The Cancer Survivors Network (CSN) is a peer support community for cancer patients, survivors, caregivers, families, and friends! CSN is a safe place to connect with others who share your interests and experiences.
15 years later - still going strong!
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I love hearing good news!
I like to think I'm am optimistic person, but once in a while I have a morning when I wake up and wonder if I'm going to make it through this cancer thing. I'm a stage 4, and whenever I hear about one of you who has made it 7, 10, 15 or more years, I really believe that I can too. Believing makes a huge difference!
THANK YOU for sharing your milestones. They mean more than you know.
Thomas
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Sorry to see noone respondedEissetB said:It so nice and uplifting to
It so nice and uplifting to read your story. I have stage 3 also, two massive tumors were removed so then I had to have the resection, and be on 12 sessions of FOLFOX for 6 months. I will have the 3rd session on May 12. Been in so much pain every time I have the pump going. Then I am now freaking out because of my hair thinning...I am so scared!! I still have 5 more months to go to complete the chemo treatment. Can you tell me what to expect while on this therapy?? A head's up is appreciated. God bless you.
Sorry to see noone responded to your questions. I didn't have any surgeries, so do not have the same experience as you. I have heard the surgery is really hard to recover from. The infusions are terrible on their own, so can only imagine how hard it was for you with the surgery too.
Your post was 6 weeks ago, so I hope you are doing better as time goes on.
I was diagnosed at stage 4 February 2016 and was only had 8 infusions with Oxaliplatin, Leucovorin, and Avastin, then the 5Fu pump for 2 days. I started losing hair after about a month on the chemo, and as it kept thinning, new hair started growing in at the scalp after the Oxaliplatin stopped - That was in July 2016 I went on maintainence chemo consisiting of Avastin infusions every 3 weeks and 5 Xeloda tablets for 14 days on and 7 off.
You may have already gotten your answer in another post, but if not you can also repost or send private messages to others with similar diagnosis and/or treatment plans.
Joan
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