u/ib4m2es

Currently on my 1st reoccurrence and they are having to swap my taxol as I keep reacting to it no matter how much steroids I take before and get during. They said it might mean I have to come in every WEEK for it. Has anyone else had to do that.

Is there anyone in this group that is doing clinical trials? How is that going? Has anyone heard of something that looks REALLY promising. I get tired of hearing “they are having break throughs all the time…” but we still seem to be treating OC with the same drugs they were 40 years ago. It doesn’t seem like we are any closer to a cure

Is it ok to make up a bottle of citric acid to have on hand instead of making it up each time? Or does it not keep well? TIA

Soooo many eggs and we can’t eat them fast enough. Whats the easiest way you store your eggs? What else can I cook with them. So far we have egg salad, quiche, breakfast egg, deviled eggs….

How were you told to count “chemo days”? I was told the day you get chemo is day 1 then so on. Hubs says no way. Chemo day is day zero, day 1 is the day after. Settle this debate!

I’m on my first reoccurance after almost 4yrs of NED. My first round of chemo is down. I always have hot flashes as I had my total hysterectomy with the first occurrence. They are well controlled with Effexor (not gone but tolerable) but man alive-chemo is making them come on with more frequency and intensity!! Is this just the steroids or the chemo itself? I’m getting the taxol/carp and I start Bev with the next treatment