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The clinic is a one-day visit clinic. You go there with your medical records (or of the person you are going there for). They analyze everything and at the end of the day they call you in for a second meeting, explain which herbs etc. you need to take. By buy those there, enough for the next 6 months. After 6 months you are expected to go back for a follow up check. Can you share any important tips for anyone considering this clinic? Call them to plan a visit. The 6 months treatment, depending on your type of cancer and stage, costs are around US$ 2,000.

They do a lot of adjuvant therapies, oxygen, vit c, curcumin, the chiropractor is excellent, they have a good psychologist, 6 pools [those were great for me as I am a water baby and exercise for me means- water]. You can receive all school medicine treatments there too. Can you share any important tips for anyone considering this clinic? It is very expensive 35k for 3 weeks, most of those adjuvant therapies can be had elsewhere cheaper. They charge $600 per room.....basically if you think the more "alternative" orientation leads to less greed you are mistaken. In addition, the food there and how it is served is only good for true believers.

I was happy I was there. But the tumor did not shrink. It was only stabilized. Can you share any important tips for anyone considering this clinic? I felt totally safe while I was there. After 2 weeks in a hotel, we found an Air bnb for the next 3 weeks.

My mom had breast cancer. They have her tonic, advised her to change her diet, had her take i3c and ester C. I wondered why i3c and ester-C, they said i3c helps block the estrogen from converting into a cancerous form of estrogen and the ester C helps make the body more alkaline. Doctors there were very knowledgeable with actual medical degrees. Made time to listen and help in understanding things. Thanks to Hoxsey, my mom is still cancer free for over 15 years! Can you share any important tips for anyone considering this clinic? We hitched a ride with this guy who carpools people down there. He does this daily. And he’d wait there till everyone was done and he drove us back.

I did CT scan after 7 months being on the treatment - all is fine Can you share any important tips for anyone considering this clinic? Don't be afraid of crossing Mexico boarder, remember that you will need to go back every 6 months for a check up first 2 years. This is arguably the most affordable alternative clinic you can find in Mexico.

My husband was treated for pancreas cancer and was clean for 9 months, but then the cancer came back with a diagnose of pancreas cancer stage 4. The oncologist offered chemotherapy. For 4 years we tried different chemotherapies and he was responding well, until it stopped working. My son did all the research and found oasis hospital. We sent all his medical records and the hospital advised us to come. They picked us up from the airport and we arrived to the hospital. It was like staying in a 5 stars hotel!. Very clean and nice. You don't feel like a patient. There is a nice restaurant you can dine in or have the meal in your room. We spent 3 weeks at the hospital and met many people that were cancer free. People from all over the world. Unfortunately, it was all too late for my husband. He was very weak by the time we got there. It still made him feel good though. Especially the hyperthermia.

I arrived at OASIS in October 2017 for an initial 3 week treatment (2 weeks oxidative treatment, 1 week Cell therapy vaccine. Accommodation on site is very good. Treatment facilities were of a high standard. The various treatments keep you busy most days. The 3 meals a day are great and of high standard. I was provided a timetable on the 1st or 2nd day and had a few meetings with the Doctors along the way with a final meeting before I left to discuss a plan moving forward. A take home plan including Nutraceuticals etc is given to you before you leave. Overall I had a great experience at this clinic. Can you share any important tips for anyone considering this clinic? Great clinic, only con would be to make sure you or your carer has an idea of whats planned for you on the various days, just so you don't miss out. At the end of the day you need to be aware of whats going on treatment wise, thats all. Not such a major concern.

On April 8, 2018 my father was diagnosed with Stage 4 lung adenocarcinoma - primary tumor 12.5cm by 10cm in right lung with metastases to left lung, hip bone, neck and lymph nodes. On April 24th he chose to receive treatment in Sloan Kettering in NYC. He received one dose of Keytruda, Alimta and Carboplatin. The next 3 weeks were miserable for him. He could not walk, had constant vertigo, bone pain, low grade fever, neuropathy, insomnia, no appetite. When we returned on May 15th for our follow up appointment at MSK the oncologist said my dad did way worse than she expected and attributed all the symptoms to Keytruda the immunotherapy and said our options were palliative chemo to extend life approximately 12 months or to stop treatment altogether. My father chose not to do the palliative chemo and instead we decided to go to CHIPSA. We knew about it from my friends and heard good stories of people currently treated there. Before getting to CHIPSA we had a call with the intake coordinator who explained all the logistics, room booking, schedules and prices. She arranged a phone consult with one of the doctors in the hospital. We had a long conversation to determine a tentative treatment plan. Getting to the hospital in Tijuana was a seamless experience. Our intake coordinator was with us every step of the way. Once at the hospital, we were shown to our room, given a tour of the hospital, had an orientation, met with nurses and physicians, had preliminary lab work, x rays and learned about the Gerson therapy that my dad would be following as part of his treatment. After xrays showed the mass unchanged from the month and half prior in NY and blood work results examined, a treatment plan was drafted and followed for the next 3 weeks. Aside from Gerson Therapy with juices and coffee enemas, my Dad received IV ozone, Apatone, B17, chelation, an immuno-oncology vaccine ValloVax and many other treatments. 2 weeks into the treatment we went to an imaging facility to get a CT scan. To everyone's surprise my Dad's tumor was 35% smaller. We were amazed with the results. My Dad was feeling and looking better. We went back to NY and continued the protocols he was given to follow at home with the Gerson therapy and custom tailored supplement plan. We returned for a 2nd 3 week stay at CHIPSA and after that stay my Dad's tumor was down to 4cmx4cm and all metastases down to tiny nodules. My dad was feeling so good he went back to work full time for the few months at home after our 2nd stay at CHIPSA. We are now 6+ months post the diagnosis day when the oncologist told my Dad he had no options. We have a lot of hope and see the improvements every day. His tumor markers are in normal range and we are excited to see future scans. Can you share any important tips for anyone considering this clinic? Everyone at CHIPSA has been exceptional and we could not recommend them enough. There are options out there and don't let anyone tell you otherwise. They offer the option to tour the hospital before enrolling. For us, every day of inaction with that rapidly growing tumor was a day setting us back a lot so we jumped into action fast and did not waste time on tours etc. BUT if you can afford the time I think touring gives people some peace of mind knowing where they're going beforehand.

Positives After much searching I settled on CMN hospital because I felt wanted but not pressured, the Skype interview was thorough and relaxed and the contact was courteous and prompt but without coming across as desperate. Upon arrival and throughout my stay I was treated very well, promptly and with care and love by all the team who genuinely seemed engaged with all patients. Food was varied, cooked well and very very nice, really enjoyed the food. The hospital did not make money an issue when my bank fouled up payment, it was mentioned, (I had just found out myself via the bank) but at no time did I feel pressured and it soon got sorted. They offer a great range of treatments. Meh It’s location isn’t exactly a beauty spot but, since I was going to get treatment and not take my beach towels, it was something I was prepared to put up with. Could do with some gym equipment although dr payan argued that he wants to create a relaxed atmosphere for his patients, it can leave the partners a little bored. Negatives Note - This should be taken in extreme context of a specific condition. Amongst the success stories there are failures, of the 3 patients who attended including me only 1 had a suessful remission. 2 got worse, including me. So on that very ridiculous market survey it has 33% success rate. All patients take the same protocols, the programme isn’t patient specific, which I appreciate would be difficult, but, the fact remains that not all will respond positively. My specific cancer type requires immunotherapy. If you know you are PD1 positive please do not take any other treatment or attend any alternative clinic, none of such similar clinics will work. (I hadn’t been confirmed such beforehand mores the pity). Being picky Having become adept working with bio resonance over last year I’d say dr payan under uses this therapy quite dramatically. It does have great effects if you believe your cancer to be pathogen led, for PD1 the programmes are sadly ineffective. Proteolytic enzymes - uses a great product, I still take it today but, if enzyme therapy is the key to your specific cancer type (pancreatic cancer particularly) you need up to 100 a day, at CMN you get 3. Dendritic cell therapy is unfortunately far too weak for PD1 cancer, peer reviewed papers prove this beyond doubt. Conclusion You will be greatly loved and respected at CMN but it’s one treatment for all style will not heal everyone. For those like me who are PD1 I would strongly advise to take immunotherapy, like keytruda for example and avoid such types of clinics. Some of the protocols at CMN are useful but, appear from other reviews to be much more potent for breast cancer patients. So, in that, some hope and confidence should be taken. Before visiting any clinic and spending your life savings Please know EXACTLY what is wrong with you before committing, a histology report from a biopsy will show this.

In 2012 I was diagnosed with stage 2 ER+ breast cancer at the age of 34 and went through conventional treatments (2 surgeries, chemo, radiation, followed by hormone therapy (tamoxifen). After a year I was released from the Cancer Center at home. And just a few years later my secondary cancer was found by accident (April 2017) upon which time I was seeking treatment in conjunction with some conventional hormone therapy. Quality of life had become my biggest concern which led me to do a little research into alternative methods. I was ultimately introduced to the Hoxsey Clinic by a trusted friend so I didn’t hesitate in going. I went within a month of my diagnosis. I was nervous and scared and had no idea what to expect. But I was met by smiling, friendly staff and when I saw the doctor there for the first time, I knew I was in the right place. He gave me the hope that I needed and ultimately the path to follow to my healing. It was the first time I had heard that my tumors could ultimately be shrinking within a years time. And they did. They started shrinking immediately. I am still currently in the treatment and I am healthier than I ever been, aside from having cancer. My tumors are not gone, but I live my life just as I did before and that is very important to me. Can you share any important tips for anyone considering this clinic? Definitely, use one of their drivers or stay at one of the hotels that have a shuttle. And always bring extra US cash in case you need supplements from the botanical or pharmacy outside the clinic.