Diet restrictions with Lanreotide?
I had my first Lanreotide injection four days ago on Monday, but was not told of any diet restrictions. I've seen that I should eat lean protein and lots of vegetables, but I read in the past that I need to stay on a low fiber (not many veggies) diet to reduce diarrhea due to the tumors in my cecum and small intestines. Now that I'm on Lanreotide, am I allowed to have veggies, my favorite foods in the world??? Will the Lanreotide keep me from having diarrhea if I do eat cruciferous veggies? I've never eaten much meat, and I'm really having a hard time eating the low fiber diet, that I feel is not a healthy diet! I haven't had any side effects from the injection other than a horrific headache about 4 hours afterward that lasted about 5 hours. Then another headache on the second day that lasted a couple of hours.
I chose not to have any surgery. I have NETs in my cecum, small intestine, lymph nodes, liver and heart. Lanreotide stopped my diarrhea the first day of treatment, and I am so darn happy about that!
Anyway, I would love to hear what diet y'all are following while on the Lanreotide! Best of luck to you all...my prayers are with you!
Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.
"My question is simply, would not eating these foods if I am not having problems change my prognosis at all."
Based on my experience as a NET patient and having talked to no less than 10 surgical and medical oncologists over the course of this journey, I don't think so. My Surgeon said " eat what you want to". That's what I do. Your diet just sounded strict to me, but it may have been your diet without a NET diagnosis anyway? Information and recommendations surrounding this cancer is always changing though. When I read recommendations, I always look for a date on that information.
On the subject of the drug Lanreotide and your diet, I found it to really help me digest food before NETs small bowel surgery (I had 3 constrictions) . I continue to believe that I benefit from it in that regard today. I currently do not have any problems. It sounds like your current diet is working well for you. That's what counts.
Dougt - There is a good website you might checked out http://www.netrf.org (Neuroendocrine Tumor Research Foundation) that has a link - Nutrition & NETS that might be very helpful for you.
It's not so much about food and the Lanriotide, but foods and your body - particularly if you've had intestional surgery. Your system just cannot digest and process foods like it used to. Vegetables with skins on are harder to digest, and some (brocoli for example) can cause more gas).
I was diagnosed with Stage 4 neuroendocrine cancer in March, 2018 when I had a blockage in my small intestine that was a neuroendocrine (carcinoid) tumor. They removed 10". This was after eleven years of misdiagnosis. In July, 2019 I had another blockage in my large intestine and lost 11". So I've lost 21" total. So I certainly can't eat like I used to.
There are several other sites that also have information about eating/nutrition while dealing with this cancer. LACNETS.org is a great source of helpful information.
I hope this is helpful.
Some diet restrictions are because the Nets have caused a possibility of bowel obstruction so raw veg is avoided for these people
Phyllisden, thank you for the information. At this time, I will continue with no diet restrictions as I don't seem to have any symptoms of blockage or carcinoid syndrome.
My situation is similar to yours. After 15+ years of being told my digestive issues were all in my head or related to "micro-colitis" or IBS, I landed in the hospital to have a blockage removed along with 16 lymph nodes and approximately 34-inch of small and large bowel combined. Spent over 30-days in hospital and an additional 2-weeks in rehab. That was 8 years ago this month. Until a year ago, things seemed to be going well and then I was diagnosed with stage 4 carcinoid with tumors on liver, pancreas, mesentery, and bone. My diet has slowly returned to what it used to be. However, I no longer consume alcohol or spicy foods.
Have any experience symptoms of loss of taste food taste better
I am taking the lanreotide injection every month
Hi, I have been on lanrwotidw over 4 years. I started with a banana sized net tumor in my ascending colon with mets to my liver stage 4. Carainoid syndrome as well.
Surgery left me with some left in my liver. 4 yrs later I am going for alblative surgery for 1 spots growth.
I follow a healthy diet. I find the info contradicts itself so I eat what I know is good that doesn't cause stomach issues. ( no alcohol, fried, processed etc)
I have my shot every 3 weeks.
I'm tired, workouts are hard but I persevere with free weights, indoor bike (10-15 min) and the new vibration plate . All keeps me from being completely out of shape. I do small bits daily.
I'm a cpap user.
I am fighting and finding it difficult with meds to control my diabetes, which I did t have prior. Appreciate any thoughts?
Positive attitude ,for me is everything.
I agree, having a positive attitude & outlook on life is key! I try to live every day like it’s my last, some days energy is low, but I keep forging ahead. I am retired & keep myself busy in my greenhouse. It’s a very uplifting atmosphere that keeps my mind off of NETS.
Good luck to you!
I have been on lanreotide for more than a year. I have no dietary restrictions. My symptoms, like diarrhoea, come and go. I experienced sporadic bloating, though, which lasted for two weeks.