Invasive Metaplastic Carcinoma
I was diagnosed with an Invasive Metaplastic TNBC in Dec
2018, and had wide local excision & SNB performed January, with nodes clear
and clear margins (though only just, on one side). Currently just...
Forum Discussion
Hi. Just popped in to introduce myself.
I was diagnosed with Metaplastic carcinoma on April 1st..no joke! My 65th Birthday was April 2nd. Great! NOT!!!
Im not familiar with medical term abbreviations I see used in posts, so I’ll just use old fashion ‘plain speak’.
The tumour 3cm at 1st scan, was removed along with sentinel lymph nodes. I think additional surgery is called ‘reduction’ or ‘lift’. So far so good. Im managing the aftermath Ok, perhaps because I’ve been down a similar path with colon cancer 10 years ago. That doesn’t mean I’m not frightened of the results of pending pathology report. My 1st cancer was detected early & wasn’t life threatening. I had bowel reconstruction and 6 months voluntary chemo. I really thought I beat cancer forever. Obviously not.
Im wrestling with having to do chemo again...IF I have to. I quit smoking a year ago to get toxins out of my body! I wish there was a healthier, safer option for all of us....similar to practises used in Eastern medicine. I’d stick out both arms for a Vitamin C injections, and take my coffee black without complaint, if it meant getting those demon cells out of EVERY nook and cranny via my backdoor. I’d gladly lend my body to be a pin cushion for acupuncture, or be subjected to polar bear baths rather than chemo or radiation, if I had those options under Medicare. A girl can dream.
Dont get me wrong, I’m grateful for any treatment(s) available under our medical system. I feel for those who have to pay for every step out of pocket, or high cost insurance.
I’m grateful too for websites like this, where I can access information, share, vent, learn, find new hope, support, friends.
I’ve support from distant family and friends, however
no (physically) close friends to share this with, other than my housemate, an older man.
Just knowing of anyone on the Sapphire Coast NSW, I’d feel less alone.
I was diagnosed with Metaplastic carcinoma on April 1st..no joke! My 65th Birthday was April 2nd. Great! NOT!!!
Im not familiar with medical term abbreviations I see used in posts, so I’ll just use old fashion ‘plain speak’.
The tumour 3cm at 1st scan, was removed along with sentinel lymph nodes. I think additional surgery is called ‘reduction’ or ‘lift’. So far so good. Im managing the aftermath Ok, perhaps because I’ve been down a similar path with colon cancer 10 years ago. That doesn’t mean I’m not frightened of the results of pending pathology report. My 1st cancer was detected early & wasn’t life threatening. I had bowel reconstruction and 6 months voluntary chemo. I really thought I beat cancer forever. Obviously not.
Im wrestling with having to do chemo again...IF I have to. I quit smoking a year ago to get toxins out of my body! I wish there was a healthier, safer option for all of us....similar to practises used in Eastern medicine. I’d stick out both arms for a Vitamin C injections, and take my coffee black without complaint, if it meant getting those demon cells out of EVERY nook and cranny via my backdoor. I’d gladly lend my body to be a pin cushion for acupuncture, or be subjected to polar bear baths rather than chemo or radiation, if I had those options under Medicare. A girl can dream.
Dont get me wrong, I’m grateful for any treatment(s) available under our medical system. I feel for those who have to pay for every step out of pocket, or high cost insurance.
I’m grateful too for websites like this, where I can access information, share, vent, learn, find new hope, support, friends.
I’ve support from distant family and friends, however
no (physically) close friends to share this with, other than my housemate, an older man.
Just knowing of anyone on the Sapphire Coast NSW, I’d feel less alone.