While in Germany, I tried whole body hyperthermia. Hyperthermia is a cancer treatment where the whole body is heated to a high enough temperature that it can damage or kill cancer cells. The maximum temperature used is dependent on the clinic - at Hallwang it was 40 degrees celsius or 104 degrees fahrenheit. From what I understand, other clinics might go to 43 degrees celsius but a sedative is used so the patient is more or less asleep for the procedure. At Hallwang, you are wide awake for the whole thing which scared the crap out of me at first.
To start, you sit in a hot bath to gradually bring up your temperature. Then, once it is high enough, you move into a tent with heat lamps that reminded me of an incubator. Thank god your head pops out the top so it is not affected by the heat. The nurse stayed in the room the whole time, monitoring my heat rate and blood pressure every 15 minutes or so. They also give you fluids to replace the massive amounts that you are losing by sweating profusely.
After spending 45 minutes to an hour in the incubator, the sides are folded on top of you to make a sort of body bag which you stay wrapped in for another hour. Now that I am typing this, the whole process sounds like some sort of cruel and unusual torture but really the worst part of it was my anxiety over needing to pee after all of these fluids had been pumped into me. Luckily I was able to hold it but the nurse did offer to put a diaper on me if needed, haha.
Unfortunately whole body hyperthermia is not available in Canada. Some Naturopaths or alternative medicine clinics might offer local hyperthermia which is done with a machine that treats a specific area. This can be effective on a tumor but if you are trying to treat circulating tumor cells like I am, whole body hyperthermia is the only option. I found that a lot of people at the clinic had not tried it but it is something I would definitely recommend. Call me weird but I actually enjoyed it...maybe not the treatment itself but the feeling you have after is unreal, like you have just sweat out every single toxin in your body.
Many people go to clinics in Germany for this treatment alone or it can be even more effective when combined with other therapies. This video gives a good overview if you are interested: https://www.youtube.com/watch?v=qGzXCS-UbVo
I am 30 years old and was diagnosed with breast cancer, specifically invasive ductal carcinoma. Before my diagnosis, I didn't even know what that meant. Now I have been forced into a reality where I not only know what it means but my doctors appointments and daily thoughts are filled with other previously unfamiliar words like neoadjuvant therapy, metastases, HER2 and triple negative.
I started this blog in hopes that some of the information I share may be helpful to other young women in a similar situation. Rather than posting my day to day experiences, feelings and progress, I plan to share some of the things I have learned along the way. Being dealt this hand in life at 30 years old brings with it some unique issues and questions. Will I ever have kids? How will this affect my relationships with my husband and friends? What is my long term prognosis?
Through this site you may find that my way of dealing with things is a bit different. I want to be educated about my disease and take an active role in my treatment and recovery. I want to understand every part of my pathology report, what it means, and feel confident that my doctors are recommending the best course of action. At each stage in my journey, I have experienced challenges with finding answers to my questions and ensuring that the medical professionals treating me really understand who I am and why my way of dealing with this disease may be unlike other women. My hope is that people will be able to relate to my experiences, learn from them and find some comfort that they are not alone.
I started this blog in hopes that some of the information I share may be helpful to other young women in a similar situation. Rather than posting my day to day experiences, feelings and progress, I plan to share some of the things I have learned along the way. Being dealt this hand in life at 30 years old brings with it some unique issues and questions. Will I ever have kids? How will this affect my relationships with my husband and friends? What is my long term prognosis?
Through this site you may find that my way of dealing with things is a bit different. I want to be educated about my disease and take an active role in my treatment and recovery. I want to understand every part of my pathology report, what it means, and feel confident that my doctors are recommending the best course of action. At each stage in my journey, I have experienced challenges with finding answers to my questions and ensuring that the medical professionals treating me really understand who I am and why my way of dealing with this disease may be unlike other women. My hope is that people will be able to relate to my experiences, learn from them and find some comfort that they are not alone.
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