It’s been a while since updated on how things are going, we have just had the second course of chemo the first week was really sick the second felt really well in fact people could not believe I was sick and my MS SYMPTONS. We’re virtually nil my walking was really good better than it had been for a while, then week three when my immunity was at its lowest was so tired, Well had the second was on Friday I The sickness has not been so bad but they have given me about 6 different types of anti sickness for the first few days So many thanks to those that asked how things had gone
Glad to hear that thingds the second time round weren’t so bad. Keep being strong. You will get there.
Sending hugs.
Anne
x
Good to hear you are well on the way to getting through the treatment. Good luck with it all. Alison x
Hi, thankyou for letting us know how the treatment is going. I am glad to hear you are doing not so bad.
My sis-in-law, in Canada, is also undergoing chemo. I spoke to her yesterday. She sounded bright, but when I asked her how many sessions she has to go (only had one weeks worth so far), she said shed finished the whole course. But her OH reminded her she has another 3 sessions to go.
She said Damn, I thought that was it. She is having some short term memory problems.
She had a brain tumour, which was successfully removed and a lung tumour. Part of the affected lung was also successfully removed.
I hope your treatment is successful and that you recover well.
luv Pollx
Glad to hear that it is going not too badly. Stay positive and look forward. Thanks for the update. Cheryl:-)
Good luck , stay strong you will get through it. Hope x
Hello Tattybear,
It is great to hear that your chemo. isn’t half as bad as you feared. I haven’t been on the forum for a few weeks now because I have been very busy visiting hospitals as I now have/had breast cancer. The 3cm tumour I had has been removed (though the stitching looks like something ‘James Herriot’ would have done!) but I now have to have chemo. because some cancer was found in my lymph nodes. I have to have all of these nodes out, chemo, radio and Herseptin as well as immuno boosters (I wonder who will win the fight between the immuno boosters and the immuno supressents that I take for the MS!). 2013 will be a heck of a year but we will come out smiling won’t we? I still feel as if I am in an outer body experience, but I am getting used to the mountain ahead of me.
Best wishes and good luck,
Moira