In the name of God the Merciful Dear Sirs. This subject concerns all patients with muscular dystrophy and researchers all over the world, and all those interested in this matter. I have three ideas ready for sale ... cocktail syrup for the treatment of vascular disease problems, a syrup for the treatment of muscular dystrophy, and syrup for the treatment of malnutrition. I hope you visit my site baraa-b.net where you can find cases of those who drank cocktail “Baraa-E”, and find answers to your questions. I do not have syrup for a final sale. In order not to be understood that this is a kind of propaganda to offer this product for sale. I hope you understand this very well. For more than thirteen years now, I have been trying to connect with research centers and pharmaceutical companies, but in vain. I have extended my hands but no hand has been extended to me. I am still seeking to help to make children happy and live happily in peace with their families. Unfortunately, nobody responded to me offers, and I am now waiting for a hand to help and support. During this period, I have participated in three Fairs dedicated for creativity and invention. I have applied for two patents, but unfortunately, I could not meet the requirements. I am quite sure that this cocktail syrup “Baraa-E” will help a lot those patients suffering from muscular dystrophy, especially those patients who have reached the stage of weakness of the heart muscle and lungs. Therefore, if the research centers are not prepared to accept this cocktail syrup for any reason, I have a proposal to make which can help me make it know for the public so that every child in the world can benefit from it, and relieve those children and patients from the painful life they live. If this cocktail syrup “Baraa-E” helps improve the lives of these children and help them, even at the rate of 10%. Why should it not applied and used untilthe research carried out by scientists and laboratory experiments while time passes. I am confident by God that this syrup cocktail will be much more useful than you expect. What is important is either a club or a charity dedicated for the patients with muscular dystrophy, or a businessperson who has the moral and material ability, as well as a medical doctor who is ready to attend a patient and provide him/her with the necessary treatment. The patients family is the best to know about their patient, and his/her sufferings, especially the mother. They can observe accurately what goes on. Let us give five patients the cocktail syrup (Barra-E) for a period not exceeding three months only, every 5 hours at the amount of 5 ml. With the control and monitoring of the parents and the doctor. If there were an improvement, even on per thousand, we carry on with the syrup so that to benefit the largest number of patients, then we thank God that the results are positive. We can prepare “Baraa-E” syrup to benefit the greatest number of patients. Then it can be put for experiment at research centers. Baraa-E syrup has no negative effects. Through experience, I can say it is as useful as fresh water. You can learn about its ingredients through the link to the website. https://youtube/watch?v=_p9EHJoC86E&list=UUHi46W5blnOfDt5I9sPNJOg I am looking forward for your support and not your quick judgment. Your support to me is by spreading this message to the biggest number possible to those who know about patients and civil societies associations, clubs in any country and at all social networking. Your participation can reach the goal that we are looking for. Your help will be for the benefit of our patients and children. We will our best to help those who suffer and need help. Hamed Al jabilil Syria – Aleppo baraa-b.net
Posted on: Sat, 16 Aug 2014 17:17:56 +0000
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