I wanted to let everyone know that I started going to Dr. Enlander in February of 2012. He recommended going to 100ng of GCMAF slowly over time along with other things. After reviewing my bloodwork, I asked him what percentage chance I had of becoming 100% well and no longer needed medicine and he said 100%. I was shocked. He has had many patients (CFS up to 14 years) who respond to GCMAF take the higher doses of GCMAF and recover to the point of complete remission. I didn't believe him until I saw the results. I went from 40ng to 80 ng over the course of a month and a half. I have almost completely recovered and am averaging around 70 hours a week now which is where I was before I got sick.
I didn't want to wait until I was 100% well to get the word out about this new dosing schedule since I am almost there now. Dr. Enlander takes patients gradually at the pace they can tolerate it up to 100 ng and then slowly brings them down as they no longer need the medicine. I found that at the higher levels, not only do I not feel tired anymore but my reaction to the GCMAF shots has changed. I am no longer in bed every weekend all weekend once I take the shot. Now, I work on the weekend and clean the house like crazy and go on long trips and have tons of energy all weekend which is very different for me. I have been on 25 GCMAF from December 2010 to January 2012 and was in bed every weekend completely knocked out by the shot. Before the higher doses, some weekends I could go somewhere before 4pm on Saturday (I take it on Friday night) but had to come home by 5pm since by 6pm I was in bed or on the sofa until Sunday night at 8pm. Ironically, the higher doses make me feel even better when I take the shot. Now, the first weekend of the higher doses of .7, I couldn't lift my head off of my pillow but after that one weekend, it was amazing. I am now up to 80 ng now and find that I don't react at all to it other than getting more energy.
I have heard that GCMAF doesn't work for everyone but for those that it works for, it seems that this may be a solution. In April 2010, 5 months after I got sick (one day after the swine flu went away) I had to use a wheel chair to get around in public. There were days I couldn't walk across the room and when it came time to pull together my tax information, I had to ask my husband the name of the company I worked for. I thought I was going to die since the pain was so bad. However, I went on Dr. Cheney's protcol and got 1/3 better. Then I went on GCMAF on the normal dose along with the Cheney protocol and got another 1/3 better. Now the higher doses of GCMAF are getting me the other 1/3 of the way there to completely home. I am also following Dr. Enlander's other protocol of MAF 878 (several days a week - but supposed to do it 7 days a week) Heppapressin with other stuff in it shot once a week, Cheney's B12 and magnesium and Taurine shots daily (extra if I overdo it) and other stuff like occasional artesunate if I travel and get in very late at night and have meetings early (maybe once a week) and other things in Dr. Enlander's protcol. This week I worked all but 4-5 hours a day (20 hour days) for Sunday-Wednesday and was weak for the first time in a month on Thursday and Friday but that was stupid to work till 1am and then start again at 5:30am for several days straight- just dumb of me.
I didn't believe Dr. Enlander when he told me I would be 100% well and there was a 100% chance of it. However, now that several months have passed under his care and protocol, I realize that he is right. I am becoming 100% well very rapidly. For those that tolerate GCMAF, this may be the way to go and maybe it makes sense to have your doctor talk to Dr. Enlander. I have found him to be 100% dedicated to this illness and its victims - Innocent lives disrupted without hope. I would like to be able to donate to Dr. Enlander and his research once I am well.
