At the risk of sounding like a Nike ad, JUST DO IT! DH and I are back from a week in Florida which included a day at Disney Springs, a day a Universal City Walk, and a day at Kennedy Space Center. Two hours via plane each way, driving around, staying in a hotel, eating out, shopping: all handled with planning and afternoon naps. We took extra stoma supplies, phone numbers, and over-the-counter medications. We stocked up on bottled water. We took breaks often.
Thinking about NYC for Christmas. I have even called our travel agent and placed a deposit for a cruise in April (with really good travel insurance). Then we will head to 2 college graduations in May. Travel has always been one of the greatest pleasures for us and by golly cancer is not taking it away!
So if you are worried about travel/whatever with a stoma or while on chemo, talk to your doctor, and then JUST DO IT. What is YOUR greatest pleasure? JUST DO IT!
Caregiver to DH, dx @ 50, mets to liver/lungs/lymphs, MSS, quad wild
9/16 CEA 114, partial blockage, left hemi, perm. colostomy
11/16 port in, FOLFOX + Avastin
4/17 CEA 11
6/17 CEA 15, 5FU + A only due to neuropathy
11/17 CEA 38, CAPOX + A
1/18 CAPOX caused hi bilirubin/bad hfs, back to FOLFOX + A
5/18 growth/ascites; change to Vectibex + 66% Irinotecan dose
9/18 CEA 31, shrinkage/no ascites