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http://rayandmave.wordpress.com/ My Chemo has been sorted for the New year so I can enjoy xmas
After having chemo all this year, (and most of the last two), I have at last got my CA125 count down to 19, and the oncologist has said I can have a break from chemo until things go down hill again. My cruise for christmas is a present I never thought I'd get. Here's hoping these drugs have done their job and it stays under control for longer than the 3 months it normally stays away.
Stay positive and never give up hope.
A quick blog to update the past week and let you all know that my Dad died on Sunday 1.40am. But i'm not going to be morbid or upsetting. I don't think it's fair to express with too much detail the process of palliative care and my personal experiences; some of you on here may be going through as patient or carer the same experience and don't want the reminder thanks very much! And if you do, P.M. me to share.
All I want to say, is though the past few weeks have been tiring both physical...
I was diagnosed with Carcinoid Cancer in March 2010. I had it in 2004 as well but had both tumors removed. My surgeon was 110% sure he got it all! Wrong! This time there is no chance of surgery, to many tumors. When I was diagnosed I was told I had 4 inoperable tumors between my right lung & my liver. I thought my life was over at that point. I decided to go to CTCA (Cancer Treatment Centers of America) for a 2nd opinion. There I had a PET Scan. This showed that I didn't have 4 tumors, I had 20 to...
The weekend after session 3 of FEC, On the positives I still have my hair, my teeth, ny gums and most of my stomach contents. However I'm incredibly tearful at anything and nothing. Many of my friends seem to have lost parents over the ast few months and so I am very luckyt to have 2 able and fighting fit parents who are taking care of thmselves and able to give me support via webcam and phone from 500 miles away. Children's nativity pays and toy services hve me bawling my eyes ot and last night...
It is two forty five - in the morning...and I am angry.
So... I have written and deleted everything I want to say - because my anger won't help me/my husband or anyone else - and I could get sued...
All I WILL say to any "professionals' reading this - treat the individual not the cancer.
This week has been such a rollercoaster of emotions and events it is difficult to get it all in order,but here goes. If you read the last blog you will know I had a bit of a downer after my last clinic visit but as always yours truly has picked herself up etc etc. Some time ago just after my diagnosis I put in a claim on the terminal illness section of my life policy...on the one hand I was really hoping I would get the money as anyone would but on the other I knew that to get it my life expectancy...
Hi My name is Karen and I have been Diagnosed with Anaplastic large cell Lymphoma.I amabout to have my 2nd Chemo, I have 2 kids 13 and 15 who are not coping to well now my hair has started to fall out. Although Iam not curable Iintend to give it the biggest fight of my life and go into remission. I have been reading other blogs and it is good to know that I am not the only one scared out of my wits and the confusion I am feeling is so normal. Anyway just wanna say hi and would love to get to know...
