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Let it Go

It’ll soon be five years since I was diagnosed. Five years of learning about this weird condition and my own particular version of it. Five years of working out what I can and can’t do; what I want and what is still left to strive for. And recently I have been thinking more about what I want – what I want to achieve, what I want to do work-wise, how I want to live, who I want around me.

 

In December I changed job roles (again – the shifting nature of the junior doctor years goes on and on!) This time I was to find myself in A&E, a notoriously difficult place to work – very physical, horrible rotas, facing crisis every day. Whereas I had been very well in my sit-down, office-based GP world with long but regular hours, the very thought of this new change made the fatigue kick in and the legs give out (more on the effects of stress and anxiety on my MS in a future blog I think.) So to be proactive I decided to seek some adjustments at work. Although I would ideally work part-time I feel the pressure of my age and unpredictable heath to complete this final stage of my training as quickly as possible. So off to Occupational Health for me to ask for “reasonable adjustments to my hours.”

The result was satisfactory – limited to 50 hours a week, no more than five working days each week and a reiteration that I don’t have to work nights. The process was generally smooth, the occupational health doctor was lovely and I found the whole experience … deeply upsetting. Why? Because I had to sit in a room with a stranger and talk about all the ways in which this disease makes me feel not quite normal. To everyone else I downplay most of this stuff; brush it off with talk of “feeling a bit rough.” Here I had to talk in detail about the days when my legs wobble or the days where I have electric shocks shooting around my body. The days where getting out of bed feels akin to climbing a mountain, or the days where I should be using tena lady (but refuse because I am too damn proud) or the awful, awful moments where I can’t think of the word I need (this is increasingly the most distressing part of my condition – I forget words daily now and apologise here to the friends who have to put up with my blather. My husband has developed the habit of finishing my sentences for me – I am not enjoying hat much! )And I had to explain all of this whilst desperately hoping that she wouldn’t say I had to stop being a doctor. Because I think I am a good doctor. I am even a pretty good A&E doctor if I don’t have to move too fast!

And she didn’t say that. Of course she didn’t. I am “mildly” disabled most of the time and patient care isn’t affected. But it shook me and I had been feeling a little low and anxious since. A friend and colleague recommended a website called moodgym (an Australian website which is CBT-based) and it has proved very useful. There are core erroneous beliefs that we all cling to despite them being unhealthy, and in times of anxiety they manifest themselves more strongly. So my new year’s resolution was to challenge those “wrong” thoughts, to try and eradicate unnecessary stressors and to “take it easy on myself.” When your body is unpredictable the rest of your life needs to be much more so. As dull as it is I need routine and regularity – routine hours, regular activity, stable relationships and a reduced to-do list.

So I have made a NOT TO-DO list

  • Stop working shifts. This is relatively easy to achieve as I have just finished my A&E work. But for future work planning I need to remember that what my body needs is to generally get up at the same time each day and go to bed at the same time. It needs food at regular and predictable intervals. Daytime sleeping makes the fatigue worse and my mood lower.
  • Stop the physical challenges. I gave up PE when I was 12. Before I was diagnosed the only exercise that I actually enjoyed was dancing and possibly a bit if swimming (if it wasn’t too cold … and there wasn’t anything good on the tele…) After diagnosis I seem to have been sucked into a world (of my own creating) where I need to be one of those people who will “defy the odds” and run marathons/do open water swims/climb mountains. I decided I was going to train for a 10k run in a couple of months – partly driven by the desire to shift some excess weight, but also by the “need” to prove that I am still physically capable. But I never was physically capable! And I definitely am not now. I started training and took to my bed. So I’m not going to do it. I have nothing to prove to anyone. I do enough as it is (50 hours working week is still pretty full-on!)
    I will still do the long bike ride in the summer that I have planned with my lovely friend, but we can take that steady, and eat Mars Bars on the way.
  • Stop obsessing about other people. I am VERY bad at this. I am quite a jealous person and also quite an over-sensitive one. Slights cut me deeply and it takes me ages to move on. I waste a huge amount of emotional energy fretting and it is starting to sap my physical energy too. So it is time to put a stop to it, and to remove myself from some friendships that are only causing me anxiety and, in some cases, anger. As a wise friend said to me the other day “you only have a limited amount of free time, why waste it seeing or thinking about people that you don’t even really like or have been mean to you or yours?”
  • Stop filling every moment. The cult of busy is strong in this house. The children are crazy busy and keep pestering to cram more in (although the boy child, recently turned 9 did burst into tears the other day because he “didn’t have enough time to play Fifa!” We had a chat about first world problems.) I like a nice full calendar – I like to see my friends, I like to sing in my choir, I like to eat in restaurants and have people for dinner. But I am approaching burnout. Me and Mr C haven’t spent an evening in together since Christmas. So I need to balance seeing the people I love who don’t live with me (and who are a great factor is keeping me steady – in “lifting me with love”) with the seeing of the one who does.

 

So my theme of February is “Let it Go.” Let go of guilt, let go of toxic relationships, let go of frantic busy-ness and, hopefully, let go of this anxiety.

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3 thoughts on “Let it Go

  1. I really enjoyed reading your post. Thanks for being so positive about adapting to life so that it’s more manageable, but of course, still fulfilling. Its made me reflect on my own life, which involves pushing myself beyond what really feels comfortable, but having a sense of guilt when I think about making changes. Maybe it’ll be my year for some changes too!

  2. I completely understand what it’s like to feel sad and resentful when you know your illness means you have to make changes to your life. I’m sure though that ultimately you will feel better for living a life that’s more manageable. I’m always setting myself goals so absolutely love your idea of a not to-do list, what a great way to take the pressure off!

  3. Thank you for this. As someone who is a big list maker, the idea of making a list of what NOT to do makes so much sense to me. Not only is it a reminder but it acknowledges the behaviours I need to work on in hopes of actually changing and not denying them

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