Introduction
Sunny Hostin is a familiar face on television, serving as a co-host on The View and as a legal analyst on various news programs. However, she is also a rare disease warrior. Hostin was diagnosed with antiphospholipid syndrome, an autoimmune disease, in 2016. This diagnosis rocked her world, as she had to learn to navigate life with a chronic condition. Hostin has since spoken out about the need for increased awareness about rare diseases, and her advocacy work has had an impact on many people’s lives.
The Unseen Struggle: Inside Sunny Hostin’s Battle with a Rare Disease
Sunny Hostin’s journey with antiphospholipid syndrome began in 2016. She experienced a pulmonary embolism, a type of blood clot that occurs in the lungs. Doctors then discovered that she had antiphospholipid syndrome, a rare autoimmune disease that can cause blood clots, miscarriages, and cognitive issues. Hostin has also noted that she experiences chronic pain and fatigue, which can impact her daily life.
As she has shared in interviews, Hostin’s disease has had a significant impact on her professional and personal life. She has had to adjust her work schedule and take time off, and she has also had to navigate her condition with her family. As Hostin has noted, “I have a wonderful family and support system. But when you’re living with a chronic illness, it can be a lonely place. Even with those who love and support you.”
Sunny Hostin Speaks Out About Her Life-Altering Diagnosis: What You Need to Know About Her Disease
Antiphospholipid syndrome (APS) is a rare autoimmune disease that can impact multiple systems in the body. According to the APS Foundation of America, APS affects approximately 1% of the population. The disease is often difficult to diagnose, as its symptoms can mimic other conditions.
Symptoms of APS can include a range of issues, including blood clots, stroke, miscarriages, and cognitive issues. In some cases, individuals with APS may also experience chronic pain, fatigue, and other symptoms. Treatment for APS often includes blood thinners and other medications. For women with APS who are pregnant, there are additional treatment considerations to help prevent miscarriage.
From Journalist to Patient: How Sunny Hostin is Raising Awareness About Her Disease
Since her diagnosis, Sunny Hostin has become an advocate for increased awareness and research funding for rare diseases. She has spoken out about her journey with APS in various interviews and has shared her story with others who may be going through similar struggles.
Hostin has also been involved with the APS Foundation of America, working to raise awareness about the disease and fund research for better treatments. In a 2019 interview, Hostin noted that “I want to be able to find a cure or at least better treatment options for people like me who are suffering from a rare disease.”
Learning to Live with a Chronic Condition: Sunny Hostin’s Story
Living with a chronic disease is no easy feat. Sunny Hostin has been open about the emotional and mental toll that her disease has taken on her. In various interviews, she has shared that she has had to adjust her expectations and learn to prioritize self-care.
Despite the challenges she’s faced, Hostin remains positive and determined. In an interview with the New York Times, she noted that “I have a lot more I want to do in my life. I’m not going to let this define me.” To cope with her condition, Hostin has utilized various self-care strategies, including exercise, meditation, and spending time with loved ones.
Sunny Hostin Opens Up About Her Disease and the Importance of Advocacy
Sunny Hostin’s journey with APS has inspired her to become an advocate for rare diseases. She has spoken out about the need for increased awareness, research, and funding. As she shared in a 2019 interview with Parade, “I want to be a voice for the voiceless…for those people that don’t have the platform to talk about rare diseases.”
For Hostin, her advocacy work is about more than just her own disease. She wants to help others who may be going through similar struggles. As she shared in a segment on The View, “I want people to know that they’re not alone, that there is hope. And, you’re strong enough to handle this.”
Conclusion
Sunny Hostin’s journey with antiphospholipid syndrome has been a challenging one, but she has not let it define her. Instead, she has become an advocate for increased awareness, research, and funding for rare diseases. Hostin’s story serves as a reminder of the importance of advocating for those who may not have a voice. By sharing her story and raising awareness, Sunny Hostin is making a difference in the lives of many.
