After a sense of hopelessness and anxiety that life was never going to be the same again on Monday, I now feel a whole lot better.
The pain I experienced while going to the toilet and afterwards has either improved significantly or the Morphine, Codeine and Paracetamol is doing an even better job at managing it. Maybe it is a combination of both.
I definitely made a mistake at trying to come off all three meds in one go, I’d say cold turkey but as a vegan, maybe I should say, cold Tofu.
Reading everyone’s responses to my feelings of despair and anxiety really helped me. It enabled me to put everything into perspective and also reflect on how I was caring for myself.
I have had two normal days. Wednesday this week was the first time I actually got up, showered, dressed and went out for a gentle afternoon dog walk, meander round the shops and ended the day with chips, mushy peas and bread. Small things are such luxuries.
Today (Thursday) I am more tired and I have been for an afternoon nap but I am still dressed and feeling better.
I now also have a date for my first follow up appointment since finishing to chemoradiation. This means that on the 11th March I will know what the next steps will be regarding tests, scans etc.
The only fly in the ointment is that on the 19th March I am having surgery to remove a cancerous lesion from my arm. The referring Nurse Practitioner told me that she thought the chemotherapy may have irritated the mole and caused the change. I don’t know how true that might be but it is certainly something I could do without right now.
So ten steps forward and four steps back. It could be worse I could be just about to start treatment.
Thank you everyone for your kindness and support.
xx
Hello LCraig
I am so pleased to hear you are feeling more positive and well done for getting out and about. And there is nothing wrong with having resting days (lots if you need them), you are so early in your recovery.
I can imagine how you feel about the lesion on your arm, I will be thinking about you, so please let us know how you get on. Yes, you could really do without this, life just throws things at us sometimes.
Big hug
Irene xx
Hi Irene,
Thank you, I really appreciate your kind comments and thoughts for the 19th. I will be glad to get it all over and done with.
I really hope all is well with you.
Xx
Hi Bungle1 ,
Thank you so much.
I think you are absolutely right about taking it one day at a time and self care. I do not want to feel disappointed if I wake up one morning feeling washed out again but rather see any ups and downs as just being all part of the process of healing.
I know that last weekend I was frightened that this was my lot in life. This week I am hopeful and positive.
I hope all is well with you.
xx
.
Hi LCraig,
So good to hear that you’re starting to turn the corner. Those very early days are so difficult and I’m not at all surprised you were feeling a sense of despair.
It’s still early days for you and probably wise to continue using the pain medication while you’re still suffering. While it was brave to stop your body was telling you otherwise.
Great that you have had some moments and hours of almost normality and I can remember how wonderful that feels. There will be good and bad days but hopefully now the good bits will get longer and you will start regaining your sense of self rather than feeling defined by the AC.
Best of luck for the 11th and for the 19th although I’m sorry you have this additional challenge. Last thing you need.
Keep being kind to yourself x
Hi LCraig ,
It’s great to hear that things are improving & that you’re in a more positive headspace. Over time you’ll find you have more good days & the gaps between the rest days will grow. Having said that don’t rush it just let it happen, you’ll soon be back to being able to do what you want when you want to without considering the fatigue. Not too long to wait for that first appointment.
I’m sorry you’re having to go through the surgery on your arm though, it’s an added worry you don’t need right now isn’t it? I had to have 2 lesions removed from my back shortly after I’d finished my treatment thankfully they turned out to be Basel Cell Carcinomas & were easily dealt with, another lady I had contact with through the forum also had something similar removed from her nose around the same time so I do wonder about what your nurse practitioner said.
Try & stay positive & know we’re always here.
Nicola
Hi Nicola,
thank you again for sharing your insight. Very interesting about the shared issue with lesions. Maybe there is something in what the practice nurse said.
My new issue is not being able to poop easily without laxatives. I feel restricted and it hurts, so I am wondering whether I may have stenosis. So, back to laxatives for me until I have had it checked out.
I am still having multiple night sweats and then getting very cold. If this is ongoing when I see my oncologist I will ask her about it. I’m wondering if this is still a left over from my treatment.
I asked to be referred to a psychologist who has some specialism in cancer therapy. I want just to talk through my new depressive anxieties.
On a really positive note, I returned to my Welsh Speaking class yesterday. Three hours of learning. I began to seriously flag after two hours but I stuck with it. It was great to be back out in the real world doing something normal again.
Hi LCraig ,
Unfortunately the chances of having a level of anal stenosis following this treatment is high. I certainly did have stenosis. I took stool softeners for approximately 3 years post treatment, my oncologist & surgeon would comment on the stenosis & I wondered if it would be a lifelong issue but it hasn’t been, the last couple of years I’ve noticed a lot of improvement, I haven’t had the need for softeners for probably 4 years now & have no discomfort or pain going to the loo. My advice would be just stick with the stool softeners for as long as you need them.
It’s good that you’ve explored some counselling options, especially with a someone that specialises in cancer related therapy. I hope you find it helps you make sense of the way you’re feeling.
It’s also great to hear you’ve ventured back into some of your leisure activities, I love this & bit by bit these things will help you regain more & more of your pre diagnosis life back which in turn I’m sure will boost your mood. You should be proud of yourself as it’s still really early days in your recovery & you’re already getting yourself back out there.
Nicola
Re pain with bowel movements. during and following anal cancer diagnosis My chemo radiation ended Oct 31 2024. I have struggled with intense pain with bowel movements . At Mayo I was given a compounded cream that contains Diltiazem with Lidocaine which seems to help. Last week I met with a general surgeon who suggested we try dilation as an in office procedure,, Its simple,, 3 different graduated size dilators were gently inserted into the rectum to try to open up that channel and sphincter. Uncomfortable for sure but I have been willing to try Anything to help.
He explained that the radiation has had this constrictive effect on the anus and rectal canal in the same way that the vagina is changed by this scarring .
I believe this is helping and I plan to go back in 3 weeks to have that repeated
Hope this helps as an option to consider , Best wishes on the journey , !!!!! How very much we do not know as we discover at each phase ... pain is real. Options vary I appreciate this forum so very much!!!
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