Hi everyone
This post will be quiet long, so bare with me cause many events had occured to me the last couple of days.
Two days ago, my cousin ( who recently knew my son had thal) advised me to pay a visit to a newly opened center that offer natural, non invasive medical therapy in different fields (ozone therapy- biomolecular therapy- neurostimulation- skin therapy using sea weeds+laser+ozone-)
The owner of this center is his friend who had a horrible five years expierence with his daughter. She had a brain cancer when she was 10 years and after horrible stories they had succeded in conquering cancer but the little girl who is now 16 years old was left blind as the chemo had affected deeply the nerve of the eyes. Anyway, he was inroduced to an Egyptian doctor who studied and lived all his life in Germany and he treated her with biomolecular therapy for one year and now this girl can see once more but no more than 6 meters till this point. I met the girl today and yes she can see. Her father said that as long as the nucleus of the cells is still alive, the biomolecular therapy can regenerate new cells and that what happened to the nerve of the eye.
When I sat with this doctor, he is now between Germany and Egypt, i told him about my son's case and to my surprise he told me that he made researches on thalassemia for seven years when he worked at Bahrain for a while as most couples are relatives and thal is widely spread there. /he had many cases that were treated by biomolecular therapy and the people who had the cost and the patience to continue the course began to make their own blood.
This treatment is offered by:
http://www.vitorgan.com/page_i.htm and this doctor work as a researcher for this company for 12 years. He told me that the treatment is made up of components of the cells taken from an ox without the nucleus of these cells. According to the company, the ox is the most suitable in its cell components compared to humans. This is what we call Live cells, hope you have idea about.
According to the doctor, Beta thal patients don't have problem in ALL the process of hb formation but only in step number 4. He said that there are 7 steps that happen in the bone marrow before the formation of the stem cell itself to form blood , the beta patients has a problem in step 4 only regardless the kind of mutation as long as it is a beta and nothing else. The treatment will do two things:
First: he told me for simplicity assume that you need a,b,c,d to form Hb, your son has a and c for example that are muted so the medicine will give him ready made a and c and the body is going to use or combine them to form healthy blood
Second:While doing this process the body will change its muted programming in this step so that when the medicne stops the body will continue to program in a correct way. When i asked him howcome and this is a genetic disorder and in this case why then we need gene therapy, he added that again it is not the original cell itself that is muted in beta, but it is one of the steps in the process of forming HB and gene therapy is still needed in other felds
When i asked him about the side effect he said none and when i told him that everything has its own risk. He said that when you exceed the dose , comes the side effect and he added that when i eat, nothing happens to me but if i eat the same food in large quantities, my stomach will hurt.
The treatment takes one year, 3 heavy months where you are injected day after the other , then twice weekly then once then once a month untile none , then finished. Some patients may need more like activation injection once a year or twice or may be not at all
The last kids that he treated where from Bahrain and they were three brothers who were major , they transfuse every 20 to 25 days and after their treatment, their Hb stablized at 9,5 and 8 and 7.5. They had never transfused for the last 5years except one of them made BT once due to an accident.
I asked him since what i hear is a miracle to me, why is this not worldwide known. He answered that this has to do with politics as the majority of the world economy goes in weapons and drug manufacturing and countries like the US manipulates all this and won't let any homupathy companies emerge as their economy will get affected.He added that when he writes a medicne for some patient in Germany, the insurance pays but when he writes homuptic medicnes, the insurance doesn't pay.
I asked him about the Rodex and that i know it is also made from bone marroow of some animals so it has the same concept as his company. I told him that Kabir-love son didn't increase much on it just one or one and half grams which is too low. He answered that he knows the rodex and i shouldn't compare as there are different compositions with different ingriedents and each company has its own research. He said that sometimes differnt brands has different effect on the body though targeting the same disease.
When asked him when do i expect a change, he said that within weeks mostly one month and when asked him should his HB increase one or two grams , he just said that he is supposed to have normal Hb for a child of his age meaning 11 or 12
I asked him when he can decide whether to stop this treatment for my son or not. he just said usually this doesn'happen but if it did , he can say this after one month. He said that there is no allergies to this treatment as he gives the body exactly the normal cell componenet that it needs.
Injections could be given on daily basis or once per week but not a shot, you stay for 4 or 5 hours taking the solution as we do when we take glucose for example
I asked him to give me reference of the patients, he gave me the web site of the company and told me that they keep a refrence of patients and i can ask them
He said he can take any thing with this treatment except hydra as it contradicts with his treatment. His philosophy is that taking a medicne with side effectas to cure something,you will turn on later with a damage in the thing that you cured
I asked him directly, is this a trail medicine or in other words is what he is offering to may son is considered trails or he knows what he will e expecting, he assured me that there are no trails and this has been known for their company and they won't lose their name in the market ofter 50 years from being there
He said that these medicine will cost from 5000 to 6000 euros for the whole year.
He insisted on examining my son's iris as he said that it tells him if there are any hidden diseases or if the malfomation of blood is due to extra factors other than thal like liver malfuncting. So he can decide that he needs energy therapy with biomolecular therapy ot not
I am going to meet my hematologist and see whar she will say, but this doctors seems very confident and above all he understands thal quiet well
Hope i didn't for get any points and soooooooooo sorry for such a loooooooong post
Manal