Mijn complimenten voor de ondertiteling. N.a.v. deze documentaire en een antwoordmail van Dennis F. Mangan van NIH, heb ik deze laatste het volgende teruggemaild:
Dear Mr. Dennis F. Mangan,
Thank you very much for your reply. It’s good to hear your goals of finding treatments and, hopefully, a cure as rapidly as possible. But it’s makes me sad that there was already a treatment available back in the nineties. In a documentary film of 1993 (here in The Netherlands I’ve seen it just now on the internetsite:
http://dutchforum.aboutmecfs.org/ ) was Ampligen a hopeful medicine for ME/CFS patients. Why can’t that drug be available for us?
I do agree on the subject that it’s not entirely up to NIH, but the government of my country doesn’t do anything at all! We have to figure it out all by ourselves. Meanwhile we’ve discovered LDN (Low Dose Naltrexone) in stead of Ampligen!
But I still have hope in finding a cure in the near future.
Yours sincerely,
Catryn