Updating about My Lanreotide Injections & CT Scan
As I promised I would after 3 months of lanreotide injections I’m reporting the results of my oncologist’s CT scan with contrast to determine whether the NETs tumor in my liver was still growing. The results showed that after a previous growth rate of 20% for the prior 4 months it now shows to be stable with no growth. I received my 4th injection today and will continue for the remainder of my original 10 month plan.
Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.
@mdmarquardt the octreotide really took my appetite away the first year or so. I'm still not hungry, but at first I really didn't feel like eating at all so I'm betting it's the lanreotide taking away your appetite. Praying for good results on your scan. It's so hard with cancer because every new pain we get, of course our first thought is wondering if the cancer is causing it.
@nana120- I too have been losing weight for about 6mo post surgery, and 5 Lan injections. Then I went stable in weight for a month, and now started gaining lbs. As the NET sites suggest you can eat most foods as long as there are no ' consequences'. I still stay away from aged cheeses( although I love them!), tomatoes, watermelon. And I eat an egg a day plus 1/2 avocado. Some days I have a tablespoon of honey ( raw or manuka) on a toast. I eat tinned sardines 2-3 times a week, and fish ( branzino, cod, flounder). I add protein powder to banana- oatmeal pancakes. I think you can slowly get back to your usual diet, just small portions and eat often. Best! And keep on fighting!🦓💜
The first thing my Dallas NETs specialist told me was that I would not be having pizza or Mexican food for a while & for a Texan that is a tough call. I have come to the realization that after my 4th injection I have reached my “new normal” & as my daughter reminds me as least I have a remainder of my life. Thanks for the encouragement!
Since banana is a “no-no” on my lanreotide list, how are you able to eat them in your pancakes? Also, I cannot have any sweets & I see you have honey. Is that what you eat as syrup on the pancakes? I cannot imagine pancakes without syrup. The rest of your diet I agree with except the sardines (personal preference). Thanks!
Just FYI, my NETs in my liver that is the largest tumor is metastatic from my lung and the oncologist & radiologist hardly pay any attention to the lung NET even though it is considered to be the original source. Sometimes I leave the office visit with more questions than before I went in. Thank goodness for a group like this to share experiences!
@nana120
So they didn’t remove your lung NET? Or had it already metastasized when first discovered?
Yes, it had already metastasized & was only determined to have been the point of origin by the pathology report after a biopsy of the tumor in my liver.
I eat banana pancakes once or 2 times a week ( 1egg, 1/4 cup of oats, vanila, 1 mashed banana). I eat them with blueberries and strawberries. Not big on syrup. I also eat avocado. What I have been really strict and not eat is smoked salmon( which I love!) , aged cheeses, and salami; only occasional sweets( tea bisquits, due to low blood sugar in emergency or a table spoon of honey). I also eat liver ( anaemic)...
I also cheat with occasional piece of dark chocolate.
Hi Nana120
I can relate to you. I am having my 3rd Lanreotide this week. I was on a 4-week spread but lost it 1 week prior, so now I am trying a 3-week spread. Just had a CT scan and waiting to hear if my liver tumors are stable (they also grew 20% in 2 months). It's all so tricky and such a balancing act for each of us. Perhaps the best news is that, due to more sophisticated testing, more people are found with NETs which means more attention given and hopefully a cure.
A huge “YES” to more education for the general public even those in the medical field. I cannot count on both hands the number of people (some even at my local oncologist’s office) that never heard of NETs. When I was first diagnosed I thought it was even more rare than I have come to find out now. We are blessed to be on the cutting edge of new medications even if we are the test cases!