The Foxs Lady
Comments
-
Yes I think of the IF in capital letters. I try to look after myself. I am doing more exercise than I ever have before. I remain overweight. But I am trying. Maybe I will be lucky and maybe the IF will never happen.
I make compromises and I live for now. I am planning the dream holiday but it can't happen for almost 2 years because my son will do the HSC next year. Family is everything to me; my health and their interests have to go hand in hand.
I do what I can. I am sure I will be here for some years to come.
0 -
Yes I think of the IF in capital letters. I try to look after myself. I am doing more exercise than I ever have before. I remain overweight. But I am trying. Maybe I will be lucky and maybe the IF will never happen.
I make compromises and I live for now. I am planning the dream holiday but it can't happen for almost 2 years because my son will do the HSC next year. Family is everything to me; my health and their interests have to go hand in hand.
I do what I can. I am sure I will be here for some years to come.
0 -
Yes I think of the IF in capital letters. I try to look after myself. I am doing more exercise than I ever have before. I remain overweight. But I am trying. Maybe I will be lucky and maybe the IF will never happen.
I make compromises and I live for now. I am planning the dream holiday but it can't happen for almost 2 years because my son will do the HSC next year. Family is everything to me; my health and their interests have to go hand in hand.
I do what I can. I am sure I will be here for some years to come.
0 -
Sorry to be slow - just saw your question. After discussions with my breast surgeon (and a family history) it was my decision to have the double mastectomy, and my surgeon agreed - but it was my choice. After chemo, my Oncologist explained that tnbc usually recurs in the soft tissues, and recommended the hysterectomy as I had already had a large cyst and an ovary removed a few years ago. He also recommends regular colonoscopies. I am now promoted to 12 month checkups and in remission. Wishing you all the best. Michelle x
0 -
My temp had dropped when I arrived at hospital, I was wearing a pain patch, because of the injection in the stomach on day 3 which was to build up the w/b cells, they still keeped me there and did blood cultures. So where are you up to with your treatment now? Deb
0 -
Hi Deanna, sorry it has taken me so long to respond I'm not very good with the social networking thing as yet. Great to see that you are a BC survivor, it gives me hope. I may be able to catch up with you sometime in the near future, still having chemo at the moment, 2 more to go and radiotherepy for 6 weeks. My older son is just about to move to St Marys so I maybe up that way from time to time. Not sure how to request you as a contact, so if you know how maybe you could request me for future reference. Debbie
0 -
Hi Deanna, sorry it has taken me so long to respond I'm not very good with the social networking thing as yet. Great to see that you are a BC survivor, it gives me hope. I may be able to catch up with you sometime in the near future, still having chemo at the moment, 2 more to go and radiotherepy for 6 weeks. My older son is just about to move to St Marys so I maybe up that way from time to time. Not sure how to request you as a contact, so if you know how maybe you could request me for future reference. Debbie
0 -
hi Leanne
All the best on 30th when you have implants. Thanks for the advice I will let the nurses take charge. Hopefully there will be a time when we can catch up.
Sandi (smead) xoxo
0 -
Hi I also live in Adelaide and would love to meet some TNBC ladies!
My story is in short, I was diagnosed with TNBC in Feb 2011, underwent mastectomy then 6 cycles of chemo. I then discovered I am BRCA 1 positive so underwent hysterectomy and removal of ovaries, then has other breast removed with expander reconstruction.
Since then I have developed decreased bone density withospeoporosis which I have to take medication for. The chemo also damaged my heart so have ongoing issues there.
I am now having surgery this month for the aneuysm in my brain. Luck me.
Some days I feel like I can not win.
Love to meet some other TNBC ladies in Adelaide
Love Catherine
0 -
Hi Catherine, similar stories, unfortunately. I too have developed osteoporosis but instead of medication my GP gave me an infusion that will last for twelve months. I had a reaction to it like chemo, and when I researched it, it is a chemo drug. I had three fractures in my legs in three months. an ankle, then both knees. I have terrible shortness of breath, exhaustion. My mum had heart disease and I'm beginning to wonder if I have some damage there. How did they test for your heart problems? I keep waiting for things to improve, I hope they do for you to,. just some semblance of a normal life would be appreciated. I have yet to go down the reconstruction side, too busy fighting all the other things that happened after treatment finished. Jo0
-
Hi Jo,
My GP sent me to a physician as I had unusual changes in my blood tests and was also also short breath, had fluid on my ankles and hands and had chest pains. I has lots of tests ECG, Cardiac Ecco and MRI of my heart.
Hope this helps I think you should get it checked out. Good luck. Catherine
0 -
Hi Catherine
I'm about to start chemo tomorrow at Flinders but would love to catch up at some stage in future. I live McLaren Vale and work in the city. What about you? I'm sure something can be arranged. Keep in touch and lets try work something out.
Love Sandi
0 -
I have an appointment with the surgeon next week and will ask her for a referral. Thanks again. Jo0
-
Girlies - just wanted you all to know in today's Guardian there is a small article about very new and very successful drug breakthrough in the treatment of triple negative cancer.
Very heartening as it says it is the combination of 2 drugs they are already using.......but doesn't mention what those drugs are.0 -
Hi Sandi,
Would love to catch up, I live in Craigmore - opposite ends of Adelaide, but I work in the city too. All the best with your chemo. Let me know how it is going, and take every day as a new one!
Love Catherine
0