Hello everyone,
I was diagnosed with Breast cancer in March 2020, 5 months to the day after nursing and losing my Dad to cancer (a devastating loss to me) I work in the nursing profession and thought I can ride this journey no problem...after all we are given tools to support patients and their relatives dealing with a devestating diagnosis.
And so (luckily for me) I was rushed into surgery as they were.closing the hospital down behind me to deal with the surge of covid patients. I kept in touch with colleagues and actually hated the fact that I couldn't.be there with them when the hospital needed its staff the most. My partner worked away and we had to make the decision that he stayed away for fear of covid being transmitted. I would not see him for months. My daughter would drop parcels to the door, grandsons waving through the window.
The only human contact was with the nurses in the cancer unit...always busy and no time to chat and aware to give patients required space to minimise cross contamination. No tea rounds from volunteers, no chat group afternoons, no wig service, just an endless round of leaflets and Webb sites. Macmillan nurses helping.elsewhere never had time to return answer machine messages (all stopped because of covid) I began to wonder if breast cancer is maybe not as serious to worry about as other diagnosis. It was the most loneliest time of my entire life, but again I focused on projects to keep my mind active and tried Not to miss human contact. I disappeared into my mind.
My treatment came with complications...reactions to the chemo caused tingling and numbing in my feet, sessions missed and dosage changed, this resulted in my treatment over running and I went straight into radiotherapy, given at another hospital further away, had to drive myself, on a return trip, whilst stationary, an elderly gentleman ran into the.back of me, writing my car off, oh the agony of trying to sort insurance when your brain doesnt function !!! That in turn resulted in hire car to get to apps, I contracted covid which put me into bed for 3 days.....on my own laying in my own sweat and unable to move. I have not been the.same since, tingling bumb hands.and feet, muscle contractionsmin my back legs.and arms. Sleep deprivation with pain. My partner so distant with me unable to cope with emotions I fear the relationship will not survive....he was so used to an independent working partner depending on no one, the glue to the family sorting the problems., not the frustrated person I have become.
And now over a year later I still await breast reconstruction (not classed as urgent) an app with neurology (6 months waiting list) my HR and Occy health depts now pushing for me to return to work or take early retirement due to ill health (apparently breast cancer comes with a limit time to heal -pressure!) there is strong feelings of having fallen off the conveyer belt and I have no idea of how to move forward from this point.
Sorry this is so long...if you have read it thankyou for your patience. Maybe I should have rung help lines and talked but I already know that ultimately the answers lie with me.
Kentbird
You really have had a rough time of it all. Staying positive is not easy. But, trying to find positives and trying to bring some positivity into your life is vital.
I am only half way through my treatments having been diagnosed in August 21. Two surgeries and now chemo to be followed by radiotherapy has certainly had its challenges. One of the hardest things to do is say ‘help’ but asking for help, seeking help is not a weakness. Having had previously suffered depression & anxiety, I absolutely knew that I had to look after my mental health and leave the experts to deal with the physical/ medical side. You, are absolutely right, that trying to find some answers within your self is a good place to start. Making yourself your first priority is not selfish. It’s about putting your own oxygen mask on first before attempting to do anything else. Please be kind to yourself, ask for help and try and ‘put your positive pants’ on. Come on, you got this ! XXX
My heart truly goes out to you after reading your story and makes me feel very fortunate to have been diagnosed with BC late last year rather than when we were all going through the earlier days of covid.
I just wanted to reach out and wish you all the very best and hope that you get the help that you so truly deserve after going through this massive trauma to both your body and mind.
Love and hugs Angela xx
Thank you so much for reading through my rant and returning your kind words ...... maybe I should just raise my head above the parapet and take a look at the bigger horizons.
Wishing you well
Kent bird
The trouble is when it’s over, it’s not actually over! But anyone who’s not been through it doesn’t understand. If I can help in anyway please just ask x
Thank you. Im so glad that you confirmed with me the feeling "that it's not over" it's difficult to get people involved once the chemo/radiotherapy finishes and are technically signed off from the oncology department. Where (apart from the chat groups) do you go for the after effects, how long do you give everything to "settle" all the booklets & leaflets will just say that everyone is different and will react and heal at their own pace
But the health system doesn't allow anyone to be treated at their own pace...the support is lost. most of the time I'm just told to ring my doctor-not easy on a stretched overworked surgery!!?
I just feel I'm constantly angry and in pain.
My goodness. You’ve had such a struggle, I commend you for getting it all out there and for getting yourself through this despite all those obstacles and challenges. Ring those helplines now. MacMillan offer counselling, courses in life after cancer, support with work, you are still in huge need and your situation is exactly what they are there for. Things are starting up again now and there are support networks out there. There’s all of us here, keep posting, keep processing it all and one day you’ll just realise you’re starting to feel better, massive hugs xx
Thankyou Anna for.your reply...I really appreciate that you have taken the time to reply with your words of support. Asking for help has never been easy for me a result of not being able to converse a cry for help as a small child......I learnt to withdraw and deal with problems on my own. Probably why I went into the caring profession?
I think the problem with physical pain is that it cant be shoved into a box to the back of your mind while you keep yourself incredibly busy. Pain consumes the body and stops it in its tracks giving me too much time to think!!! My survival modes compromised. My frustration is Born out of wanting a diagnosis and cure for this pain and to get my life.back but as you say doors are slowly opening again so hopefully steps can be taken to get back on track....journeys have a beginning and an end, I just need my first step!
Wishing you virtual hugs....Kent bird
Thank you for sharing. I can't really add to what's already been said here except that this is a safe place to unpack and discuss what you've experienced. Macmillan nurses are amazing and can access support for you from avenues you won't have thought possible.
Hang in there, you've got this
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