I have sjogrens and have had surgery for breast cancer. I should like to know how treatments effected your sjogrens symptoms, temporarily and permanently? I am particularly interested in learning about
your experiences after having had chemo and/or /Tamoxifen. Also radiation.
It would be also be great to hear from you if, like myself, you are not on medication for sjogrens and so are aware 100% of what your body is telling you and the side effects experienced.
I live in Africa and so, would also would like to know if there are any other breast cancer treatment options available there that are kinder to us with sjogrens?