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Patients Neuroendocrine tumor
How are your NETs being treated?
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Courtney_J
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Courtney_J
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Last activity on 08/08/2022 at 11:09 AM
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1,340 comments posted | 5 in the Neuroendocrine tumor Forum
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Hello Michel, thank you for opening this discussion. That's great that you've started to see some improvement with the lanreotide! Let me tag some other members who can possibly share with you.
Hi everyone, how are you today?
As you know, treatment options for neuroendocrine tumors tend to vary and range from surgery, cancer treatments like radiation and chemotherapy, to targeted drug therapy and more.
What treatments have you undergone for your neuroendocrine tumors? Have they been effective?
@Dh3510 @TerriEngels @mauidennis @JENN723 @Beckybarsness @Joonbug @Kurlee @Virginian @kathleenwis @Bhnt1109 @Vlinan6971 @BarbaraH @Shyro73 @Robmac @Hitch55 @RBO0813 @Cmloretto @Cats22 @sgyle1
Feel free to share with us here!
Take care,
Courtney
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Courtney_J, Community Manager, Carenity US
micheldequevedo
micheldequevedo
Last activity on 02/06/2023 at 4:47 PM
Joined in 2021
4 comments posted | 3 in the Neuroendocrine tumor Forum
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Hello again,
Quick update, I am going for surgery tomorrow morning ( December 14th, 2021 ) Getting a bowel resection and debulking as much as possible, my doctor says they are hoping to be able to remove 70% to 90% of the disease. I wont be Cancer free but I like those numbers!
I'll post another update whenever I can.
mauidennis
mauidennis
Last activity on 01/16/2024 at 6:11 AM
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1 comment posted | 1 in the Neuroendocrine tumor Forum
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I am a 71 year old male, I have known about my cancer since the begining of the pandemic, I have carcinoid syndrome of the liver, my liver is now about two or three times the size it was. I had two tumors, the largest was 11.5 cm x 9 cm, the smaller one 3cm. I had the two tumors embolized. The large tumor was very painful, thank goodness for drugs! Then I learned I had many small tumors, so many you could not count them .I started with Everolimus (afinitor)then later with oxterotide LAR, both do a great job of eliminating the side effects of NETs, the Octeotide perhaps a tiny bit better. But they do not stop the tumors. There are studies where they are used together, I have not tried that due to cost and my age. Which say that with one you get 16 months average, l think, with both 27 months. The only one that actually kills the Nets is a procedure called PRRT, where radioactive particles are injected into you and attach to the samosatin positive tumours, the rest are just peed out. It is effective as I had a friend who died a bit ago ( he lived for over 15 years since his cancer was discovered) and he did PRRT. The cost of PRRT is a lot so you need to get on a study or you have a good insurance company. Hope this helps.
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Dennis foster
Laurell410
Laurell410
Last activity on 07/31/2024 at 2:59 AM
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4 comments posted | 1 in the Neuroendocrine tumor Forum
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I receive 20mg injections of octreotide every 28days.
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Laurell Watson
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DCline3dogs
I completely understand as I don’t have anyone to talk to also. I’m a widow & I live alone. My oldest son died in 2021 & my youngest son & his family live 3 hours. My father is dead & my mother has chronic back pain & is immobile. My younger sister lives with our mother & she is going through a divorce from her husband who abandoned her. My sister doesn’t visit me, help me, call me & rarely texts me. I have various cousins, a niece & nephew that are spread out in nearby states but are hours away from me. After I told my friends I had cancer, they quit contacting me. I have learned how to be my own care giver. It has been very difficult. I’ll admit I’ve been depressed, cried a lot, felt sorry for myself but I never gave up. I prayed & read my Bible everyday. Then I found cancer groups online like this one where I could share what I was going through & got empathetic responses. That really kept me going. I hope you find someone to talk to but I highly recommend the online cancer chat groups.
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DCline3dogs
I completely understand as I don’t have anyone to talk to also. I’m a widow & I live alone. My oldest son died in 2021 & my youngest son & his family live 3 hours. My father is dead & my mother has chronic back pain & is immobile. My younger sister lives with our mother & she is going through a divorce from her husband who abandoned her. My sister doesn’t visit me, help me, call me & rarely texts me. I have various cousins, a niece & nephew that are spread out in nearby states but are hours away from me. After I told my friends I had cancer, they quit contacting me. I have learned how to be my own care giver. It has been very difficult. I’ll admit I’ve been depressed, cried a lot, felt sorry for myself but I never gave up. I prayed & read my Bible everyday. Then I found cancer groups online like this one where I could share what I was going through & got empathetic responses. That really kept me going. I hope you find someone to talk to but I highly recommend the online cancer chat groups.
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micheldequevedo
micheldequevedo
Last activity on 02/06/2023 at 4:47 PM
Joined in 2021
4 comments posted | 3 in the Neuroendocrine tumor Forum
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Hello,
The purpose of this discussion is to learn about different treatment options Neuroendocrine Cancer patients have.
I have stage IV, GI Neuroendocrine Cancer. I have several grade 1 tumors ( 2 of them over 4 cms!) in my omentum, small bowel, appendix, liver and right lung.
I am been treated with Lanreotide injections, 120mg, every 28 days and, so far, it has reduced my carcinoid syndrome symptoms drastically. I’m too early into my treatment to show any other progress (I was diagnosed just 2 months ago) and I am still waiting to get a Dotatate Scan to determine if any of the tumors can be surgically removed or recessed, as well is other treatment options.
I’ve read about different treatment options, both conventional and alternative, and I am wondering if you will be willing to share your experiences so to help new patients like me learn about the different options we have.
Thank you.
Michel.