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Service
Social Services
https://www.shrinerschildrens.org/en/Pediatric-Care/Social-ServicesAt Shriners Children’s, our specialists in social services are with you every step of the way, helping you deal with challenges and providing the resources you need to feel encouraged and empowered.
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Condition
Gaucher Disease
There are three variations of Gaucher disease, an inherited metabolic disorder. Treatment options depend on which type a child has and are tailored to prevent or lessen symptoms with an overall goal to improve quality of life.
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Condition
Lyme Disease
Lyme disease is a bacterial infection typically spread by tick bites. Months to years after a bite, symptoms may include inflammation of joints (arthritis). Shriners Children's treats arthritis caused by Lyme disease.
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Extension Clinic
Shriners Children's Medford Clinic
https://www.shrinerschildrens.org/en/Locations/Portland/Clinics/Medford-ClinicShriners Children's Medford Clinic is an extension of Shriners Children's Portland, conveniently located for families in southern Oregon.
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Extension Clinic
Shriners Children's Rapid City Clinic
https://www.shrinerschildrens.org/en/Locations/Twin-Cities/Clinics/Rapid-City-ClinicThe Rapid City Clinic of Shriners Children's Twin Cities is convenient for those who live in the Rapid City, South Dakota area.
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Extension Clinic
Shriners Children's Fairbanks Clinic
https://www.shrinerschildrens.org/en/Locations/Spokane/Clinics/Fairbanks-ClinicThe Shriners Children's Fairbanks Clinic is convenient for those who live in Alaska.
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Outpatient Clinic
Shriners Children's Tijuana Clinic
https://www.shrinerschildrens.org/en/Locations/Mexico/Clinics/Tijuana-ClinicThe Shriners Children's Tijuana Clinic is convenient for those who live in Baja California, Mexico.
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Condition
Hirschprung Disease
Shriners Children’s provides comprehensive care for children with Hirschsprung Disease, a birth defect that most commonly affects the colon (large intestine) and causes problems with passing stool.
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Condition
Ollier Disease
A skeletal disorder characterized by abnormal bone development. While this disease may be present at birth, symptoms such as limb deformities or improper growth may not appear until early childhood.
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Condition
Werdnig-Hoffmann Disease
Werdnig-Hoffmann disease is a severe form of spinal muscular atrophy. This rare genetic condition causes muscles to weaken, leading to minimal ability to move.
