365 days later after surgery to remove esophageal cancer at Mayo
Word of thanks , thanks to Dr. Wigal and his team a year ago today , I had my Esophagus removed stage 3 cancer . It’s been a bumpy road for me as I like to eat and it was a struggle getting used to the NEW ME ..after about 6 months , I was told I had Ulcerative Colitis and was prescribed meds for that , (so far its under control ), after losing 70 pounds im finally gaining some weight back , went from 255 before surgery to 175 after ,now at 190 . Hopefully Im on the right track now feeling good and blessed . Id like to thank the people that helped me at ST Marys , Greg , Brice, Avery , Dr Wigal's team God Bless and KEEP DOING WHAT YOU DO ….. SAVING LIFES ….. John
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Thanks johnstawicki,
I’m so sorry for all you’ve been through and I’m so happy to hear you’ve had your wife’s steadfast support. That, despite all else, is a beautiful story.
Unfortunately, by the time the diagnosis came, it was Stage 4, it had spread. The surgeon said surgery wasn’t an option.
Chemo started today. Only learned the prognosis 4 days ago. Read about the side effects tonight.
“This is not the end, it’s just a chapter in the story.
Joy is on the way.”
~Laura Souguellis’ lyric
I had a J tube for a few months following Stage 4 Esophageal Cancer surgery. The last few months were spent in nursing facilities which I found to not be very good for patients. Of the 4 places I was in, 95% of the nurses caring for patients didn't know the difference between a "J" tube and a "G" tube. Consequently, they thought nothing of crushing my meds and running them thru my J tube which clogged it up like cement. The G tube is larger & goes into the stomach & the smaller J tube goes into the intestine. Unclogging rarely worked and twice I had to go to ER to have the damaged tube removed and replaced with a new one. One nurse tried pouring hot water from the coffee maker into the tube which then exploded and the extremely hot water seriously burned my abdomen. I was so glad to get the tube removed after I finally returned home after 7 mo. of confinement.
ABSOLUTELY.
Holy cow... you've gotta be shttin' me! That's some crazy story. Horrific care.
So, I've forgotten... are you the one with the stent being installed?
johnstawicki, I also had Dr. Dennis Wigle and his awesome team at St. Mary's do my esophagectomy!!!! April 2020. 2 weeks as a guest at the hospital (I encountered infection in one of my drainage ports after removal).
HOW HAVE YOU BEEN DOING SINCE .
@l1krieger, hearing that you have cancer sends you reeling. Despite that emotional rollercoaster and the stress of that news, you are forced to learn a whole new language, move in an alien world of medicine, doctors, tests and hospitals. Not to mention sharing the news with people who you want to tell and sometimes having to comfort them and manage family communications. It's a lot and you and your wife have had little time to adjust.
I'm glad that you've come here to ask questions to help make sense of things or even to figure out what questions you can and should be asking your cancer care team.
Chemo, radiation followed by surgery and immunotherapy is a very common course of treatment for esophageal cancer as @zzonner and others can share. You can read more on Mayo Clinic's website
- Esophageal Cancer treatments https://www.mayoclinic.org/diseases-conditions/esophageal-cancer/diagnosis-treatment/drc-20356090
For some people, like @dsh33782 and @justtrust, surgery is not necessary or not an option. But chemo, radiation and immunotherapy are still options.
I'm concerned about your statement that someone said they took "strong medicine", no further treatment and they are cancer-free now. If it sounds too good to be true, it probably isn't true - although I wish it were. Always research what you read and make sure that it is evidence-based from a trusty medical source like Mayo Clinic.
Yes, esophageal cancer treatment is tough, but as you can read from the stories like that of @johnstawicki @dsh33782 @aheid @mrgvw @lori57216 and many others here, there is hope and healing.
Like @aheid said, I think that many members in this group would appreciate your recipes and tips for blender and pureed foods. As you experiment, I encourage you to start and new discussion where you and others could share recipes and tips for eating while on treatment and after treatment.
How are you doing today? How's treatment going?
All I eat is real food , those protein drinks are way to sweet for me and give me dumping syndrome ….I found a protein water I like protein20 …