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Selma Blair's Lifelong Battle with Undiagnosed Juvenile MS Inspires Advocacy

Summary

  • Selma Blair diagnosed with relapsing limiting MS in 2018
  • Experienced symptoms like pain, fatigue, and neurological issues from childhood
  • Doctors dismissed her symptoms as "growing pains" until her 40s
Selma Blair's Lifelong Battle with Undiagnosed Juvenile MS Inspires Advocacy

Selma Blair, the 53-year-old actress, has been open about her lifelong struggle with undiagnosed multiple sclerosis (MS). It turns out that the symptoms she experienced from a young age, including pain, fatigue, and neurological problems, were signs of juvenile MS that went unrecognized by medical professionals for decades.

Blair was finally diagnosed with relapsing limiting MS in 2018, but she recalls a long history of unexplained health issues. As a child, she had frequent fevers, headaches, and "bone crushing fatigue," yet doctors often dismissed her symptoms as "growing pains" or related to her menstrual cycle. Even when her mother requested MRI scans, the tests were denied, with the doctors claiming Blair did not need them.

Despite the challenges, Blair has found solace in sharing her story and connecting with others facing similar health battles. She has been vocal about her journey, using social media to thank supportive colleagues and raise awareness about the realities of living with chronic illness. Blair's openness has resonated with many, providing a sense of community for those who feel "seen" by her experiences.

Now in remission, Blair continues to make progress, recently finding success with a new therapy called Mavenclad. Her perseverance and willingness to advocate for herself have been instrumental in her journey, inspiring others to be their own best health advocates.

Disclaimer: This story has been auto-aggregated and auto-summarised by a computer program. This story has not been edited or created by the Feedzop team.
Selma Blair experienced symptoms like pain, fatigue, and neurological problems from a young age, which were later revealed to be signs of juvenile multiple sclerosis.
Selma Blair's doctors often dismissed her symptoms as "growing pains" or related to her menstrual cycle, even denying her requests for MRI scans.
Selma Blair's willingness to share her story has provided a sense of community and inspiration for others living with chronic illnesses, making them feel "seen" and understood.

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