FDA should give CFS patients access to Ampligen!

Help is desperately needed for these neglected and stigmatized people!

Why has this illness with millions afflicted, including myself, been so ignored when funds are allocated for diseases with far fewer sufferers and in some cases, less illness? It really is a mystery to me and it is cruel and unethical to make so many of us suffer for so long.

Please approve this drug, and spare me from this slow, agonizing death.

Please sign this petition for all the chronic fatigue / fibromyalgia. I've suffered forty years with nothing to benefit us. This is a debilitating disease which has caused me to be home bound. Please help.

I am 74 a have suffered 40 years since I had infectious mono. I was hospitalized 2 was. I had a temp of 105 they had a difficult time getting down. I am home bound most of the time. I would like to live healthier for whatever time I have left.

I have been suffering from PVCFS for many years. My doctors and I believe this medication will help me to improve my health, in order to enable to me to return to work and care for myself and my family. Which I am currently unable to do in spite of being highly WILLING, SKILLED AND EDUCATED. Please help! Dawn Rubio Lazar, 3170 Wilson Ave, Bethlehem, PA 18020

there is no FDA treatment for ME/cfs, why???

This medication is needed so much

Why can't ME/CFS sufferer be treated with Ampligen when others can?! Doesen't make sense.

My wife is sick in ME/CFS

I have chronic fatigue and would definitely take amplified if it were available!

I've lived with ME/CFS for thirty years. the disease has robbed me of my young adulthood, I missed out on raising my children properly, rather survival mode. The disease causes me to feel flu-like every day of my life, the first 6 years was sever flu symptons, especially nausea. To this day, I'm not quite sure how I hung onto life during that time. It was a constant battle in my mind, to stay in this life with chronic illness or to leave it behind. Can you imagine waking up every day of your life with swollen glands, chills, diarrhea, extreme nausea and exhaustion and then wake up for the next six years with the same severe symptoms. On top of dealing with the symptoms I had three children that needed me and I had nothing to offer them except hugs. They had to deal with the constant flow of baby sitters and disappointments, when I had to tell them time and time again that we wouldn't be able to attend sport practices or any events really. I think the only reason I'm writing to you today is because I didn't want my children to have the legacy that their mother committed suicide. I've lived to see better days due to IVGG treatment monthly. My flu symptoms are a little quieter, but they refuse to ever give up completely. I've also learned to cope better with chronic illness and find joy in life. However, on the bad days, it's so hard to stay positive. I pray answers to what the disease is and a cure come soon for all of us patients and families who care for us so that another young mother of three children never has to lose so much again.

Fuck, just do it!

I have suffered from this disabling illness for 25 years and have tried every thing under the sun to cure it. I think we CFS patients should be allowed to try it.

I was part of the ampligen study several years back. It worked for me. Please approve this drug.

I have had chronic fatigue for 8 years now this could be my last hope

help us wide ME!

Want to have my life back!

Please, give us our lives back!!!

I hope my wife, who is suffering from ME/CFS will be cured. I belive in Ampligen!