Sorry, I finally finished editing this for the 100th time. It's barely recognizable from the draft, links have also been added showing proof of FDA patent uses infant thymuses <9 mos age to make their pharmaceutical drug.
This is the first time I could write about their future plans. Usually I email myself articles, sit at my computer and break down crying with feelings of hopeless, helpless. I'm surprised I got through this. Almost like a force outside myself helped me because just as I finished I broke down in tears. I wrote it, for what it's worth. Every thymus article tears my heart open and makes it bleed for my son and all these innocent babies, what their futures hold.
Good work. But, please, don't give them any ideas about intestines. They will be selling them for sausage casing. I mean, the average small intestine is twenty-six feet long. They will be thinking, "Surely the patient won't miss a few feet." As a Crohn's sufferer I have fortunately been able to keep all mine, but others have have not been so lucky.
My son has crohn's, after several surgeries they eventually completely took out his colon. I don't think they would want to steal it, it was a mass of blood.
Twelve years ago my son's was about there and was close to doing the same. Biologics had come onto the scene and reversed his condition. He is in his early forties now, goes every six to eight weeks for an infusion and seems to be doing fine. They are expensive, however. My dad had an older sister who had to have her colon taken out when she was thirty-six. She was born in 1927 and lived to be seventy-eight In the intervening years after having her colon remove, she had about half-a-dozen more surgeries. About age seventy-four she had to have a feeding tube installed because she did not have enough small intestine left to absorb the nutrients she needed. I feel so fortunate that I was able to respond to medication and only have symptom sporadically. An old immune-supression cancer drug, Imuran, has kept mine under control.
Intravenous immunoglobulin (IVIG) is a pooled antibody, and a biological agent used to manage various immunodeficiency states and a plethora of other conditions, including autoimmune, infectious, and inflammatory states. The ultimate goal of this therapy is to normalize a compromised immune system."
My son has been on two. I do not remember the names. I will try to run him down and get that. The first one did such a good job, that after a few years the doctors thought he was in complete remission and stable enough to take him off it. Well, . . . that state lasted less than two years. Once off the med your body builds up antigens to it and he had to go to another medication. That is how he explained it to me, and he is a nurse practitioner.
The white blood cell is one heck of a mechanism. Our immune system is a most mysterious thing. It is like Goldilocks and the Three Bears. Either too much or too little and we are in trouble. It has to be just right.
Remicade was the first thing they tried, but he did not do well on it, so he was put on Humira, which did work. I think he was giving himself the Humira injections. He is now on IV Entivio every eight weeks. Toward the end of the eight weeks he can start to feel joint stiffness, but so far it has worked well.
I read late, and sometimes go to bed thinking about you & your son. As I grow older I try to not look away. I think most people have something almost button-like in their brain, that just turns off at meeting Big Evil. The deeper your truth, the more people flee. I was that way too. I didn't technically know about Thymectomy until reading you. Then, I realized, at some level I did. Know so much was wrong. I know several children with severe health issues, and complicated involvement with hospitals. This newest article answers part of my question "what do they do with the body parts?" I have nothing to offer you except to say I am your witness. And to acknowledge your indomitable spirit. Lately I've had a chance to offer care in a couple of difficult situations; you have inspired me. Many thanks💛
And the Germans supposedly performing hideous and barbaric acts against people under the guise of medical experimentation was a reason for going to war against them. We've surpassed their alleged crimes exponentially. And that's just what we know about.
Sorry, I finally finished editing this for the 100th time. It's barely recognizable from the draft, links have also been added showing proof of FDA patent uses infant thymuses <9 mos age to make their pharmaceutical drug.
Hard to imagine how you can keep your rage under control.
🎯🙏
I needed rage to make this post.
This is the first time I could write about their future plans. Usually I email myself articles, sit at my computer and break down crying with feelings of hopeless, helpless. I'm surprised I got through this. Almost like a force outside myself helped me because just as I finished I broke down in tears. I wrote it, for what it's worth. Every thymus article tears my heart open and makes it bleed for my son and all these innocent babies, what their futures hold.
Good work. But, please, don't give them any ideas about intestines. They will be selling them for sausage casing. I mean, the average small intestine is twenty-six feet long. They will be thinking, "Surely the patient won't miss a few feet." As a Crohn's sufferer I have fortunately been able to keep all mine, but others have have not been so lucky.
Thank you Carl. 🙏
I'm happy to hear you've kept all your intestines! 💞
My son has crohn's, after several surgeries they eventually completely took out his colon. I don't think they would want to steal it, it was a mass of blood.
I'm sorry about your son. I hope he's doing well. 🙏❤
Twelve years ago my son's was about there and was close to doing the same. Biologics had come onto the scene and reversed his condition. He is in his early forties now, goes every six to eight weeks for an infusion and seems to be doing fine. They are expensive, however. My dad had an older sister who had to have her colon taken out when she was thirty-six. She was born in 1927 and lived to be seventy-eight In the intervening years after having her colon remove, she had about half-a-dozen more surgeries. About age seventy-four she had to have a feeding tube installed because she did not have enough small intestine left to absorb the nutrients she needed. I feel so fortunate that I was able to respond to medication and only have symptom sporadically. An old immune-supression cancer drug, Imuran, has kept mine under control.
I wish you and your son well, Margie.
I'm not certain if he is getting IVIG (the treatment my son was refused). IVIG is the biologic infusion used in Chron's and other autoimmune diseases.
https://www.google.com/url?sa=t&source=web&rct=j&opi=89978449&url=https://www.healthline.com/health/crohns-disease/ivig-crohns-disease&ved=2ahUKEwj9p8a0tYSGAxUrmYQIHYxYCssQFnoECB8QAQ&usg=AOvVaw3Ch4da63iH0trzqVGKyDxr
https://www.google.com/url?sa=t&source=web&rct=j&opi=89978449&url=https://www.ncbi.nlm.nih.gov/books/NBK554446/%23:~:text%3DIntravenous%2520immunoglobulin%2520(IVIG)%2520is%2520a,normalize%2520a%2520compromised%2520immune%2520system.&ved=2ahUKEwjtvcPftYSGAxWdpIQIHatHDYEQFnoECBUQBQ&usg=AOvVaw0OuJjbUfJV4Blrv8vwLy4j
Intravenous immunoglobulin (IVIG) is a pooled antibody, and a biological agent used to manage various immunodeficiency states and a plethora of other conditions, including autoimmune, infectious, and inflammatory states. The ultimate goal of this therapy is to normalize a compromised immune system."
My son has been on two. I do not remember the names. I will try to run him down and get that. The first one did such a good job, that after a few years the doctors thought he was in complete remission and stable enough to take him off it. Well, . . . that state lasted less than two years. Once off the med your body builds up antigens to it and he had to go to another medication. That is how he explained it to me, and he is a nurse practitioner.
The white blood cell is one heck of a mechanism. Our immune system is a most mysterious thing. It is like Goldilocks and the Three Bears. Either too much or too little and we are in trouble. It has to be just right.
I'm sorry that happened, happy to hear he found a second that worked. 🙏
I look forward to hearing back if you happen to find out. 🙏💞
Remicade was the first thing they tried, but he did not do well on it, so he was put on Humira, which did work. I think he was giving himself the Humira injections. He is now on IV Entivio every eight weeks. Toward the end of the eight weeks he can start to feel joint stiffness, but so far it has worked well.
Sorry for the language, but this is fucking horrifying.
🎯🎯🎯🎯🎯🎯🎯♾
I read late, and sometimes go to bed thinking about you & your son. As I grow older I try to not look away. I think most people have something almost button-like in their brain, that just turns off at meeting Big Evil. The deeper your truth, the more people flee. I was that way too. I didn't technically know about Thymectomy until reading you. Then, I realized, at some level I did. Know so much was wrong. I know several children with severe health issues, and complicated involvement with hospitals. This newest article answers part of my question "what do they do with the body parts?" I have nothing to offer you except to say I am your witness. And to acknowledge your indomitable spirit. Lately I've had a chance to offer care in a couple of difficult situations; you have inspired me. Many thanks💛
Thank you RT. 🙏🌹💞💞💞💞💞
this is horrifying and enraging.
😪🙏🎯💞
How can we ever trust the medical establishment again!
🎯🎯🎯
And the Germans supposedly performing hideous and barbaric acts against people under the guise of medical experimentation was a reason for going to war against them. We've surpassed their alleged crimes exponentially. And that's just what we know about.