So, yesterday (as I posted earlier) I joined a gym.
I did light exercise, 20 minutes on 'easy' on a cross trainer. About 5 minutes doing some rowing on the rowing machine and then a couple of lengths swimming, jacuzzi time and then steam room.
I felt amazing. I expected to be a little sore today and I'm pretty happy to report that I'm only ever so slightly more sore than I usually am.
After I did a blog post, I decided to go for a walk into town to purchase some gym appropriate clothing. I found what I wanted, got some food and came home... where I promptly crawled into bed. So, although I felt really pumped and awesome, I'm certainly paying for it now. I'm exhausted and worn, but it is not going to put me off. My body hasn't been worked in a very long time and I'm determined to see this through. (I have a 6 month contract!)
Bring it on.
Showing posts with label exercise. Show all posts
Showing posts with label exercise. Show all posts
Tuesday, 15 January 2013
Officially a gym member!
Shock horror. A girl with ME/CFS has joined a gym.
It's absolute madness I know, so hear me out;
Yes, I am constantly fatigued, in pain and all the fun symptoms that you have with having MECFS. However, before (and the first few years that) I was unwell I was also incredibly... dare I say addicted? to exercise. I absolutely LOVED dancing. I even took up martial arts (had to drop it quite early on however...). I used to compete nationally in a team. I'd be dancing three days a week and then practice when I wasn't at the studio! I used to go on long walks, help muck out stables, I even (last year) took up horse riding but unfortunately money and Perrin treatment collided and I had to stop.
So anyway, I've always been an exercise nut, I enjoy the workout, the feeling you get after pumping your body. Especially if it's dancing, or with animals. Heck, if I had a dog you could count on me doing agility trials with them!
The exercises I'm doing at the gym are quite light. Least resistance, short times etc. Mainly walking exercises, such as the cross trainer. I'm also quite taken with the rowing machines and used that for the first time in a very long time yesterday!
So overall, my gym work outs are going to test me, but they're going to be incredibly 'laid back' work outs. I just feel that I need to get fitter. I can climb a set of stairs and then be out of breath and I honestly don't think it's helping my MECFS with me being so unfit! So I'm hoping I can hit just the right amount of balance for me to not kill myself at the gym, but to get fitter and improve my symptoms.
There is also a pool there which is fantastic as it helps ease the pains in my joints etc. After the pool you can also use a jacuzzi... the warmth is SO SO soothing after doing a work out... and the finally a steam room. My boyfriend said I was practically glowing after being there.
I've signed up for 6 months for a whopping £38 pcm. Eeek! So my pay slips are taking quite a bashing. But I'm thinking that it will be worth it. It also gives me and my boyfriend a chance to do something together away from the house; we struggle to find time for each other at the moment so it's nice to set a few hours aside for us to work out side by side (occasionally ignoring each other for music!). It's great so far and I love it.
I just need to invest in some real gym clothes as mine arn't really that appropriate!
It's absolute madness I know, so hear me out;
Yes, I am constantly fatigued, in pain and all the fun symptoms that you have with having MECFS. However, before (and the first few years that) I was unwell I was also incredibly... dare I say addicted? to exercise. I absolutely LOVED dancing. I even took up martial arts (had to drop it quite early on however...). I used to compete nationally in a team. I'd be dancing three days a week and then practice when I wasn't at the studio! I used to go on long walks, help muck out stables, I even (last year) took up horse riding but unfortunately money and Perrin treatment collided and I had to stop.
So anyway, I've always been an exercise nut, I enjoy the workout, the feeling you get after pumping your body. Especially if it's dancing, or with animals. Heck, if I had a dog you could count on me doing agility trials with them!
The exercises I'm doing at the gym are quite light. Least resistance, short times etc. Mainly walking exercises, such as the cross trainer. I'm also quite taken with the rowing machines and used that for the first time in a very long time yesterday!
So overall, my gym work outs are going to test me, but they're going to be incredibly 'laid back' work outs. I just feel that I need to get fitter. I can climb a set of stairs and then be out of breath and I honestly don't think it's helping my MECFS with me being so unfit! So I'm hoping I can hit just the right amount of balance for me to not kill myself at the gym, but to get fitter and improve my symptoms.
There is also a pool there which is fantastic as it helps ease the pains in my joints etc. After the pool you can also use a jacuzzi... the warmth is SO SO soothing after doing a work out... and the finally a steam room. My boyfriend said I was practically glowing after being there.
I've signed up for 6 months for a whopping £38 pcm. Eeek! So my pay slips are taking quite a bashing. But I'm thinking that it will be worth it. It also gives me and my boyfriend a chance to do something together away from the house; we struggle to find time for each other at the moment so it's nice to set a few hours aside for us to work out side by side (occasionally ignoring each other for music!). It's great so far and I love it.
I just need to invest in some real gym clothes as mine arn't really that appropriate!
Tuesday, 4 December 2012
Update: Perrin Technique
Last November(?), I started a treatment for my MECFS. The doctor was fantastic (Dr Perrin). He explained the treatment and the potential cause for my illness so well and in so much detail I genuinely believed he has a grasp on this whole thing. He does not parade around that he has some magical cure, it's a long and gruelling process to even feel better (with plenty of lows in between the highs) but it is something more than nothing. And a whole lot of nothing is what we've all had so far.
Dr Perrin has a book out, which I borrowed from my local library before I started treatment; I'm not one to rush into things and believe it's going to fix me, so I was incredibly anxious and non believing about it. After reading the book, as did my boyfriend and also my housemate. I got given their verdicts and then I decided to go for the treatment.
Whilst I was on this treatment, I felt horrid. I was told that because of how it works (probably a post for another day, running on limited energy!) I am going to feel a lot worse as my body gets rid of a ton of crap, before feeling better. I was bed bound, I was sick, my stomach was horrid to me, my energy was lower than low... and then I started feeling better. Whether this coincided with it getting towards spring and then summer, I'm unsure... but it felt like it was working for me.
Unfortunately we moved at the end of February to somewhere where it made it really difficult to commute to see any of the therapists for me... so I had to give it up. Needless to say, I've gotten worse since giving it up.
It is a hard therapy to go through and requires a lot of effort and energy on your part, which made it very difficult during the 'lows'. But if I had the money and the support that the therapists gave me, I'd certainly try it again without a doubt. There are some things in the pipeworks that may mean I can start up the treatment again... so fingers crossed. I'd love for in two years for me to be able to do things like a normal girl of my age, with just a minor set back of needing to rest more than others!
Dr Perrin has a book out, which I borrowed from my local library before I started treatment; I'm not one to rush into things and believe it's going to fix me, so I was incredibly anxious and non believing about it. After reading the book, as did my boyfriend and also my housemate. I got given their verdicts and then I decided to go for the treatment.
Whilst I was on this treatment, I felt horrid. I was told that because of how it works (probably a post for another day, running on limited energy!) I am going to feel a lot worse as my body gets rid of a ton of crap, before feeling better. I was bed bound, I was sick, my stomach was horrid to me, my energy was lower than low... and then I started feeling better. Whether this coincided with it getting towards spring and then summer, I'm unsure... but it felt like it was working for me.
Unfortunately we moved at the end of February to somewhere where it made it really difficult to commute to see any of the therapists for me... so I had to give it up. Needless to say, I've gotten worse since giving it up.
It is a hard therapy to go through and requires a lot of effort and energy on your part, which made it very difficult during the 'lows'. But if I had the money and the support that the therapists gave me, I'd certainly try it again without a doubt. There are some things in the pipeworks that may mean I can start up the treatment again... so fingers crossed. I'd love for in two years for me to be able to do things like a normal girl of my age, with just a minor set back of needing to rest more than others!
There was one thing that really stuck in my head about Dr Perrin; and that was his not yet published research and findings that he showed me. His researched showed that people around my level of disability with MECFS (you do a chart/questionnaire in your first sessions) that after a year people have significantly improved, to the point they were leading a relatively normal life with less pain and rest so they didn't overwork themselves and after 2 years, not cured, but better still. I think it was something like 90%(ish I can't remember exactly) of people going through his treatment had improved. So fingers crossed for all those who're going through it right now.
I'm usually rather dubious about treatment; I refused outright the LTP because I knew it wouldn't work for me, I didn't see it as a treatment, I saw it as mind games to make you think you were okay. & since speaking to some people and their family and friends, I truely think it is just hypnosis at it's best. But unfortunately, it's not just a mental attitude to this illness that makes it as bad as it is, it IS a physical problem. So mind games will not work.
Anyway, point to this is, I've tried the Perrin Technique, is began working for me, I had to stop, but can't wait to go back because it seemed so promising!
I'm usually rather dubious about treatment; I refused outright the LTP because I knew it wouldn't work for me, I didn't see it as a treatment, I saw it as mind games to make you think you were okay. & since speaking to some people and their family and friends, I truely think it is just hypnosis at it's best. But unfortunately, it's not just a mental attitude to this illness that makes it as bad as it is, it IS a physical problem. So mind games will not work.
Anyway, point to this is, I've tried the Perrin Technique, is began working for me, I had to stop, but can't wait to go back because it seemed so promising!
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