Diagnosed with aggressive NET. Happy to see this group!

Posted by Justin B @somefan, Aug 3, 2017

I was diagnosed in May with aggressive NET, which started in the colon and had already spread to the liver with a 6 inch tumor. I started in the ER at Rush University Hospital in Chicago where I received my first infusions inpatient, but have since moved to Northwestern, which is the best in Illinois. As soon as I switched, I was given the sandotatin injection along with daily dexamethasone. Between those two my quality of life has really improved. I know many say that chemo is worthless with this cancer but both oncologists I have had insist it be given a shot with how large my tumor was, and I certainly haven't done any oncology residencies myself to argue.

My legs are like Jello most days and I'm fairly certain it's caused by the chemo (as leg weakness is an occasional side effect of carboplatum (and it gets a little worse after each set of infusions). I've noticed ankle swelling for the first time tonight (though am not feeling any cardio/breathing issues and I have been on my feet most of the day) and I'm fighting chronic diarrhea. However I actually feel really good--far better than before I was diagnosed, unquestionably! I've continued my MBA through all of this and will graduate in December, and still work pretty normally with the exception of my infusion week.

I would certainly go to Mayo if they were closer but I can't justify it at the moment. I have a couple more rounds of chemo in the original treatment plan and if I feel I'm getting nowhere at that point I'll probably consider it but I really do love my treatment team and feel they are giving me loads of attention and help. I have a lot of confidence in them.

I've learned from this experience that attitude is everything, and really do value each relationship (work, spouse, friends) so much more now. I'm far more aware of the responses I give daily in reaction to petty nonsense. My perception of what matters has changed, for the better!

Anyway, I just wanted to introduce myself. I don't know how long I have left on this earth but I was delighted to read about many of your experiences and it has given me what I needed most; hope! Thank you! There's so much old information out there online that gives me an abysmal chance at three years so I already love this group! I'm not so worried about when I will pass on; but it's really great to to see that it might not be over just yet! 🙂

Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.

@mollie59

Welcome
I too am a new to NETS, just being diagnosed in late May. My Carcinoid cancer attacked my heart so I am preparing for open heart surgery in 3 weeks to replace 2 valves. I had my injections of Sandostatin last Thursday and am feeling much better now. My liver is full also.
I bought the book "But You Look So Good" as well. The beginning is very informative and resourceful, the personal stories reinforce the importance to stay focused, and how staying positive is the name of the game. We all have doubtful days, but we do need to learn to quickly shake it off and find our smiles.
Best of luck to you, stay strong, ask questions, and find a doctor you really trust.
@mollie59

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Mollie59,

I have a friend who had open-heart surgery last year and it was amazing to see just how fast she recuperated and went back to work in less than 6 weeks. I'm hopeful that you will have a similar outcome and it is comforting knowing that you will be in the hands of the Mayo Clinic.

I'm just short of nine years living with carcinoid and I also have a liver this is full of mets. I'm also living with heart disease (unrelated to carcinoid) and I'm praying that the injections will continue to keep the carcinoid at bay.

I agree with you about the doubtful days and shaking it off, staying positive and resourceful. I often tell people, “I may have cancer, but cancer does not have me.” I refuse to give cancer the power to control my outlook on life.

I have put your surgery date on my calendar and will send positive energy and thoughts your way. I'm confident that all will go well and that the treatment your doctors have in store for you will greatly improve your quality of life.

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@mollie59

Welcome
I too am a new to NETS, just being diagnosed in late May. My Carcinoid cancer attacked my heart so I am preparing for open heart surgery in 3 weeks to replace 2 valves. I had my injections of Sandostatin last Thursday and am feeling much better now. My liver is full also.
I bought the book "But You Look So Good" as well. The beginning is very informative and resourceful, the personal stories reinforce the importance to stay focused, and how staying positive is the name of the game. We all have doubtful days, but we do need to learn to quickly shake it off and find our smiles.
Best of luck to you, stay strong, ask questions, and find a doctor you really trust.
@mollie59

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Thanks for all your encouraging words, they come at a good time. I will keep you in my prayers, as I do for all Carcinoid patients

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I am so glad you have found hope in our group as I believe I see it in so many of the patients I read about and with on this site. I completed my MBA about 25 years ago and could not imagine trying to get my brain to function at that level while dealing with your current circumstance; I am awed. Very happy you have found us, I pray we continue to show you hope, and best of luck on your MBA completion, but I don't think you need any luck!

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Hello Justin @somefan

How are you feeling? When we last heard from you, you were having some vision problems and you weren't sure if they were related to your infusions.

Do you have any answers for that problem, yet? We would enjoy hearing from you as you have time.

Teresa

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