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Glasgow teen diagnosed with gastroparesis after severe stomach pain

A Glasgow teenager with PoTS was diagnosed with gastroparesis after worsening symptoms, highlighting patient experiences and support efforts.

August 18, 2025 at 05:49 AM
blur Glasgow teen had 'severe stomach pain' before life-changing diagnosis

A Glasgow teenager shares her journey with gastroparesis after a late diagnosis linked to PoTS, highlighting treatment challenges and support.

Glasgow teen diagnosed with gastroparesis after severe stomach pain

Lucy Main, 19, from Glasgow, was diagnosed with Postural orthostatic tachycardia syndrome PoTS at 14. Last year her symptoms worsened and she was admitted to hospital with nausea, low blood sugar and severe abdominal pain. Doctors initially attributed the issues to a virus or the PoTS, but further testing suggested gastroparesis, a rare condition that slows stomach emptying. She found information and solidarity through Guts UK, which explained the condition in simple terms and connected her with others who share similar struggles.

Her initial treatment included dietary changes, medication and nutritional supplements. After a period of weight loss and continued symptoms, she was admitted again in early 2025 and told she would need an NJ feeding tube. She recalls feeling scared and crying at the thought, yet she says the tube now provides energy and stability. The feeding tube bypasses the stomach and runs overnight for about 13 hours, improving her overall health and enabling her to pursue university studies in Politics and International Relations. The story also highlights Gastroparesis Awareness Month in August and the role of Guts UK in raising informed discussion about the condition, which affects about 14 in every 100,000 people in the UK.

Key Takeaways

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Gastroparesis can co-exist with PoTS and may be missed without thorough testing
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Early information and charity support can help patients navigate rare conditions
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Feeding tube therapy can significantly improve energy and nutrition for some patients
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Awareness campaigns reduce stigma and build community among patients
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Young people with rare diseases face education and career planning alongside treatment
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Public information campaigns are essential to demystify complex medical care
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Patients benefit from patient-led resources and peer connections

"I just remember crying, I didn’t want a feeding tube at all."

Lucy on facing the NJ feeding tube

"There isn't a cure, and that can be scary."

Lucy speaks about the nature of gastroparesis

"Guts UK was the first charity I found when looking for information"

Lucy on the role of the charity

"I have so much more energy now and I feel more like myself"

Lucy on improvements after feeding tube

Lucy’s experience underscores how rare conditions can be missed or misattributed, especially when symptoms overlap with more common illnesses. It also shows the vital role charities play in helping patients understand complex diagnoses and access practical support. The piece invites readers to consider the long road from diagnosis to daily life, including the emotional impact of treatment choices like feeding tubes and the importance of clear information for patients and families. While medical care can offer targeted therapies, awareness and accessible information remain key to improving outcomes for those with gastroparesis and related disorders.

Highlights

  • Gastroparesis is not well known but it changes every day.
  • A feeding tube felt scary at first now it means I can dream bigger.
  • Guts UK was the first charity I found and it helped me learn.
  • Take each day as it comes and don’t fear the unknown.

Awareness can turn private struggle into shared support.

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