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hi sarah been to docs and everything seems ok at the which is great.
1 of the doctors thinks she has osteoperois so waiting for an appointment to come thought for a full body scan.
well as i thought and my oncologist thought too surgery isnt an option so she has decided to put me on chemo radiotherapy, cistplatin weekly with the radio for 6 weeks. plus internal radiotherapy afterwards. This new treatment is to start in 3 weeks or so once my bloods are back to normal and scans are done ( i have pet scan on 19th). i am not sure how i feel about all of this just scared,worried, nervous, alone everything to be honest. my mind is in overdrive about what ifs and all that and i am...
I had an allergic reaction to the antibiotics I was given on Monday! I woke up Tuesday morning with the most horrendous headache and a rash from top to toe. I know I am allergic to erithromycin and can now add penicillin to that list too. I havent had antibiotics many times in my life so I think thats why this is only becoming apparent now...it never ends does it!!
So its now Thursday and I still have a headache and I went to my GP this morning who didnt seem too worried but neither did she give...
I always feel like im moaning on here, but i think we just having a really bad time at the moment , another really bad night ,we slept on sofa together till about 11.30, then went to bed but hubby is waking up every hour which i knew so will try sleeping tabs tonight, but what i didnt know is whats going round in his head which i could have guessed, but is fear , he admitted it to our macmillan nurse today,while i was their, he also said he had no quality of life which i also knew but was so hard...
Now that the snow and ice have gone, I have been going out for walks every day for about an hour or an hour and a half.
We live in a village so there are plenty of walks close by.
I will have to get in the habit of doing this, it seems like regular exercise is good for stopping bowel cancer returning. Don't know if that is true but it can't do any harm.
I guess healthy eating, exercise, low cholesterol, lower blood pressure etc are good for all conditions including dementia - according...
So here we are, almost 6 months since we were warned to 'expect the worst' when Dad struggled to survive pneumonia and sometimes it feels as if we're all caught in some sort of No Mans Land. As there is no more treatment possible, there are no more hospital visits, x-rays or scans - indeed, there's probably not much point.
But for those of us watching him in his daily struggle to have some sort of quality of life, it's extremely hard not knowing what we're likely to face in the next...
Hi
I have been supporting my father since August when he was incorrectly diagnosed with pancreatic cancer. He was not strong enough for chemo and although the gastro doctor put in a metal stent it did not clear the bile that had caused his jaundice.
He has now been referred to another hospital and a very good team that have biopsied his liver to try and confirm PSC a liver disease and they plan to remove the metal stent he does not need.
What a few months! I thought getting into a new year things...
Well I guess the news is good.
They said they have found the tumor early and I have been officially staged as 1B.
So they have booked me in for a hysterectomy. If my lymph nodes are clear then than that is all the treatment I will need so I guess I should be grateful that it looks like I wont need chemo/radiation, but am just struggling so much with the fact that we wont be able to have a family. It just seems so unfair, and to have that snatched away from you so quickly just makes what should be good...
I have had my fourth chemo today. my Oncologist is very pleased with my responce to Caelyx. my blood tests had been going up so l had a ct scan to see if it was working which it is so l am very pleased because l had thought l might have to be starting again.
so l am planning a birdwatching trip to celebrate.
Rosie
Well, my husband had his 10 days radiotherapy in Dec.09 (not Nov.as I said previously) which he sailed through with only minor tiredness.
Christmas and New Year were spent very quietly, on our own. How difficult it is to make conversation when both are watching the same television programmes and only talking to the MacMillan Nurse every ten or so days.
The only follow-up appointment my husband has is with the Oncologist on the 18th Feb. Our Mac Nurse says that this is only to ask, 'How did you cope...
