I am a 30-year-old female living with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), a complex and debilitating neurological condition that has forced me to pause my life, watching everyone from the sidelines.

I never thought at the age of 30 that I would be bedbound, relying on family to care for me. I miss the simple things, like walking our dog and dancing around the kitchen acting silly with my husband.

This condition is not widely understood or researched and there is currently no treatment or cure available.

ME/CFS is characterized by profound fatigue that is not improved by rest and may be worsened by physical or mental activity. Other common symptoms include post-exertional malaise, unrefreshing sleep, cognitive difficulties, and various symptoms affecting multiple body systems.

ME/CFS affects an estimated 17-24 million people worldwide, yet it remains one of the least funded diseases in terms of research money per patient (Source: ME Association). The lack of understanding about this illness means that many patients are left without effective treatment options, leading to a decreased quality of life.

The need for increased funding is urgent. We need more research to understand this disease better, develop effective treatments and ultimately find a cure. It's time for our governments and health organizations to recognize the severity of ME/CFS and allocate appropriate funding towards its research.

By signing this petition, you are advocating for millions like me who suffer daily from the effects of ME/CFS. Let's push for change together - sign today to demand increased funding for ME/CFS research!