Rare Disease Education
Accelerating diagnosis and referral in X-Linked Hypophosphatemia (XLH)
Educational Objectives
Education is critical to earlier identification, referral, and diagnosis.
Awareness and education is critical to reducing diagnostic delay, improving care coordination and providing the best treatment and support to patients with rare conditions.
Our client wanted to impact diagnosis and referral of patients with X-Linked hypophosphatemia (XLH), reaching a broad audience with disease awareness strategies, while supporting peer-to-peer discussion among specialists in a secure network.
Our Approach
Multidisciplinary target audience
To address the educational needs of a broad audience of healthcare professionals, we connected specialists and generalists through case discussion and peer learning opportunities.
- Endocrinologists, nephrologists, rheumatologists
- General practitioners / family physicians and pediatricians
- Europe and the Middle East (EMEA)
Case-based education
Very few physicians have experience managing patients with rare diseases such as XLH, so case-based medical education is critical to improving diagnosis and management.
- Secure, online discussion group, enabling doctors to reflect on cases and ask questions
- Educational cases designed to help doctors recognize XLH in adult and pediatric patients
- Targeted omnichannel amplification
MedShr's medical education programs are tailored, localized, and targeted
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