Editor’s Note: In honor of Cystic Fibrosis Awareness Month, we asked Jacqueline Washle, Ambry’s Community Outreach Manager, to tell us about the Mauli Ola Foundation, which supports people with cystic fibrosis and other inherited conditions as part of its mission. Did you know that going to the beach is not only a fun pastime for…
Technology is everywhere. It has become pervasive in our lives. Phones and computers became smaller, smaller, and then somehow bigger and bigger again as our phones become our new computers. Increasing technological advances are also propelling healthcare: newer techniques, smarter robotics, and new drugs. Within genetics, testing techniques…
Editor’s Note: As National Autism Awareness Month continues, we conclude our 2-part interview we began with Kieran Best, a young man with an autism spectrum disorder. His mother, Christina DeRochemont, shares candidly about what life was like early on with Kieran, how they received his diagnosis, and offers tips for other parents in a similar…
Editor’s Note: We are so pleased to continue introducing new voices into the Ambry patient blog. This week we are honored to have Jon Rodis, patient advocate, tell us what it was like to be diagnosed with Marfan syndrome, an inherited condition that can cause heart problems, many years ago – well before genetic testing became available…
Editor’s Note: To help support National Autism Awareness Month, we are sharing our interview with Kieran Best, a 14-year-old young man with an autism spectrum disorder. Kieran graciously shared insights into what his day-to-day life is like and offered words of wisdom to others who may be in his situation. Check back in two weeks to read our…
In my role as co-founder of AliveAndKickn, people ask me for my opinion all the time. Topics range from how to manage pain, how to navigate post-cancer survivorship, to whether or not the U.S. will ever become a world soccer powerhouse. (No, I’m not kidding.) I’m not big on giving advice, but I try to answer as honestly as I can. First,…
Editor’s Note: In recognition of National Colorectal Cancer Awareness Month, we are re-posting this piece by an Ambry genetic counselor. His many years of clinical experience working with families affected by hereditary colorectal cancer helped him understand the importance of expert care teams, and how they can help you. My name is…
Several years prior to my breast cancer diagnosis, I started to think about the right time to liquidate my business and sell the real estate. At the time, my brother and I owned two Ace hardware stores in the Milwaukee area with approximately 100,000-sq. ft. of retail space, warehouse and offices. I knew it would be a physically daunting undertaking…
As a genetic counselor specializing in cancer genetics, I’m happy to be contributing to the Ambry patient blog during National Colorectal Cancer Awareness Month. Colorectal cancer can happen by chance, but it can also be inherited. Your doctor or genetic counselor can evaluate your family history to determine if you should consider genetic testing…
In honor of Colorectal Cancer Awareness Month, I would like to discuss the most common cause of hereditary colorectal and uterine cancer – Lynch syndrome. In fact, this post is dedicated to my brother Jimmy, who died of colon cancer due to Lynch syndrome at the age of 36. Lynch syndrome is a hereditary cancer condition passed down in families…