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Hello to anyone interested, I've had nothing major to say on my recovery recently. After Ivor Lewis procedure on 3rd October, discharged on 15th October first two weeks eating was going well then at end of October started to get swallowing difficulties. I phoned hospital and was told that it was part of the healing process and too soon after the surgery to do anything. Had my follow up appointment with consultant surgeon on 25th November told me I had a 20-25% chance of survival up to 5 years. I...
I have been fighting this fight for a few years and winning I might add, but today I felt drained from the inside out, i don't know if it's the build up to christmas or work or family or all if it, but if I had a button I'd want someone to turn me off for the night, switch me on in the morning .
So it's a year on
I named my tumours the twins as there were two of them and they were growing really fast. My initial diagnosis was grim and for two months life was a whirlwind of tests, consultations, bad news, a radical hysterectomy, a wedding.....then great news my tumours were of low malignant potential. Christmas came and went. I went back to work and just muddled through trying to come to terms with it all, my new body (the scar is impressive) and the menopause, not just any menopause...
So….here I am in my kitchen with a cup of tea, once again the fluttering, flapping wings of Cancer muffling all my other thoughts. It’s so irritating! They quietened a little after my first blog entry so worth another try.
I’m on day 18 of my first cycle - round 2 is on Thursday - so it’s a good time to summarise my Cycle 1 experience. There’s a fair amount to say so I’ll just start with Treatment Day - Day Zero:
Treatment was EC90 - Epirubicin (aka Red Devil...
We were given the worst possible news last Thursday that my dad has cancer in multiple places. He's 81 years old and I am 39. He won't be having any treatment just pain relief. I'm really struggling to see his decline and as he didn't want to know a timescale, I'm terrified that he will go very soon. It's really hard to stay strong for my children, mum and dad. All of us are staying strong, dad included. As he has said, he's not ready to go and neither are we to let him. With Christmas this coming...
Last week was my three year 'check up from the neck up' and relieved to say am still in remission and making good progress now from the throat cancer and RT that took away a year of my life in 2014... Sure the nerve damage and feeling to the neck, shoulder and back will never get any better now but I am back playing squash to a reasonable level and am learning to fight judo left handed!...Still wish for a solid 8 hours sleep without waking up with a dry mouth, and would love to eat something...
Sunday 18th December.
Today has been a day of passing time until tomorrow, much like yesterday. I will have the blood test tomorrow morning and then have to wait until possibly the evening to find out the result. It all seems so cruel the waiting. It's exhausting. But what will be will be and there's nothing I can do about my white cell count. If I hear nothing by the evening then all is good, so I will not be wanting any phone calls tomorrow from late afternoon onwards...more stress. ...
Hi all
Can anyone advise I'm on weekly paclitaxel and have had 2 sessions. Yesterday I woke up with a rash on my face and chest. It is very itchy and red can anyone suggest anything that I can put on it. I'm seeing the oncologist tomorrow so I'm hoping they can suggest something. I think it is like an allergic reaction not sure.
Jane
So I find myself here following a diagnosis ofobular breast cancer. Apparently I'm lucky, because lobular breast cancer is almost impossible to diagnose untill it has spread.
I found myself at the Brest clinic following months of visiting my GP feeling like I had the flue, and fringe tiered. I was o. And off antibiotics for two years. Told I had a virus. My bloods showed slight I famation but nothing to worry about. Untill I noticed my left nipple was looking a bit squished. At first I thought...
I'm now one month in and, if the general consensus is to be believed, the fatigue and nausea should soon start to lift. I'm searching for the light at the end of the tunnel because after a month of feeling ill everyday I am beginning to tire of this.
I saw the docs last week - a very nice registrar who said he'd not seen anyone on Rucaparib hammered with fatigue quite so hard. If the onset had not coincided so exactly with starting Rucaparib, he said, they'd need to investigate whether...
