The Focus on Sickle Cell Foundation (FoSCel) has raised concerns over increasing distress calls from persons living with sickle cell disease and their caregivers across Ghana as the rainy season worsens health challenges associated with the condition.
In a statement issued on Wednesday, July 1, 2026, the Foundation said changes in weather conditions, particularly cold temperatures, have contributed to a rise in painful sickle cell crises, infections and other complications, leading to increased hospital visits and placing additional emotional and financial pressure on affected families.
FoSCel noted that while many patients require urgent medical attention during crisis periods, some continue to face difficulties accessing timely healthcare services and essential medications.
The Foundation is therefore appealing to the Government of Ghana, the Ministry of Health, the National Health Insurance Authority, healthcare providers, development partners, corporate organizations and the general public to provide immediate support for persons living with sickle cell disease.
It called for improved access to quality healthcare, availability of essential medicines, increased public education and stronger emergency support systems to reduce preventable complications and improve outcomes for patients.
FoSCel also encouraged sickle cell warriors and their caregivers to take additional precautions during the rainy season by keeping warm, staying hydrated, taking prescribed medications regularly, limiting exposure to cold conditions and seeking medical attention promptly when symptoms of a crisis appear.
The Foundation emphasized that sickle cell disease remains a significant public health concern in Ghana, with seasonal weather changes increasing the vulnerability of affected individuals.
“No sickle cell warrior should suffer or lose their life because timely care and support were unavailable,” FoSCel stated.
The organisation reaffirmed its commitment to working with government agencies, healthcare institutions, the media, civil society groups and development partners to increase awareness, strengthen support systems and advocate for policies that protect the lives and dignity of people living with sickle cell disease.
Source: www.kumasimail.com
