T-5 and counting. Returning to work after 10 months off...eek

2 minute read time.

Over the past couple of months I have been planning my return to work and finally got the last sign off yesterday. This is something I have been pushing for in my quest to get back to normality but now it is getting close, I confess to being a little apprehensive. I am due back on 1 August and that is only a few days away...

After such a long time, most of which was spent not having the energy or inclination to do very much  I do wonder how I will cope! I am only doing 3 hours a day for 2 or 3 days a week for the first couple of weeks, increasing my hours/days over a long period of time until I am doing my contracted hours. When putting together the plan, I thought at the time that it wasn’t enough. Now I realise it is not just being at work, it is reconnecting with my work colleagues, understanding the changes  - I work in IT for a large FSA company and change was constant and fast when I was full time, not just technology but rules, laws and regulations that IT had to comply with and often time bound - and being once again thrust into a hectic and challenging role. The role was always mentally challenging, knowing there could be financial or reputational damage for the company if my decision making wasn’t sound or project timelines and milestones were missed. Looking back at my return to work plan now, I am relieved that I will be easing very gently into my role and full time hours! 

I haven’t shed a tear, not one, since diagnosis and part of me wonders whether I have bottled up all of those emotions and at some point when I am back doing the things I was doing pre diagnosis the top will come off! I am always good in a crisis but have been known to turn into a shaky mess once the crisis is over. I know that my work colleagues will be there for me if that happens but I certainly do not relish the thought of having a meltdown anywhere, let alone amongst my colleagues. I am not someone who cries...in fact I can’t remember the last time I had a good bawl. What I do know is thatI am an ugly crier! Red puffy eyes, snotty nose, the whole works! Nope, don’t want to do that in front of anyoneGrimacing

Que sera, sera. 

Anonymous
  • <p>Hi there - Lucky you! :-)</p> <p>By &#39;lucky&#39;, I mean lucky to be over the worst now and looking forward to getting back to work and on with the rest of your life!</p> <p>I&#39;ve just had my very first session of Chemo - 3 more to come - then a full Gastrectomy, then more Chemo. At least I can take courage from knowing that you have already had the experience of having your Christmas Dinner through a straw and have survived it! LOL I can&#39;t wait!!! ;-)</p> <p>Seriously though, I&#39;m sure you&#39;ll be just fine getting back in to the swing of things. Don&#39;t forget, your work colleagues will be nervous too and may feel the need to tread on eggshells when you return!&nbsp;But just think of all the catching up you&#39;ll have to do.</p> <p>No, I reckon you&#39;ll be fine and so what if you shed a few tears - and if you&#39;re a &#39;bawler&#39; - that just confirms that you&#39;re human and alive!</p> <p>Have a great few days and all the best for your return.</p> <p>Kindest regards</p> <p>George.&nbsp;</p> <p></p>
  • FormerMember
    FormerMember
    <p>Thanks for your message George.</p> <p>I am very fortunate to work for an excellent employer with a lot of support mechanisms in place to help me get back to work. I have also visited the office a few times during treatment and my immediate colleagues set up a What&rsquo;s App group where we all keep in touch and generally take the piss...exactly how it is in the office! Many other colleagues have also kept in touch or met me for coffee etc so hopefully we are all comfortable enough that it won&rsquo;t be too strange going back after all this time.</p> <p>Hopefully you aren&rsquo;t suffering too much following cycle 1 and are geared up ready for the next one. I just listened to my body and if it said to lie around all day, I did exactly that. There were enough good days to balance this out when I was able to do stuff. Fingers crossed that your treatment goes ok and you get to the same stage I am at now. I feel remarkably well although too skinny.&nbsp;</p> <p>One big tip...try to build up your strength, stamina and weight pre surgery. You will only have a few weeks to do this once pre op chemo is complete but it certainly helped me get through surgery really well and the additional few pounds I put on gave me a bit of a cushion in the weight loss department.</p> <p>All the best</p> <p>Karen</p>
  • FormerMember
    FormerMember
    <p><strong>Website:</strong><br /><a href="www.londoninterventionalclinic.co.uk/.../p>
  • FormerMember
    FormerMember
    <p>Glad to hear your story, I am happy for you :) I have Stage 4 esophageal cancer. Diagnosed in November 2017, I was given six months to live. 20 months later I&rsquo;m still here and feeling great. Yes, I will probably have cancer the rest of my life, but that is fine with me. I am getting my treatment done by doctors at www.chwchospital.org</p>
  • FormerMember
    FormerMember
    <p>Hi AvaW123</p> <p>&nbsp;So sorry to hear you have stage 4 cancer. I can&rsquo;t imagine what you must be dealing with every day.&nbsp;You sound like a fighter...good for you. Never give up.</p>