JL2Party
Well-Known Member
- Joined
- Mar 9, 2013
- Messages
- 47
- Reaction score
- 14
Prayers for you and your family.
Can WE as a group do something for John and his family. I cannot imagine my wife and her needs if I were in his situation.
If anyone has any ideas, please put them up here.
Hey everyone. I'm home now and resting. Words cannot express how much I'm touched by all of the kind words you all have posted. I will be updating the thread when I'm feeling a little better and ill give more detail at that time. Thanks again so much. You guys rock.
John we have never met, but if you need any help around the house or something like that I'm just a phone call away. I live in Waddell now but used to live in Peoria so it won't be an issue to stop over.
Tracy
623-256-5776
John stay tough. You will beat this.
I noticed you said the surgeon was a she. I wonder if it is Adrienne Forstner? If so you are in great hands. I was actually going to recommend her to you but since your operation was scheduled I did not.
My father has beaten Cancer twice. He is in remission now with a very rare form of Lympothia. Continue to be proactive. Don't be shy about asking for options, studies and investigate Centers of excellence.
If there is anything I can do for you please do not hesitate to ask.
Take care of yourself. Prayers sent.
Well, today will be one week since I woke up from my TME surgery. When I awoke and realized that only 2 hours had gone by. I was confused. It was supposed to be a 4 hour surgery. I reached down and felt that there were bandages on my abdomen but no ostomy port/bag. Even more confusing. A few minutes later my wife walked in and she looked worried. She said the surgeon needs to talk to us but we would have to wait 30 minutes or so. I knew something was very wrong. I asked her to tell me now because I could not wait. She was hesitant but after I repeatedly asked her, she told me the worst news of my life--the surgeon found that my rectal cancer has spread to my peritoneum.
The peritoneum is the interior lining of the abdominal cavity. This is the chamber that the stomach, intestines, liver, and other organs reside in. Peritoneal cancer is very rare and can be primary or secondary. In my case, it is the secondary variety as the cancer was confirmed to match the original rectal tumor site pathology. After the surgeon came in she explained that they had found about 15-20 breadcrumb size clusters of cancer cells on my peritoneum. They are much too small to show on any scans, PET, CT, MRI, etc. In fact, had the surgery not been laparoscopically performed, they would likely have gone unnoticed. The magnification of the laparoscope camera was able to view these much easier than the naked eye. My surgeon is one of the few in the world that is qualified to do a TME surgery laparoscopically so I am grateful for her finding this. But the discovery leaves me facing a stage 4 cancer battle now. Stage 4 is hard to beat. I am not sure what lies ahead but i know it will be rough. I meet with the oncologist this week to discuss my options.
In the mean time, I'm healing well from the surgery. Basically what happened was the surgeon found the cancer, halted the operation and consulted the oncology docs while I was on the table. They mutually agreed that I need to have more chemo before doing the TME procedure. Had the TME been completed they would not be able to treat the spreading cancer for several weeks due to the healing process. While she was in there she scoped all the visible organs and found that there has been no vital organ spreading so that is some good news. However, it is very close to these organs which is scary.
The last 5 months have been a roller coaster of lows and highs. I shook off the initial fear and depression pretty quick when the prognosis looked good and the cancer was initially staged at a 2-3. Now, at a confirmed stage 4, it is a nightmare I wake up from every morning and wish it were just a bad dream. I have to admit that for the first time since I started battling this I am really starting to contemplate my own death, what will become of my family if I'm gone, and what they will have to go though. It is a rough spot to be in. I'm replaying my life choices and wishing I could turn back time and do a lot of things differently, including living healthier and buying better life insurance.
Anyway, I know this is a very depressing post and I don't want to weigh the board down in such depressing thoughts. After all, RDP is a place to come to escape and have fun. I just wanted to update everyone on my situation and sincerely thank all of you for your support, prayers, and offers to help out.
John
Waldenstom's?
Waldenstom's?
Adrienne Forstner-Barthell
Started my IV chemo yesterday. This shit is nasty compared to the pill form I took with my radiation in June/July. It was a 7 hour day in the hospital yesterday and 46 hours on the take-home pump (wearing a fanny pack deal until tomorrow). I was in the hospital 8 hours Tuesday having a port installed in my chest/jugular vein--weird shit. Anyway, I feel a little better today than last night and I'm hoping the feeling shitty part does not get much worse. I have 8 treatments 2-weeks apart, 1 down, 7 to go. After that it is more scans and maybe another lap surgery to check it out before making the next move.
After meeting the onc doc last week with the wife I have been in a bit of shock. The wife cried for 2 days. The docs tell me if I don't treat I have a year to live. With treatments (chemo for life) I have 20% chance to make it 5 years. My first thoughts are no way I want to live my last 5 years on chemo feeling like shit and suffering. I was super depressed for a week. Now I'm getting back into fighter mode and digging deep into my soul and calling on God. I have decided to fight and explore some alternative treatments after the 4 months of chemo is done. I am going to prove the docs wrong. I have no choice. Thanks for all of your support, especially the stories about beating the odds. Dave, I will be calling you about the Mexico place. I am pretty sure I know the place but would love to get more details.
Thanks again everyone.:thumbsup