Thank you! I’m I should have know that!!!
Thank you I should’ve known that!!
I have been fighting TNBC for years. It started in 2004 when I was six months pregnant. I was in remission for 17 years before having it return with a vengeance! It has metastasized throughout my body including my bone, brain, kidney, lungs, and liver. The bone Mets are excruciatingly painful. I was recently hospitalized with nodules on my kidneys and a stent was placed to help the blockage to my ureter. I have lymphoma in my left arm due to lymph nodes being removed and have had a double mastectomy last year. I was wondering if it was common to have bloody urine after a week of clear with the new stent. It has been replaced once already due to a kink and don’t want it to happen again. I went on hospice two days ago and with the new pain can’t get any answers except to, “take more pain meds!” I understand this is what hospice does, but would like to know what is going on also. Any thoughts are welcome! Just not looking forward to a repeat process. I was also told I would have to have the stent removed, does this still happen on hospice? If anyone has any thoughts or similar situations, I would really like to know I’m not alone!!🥹