Has anyone been on Eritux? If so can you tell me about your experience--symtoms, results, how long on it etc? Were you on it alone or with a chemo therapy drug too? Id appreciate it, my Dr. wants me to go on it...Thx, Sue
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Sue I haven't been on that drug but I will check around to see if there is anyone who has... Hang in there Your in my prayers Cheryl
Hi Sue; No I haven't heard of it either but I always find going to GOOGLE will take you to sites where people blog their thoughts on varying drugs. Weezie
Sue: here is a site to go to regarding the drug you were talking about I hope this helps ..If I find any other information I will post it. Good luck Sue, I am always thinking of you in your battle. You are one brave and wonderful gal. Weezie
Sue; Here is another website. Weezie
Hi Sue, I am new to this blog. However, I have read many of the blogs over the past year and I appreciate everyones posts. It really helped me in hard times. My husband has stage 4 colon cancer with mets to the liver diagnosed Oct. 2007. His first chemo treatment was Erbitux, Oxalyplatin and Xeloda for 8 weeks. The plan was for 3-4 months but this regiment worked great on getting rid of the cancer. My husband got a rash (like pimples) all over his face and chest. We got cream from the doctor to control the rash. Some say if you get the rash that it's a good sign. The Erbitux really shrunk his tumor so that he could do surgery sooner. My husband was to take Erbitux again after surgery but was tested for the K ras gene to see if Erbitux would still work but tumor mutated. So the erbitux won't work for us any longer. My husband felt like Erbitux did the most to rid cancer compare to the others. Read about all the side effects but it can really work well. Good Luck!
I have heard of that stuff it comes imclone and costs 30000 thousand dollars a month It is the company that got Martha Stewart in trouble. I understand they have to make a profit but gee wiz if it costs that much most people will never get it, so whats the good?
testing again
I've learned my lesson to sign in. The last time I wrote a novel, I lost the whole thing. Anyway, I took Erbitux w/ the Oxciliplatin and 5FU from Dec to June '08 (6 mos of hell) for my stage 3 c colon cancer diagnosis. I have my 1 yr colonoscopy recheck in a few weeks. Trying not to think about it. I had qualified for a drug study which one 'arm' included the erbitux. Usually it's only covered for metastatic cancers. I was included in the trial because my sigmoid colon tumor fit the bill by 1 cm. Way to go tumor! yay! (ha ha) And so if your Dr says let's start this, I would not say no. Onc. felt it would give me an extra 10-15% boost on my survival rate. WHOO HOO! (but it least it's SOMETHING) Now I'd get the basic steroid and antinausea drug first, then the Erbitux by itself for the 30-40 min (in the beginning, I'd have to wait 1 hr in between...agony to have "more time" to sit at the "cancer center") but then they realized that no one was having an allergic reaction after their 1st dose. I rememeber back (and I did make notes, but one couldn't pay me to revisit that book right now...if not ever) to the evening or 2 after my 1st and 2nd dose and I called my Dr crying because I felt like I had a bad sunburn on my face and lips. The hotness feeling continued, but waxed and waned. The white pimple like spots started to crop up like wildfire on my nose and there was no stopping it. Then my chin, then my cheeks, and all over my face. I tried Clindomycin (sp? which was too drying), Triminacolone cream (beware, steriod cream takes redness away but is like fertilizer to acne), Elidel (studies have shown can cause cancer! ha! and cream seemed to only feel soothing), and then the Derm. gave me something for Rosacia. The rash was localized to my face. I am 35 and never had acne. So that was fun. Now I have blotchy scaring and it's just going away, 4 mos. post chemo. The weirdest part about Erbitux was the curling of the eyelashes, eyebrows looked thicker, and not sure if it was from the chemo knocking out my fertity at the time or from the steroid face cream, but I developed fine hairs on my cheeks. It's gone now. (not really noticable though) My eyelashes are still funky when applying mascara. Most of them would grow super long but straight. My eye dr had to pull some out as they'd start to grow towards my eyes. On one occassion towards the end of chemo, I must have pulled (w/ tweezers) about 15 defunct eyelashes per eye. Strange. I'll check in more often, especially after my colonoscopy. I am rarely on this board (busy w/ 3 little ones) and I must run now! PS--major symptom w/ chemo was and is the neuropathy (fingers, hands, feet, ankles) i wrote in on this a few weeks ago feel free to email me directly if anyone has any questions i also want a t-shirt (especially a SURVIVOR one) any idea on where to find this? thanks melanie
Sue I will ask my Dr. about Eritux right now I am on Taxatere 3 weeks on 1 week off. Good luck with your treatment. Your in my prayers Cheryl
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May 1, 1952 - November 19, 2009

Vital Info


June 27, 2007

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May 1, 1952

November 19, 2009

Cancer Info

Colon and Rectal Cancer

colon cancer

June, 2003

Stage 4


Fluorouracil (5-FU)

How it hurts soooo many people!

I live to the fullest everyday.

Pray for everyone's pain and suffering.

animic--I also have lupus and this was found on a routine blood test. I had no other symtoms. Had I got a colonoscopy one year earlier at age 50, I probably would not have got cancer. Please have a colonoscopy at least by age 50! Earlier if there is a family history or if you have symtoms.

28 days after second surgery. Felt ok until the last week in which I was very tired.


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