Young Swedish Woman Battles Severe ME/CFS and Post-COVID Illness Amid Healthcare Challenges
A 21-year-old Swedish woman with ME/CFS and post-COVID illness faces severe health challenges and systemic healthcare misunderstandings.
- • Maja, 21, is bedridden due to severe ME/CFS and post-COVID illness sparked by COVID-19 and mononucleosis.
- • Healthcare providers often misinterpret Maja's symptoms as psychological issues, leading to inadequate care.
- • She has been unable to perform basic tasks for over a year but shows slight improvements with rehabilitation from a Danish clinic.
- • Maja's story highlights the systemic healthcare challenges young chronic illness patients face in Sweden.
Key details
Maja, a 21-year-old from Avesta, Sweden, is bedridden around the clock due to debilitating chronic illnesses following COVID-19 and mononucleosis infections. Diagnosed with ME/CFS, post-COVID syndrome, and POTS, she has endured extreme fatigue, anxiety, and physical incapacitation that prevent her from performing basic daily tasks such as showering or walking independently over the past year.
Despite actively pursuing healthcare, Maja has been frequently misunderstood and dismissed by medical professionals, who often attribute her severe symptoms to psychological factors rather than recognizing the chronic physical conditions involved. Her mother, Malin Rabb, shared experiences highlighting the skepticism and lack of adequate support they have faced. This has intensified Maja's emotional distress, at points leading her to express a desire to die.
Recent progress has come through rehabilitation efforts from a private Danish clinic, enabling Maja to take steps and feed herself independently, offering hope amid ongoing struggles. Her story underscores the complexities faced by young patients with chronic illnesses like ME/CFS and post-COVID conditions, particularly young women, and calls attention to systemic gaps in understanding and treatment within Swedish healthcare.
Maja's case exemplifies the urgent need for medical communities to better acknowledge and respond to chronic illness realities, fostering compassionate and informed care approaches for vulnerable young patients.
This article was synthesized and translated from native language sources to provide English-speaking readers with local perspectives.
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