If you said no, what did they not understand? No should mean no.
I’m glad it worked out for you.
I had pancreas cancer in 2019 and had Whipples and 6 months chemo. I had Neulasta with nil adverse reaction it just felt like old age in my hips for 1 day ( I was 55)
Never had issues with wcc, neutrophils or platelets.
However cancer metastasised to my lung in June this year. Chemo is knocking my bone marrow around so my wcc and neutrophils have been low, one drug stopped but levels still low.
Oncologist says I can’t have Neulasta as my regime is weekly. Even if they reduce it to fortnightly apparently that’s too soon .
The accumulative effects of chemo are toxic in on healthy, well people who have no symptoms.
I want to have it and can’t and I hate the thought that chemo may have to stop because of this.
So don’t be scared by the fear of side effects if it’s going to assist your body to cope with the effects of chemo . You need to Wright up risks and benefits and discuss with your Dr. Good luck everyone x
Neulasta is OVER used!! My cancer situation is almost identical to hers! Same age, same chemo treatment, same diagnosis. First dose Neulasta no problem! 2nd dose raised my wbc counts through the roof! Horrible side effects it felt like 3rd degree sunburn on my face,head,neck,back and both forearms! This lasted a week! Theres no antidote for it! Benadryl and Tylenol! I didn’t need the second dose according to my blood work but Dr insisted! Theres no doubt in my mind the reason I had those side effects was because of a too HIGH neutrophil/wbc count!! Third round chemo I had to refuse it otherwise they were going to give it to me again! Let me tell you I feel so much better skipping it this time! IF our blood work is good WHY are they insisting we take these poison shots!! Btw Neulasta is made with/from e-coli! Look it up! Its a money maker plain and simple!!
I was found to have fallopian tube cancer, stage 1C3. I did read your article and due to the awful bone pain, at the last 6th treatment decided I’d had enough. I’m 74, my blood cell levels were good. I did not take neulasta. My oncologist said it was ok. So far, so good. My weight ballooned to 150.4 Saturday after treatment on Thursday, and today, 5 days later, my weight is 142.8, all fluid retention. I’m done with the chemo. I want to get back to living.
I hate the effects of Neulasta and have suffered them each of 4 times so far that I’ve had chemo infusion. I have 2 more to go, and I am strongly thinking of refusing it. I am over 65 but have no “health conditions” other than the stage 2 ovarian cancer I’m being treated for.
I did have a debate with the Onc nurse wanting to give me Neulasta on the third infusion. My WBC was high before the second infusion at 19, when 10 is top normal. Then just before the 3rd infusion it was 30.8 which is 3times high normal and several other measures were out of range as well. Also kidney function measures were off. Finally she said she would consult with my Onc doc who is very hard to reach. Onc Doc agreed with me and we are skipping the Neulasta on this 3rd round. I am 74 so I fit the criteria for the drug. We will see what the WBC drops to before the 4th round. I already have an enlarged spleen so WBC spikes might not be a good thing.
Mine gave every patient neulast without asking us first.
I had severe side effects within 5 minutes of the injection going into my bidy, mine was the on- body injection.For 2r hours, I had no issues with my chemo drugs..My oncologist told me it was NOT the neulastam but I know it was..I still have adema and bone pain which I never had until my breast cancer treatments.
I vomited up black blood 68 hours after the neulasta…that stuff would have killed me…
They charged me over $11,000.00 for the drug, I owed over 3,000.00 after Medicare paid…I am still paying it out.
I was not offered any kind of co pay card…and on tv they offer a 5.00 co pay card..
I don’t recommend anyone getting the Neulasta drug.
I felt the same as you! I told my Dr I wasn’t taking it anymore! They said well it may prolong you treatment. I said I don’t care!
This was the worst product for. I had such severe bone pain, I couldn’t walk. Had to go to ER 4 hours of morphine just took the edge off. 9 days to get through my system. Some bone pain is what they say, but know it can vary from person to person just know this going in! Dr poo-pooped
Any of the information I would have wanted before using this product. If it works well for you, then that is fantastic!
I am a cancer patient and big advocate of talking with your doctors and driving your treatment. One note on Neulasta, it can increase lymphocytes and even T-cells which may dramatically increase the immune response and the ability of your immune system to fight cancer and prevent recurrence. I want it when I start chemo again soon.
Thank you. I was given Neulasta after I said no to it. It has made me so weak and caused severe bone pain, headaches, feeling ill, shortness of breath, and that someone stole my body and made me frail. I feel Taxol will continue to cause this as I still have not recovered after 4 weeks.
Question for for Amy and Christina. Same horrible reaction to Neulasta. I am 50, healthy prior to diagnosis. Did your Dr. let you stop Neulasta? Amy, thank you for the article. I am going to give it a shot of talking to DR. I was walking 2-4 miles a day on non chemo days and then Neulasta I couldn’t walk at at all for 5 and the pain was not touchable by any meds.
Thank you so much for this info, the shot I have taken for my third time has made me super sick! I’ve been saying that since day one of chemo. I can’t walk or function and think I’m allergic to it. I have every side affect that is shows, it’s very scary!! Reading your post, has made it where I will be talking with my doctor to discontinue the shot. Thank you again for the info. It has made me aware to be more on top of my medical.
Hey Amy: I’m so glad this motivated you to think about your choices in your treatment and to stimulate conversations with your treatment team. This is how you take back power over your health!
Such a great article and information – THANK YOU! I have nearly the same diagnosis and am currently on a similar treatment plan (I take the Taxol every other week). I had bone pain for about a day and a half after treatment #3 of the A&C but not with the other treatments. I had severe bone pain after my first treatment of Taxol which was my 5th treatment altogether. It was incredibly painful and lasted for 3 days. Advil or Tylenol didn’t affect it or if they did, I sure didn’t notice. I really feel like it’s the Nuelasta that caused it so I asked my Nurse Practitioner if I could forgo it for my 6th treatment. I’m 49 and, aside from cancer, am healthy and fit. My blood counts have been good each time so she allowed me to forgo it. I’ll get my blood tested a week before my next treatment and if my counts are low they’ll give me a fast-acting shot that should get my counts up again in enough time for my next treatment. I’m hopeful I’ll be able to avoid taking anymore of the Nuelasta. And yes, it is CRAZY expensive. They charge my insurance $11,000 each time although I believe my insurance only pays up to $4,900 which is still an exorbitant amount for a preventative drug. Thank you again for posting – I’m sure there are many out there that may be suffering unnecessarily and hopefully this will help them as well.