Student lost half her body weight in six months after rare condition ‘paralysed’ her stomach

Student’s Dramatic Weight Loss Journey Due to Rare Stomach Condition

Shannon Dunbar-Dawe, a 30-year-old former accounting student, experienced a life-altering transformation when she lost nearly half her body weight in just six months. Shannon’s ordeal began in May 2022 when she started to suffer from bloating and nausea. Initially attributing it to excessive coffee consumption, Shannon’s condition worsened, leaving her unable to eat more than a few digestive biscuits a day without her stomach swelling significantly.

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Despite seeking medical help, Shannon’s symptoms were dismissed as anxiety or an eating disorder until she was eventually diagnosed with gastroparesis, a rare condition that paralyses the stomach’s nerves and muscles, causing delayed food digestion. Following the diagnosis, Shannon had a feeding tube fitted to aid in her food consumption, as traditional eating was no longer an option for her.

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The journey to her diagnosis was riddled with challenges, as doctors initially misdiagnosed her condition and even forced her to undergo treatments for issues she did not have. Shannon’s sister, Charelle Dunbar-Dawe, set up a GoFundMe page to raise funds for Shannon to undergo a procedure to improve her quality of life and potentially allow for the removal of her feeding tube.

Shannon’s daily life has been drastically altered since the insertion of the feeding tube. She now faces challenges such as nausea, discomfort, and acid reflux, making each day a struggle. Despite the hardships, Shannon remains hopeful that a gastric pacemaker, which is currently unavailable through the NHS, could improve her condition and eventually lead to a better quality of life.

The fundraising efforts aim to provide Shannon with the necessary treatment to manage her symptoms effectively and possibly regain the ability to eat regular food again. Shannon’s story sheds light on the importance of raising awareness for rare conditions like gastroparesis and advocating for proper diagnosis and treatment for individuals experiencing similar symptoms.

Through her journey, Shannon hopes to not only receive the medical support she needs but also to educate others about her condition. By sharing her experience, Shannon aims to prevent others from suffering needlessly due to delayed or misdiagnosed illnesses. Her resilience and determination serve as an inspiration, showcasing the strength needed to navigate the challenges of living with a rare medical condition.

As Shannon continues her fight for a better quality of life, her story serves as a reminder of the importance of perseverance and advocacy in the face of adversity. With the support of her loved ones and the community, Shannon remains determined to overcome the obstacles posed by her condition and emerge stronger on the other side.