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How I Cured Morgellons
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2/23/2019 9:48:22 AM |
This forum would not exist if it wasn't for Mel. The website would not be here and there would be no community. Nor would the knowledge needed on the 'sum of the parts' be here for everybody. All of these things are HUGE. It all took one man's tenacity and determination, he promised that if God got him well he would help others around the world. And help he does!!!!!!! For five dollars a month we have this wonderful website, Subscribe Here full of support, help, advice and wisdom. It has all the information we need in order to heal our weakened bio terrain from this disease. Also if people need that extra help and support, Mel also provides a very reasonably priced "One-on-One Coaching" Telephone service around the globe. Coaching can help people to stay on track as this is not an easy journey that we are on. From the start Mel knew to focus on health and hope and to banish horror stories. In this way our community helps to hold people up in times of distress. Mel has achieved a tremendous amount with this community. We are very blessed to have it. Most of us would have been alone otherwise, without the support, companionship, or sound advice of others. Without the knowledge or correct medicines we would not have been able to heal . And through Mel's website many have gotten well through the years, MANY!! If there was no Mel there would be none of this. Its a sobering thought is it not? He also set up the He Cures All Foundation, in order to help people to get the protocol who could otherwise not afford to buy it. He even helped me to get it and I live in Scotland!?!?! I mean, how wonderful is that!!! Anyone who feels they would like to help the HCAF (He Cures All Foundation) please donate to help those in need, please do so. Every cent matters and is greatly and hugely appreciated, believe me!! Many of us who get help from the HCAF had been sick for a long time. We had almost given up hope, until Mel came along and held out his hand to us. Mel works very hard to keep all of this going for us all. He provides a lifeline to many distressed and despairing people who are suffering terribly. In time and with help, their suffering diminishes as their health slowly but surely returns. Mel is there every Saturday and Sunday at the free weekend conference calls. He records the Saturday call for the forum so that an average of over 3,000 people a month can hear it. In this way people with brain fog can easily access the knowledge they need. It also helps people to feel less alone when they hear others with this disease talking together. Mel goes out of his way to provide a laugh or two on the calls. Or to give us funny pictures on the forum. He knows that stress is probably worse than sugar as it feeds this disease. Therefore, he tries to get us to laugh or focus on the positive His is not by any means an easy job. Day in and day out, listening to extremely distressed and often crying people must be tiring at times and taxing. But he does it year in year out. He doesn't even take a holiday (even though we think that he should have a break sometimes). When I was recovering after an operation recently it was Mel's idea to dedicate a prayer call to me. He also recorded it so I could hear it when I was able to as I was not well enough to attend. He also put beautiful pictures of angels on a prayer thread for me. He was very thoughtful and kind. I was very touched by it all :-). So I ask, that if anyone reading this feels blessed to be a part of all of this and would like to give a little back, please do. Go to Mel's Mel's Go Fund Me Account. and help Mel. Every little bit counts you know.. . And let's bring a wee smile to Mel's face, after all he tries his hardest to bring a smile to ours :-). Thanks, Chrissie. | ||||||
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