Y90 AND Captem Combo
Anyone start this treatment? With good results? My husband has PNETS G3 KI67% 25%. There is a clinical trial stating it has worked well.
Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.
A lot if times we go to the local mtns for the holiday. But I went last year and there was a heat wave so that year was also different. My Mom said she didn't feel like it was the 4th. It was quiet. We saw some fireworks in the city, my son and I. Just hanging near home and rushing around less I would say. Some boutique thrift store shopping which I would also do in the mtns. I am really trying to do things as normal as possible. I am concerned how the Y90 cycles will land. August there is a bday and October my husband's bday and our Anniversary. Maybe we can navigate around it somehow.
No problem! There has to be more fun in the future!
Do you mind explaining why other net specialists didn't want to start treatment? Was it the tumor burden? Yes, 3 years is a long time. I think for our area disability would only be a year .....
Only one specialist had that opinion. I have no idea why. We had done enough research to know there were good viable options. But it was in 2010 when there wasn't as much knowledge even among specialists.
Yes, I am hoping there are a lot more options since Steve Jobs story. But we really don't know exactly what happened. I totally remember hearing about him. So successful I had thought and this is what happened to him. Funny or not funny, here we are. I remember that day like yesterday.
Steve Jobs was originally treated at Stanford (where my husband had his pancreas surgery) but then went on a holistic approach. You just never know.