GcMAF Australia
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I hope that you see imrovements soon Daffodil
XOXOXOX
XOXOXOX
Great mate!!Hi all,
I just wanted to check back in and let everyone know how I am doing on 100 MG of GCMAF. I am still working a 80-90 hour week and have almost zero reaction to the GCMAF on the weekends. I can notice a slight difference in my energy level after taking the shot and not taking the shot but not very much. The intensive exercise problem is the only problem left and it is improving by every month. I will keep taking 100MG until I can walk 5-7 miles and can lift heavy weights again. Dr. Enlander said that when I am 100% I should start gradually taking less and less each week until i am off of it. I will wait until I can do extreme exercise and then start reducing it. Right now, if I walk over 2 miles, I feel it the next day so clearly I am not completely well. That is the only time I notice my Chronic Fatigue so will just keep going until that problem goes away as well. I still take the Heppapressin shots everyday and think they are invaluable.
That's great news Cindi!
When we don't hear from people who are trying a treatment we never know if the improvement continued or what happened to them.
Sounds like this has been a success for you and that Dr Enlander is talking about tapering off the dose. Hope that this can be done and the good effects to last.
My experience on the MAF314 is that it does wear off after I stop taking it. On my first attempt the good effects lasted for at least a month and on my second attempt it was shorter.
Then again I never get to the level of functioning you are at now so very different.
I started GcMaf shots 2.5 weeks ago via my doctor in the U.S. The first two weeks I injected .1mg and this week .15mg.
msa
. Where does one get hepapressin, do you have to work with an MD who uses it? Thanks.Thanks for coming back to report, Cindy - I often wonder if people who do well on something just disappear into their new lives and so we don't get to hear the successes. Congratulations on your recovery - I'm so pleased for you!
I'm also on hepapressin and started MAF 878 a couple of weeks ago (no GcMAF) so very early days for me, especially since I've been ill for 26 years but I'm hopeful, and it's a huge boost to read an account like yours.
. Where does one get hepapressin, do you have to work with an MD who uses it? Thanks.
. Where does one get hepapressin, do you have to work with an MD who uses it? Thanks.
It is my understanding that I have to wait until I am 100% well or I will go downhill without it so I am planning on waiting until I have zero effect from the GCMAF and can do EVERTHING I could do before. I tried running tonight and it didn't go so well so not there yet. I will keep posting and let you know once I can exercise the same as before. Also, I will let you know how the going down a little at a time works once I am at 100%. My husband is doing everything I am doing with Dr. Enlander and is at the same place that I am which is interesting. We got sick 3 months apart after getting the swine flu three months apart.
This is fantastic,I am not 100% yet but I did work over a 100 hour week not including travel time of another 8 hours this past week and didn't feel sick. For the past 3 weeks, the average has been over 95 hours a week plus 8 of travel and I didn't feel sick. However, strenuous exercise is still not possible for me. My husband started the yogurt MAF878 everyday and is almost well from it. He started doing pilates several times a week and is trying to build up into strenuous exercise. So this is the one thing that we still can't do. Hopefully, this will change as we get closer to 100% well but I wanted to check in and let everyone know the improvement that has taken place. Both my husband and I take 40ng of Heppapressin everyday Monday-Thursday and on Friday with our GCMAF shot, we take 100ng. This plus the GCMAF shot of 100ng plus the MAF878 1/3 cup makes a big difference. I take the MAF878 on the weekend only since it is too strong for me to take it and work also but I take it on weekends and vacations and it makes a big difference. My husband takes it everyday. The first week, he couldn't work. The second, he worked three days but then he felt great taking it everyday thereafter. Once he started taking it everyday, he told me that he didn't have any fatigue anymore. however, he still can't do very strenuous exercise and neither can I.
Hi CindyWillis, I keep reading your post and can't help bu think that if you stopped working 100 hour weeks you would be well already. Working 100+ hour weeks is not normal and will give any healthy person a huge predisposition of getting CFS
I am in the United States but I understand that Dr. Enlander treats patients at a distance.This is fantastic,
Which country are you in??