My Nonprofit Reviews

In the 24 years I have had ME/CFS OMF has given us the most hope. They share their research openly, use their funds as well as they can to maximise the value they get from them, have people involved who have a personal interest in seeing a diagnostic test and cure for this devastating disease. They are working for their loved ones as well as all of us. They work tirelessly, take every opportunity to raise awareness and bring help to a substantial number of people who have had lives devastated by this horrible illness. My daughter is 30 and has had the illness since 13. All her dreams on hold. We are both house and bedbound. To know that OMF are tireless and dedicated to helping us gives us more hope than we've ever had. Thank you OMF.