Today was my last day of treatment at Chipsa. I received the Vitamin C and K IV and Ozone IV treatments. I also received Myers IV. Myers Cocktail is an infusion of multiple vitamins and minerals, including B vitamins, vitamin C, calcium and magnesium. Because I am so anemic, I also received Iron IV. My go home meds include: Apatone, Coleys Shot, GCMAF Shot. All three of these medications, you cannot get in the United States. Apatone is Vitamin C and K in oral supplementation. Apatone is a proprietary therapy that exhibits synergistic anti- tumor activity and kills tumor cells. This patented technology allows up to 400% more oral vitamin C into the cancer cell. I will have to take 2 capsules of Apatone every 2 hours, 6 times a day. Coley’s Shot consists of a sterile (dead) mixture of bacteria. Using a killed bacterial suspension, mimics an infection and accompanying immune response, without incurring the risks of an actual infection. This coaxes the immune system to fight cancer. At home treatment involves giving a subcutaneous injection in the arm, leg, or abdomen. I will have to give myself an injection 3 days a week. GCMAF shot is a proprietary blend of protein macrophage activating factors. Macrophages are a type of white blood cell of the immune system that engulfs and digests cancer cells. I will have to give myself an intramuscular injection weekly. These medications will last me until my return visit to Chipsa in 3 months. All the medications, needles, and syringes were placed in a small black bag with a medical note enclosed. After I was discharged from Chipsa, we had to cross the border to get back into the United States. Because we had a medical pass, and a driver from Chipsa take us; it took us close to 2 hours to get through. Without the pass, we would have waited 6 to 7 hours. My parents, my son, and I will be staying in San Diego for the weekend before heading home on Monday. I am going to forget about cancer for 2 days and have some fun at the San Diego Zoo, Safari Park, and Sea World. I will still be following my special diet, but I want to take these 2 days and just have fun. I will post blogs 1 to 2x weekly when I am home, and give updates on my treatments at home. I will also share information that I hope can help others, such as diet and supplements to take. I am excited to continue sharing my journey, and to create awareness that there are other options treating cancer outside of the United States.
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I continue to pray for you Angela and look forward to your updates.