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Solve ME/CFS Initiative
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==Resources== [https://solvecfs.org/me-cfs-long-covid/patient-and-caregiver-resources/ Resources for People with ME/CFS & Caregivers] * As someone living with and managing ME/CFS, we know you have questions. We've compiled resources and links to information about some of our most commonly asked questions. [https://solvecfs.org/me-cfs-long-covid/resources-for-healthcare-providers/ Resources for Medical Providers] * Because it is not yet fully understood, there is no cure for ME/CFS, nor are there any FDA-approved drugs or treatments. However, there are interventions and symptom-reduction strategies that you can use to significantly improve patients’ quality of life. Providing compassionate and effective care for patients with ME/CFS can be challenging, like many other multisystemic chronic conditions. Patients and their providers must be partners with open lines of communication in order to effectively manage this illness. Visit our website for education on ME/CFS based on current research. [https://www.youtube.com/solveme Solve M.E. Webinars] * Solve M.E. provides a free webinar series to educate patients, researchers, and healthcare providers, as well as to raise awareness of ME/CFS, Long Covid, and ‘long-haul’ diseases among scientists, political leaders, and the general public. All webinars are recorded and posted on our website and [https://www.youtube.com/channel/UCzrFQHNiCc_6AMpw_GpWZOA YouTube channel] following the presentation so that you can access the content at your convenience.
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