CSN Login
Members Online: 9

Surgery, now Chemo

jsabol's picture
jsabol
Posts: 1156
Joined: Dec 2003

Hi to all. I have just found the courage to look for this site. Had a "baseline" colonoscopy in November at age 53, no symptoms, good overall health. 1 small polyp, positive biopsy, colectomy in December (surgery went very well, good recovery!), with a 1 cm polyp and 1 positive node, hence on to chemo. Chemo starts Friday, with 5 FU and leukovorin. As the day approaches, my usually upbeat attitude is giving way to a lot of nervousness. I am hopeful that this will not be debilitating, but I'm seeing wide variation in personal responses to chemo. I'd appreciate any kind and positive words from chemo recipients. I am hoping to return to my 4 day/wk work schedule in a few weeks and continue to have a life despite 26 wks of chemo. I have an 18 yr old dghtr, 17 yr old son and a very concerned husband. Sure has given me a lot to be thankful for.Thanks in advance for your help, J

aleftina
Posts: 102
Joined: Nov 2003

Judith, the main thing is not be nervous. You are going to have the chemo anyway, so what does it help? Depak Chopra said in his "Soul of heealing" lecture that there was a study done on people who receive chemo, they discovered that the white blood cells go down before the chemo, when the patient starts thinking about it. Your mind is a partner in this fight, use it wisely.

I started with 1,000 5FU, but after couple of weeks had to go down to 800, as I continued working. Looking bad it wasn't so bad, I took campazine for nausea, I was noxious for couple of days, that's all. Though everyone reacts differently, there is a lot of things you can do to help yourself. Make sure you communicate with your onc really well, he can help a lot too. Good luck with it, if you are religeous, I will pray for you. Please visit here and let us know how you are doing. Tina

KrisS
Posts: 232
Joined: Apr 2003

Judith- as Monika and Tina have said, everyone is an individual, but for me, chemo with 5-FU/CPT 11 was not bad, with the exception of diarrhea due to CPT 11 (but I worked anyway, with slightly reduced hours).

I had 5-FU Leukovorin along with oxaliplatin and managed to pretty well work through all of that too.

The 5-FU (as well as the Xeloda which I am now on) makes my hands a bit red and sore for a few days, and I get a bit tired.

There are a number of antinausea medications that are available to try if that becomes a problem. If one doesn't work or makes you tired etc. they can try others. It is important to communicate with your oncologist and the nurses. As Tina has said, they can help a lot.

I am glad to hear your surgery went smoothly... I am sure you were nervous about that too. Keep a positive attitude and you will get through this too.

Best wishes,

Kris

StacyGleaso's picture
StacyGleaso
Posts: 1246
Joined: Mar 2003

Hi Judith!

As a veteran in this arena, I can give you a few pointers. First of all, drink tons of water before and after your treatment. If you don't have a port-a-cath, you might want to look into it. I did, and it was really a blessing. I was a stage 4 patient, and today a stage 4 survivor. My chemo gave me absolutely no side effects. I got my treatment on Tuesdays, and was at work Wednesday morning on time. My kids were little when all of mine took place 2 yrs ago...they were my motivation. I was 33 at the time. Make it a situation of mind over matter. If you tell yourself that you'll be sick, you'll talk yourself into it. For some reason peanut butter was one thing I remember eating afterwards which was just the trick to combat nausea. You can also ask for campozine which is a prescription for nausea. I got my prescription filled, but never took a pill.

Ok, now here's the pep talk:

You can get through this. Failure is NOT an option. Too many people depend on you, and your job is to be here for your kids. The diagnosis and treatment is not the end of the world. Unfortunately, you are just a tough cookie who God feels can handle a whole bunch of obstacles. So be brave, and work on staying positive.

Did that help? Please let me know if I can help in any way.

Keep us posted,

Stacy

nanuk's picture
nanuk
Posts: 1363
Joined: Dec 2003

Judiths: Remember that the only disability in life is a bad attitude. I was a bad patient during my adjuvant therapy, but the attitude improved because of the attitude of my wonderful friends who became my family during that difficult time, and refused to let me do it alone. You are fortunate to have your family; let them support you. Best wishes, Bud

nanuk's picture
nanuk
Posts: 1363
Joined: Dec 2003

Recommended reading (although dissimilar cancer) "It's Not The Bike" by Lance Armstrong - the true story of his battle with cancer.

2bhealed's picture
2bhealed
Posts: 2084
Joined: Dec 2001

Just finished EVERY SECOND COUNTS...his second book....last night. After you put yourself into the 'survivor' catagory read that too. Life after cancer is a new experience requiring life adjustments as well for some of us.

peace, emily

goldfinch's picture
goldfinch
Posts: 737
Joined: Oct 2003

Hi Judith. I was diagnosed with rectal ca in Aug (47 year old female). Went through chemo (5fu) and radiation together. That was difficult-severe diarrhea. Oncologist blamed radiation, radiation oncologist blamed chemo. I'm sure it was the combo. I had surgery for removal of the rectum and now have chemo to look forward to til Sept (1 time per week for 6 weeks, then 2 weeks off. do that 6 times). I've had 2 treatments so far and haven't had any problems except a little diarrhea. I have a temporary ileostomy though and it's hard to tell if the diarrhea is relatied to the chemo or the ileostomy since i was having some difficulty with that anyway.
I agree with all those who say that attitude is important. I choose to believe that chemo is saving my life, so i will put up with whatever effects it brings.
Regarding working. I can't answer that yet as i've been out because of the surgery. i return Jan 5 and, as of now, don't anticipate any problems as my energy seems to be back to normal (despite chemo).
Every one's response is different. Here's hoping things go smoothly for you, but if you have problems, believe you can deal with them.
Good luck! Keep thinking positive thoughts!
Mary

spongebob's picture
spongebob
Posts: 2600
Joined: Apr 2003

Ahoy, judiths -

Lots of great advice here from folks who have been there, done that, and gotten their commemorative tee-shirts. One thing I didn't see anyone mention was to be sure to drink something cold or suck ice chips as they push the chemo bolus - it will help reduce the incidence of mouth sores that often accompany 5FU/Leucovorin treatments.

No reason to fear the chemo. It's there to help you get better. I am an active duty military person. I worked a 60 hour work week during my chemo, plus I was going through a nasty divorce and had to get a part-time job to make ends meet. This isn't to say that I didn't get really tired or that I didn't have side-effects, you may or may not have the same experience, what I am saying is that many people continue working and dealing with the life-bumps along the way. You will get through this and there are a bunch of people here who will be happy to lend you a hand as you make your journey.

Do it for your family. Do it for yourself. Remember this: your attitude is the most potent weapon you have in your cancer-fighting arsenal.

Be well

- SpongeBob

pattieb
Posts: 176
Joined: Mar 2003

Hi Judiths
Like evryone has said we all react to it differntly, I had no problems to speak of didn't even lose my hair, was just tired and had some nausea that I controlled with a rx, I am getting ready to go through another round of treatments and don't know what to expect but I will get through it. I did return to work during my treatments and other than being tired did ok.
keep postive.
Pattie

mrslacsr's picture
mrslacsr
Posts: 30
Joined: Apr 2002

I know that it has been a year but I was wondering how you were doing this holiday season? I had an ileostomy in January 02; still doing follow-ups every three months. Write back and let me know. I don't get many send backs. Have a good holiday. Michele

Subscribe with RSS
About Cancer Society

The content on this site is for informational purposes only. It is not a substitute for professional medical advice. Do not use this information to diagnose or treat a health problem or disease without consulting with a qualified healthcare provider. Please consult your healthcare provider with any questions or concerns you may have regarding your condition. Use of this online service is subject to the disclaimer and the terms and conditions.

Copyright 2000-2014 © Cancer Survivors Network