Cancer Support and Caregivers Who Are Trail Blazers!

[JustJo]

Originally Posted by claybaby

hey JustJo...hugs right back at ya....you & mom are in our thoughts & prayers...do you have a Hospice Center there? Those RN's are awesome and the oncologists have a "protocol" or "regimen" of drugs and having Hospice involved insures your getting, having, and with access 24/7 to ANY med she may need. She needs to have an rx for Zofran (generic is: ondansetron) 4 mg. disintegrating tablets...to use every 4 hrs.....as needed....for the nausea...AND sounds like she would be an ideal candidate for Oxycontin...and it comes in liquid...the Morphine is horrible. I initially had a pump of Dilaudid IV for pain and an epidual with pain cotrol meds in it....and had to switch to MS (morphine) which I HATED to take..I only pushed my "button" for that med a total of 20 times in the whole 12 days I had it...smiles....(HIGH tolerance) to pain..smiles...
Anyway I am certainly not trying to prescribe or "manage" BUT offer you some suggestions..smiles....I am a nurse....smiles....
Take care..and YOU are doing an awesome job....give yourself a pat on the back...Clay

Thank Clay. She is on the Zofran, which helps a little but not completely.
Hospice can't/won't do anything until she rejects all chemo treatment...and she's not quite ready to do that yet.

Her current/new oncologist down here is proposing modifying her chemo to something that will be less hard on her and only every 3 weeks (since she can't be cured anyway)....and she wants to see if that helps her quality of life.

Right now we're just one step at a time...but it's an uphill battle.