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Young woman's health crisis sparked by misdiagnosis
Charlotte Kent is struggling with a rare heart condition after years of being mistaken for bloating.

Charlotte Kent is facing a dire health battle after a rare heart condition was misdiagnosed as bloating.
Active daughter suffers from undiagnosed condition leading to severe health crisis
At just 25 years old, Charlotte Kent is confronting a life-threatening condition after years of misdiagnosis. The daughter from Earith, Cambridgeshire, has been battling superior mesenteric artery syndrome, a rare disorder where a major artery compresses the intestine, causing severe digestive issues. Her parents initially attributed her recurring bloating and stomach distension to growth spurts and exercise, but as her symptoms worsened, it became clear something significant was wrong. Charlotte, reliant on a nasogastric tube for nourishment, has spent 47 of the last 60 months hospitalized. Despite her plight, health professionals in the UK were unable to recognize her condition for years. A private consultation eventually led to the diagnosis and the discovery of a potential remedy, the Alvear procedure, which remains unavailable through the National Health Service in the UK.
Key Takeaways
"Charlotte is dying before my eyes, her body is just slowing down."
Charlotte's mother expresses her anguish over her daughter's deteriorating condition.
"Because SMA is so rare, doctors in the UK have little understanding about it."
Leanne reflects on the lack of awareness among healthcare providers about Charlotte's condition.
"It’s her only hope."
Leanne emphasizes the urgent need for the Alvear procedure for Charlotte's survival.
"I feel stuck while the rest of the world moves on."
Charlotte shares her experience of isolation due to her illness.
Charlotte's story reflects the tragic consequences of healthcare delays and misdiagnosis, especially regarding rare conditions that are poorly understood. The struggle to secure timely treatment highlights a systemic issue where doctors may overlook severe symptoms in younger patients, attributing them to less serious causes. Charlotte's determination to seek help shows the power of advocacy and resilience amid frustrating barriers. Without immediate action, her situation serves as a poignant reminder of the urgent need for improved awareness and understanding of rare medical conditions among healthcare providers.
Highlights
- I feel like my life has stopped while the world continues to go round.
- I wouldn't wish this on anybody, I just want a normal life.
- Watching my daughter struggle is the hardest thing I've ever faced.
- I just want to give my daughter a second chance at life.
Sensitive health crisis raises concerns about medical awareness
Charlotte's misdiagnosis highlights gaps in understanding rare conditions among healthcare providers, which can lead to severe health implications.
Charlotte's journey underlines the importance of awareness in rare medical conditions.
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