Living with colorectal cancer - Meet others & come say hi
Welcome to the Colorectal Cancer group on Mayo Clinic Connect.
This is a welcoming, safe place where you can meet people living with colorectal cancer or caring for someone with colorectal cancer. Let's learn from each other and share stories about living well with cancer, coping with the challenges and offering tips.
I'm Colleen, and I'm the moderator of this group, and Community Director of Connect. Chances are you'll to be greeted by fellow members and volunteer patient Mentors, when you post to this group. Learn more about Moderators and Mentors on Connect.
We look forward to welcoming you and introducing you to other members. Feel free to browse the topics or start a new one.
Let's chat. Why not start by introducing yourself?
Interested in more discussions like this? Go to the Colorectal Cancer Support Group.
Dear @Ikissinger, I am so sorry to hear about your father. I keep on praying for your father and please keep positive and follow up with necessary arrangement with hospice. I would also suggest to discuss with the doctors that how they can make this lemon sized tumors to be shrunken if they are inoperable. Please find out ways. There is always a way if there is a will. I will keep you and your father in my prayers. Soul
💋thanks
Yes. Thankfully my brothers wife does hospice care so navigating should be a little easier on us. 💋
Hi im james. I had colon cancer 10 yrs br4 i would do anything about it cause i did not want a bag on me. Worst mistake could have made. I was loosing so much blood and food was going straight through me was weigh less than 100 lbs my red blood cell count went so low i couldnt stay awake and would sleep 18 hrs a day. My dad came by and took me to hospital. With in one yr with no insurance or anything had all my intestines taking out. Im 48 yr old did heating ac refrigeration work over 30 yrs all i know how to do.after all the testing and taking blood mris and all other test ever 2 days all over la. They told me would be a 6 hr surgery. Would only have bag on me a few months. Was over 12 hrs long. Didnt wake up tell day later. Said i would be walking in two days. Was 2 wks. Was in hospital almost 2 month and left with stitches and staples in my rear.felt like barb wire. Needless to say im stuck with for life. I now have all my small intestine full of polyps and have to have some cut out ever yr. I applied for disabily 2 yrs ago. Just got aproved.i had to sell everything and more just to survive.been long road for me. Just want a break. Im just getting used to myself
Moved to la. From Texas cause texas would not help or do anything about tell i was dying. And would not give me medicaid. I was buying my ostamy supplies out of pocket i got medicaid finialy and got liberator to start sending me supplies. Has been very long road. I get my ssd settlement money this month. Suppost to have another surgery on 28. I really just thinking on taking a break or vacation ..
If you think you have any problems have it checked and dont put off cause of temporary bag. I went through. Depression and have to be on 16 medications now. And so much worse than if would have taking care of.
Welcome to Connect, @sockwelljames. I'm grateful that you posted your story to tell others about the importance of getting checked. Colon cancer can be effectively screened, but many are afraid to do it because they fear bad news.
What surgery are you supposed to have on the 28th? Have you discussed taking a break with your surgeon?
No i have not. Now dont have any large intestines. And now have polyps in small intestines. 1000s to be extact. Exery yr have to have some cut out for rest of life they told me. Last one was 2 inches at the y .were pankrus and gallbladder drains to small intestine. Cut it out put stint in pankrus .got pankritus 2 wks later back in hosiptal. But no have not discussed it. .my doctor first came to me crying saying it was too big for her to handle and got me set up with who she said is the best in new orleans. I still love the lady and respect her honesty so much.
All my family in texas. Done got all my doctors and medicaid and just getting ssd. Too much to change and doc that know me . make it hard to move back. Even though texas would not help me and la did .still texas feels like home
Nice to meet someone who's in a similar boat. I am 44. I was diagnosed with Cecum cancer August 23 2018. My colon resection surgery was on Sept. 5 2018. they removed 18 inches. I was at a stage 2 T3.
so far all tests indicate my surgery was a success. i also have to follow up with blood work every 3 months for my CEA levels, yearly colonoscopy and CT scans for 3 - 5 years. No chemo was needed.
My cancer was found by fluke. it's important to be your own advocate. I originally had a colonoscopy at age 41. I have a dairy allergy and a few other bizarre food allergies which led to some rectal bleeding. as a result of my first colonoscopy, polyps were found in my cecum. Cancer was found at my 3 year follow up.
I feel very fortunate to have this discovered so early.
i'm still dealing with stress from my 5 month journey to date and the fact that my best friend died from colon cancer shortly after my first colonoscopy. i feel so much better post surgery but recently i've been feeling very tired. I'm writing it off as being new to this whole testing process which i find stressful. As I progress through my follow ups and my CEA levels remain low (it was 0.6 in October, 0.9 as of today) i'm certain my mood will improve and the anxiety will go away.
i just wanted to say 'hi'!
Hi @michelle74, and welcome to Connect.
I’d like to introduce you to @travelgirl who has shared her journey with cecum cancer in many of the discussions in this group. I’m certain she will extend a warm welcome and offer her insights soon.
In the meantime I encourage you to view these videos where Mayo Clinic experts talk screening, prevention, colorectal cancer diagnosis, treatment, and more. https://connect.mayoclinic.org/page/gastroenterology-and-gi-surgery/tab/colorectal-cancer/
I really admire your positive attitude, and am glad that the diagnosis was made early. You’re coping with a tough diagnosis, and I’m sure anxiety and worry must also be why you are feeling tired.
I’m also tagging @diannechildress @martid @ilene1 @soul @brglight @nannytart @bush @sallyg @starrlight @joannem, who’ve written about CEA levels; you can view their messages in this discussion: https://connect.mayoclinic.org/discussion/cea-levels/
I wish you all success, @michelle74 and look forward to hearing back from you – updates, questions, concerns – the Connect community is here, listening.