The good news is the previous TBI risks cancel out the risks of not having radiotherapy again (and the oncologist radiologist is cuuute). So therefore I am having radiotherapy after surgery.
The bad news is it will be for at least 5 weeks (not 3 or 4) and won’t start potentially until April (my birthday month).
On the flip side when all this is said and done the risks if it reoccurring are down to 1 – 2% and the only reconstruction option is flap reconstruction after radiotherapy, so all the choices I have made so far have been serindipidously correct.
Dr Dreosti has also agreed to reduce cost of out of pocket expenses!
Murray arrives tomorrow.
Happy days xx
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Published by Debra Mesecke
I was 21 and I was planning a wedding, buying a house and had a job interview for the job of my dreams on my 22nd birthday. You see I was being made redundant and had to find a new job by August. Especially with the new mortgage now. It was April. I worked for CML and my new job was a done deal. All I needed was a medical. And with that, just like that....my life was turned upside down and I was diagnosed with CML, ha ha, I know the irony. My hematologist had a laugh at that too. I had Chronic Myeloid Leukeamia, which was normally reserved for 70 year old men. Quite rare for a young adult to get, so how would they treat it? I underwent two separate trials until finally it was decided my best chance of survival (all be it only 50% chance), would be a MUD BMT (matched unrelated bone marrow transplant), now known as VUD Allograt (volunteer unrelated donor). I was told 21 years ago the chance of finding a match was 1 in 20,000 (and that is everyone was on the bone marrow donor registry). Scary odds. So being the risk taker I am I said "go for it". They found a match and that was my first miracle in this journey. The second miracle was, it worked - new blood type, two different DNA profiles and the miracle of medicine was reborn inside me. The third miracle is my son.
25 years on, I now face a new challenge. Breast Cancer. Certainly not the first person to have cancer, to have invasive ductile cancer, hormone receptive and HER2 +, or to even have a dual diagnosis. But this is not another Webiste about a cancer survivor, this is just my excuse to finally publicly write. Along the way I am hoping I can share some insights I have learnt over the years and at the same time, give you a good belly laugh.
View all posts by Debra Mesecke
Silver linings – got to love them. 1-2 % chance of reoccurring is brilliant news – makes me VERY happy. Can’t wait to meet Murray xxxx
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