Kutapressin Helps So Very, Very Much!!
I had a primary care doc who knew the specialists had used Kutapressin in early trials with CIFDS patients in the 80's. He prescribed it for me nearly two years ago. Unfortunately, I had to pay for it...just about the price quoted online in the U.S. I paid, got better, paid, got better until I was at least 40% better. I could cook, clean, even garden again. I was getting better and better, but on a higher dose and for longer than was ever given before. It was a miracle worker. I ran out of money, and therefore, with tears in my eyes told the pharmacist he might as well quit ordering it for me. ... more »
I had a primary care doc who knew the specialists had used Kutapressin in early trials with CIFDS patients in the 80's. He prescribed it for me nearly two years ago. Unfortunately, I had to pay for it...just about the price quoted online in the U.S. I paid, got better, paid, got better until I was at least 40% better. I could cook, clean, even garden again. I was getting better and better, but on a higher dose and for longer than was ever given before. It was a miracle worker. I ran out of money, and therefore, with tears in my eyes told the pharmacist he might as well quit ordering it for me.
I'm waiting to go to Mexico, as I have gone before to a clinic and really gotten 70-80% better. But one has to take the Kutapressin injections 2-3 cc's every day for at least 3-4 months, take a short break, then continue. I think if Icould have continued for a whole year instead of my three months worth, I might still be well today. I don't know where to go or exactly how to find out if Shwarz Pharma has a program for
poor people on disability, nor if the Mexican pharmacies even have it.
BUT if you have CFIDS, you should definitely try the shots every day for months, with a little breather in there if the doc finds your enzyme levels not Kosher. I had absolutely NO (I mean NONE) side effects and my liver, kidneys, et al held up really well. I'm dying to get my hands on some, but we just can't afford American pharmaceuticals.
There is no reason this drug is kept from us, especially those of us with health insurance. Also, it should be at a reasonable price for humanitarian reasons. I think it didn't work for those early using it simply because it wasn't the right dose. My doc let me decide how it worked best for me...and everyone should. But this is a drug that might save lives until or unless something better comes along. It might just do the job all by itself, but in the higher doses in everyday injections.
Please tell me what you think. I've had CFIDS for 14 years, and nothing besides a "questionable" Ozone treatment in Mexico which worked immediately, then fell off at 4 months made me mostly well. I've tried everything else I know of. Thanks for reading this. We need to demand this drug and Ampligen,
as they DO work for us. We deserve to live a life. Right now, I have no life, even though I'm still married. I rarely get dressed, I can barely take a shower, and yet I haven't given up hope. Thanks. Susan R. Jones, Deneb@lvcm.com or Deneb@cox.net. Same address, just updating their address for the cable modem system. I'm in Las Vegas, NV. by the way
