Hi,
I am nearly one year post surgery and currently awaiting my first annual CT scan and due a colonoscopy soon. Like most people on here that have or is going these checks my anxiety levels have increased and despite all attempts to keep busy and positive it's always at the back of your mind. I had adjuvant chemotherapy which consisted of several cycles capecitabine. I finished treatment in Nov 24, however within the last fortnight I have been experiencing a number of symptoms similar to when I was having chemotherapy; dry skin, particularly my hands and feet, tingling, pins and needles affecting my feet and hands. I thought I was over these symptoms but noticed they have come back with vengeance in the last 2 weeks, has anyone experienced this and if so what helped or is this something which is permanent? I've mentioned in a previous post my experience of fatigue and brain fog and hope this will pass but I just wanted to know other people's experience?
Hi Carlos80
I’m Anne, one of the Community Champions here on the Online Community and, although I'm not a member of this group, I noticed that your post hadn't had any replies yet. Responding to you will 'bump' it back to the top of the discussion list again.
Wishing you all the best with your upcoming scan and colonoscopy.
PS your anxiety is completely understandable. I had my first follow-up scan in Jan and I was a total wreck. Same thing when I had my second follow-up scan and a colonscopy in April. I now get a 6 month pause but I anticipate the anxiety will return in Oct. It feels like I'm living my life between follow-ups.
Hi, I have my first colonoscopy post op and 3 wks I'm and still no CT scan results. I'm tempted to ring the team but scared at the same time, thinking it's not good news and the colonoscopy will probably confirm my fears. I hate to sound so negative but this time of the year just brings it all back and I don't want to go through it again. I'm back at work but don't feel the same anymore and feel I may have rushed back too soon. Anyway thanks for the reply and advice and I'll definitely be following up the neuropathy symptoms I am currently experiencing
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