I had WBR 4 weeks ago and thought the side effects of the brain mets should have mostly gone down by now. It is better now than it was but I’m still getting the occasional stabbing headache (lasts seconds and goes)and the onc said it would be 6 weeks before the rads have had their full effect but I assumed that I would have had most of the benefits by now or does it take longer?
Is this the kind of thing the helpline can help with? I’ve never called them.
Cheers
Hope you all have a stunningly beautiful and fun weekend.
Angie
Hi Angie
Yes, absolutely, the helpline will be able to offer support and information regarding WBR, just give them a call, they’ll be happy to help or just talk through any concerns you have.
The number is 0808 8006000.
Kind regards
Louise
Facilitator
Hi Angie - I spoke to my sister tonight, she had her WBR about 6 weeks ago and for the last week she has been feeling sick and has lost her appetite though she feels fine in herself. Apparently this is due to the WBR reaching its full effect.Just so you know you are not alone in delayed side effects… She has been given protein drinks from her GP so that she keeps her nutrition in check xx.
Thanks Holly.
I’ve also been on the old protein shakes etc but I’m finding I can handle these foods and enjoy them.
Jelly
Simple omelette (with mushrooms good as loaded with protein)
fruit (this is my fave at the moment).
Just thought I’d share as it’s no fun being knocked down by radio and then feeling a little extra kicked in the teeth by your own lack of energy.
I only had 2 small doses so I think I may be recovering faster.