) and talk to your doctor.


Join Fight CRC for their virtual Call-on Congress event


Did you know March is Colorectal Cancer Awareness Month?

Fight CRC is excited for its annual Call-on Congress event. In December, they held their first Path to a Cure that identified priorities and innovative research ideas focused on advancing treatment and developing a cure for stage III and stage IV MSS colorectal cancer patients. Fight CRC’s Screening Mini Mag is a great resource for anyone preparing for or on the fence about preventive screening and the newest edition of Beyond Blue is also out!

Make sure to follow them @fightcrc on Instagram and Twitter, and Fight Colorectal Cancer on Facebook to stay up to date on all of their advocacy, research, and patient-centered updates


Join the Melanoma Exchange Patient Forum in-person and virtually

Melanoma Reasearch Alliance

Join the Melanoma Research Alliance on March 9!

MRA’s Melanoma Exchange Patient Forum, held in-person in Washington, DC and virtually on March 9, will bring together melanoma patients, survivors, advocates, and their loved ones to provide lay-friendly, state-of-the-science education, promote collaboration, and provide networking opportunities across the melanoma community.

Throughout the event, you’ll hear from leading experts in the melanoma field and have the opportunity to ask questions, discuss, and network with other people who are going through their own melanoma journey. Each session will provide information, insight, and strategies to help navigate melanoma diagnosis, treatment, or beyond.

Register Here


Dysautonomia Support Network

Dysatomonia Support Network
Dysautonomia Support Network has a new website. The website is a labor of love for all those that struggle with dysautonomia. As patients, caregivers, and supporters, we designed the site with what we ourselves hoped for when we started our own dysautonomia journey. Make sure to check out our:

We hope you will take the time to look around our DSN Website and share your feedback!


Join our Myeloma Online Support Community

Leukemia Research Foundation

March is Multiple Myeloma Awareness Month wich is a great time for individuals to take actions that positively impact the myeloma community. If you or a loved one is living with myeloma, we encourage you to join our Myeloma Online Support Community today to connect with others, and get or give support.

Monthly Dose Quote

“What you do makes a difference, and you have to decide what kind of difference you want to make.” – Jane Goodall

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