Відео

I have to share one thing who's friends or family diagnosed or suffering with cancer plz help them ....I'm from Hyderabad our hospital giving treatment s to all stages of cancer ....it will be cure ....so plz save the life...🙏

Supporting cancer

I have never seen a generous and helping being like Doctor Madida who handles to me the cure to Tinnitus and vertigo condition and this 🌿🌿medicine perfectly healed me of my Tinnitus and vertigo.✅✅✅All thanks to God for helping me find doctor Madida on UA-cam😊😊

CORTICO STEROID ITSELF CAUSES CANCER

Shoutout to the 9 people who disliked this love you guys always

I’ve been diagnosed with early stage liver cancer. I have not started treatment yet which will be ablation surgery. A few months ago, I started feeling fatigue before the diagnosis. Is this possible or just some sort of mental issue. I also find if I do something like walking 3-4 miles, it takes me twice as long to recover. This used to be easy for me golfing. I would walk 18 holes. Now it takes two full days to recover. That being said I am 72 yrs old.

Did you know that the clinic is suppose to have the chemo patients given a injection to boost their immune system after chem. I know they can because when i hired on at a hospital my white cells were very low and they insisted i get a injection to boost it. I didnt. Ended up so ill. I should have.

Keytruda is a dangerous drug. I lose eyesight second day of treatment. Now my left eye stays blurry. Lung infection. Itching. Bone pain. Barely walk. Garbage. I stopped it. Know why they push it? Cost is 56,000.00. a session. I had full hysterectomy. 6 months later both clear cell and endometrial cancers came back with a third. Tissue. I was suppose to get radiation. Oh no they cant makw money off of that so they tell me chemo for 6 weeks plus immunotherapy. After i told them no to keytruda. The cancer center called and called to get me to change my mind. A person who works for their finance department said dont worry meficare covers 80% we'll pay the 20% . 2,400.00. Then she said I told them to go ahead and continue to give it. I called the doctor. Dr. Wouldnt talk to me. So i told her nurse NO!. Their not profiting off of me.

Understanding the costs and benefits of investing in cancer Posted by: Brian Ferguson, Posted on: 1 November 2016 - Understanding the costs associated with cancer is vital in order that resources are used for maximum effect. And investing in prevention and early intervention is critical if we are going to reduce the emotional and physical impact of cancer on individuals, families, friends and those that care for people with cancer. Calculating the health care and wider costs of cancer - as well as assessing the cost-effectiveness of prevention, early intervention and treatment - is a fundamental challenge faced by decision makers across the health and social care system. The costs of cancer can be felt at an individual level: work by Macmillan has shown that most (83%) cancer patients incur an average cost of £570 per month as a result of their illness. It can also be felt in the national economy: Oxford University estimate the cost of cancer to the economy is £7.6 billion a year due to premature deaths and time taken off work. Costs and the health system The Independent Cancer Taskforce Report (ICTR) set out the need for there to be clearer accountability of spend on cancer and emphasised the need for action in prevention and early diagnosis to reduce the longer term burden on the health system. It says: “The National Audit Office has estimated cancer services cost the NHS approximately £6.7bn per annum in 2012/13. The Five Year Forward View projections indicate that this will grow by about 9% a year, implying a total of £13bn by 2020/21.” Recommendation 95 in the strategy specifically asks that: “NHS England and Public Health England should work with Monitor and other bodies to consider how to develop better health economic evaluation of new service models and interventions.” We have a dedicated health economics team that commissions work to assess the economic impact of prevention and early intervention, and an example of this is recent work on bowel cancer in direct response to Taskforce Recommendation 95. This work has summarised the available cost-effectiveness evidence. Cost-effectiveness is a key concept in health economics and is concerned with the value we get from the money spent - where value is often expressed in terms of improving both survival and quality of life. For instance if we invested resources in the best possible way in bowel cancer then we would see improvements in survival, and also improvements in the quality of life of individuals who are staged earlier and therefore do not suffer the more unpleasant effects of treatment that could potentially be avoided. This is why a ‘return on investment’ (RoI) type approach has been followed in this work: how do we make sure that resources are invested in such a way that we achieve health gains at the same time as avoiding health care and other system costs further down the line.

Is targeted therapy useful for stage 3 cancer?

Well this killed my mom.the dr admitted it she would of still been alive if it wasn't for this treatment she got her first treatment couple days later on hosptis care couple weeks later she passed this might work for some people some people it dont

One thing I wish I knew before being involved with my friends final care was that the hospital didn't want her to die in the hospital. At the very end we were abruptly moved to another facility for her death. They were concerned about their treatment statistics and their rating with the insurance providers. In my opinion it was abrupt and stressful for her to be transported in moved within hours of her death with the only purpose being to protect the hospitals death metrics.

Head and neck cancer on the rise in your claiming that it's tobacco I believe it is the fast food industry that has given young people head and neck cancer really I don't believe it's tobacco at all I believe wholeheartedly it's their diet and the way people live today everybody lives on fast food

thank you so much for sharing this - we recently started sharing our story on our channel with hopes of connecting and helping one another heal after hearing this diagnosis!! we are in this together!

Riteshkumar

Ggg

A bit of common sense

The doctors make these procedures sound easy for the patient. I wish the doctors would go into a more detailed explanation of what will take place before and after transplant. They don't tell the patient about the injections to make the body produce more stem cells, that it can take up to three or more days to harvest the required amount of stem cells, that the drugs they use for the chemo treatment before transplant can be more dangerous than the procedure. Most of all, the various outcomes that can happen after transplant.

Michael Link is a great doctor he was my doctor when I had rhabdomyosarcoma 33 years ago

my brother passed away from rhabdomyosarcoma 7 months ago, at the age of 33. he really wanted to have his affairs in order, giving directions who should have his money and cars... I think managing this gave him some peace. He wanted to talk about death and I'm glad we managed the strength to talk about it with him. he hated hospitals with all his might and I'm very grateful he could die at home with us. On his last day, he knew. Even though extremely weak and hallucinating prior, he came to for a brief period of time and he hugged me hard and I got to say that I loved him and that is a moment I will never ever forget. I know you're with the stars now, Matko, and I hope you check on us from time to time. I love you and think about you all the time. your sister, I.

Separation anxiety sucks!

I finished radiation and started hormone blockers for breast cancer. I was always active but now fatigue and sleeping issues is robbing me of the energy to do the things i need to do i can't seem to get the things i need to do done .

It hurts 😢😢😢 all the time. Gabapentin and Tylenol and Meloxicam is all I have. What else is there unless its morphine pills which is bad on dizziness. Plus I have Meniers disease. Narcotics trigger dizziness. Geeeeeze. BRCA - IDC is mine. What the heck should I ask my cancer doctor for that will help? Thanks for this video.

Stage 3-4 endometrial cancer with only 2 weeks palliative pelvic radiation. I went Whole Food Plant based without added oils/fats. Lost my excess 20 pounds easily. But 2 years since radiation and still Extreme Fatigue. Blood markers fine, but living with uterine cancer. Too big and too Advanced to remove surgically. 🤷‍♀️

I should have this ..smoker and drink... My mother did none of that... please reach out for what she is to do next ... Immune otherpy is her wish and mine for her .. please.. please..reach out..

Can u help my exceptional loving caring mom?

sonali ru blood group A?

I must say that I have enormous respect for you Dr Apala considering the manner in which I receive my complete treatment for my HSV after taking your herbs ❤‍🔥........................

Hard to go to work or anywhere with unremitting diarrhea. Grade 2 idc, tchp

I start treatment tomorrow. I had stage 4 Kidney cancer. I had my Kidney removed a few weeks Ago. I already did the radiation for my neck. 🤞

Thank you for your help

What if now u have just the cells plus a auto immune

American healthcare is diabolical.

Family and friends who don’t call or support are the worst. Evil.

What is the reason I can't test salt in my food

The channel's insights on cancer are incredibly informative and supportive! 🎗 Planet Ayurveda's holistic approach supported me during my cancer treatment. Sharing this valuable info with others battling the same!

I’m writing a story about a hospice patient and their doctor, and I’m hoping to be as realistic and respectful as possible.

I was the sole carer for my mother when she got cancer, one of the biggest eye openers for me was those you expect to be there for you werent and those you LEAST expect to be there and help out whether emotionally or physically were there, my mother has passed now, it was a very intense year or so and am glad shes now at peace no more suffering

After 4 infusions I pulled the plug on Keytruda. I developed a rheumatoid arthritis like side effect that affected my joints. It was the worst 5 months of my life. Malaise, and multiple other issues including pancreatitis, a sinus infection that would NOT go away after multiple rounds of antibiotics, two rounds of C-Diff, a UTI, and fatigue. I haven't had in infusion for over 4 months and I am in pain nearly every day at some level.

My father is facing from HCC should we go for immunotherapy ?

i would like to share the fact the my lover lady survived BC and the mastectomy. The post treatment with Zolodex and other hormones seems very old fashioned. She is clear but suffers from numerous hot flashes and is tempted to stop taking these things. Not sure what options are out there but though i would ask non the less. My love for her is beyond the spoken word can tell and I will do anything that would make her life more comfortable post BC

There's a 13 year old boy with a teratoma (about 2 cm). His blood works are good. CT also showed his organs are good. The doctor advised to remove a testicle which has teratoma. Is it possible just to remove teratoma saving testicle?

Is there any need to give targeted therapy in initial stage ? Why nowadays doctor suggest targeted therapy at initial stage

Thank you for sharing this information with us. I do appreciate.😊

great talk well presented

During chemo I couldn’t even think about doing things. I thought I was being lazy. I slept a lot! Three months later I can at least imagine things I want to do and do some of them. I look forward to getting better and remind myself that I’m healing.

what do you do if need post cancer care because told terminal from cancer treatment complications? please help. my last oncologist who came in taking place my dr who moved just doesnt listen and I feel like im wasting her time .

2:30

I’m refusing Chemotherapy. I watched several of my relatives suffer even more and still die. It’s my body and I want to go out on my own terms.

I had a rectal net grade 1 but i have other polyps that are pre cancerous so every year i need to get a colonoscopy but they wanted to say if the net was cancer they just said you have a mass we didn't get it all out we need to go back in and remove the rest