Tag: fitness

  • Mixed feelings about this

    This arrived yesterday…

    And I have mixed feelings about it. I have no obvious disabilities and would feel guilty using this on a daily basis but having had a few occasions queuing around a hospital car park while dozens of disabled bay are staring, gloating at me where I’ve thought why can’t I use those.

    They’d stop me turning up for appointments panting and wheezing like a steam train.

    More of a concern is that its another tangible sign that I’m not my normal self any more and no amount of denial can hide it. I don’t like being unwell and have always been able to look after myself so it’s the acceptance that’s still just out of reach.

    I guess I should take anything that makes life easier with open arms, whether its a badge, some form of benefit entitlement, offers of help and swallow my pride.

  • A good few days

    Since the weekend I’ve had a good couple of days. We had a nice walk around Frensham pond in the sunshine on Tuesday, just me and Kira. I noticed that the drop in temperature has affected my breathing a little. Made it a bit harder but nothing too bad.

    Appreciate the simple things now

    Today I had a very wet walk with the dogs. If I’m honest I prefer it like that as it’s quieter.

    I’ve been sleeping well, no vivid dreams for a few days either. Depsite me not getting my new meds until today. I’m hoping this improves even more. I hadn’t realised that a lot of people have the same issue with morphine buildup in the body.

    I also need to keep my breath exercises up as my chest is very tight when I breath deeply. Not a sharp pain but just a muscle ache. I’ve been unconsciously not breathing deeply again so when I do I just feels tight. I hope the by forcing some regular deep breaths that it start to feel normal again.

    My thinking is that lungs are muscles and like all muscles if you don’t use their full range then they weaken.

  • Fitness, stamina and weight loss

    2020 has not been a great year for me for general fitness and exercise. What with recovering from a shoulder operation in December, then lockdown stopping boot camp visits (I never really liked the remote/zoom classes), then the surfacing of the cancer I think its fair to say 2020 has been a sedentary year.

    Recent years has seen me battle with weight from losing 8st in 2008 and then slowly putting most of it back on in the following 12 years to ramping up exercise with personal trainers and then boot camp sessions. I’ve always been unfit and overweight but trying to do something about it.

    Being 6’8” tall had always disguised my size and when I was at my heaviest at 330lb people were always surprised when I told them. I’m not proud of hitting that weight.

    From March to Sept this year I didn’t weigh myself at all. Not through a conscious decision but because I was scared to. I knew I wasn’t exercising and was convinced I’d piled the pounds back on and was heavier than ever. In March I was back to 317lbs 😳

    After the antics in September when my cancer was discovered I’d had a period of a few days of eating almost nothing while in hospital and worried. When I got home after that first admission I decided to weigh myself again. I was pleasantly surprised to find I was still at 317. I’d clearly been a bit higher but not that much.

    Worryingly, by the middle of Sept I was down to 310. I wasn’t trying to lose weight but my appetite had gone. Even though for almost 2 weeks I spent a lot of time lying down in bed as this was where pain was most manageable and was barely moving around much, I was still losing weight.

    I joked it was alright as I had a lot spare but I knew this could be an issue if not controlled. I was at 300lbs by the middle of October.

    At the start of October I made a conscious decision to get out and start moving a bit more. Walking was my exercise of choice and my first few walks were slow and only about 0.5 miles. Then 0.8 miles and then a mile.

    I was struggling with stamina, I couldn’t talk while walking and the slightest hill would mean I had to take a breather.

    I decided to trying some help with Nordic walking poles. These helped massively by making me stand up straight, open the chest, use arms and legs to help propel.

    The distance increased to 1.5, then 2 miles over a few days. Great!

    My knees disagreed, I’d tried to do to much to quickly. My physiotherapist told me to focus on a mile and keep to a mile until I could do it comfortably. And then try and get to my normal walking pace.

    Long story short is that now, in mid Nov 2020 I’m walking (without the poles) at my normal pace and can hold a conversation. This weekend I’ve walked 5.5 miles and joints are fine. I’m still finding hills very hard but that will come with time too. It also means I earn my naps now 😴

    As for the weight and appetite, my appetite has now come back. I’m not eating quite as much as before and if I’m honest this is mostly due to me going to bed earlier so I’m not having schnacky snacks. My weight this morning is 294lbs. That’s another 3lbs in 2 weeks. I’m 99% certain this is fine and is due to me not snacking.

    I’m still very overweight but I’m in the strange situation that I have to be very careful how I lose weight. It needs to be intentional and I have to make sure I look after myself.

  • Fatigue isn’t the same as just being tired

    The biggest side effect of my illness currently is fatigue. I’ve never experienced anything like it even though I’m someone used to having naps and enjoying sleep but also experiencing being tired through not getting enough sleep in the past.

    This is not fatigue.

    I can only describe it as constantly having a phone battery at 5% and running in low power mode. Everything is an effort, almost in slow motion. I feel drained all the time, despite eating and drinking I have no energy. Despite sleeping for what seems like 99% of the time I’m still tired.

    I’m constantly told “its you’re body repairing itself”, which I guess is partly true. It not a great feeling though.

    I’m now struggling to make it more than an hour or so without some sort of nap and when I do have a nap I have to make sure I set some sort of timer for 30 minutes to wake me up. This is so I don’t lose hours by falling into a deep sleep. I did this a few weeks back, went for a nap at about 4pm and despite waking briefly a few times was in bed until 8am.

    And I was still tired after that!

    In an effort to control my sleeping patterns I’m now going to bed very early, usually by 9pm. The amount of fluid I’m drinking each day, combined with the fact I only currently have one functioning kidney means I visit the bathroom at least 3 times a night (that’s not helping the sleep either!) and then I wake around 8am.

    I’m informed that some of the fatigue is down to medication, some is due to the illness but some is also down to lack of fresh air, lack of exercise over the past few weeks. So I’m now making an effort to rectify some of this.

    I’m trying to get out walking most days. A few weeks back I managed just over half a mile and was a wreck. This weekend just gone I managed a mile at almost normal walking pace while holding a conversation. Progress is progress but I’m still a way off being able to take the dogs out for 3-4 mile walks.

    I hope the fatigue eases but compared to some of the possible side effects I could be suffering from I’ll take fatigue every day.