The lovely BB member has been back in contact and has asked me to post this on her behalf
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Thank you al for your heartfelt replies , it's people like you that make it a nicer time and a little easier to go through. I feel for those of you who have lost someone to this horrible disease, and those who know someone going through it or who has been through it. You are all truly wonderful people.
I am still around, and my chemo is nearly over. I was sick with a virus and had to miss one week of it, so i have an 'extra' week of it to catch up on. I'm counting it injection by injection now (makes it seem like it's going faster....) so now only have 5 to go before I start my radiotherapy course.
I have spoken to my surgeon about reconstruction, and may be able to have one early to mid next year, I feel very strongly about BFand i am currently preparing to re-lactate (sorry if TMI) so I can feed my little one again in the future - this is depending on if I am having to take Tamoxifen (for 5 years!) and if it is present in breast milk. I am enquiring with as many professionals in the field (here and in the USA) as I can to find out if it will be safe for my bub, as I do not wish my strong desire to BF to in any way harm his precious little bod! if it is present in my BM, I won't continue.
My hair, eyelashes and eyebrows are making a comeback - I am having a competition with my 5 month old to see who can grow hair the fastest, and unfortunately my 5 month old is winning !!!!
It's been a hard road, but i have kept my sense of humour, and have thought long and hard about many things you wouldn't normally think of. Life is far too short not to enjoy.
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