Top 7 alternative sites to ibmmyositis.com

  1. cureibm.org
    cureibm.org
  2. Inclusion Body Myositis | Cure IBM
    Inclusion Body Myositis (IBM) is a muscle disease that causes gradually worsening muscle weakness. Cure IBM provides information for patients and physicians.
    Author: Kevin Dooley; MD

  3. doihavecidp.com
    doihavecidp.com
  4. Weakness, Fatigue, Tingling, and Numbness Can Be CIDP
    CIDP symptoms include weakness, fatigue, tingling, numbness, and more. Early detection is important. See if the symptoms you have been experiencing could be CIDP.

  5. rare-e-connect.eu
    rare-e-connect.eu
  6. RARE-e-CONNECT - RARE-e-CONNECT
    Secure multidisciplinary collaboration and knowledge sharing on rare diseases. For Healthcare Professionals and patients within Cyprus and abroad, large repository of medical centres in Europe and other countries with verified expertise in rare disease groups and rare diseases, Patient life stories, Continuous Medical Education via webinars and automated newsfeeds from key medical databases to stay up to date with important developments and clinical trials in rare diseases.
    Author: Super User

  7. forabodiesonly.com
    forabodiesonly.com
  8. For A Bodies Only Mopar Forum
    A-Body MOPAR club and forums for the Plymouth Barracuda, Plymouth Valiant, Dodge Dart, Duster and other A-Body Mopar automobiles and Mopar muscle cars, and Classic Mopar parts.
    Author: Joeychgo

  9. moreenergy.com
    moreenergy.com
  10. The Human Body is Cellular Electrical!
    The human body is made up of over 80 trillion cells that produce energy continuously; brain cells, heart cells, blood cells, bone cells, **** cells, muscle cells and skin cells. But just like anything else that produces energy, the cells need the correct fuel and a clean system to operate properly.

  11. rarevoices.org.au
    rarevoices.org.au
  12. Peak body for Australians with rare diseases including genetic disorders
    Many Voices ONE GOAL YOUR NATIONAL STRATEGIC ACTION PLAN FOR RARE DISEASES Read the Action Plan now Rare Voices Australia (RVA) is the peak national body for Australians living with a rare disease. RVA provides a strong, unified voice to advocate for policy as well as

  13. klur.co
    klur.co
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