I am a pretty much a glass half full type of girl. I like to be positive, up beat, enthusiastic, to the point of being annoying some may suggest. I don't like to sound like I am moaning, I know there are plenty people who are worse off than me. So it is hard for me to admit when the going get tough but the point of this blog is to raise awareness of EDS hypermobility so I guess I need to be honest too. To admit defeat even. Don't panic I'm not giving up.
I had a great weekend down at Mum's, although I didn't do any proper training, thanks to the mini personal trainer it was non-stop and I was pleased to still be able to show 'em how it is done on a trampoline! we went to Whinlatter (which I would highly recommend) and walked, ran, jumped and played all day. We had a great time and I kept food in check!
Bank holiday Monday I got up, went out and ran (well with some walking thrown in) 5k, I felt great. it was a really good trail run, along the river with some pretty steep hills thrown in too. I love trails! Toe dislocated for the first 1k or so and my rib popped a bit but in the grand scheme of things I felt great. Went out for lunch made good food choices, I felt positive, strong and ready to take on the Spartan challenge.
Tuesday started OK, I had already decided I would have an easy day exercise wise. Food wise I did fine, but as the day went on I got tired, really tired. Now I am mostly tired, I blame the 5 year old sleep terrorist. But this was like that heavy cloud that comes down and makes you feel a bit like you are walking through syrup, mmmm syrup. Anyway that fog that makes it hard to concentrate, to think and certainly to do anything energetic!
By Tuesday night I was shattered and I hurt - everywhere. Now there are many parts of EDS that I dislike but I think for me this is the worst. Dislocations are horrible but you can say OK I dislocated by *insert body part here* and people understand. But it is hard to explain the severity of the hurt when you just hurt everywhere. I think the only thing I can compare it to is flu, possibly even man flu! Everything aches and stiffens up. Sitting still is agony. Moving is too much of an effort. My hips gave way as I stood up. I was in a proper grump with myself. My hands turned into claws, and while it was funny when it happened in Friends......
Wednesday I resorted to painkillers and toast a sure sign that I am sore! Food was carbilicious rather than nutritious. The pain (and then the painkillers) makes me feel sick. Thank goodness for computers because when I tried to write a hand written note I was very nearly reduced to tears. However, if you had passed me on the street you would not have known anything was wrong - I looked fine. Not particularly glamorous but fine. And I think that makes it so hard to admit how tough it can be because you look OK, but all you want to do is curl up in a ball and have a good cry. Of course, life goes on. I work, I have a family, I can't just curl up in a darkened room until it passes. So there I've said it out loud, it hurt, it was hard, I hate it, it makes me want to cry. Maybe I need to say it more and stop trying to fight it but I probably wont.
Happily it hasn't lasted long and today (Thursday) I feel loads better. Tomorrow I will run. And I'll smile because as tough as it gets on my good days I can conquer the world, as long as I can walk some of the way!
Labels
Showing posts with label kids. Show all posts
Showing posts with label kids. Show all posts
Thursday, 8 May 2014
Thursday, 3 April 2014
Sitting down, standing still, moving forward!
So sometimes it hurts to move but more often it hurts more not to move! Last week I had a two days of sitting in one position for long periods of time (work conference) then a day of standing still (PTA fundraiser) and oh my did it take its toll. I am a fidget, I can't help it, it is all part and parcel of HEDS. Sitting still kills me! I am aware that for other people this is extreemly annoying and do try to minimise it, especially in conference type situations. However, by the end of the three days I was in agony. It hurt to move, it hurt to sit still. So rather than run as normal while Chloe was at swimming I went for the rest option and planned to keep it that way. So thank goodness for my mini personal trainer. We made it until about 14.00 untill she could be contained no longer (she had already been swimming that morning) so a bike ride it was. Except my finders were not working and my bike needed a new saddle. Not one to be easily deterred, little miss declared I could run, and she promised not to go too fast! So an hour later, she kept true to her word and I walked most of it, with the occassional run thrown in I felt......so much better. If it hadn't been for her then I would have lazed around and probably still felt rubbish on the Sunday. So moving is the way forward.
I did however get up at 6.30am, when I was staying in a hotel without the sleep terrorist, to go for a run! I feel like I am dedicated :-)
Got really quite excited as my EDS running vest arrived - you will definately be able to spot me in a crowd! Just need to get it back from the little lady now.
I did however get up at 6.30am, when I was staying in a hotel without the sleep terrorist, to go for a run! I feel like I am dedicated :-)
Got really quite excited as my EDS running vest arrived - you will definately be able to spot me in a crowd! Just need to get it back from the little lady now.
But for now I'll just keep on moving forward!
Labels:
#WobblesWednesday,
diet,
EDS,
exercise,
fitness,
health,
HEDS,
hypermobility,
kids,
motivation,
pain,
running,
Spartan
Friday, 7 February 2014
The fog
It is not the fog outside that is hampering my progress, although going out in the freezing fog is not that appealing! But the brain fog. One of the issues with Hypermobile EDS is tiredness. Which sounds a bit pathetic doesn't it? I mean everyone gets tired. I have a 5 year old sleep terrorist so I am permanently at some level of tiredness but when EDS tiredness hits it is on a different level.
This week it hit, I can only describe as being a bit like when you have flu, you know when everything aches, and you are just so exhausted you could happily cry. Even the thought of actually walking upstairs to go to bed is a bit much of an effort and you think twice about having a drink of water because lifting the glass just seems like an impossible task. So once C has been in bed this week I have barely moved off the sofa, tea has been drunk and not much else has been achieved.
I have stuck to my 30 minutes a day but this has mostly been walking and I really need to up my game. Food wise has not been too bad have resisted the extremely strong urge to survive off toast and toast alone.
On Monday I did venture off the sofa and have a clear out of clothes - I have a vac pack of stuff that is a wee bit too tight, it will be opened at the end of April and my word it had better fit!
So the moral of the story is I need to man up, I genuinely think if I can push myself to be more active through the day I will be less tired at night, if I can strengthen my muscles it will not be as much of an effort to hold everything in place. That's the plan anyway - I'll keep you updated!
Please give me a kick and make sure I move my bahooki!
This week it hit, I can only describe as being a bit like when you have flu, you know when everything aches, and you are just so exhausted you could happily cry. Even the thought of actually walking upstairs to go to bed is a bit much of an effort and you think twice about having a drink of water because lifting the glass just seems like an impossible task. So once C has been in bed this week I have barely moved off the sofa, tea has been drunk and not much else has been achieved.
I have stuck to my 30 minutes a day but this has mostly been walking and I really need to up my game. Food wise has not been too bad have resisted the extremely strong urge to survive off toast and toast alone.
On Monday I did venture off the sofa and have a clear out of clothes - I have a vac pack of stuff that is a wee bit too tight, it will be opened at the end of April and my word it had better fit!
So the moral of the story is I need to man up, I genuinely think if I can push myself to be more active through the day I will be less tired at night, if I can strengthen my muscles it will not be as much of an effort to hold everything in place. That's the plan anyway - I'll keep you updated!
Please give me a kick and make sure I move my bahooki!
Labels:
#WobblesWednesday,
diet,
EDS,
fitness,
health,
HEDS,
hypermobility,
kids,
motivation,
Spartan,
tiredness
Wednesday, 29 January 2014
And so it begins
Well I am now signed up to do the Spartan Sprint! Although having a slight issue getting the team set up but am sure we'll get there.
It is not until September 21st so I have plenty of time but I have a lot to do. The challenges are actually not phasing me too much - yes they are going to be tough. However, the thought of running 5k (I know it is really not far) makes me want to cry a little.
So I am starting gradually, I will do at least 30 minutes of exercise a day. This may be anything from Insanity to a brisk walk, dancing with C (which is more of a workout than you would think, there are a lot of lifts involved) to, gulp, going for a run. But I will do it. Everyday.
Everyone struggles to get motivated to exercise, there is always something better to do, like I don't know, waiting for facebook to update. however, it is extra tough when you are already hurting, the sofa seems like a far better option. After all when you ache all over why would you want to add to it? But, really what is the alternative? Yes sitting on the sofa is and immediate relief but in the long run being fitter and stronger can only be beneficial. So, for now I will be doing my 30 mins a day, by March when I am in the habit and it is, hopefully, second nature, I will start regularly running. yes, me running. Remind me again why I am doing this?
There is no point in getting into the regular exercise habit if I do not eat right. Now overall my diet is not that bad. I don't drink alcohol, mostly drink water, cook most of our meals from scratch, watch sugar and fat intake. I'll not lie sometimes this just means watching chocolate go from packet into mouth :-)
One of the reasons I am doing this crazy race is to show C that you can do anything you set your mind to and to be a positive role model to her. It occurred to me the other day that we do a lot of moaning about advertising aimed at kids and the amount of junk that is sold solely with kids in mind. While I agree there is way too much rubbish out there marketed at kids, actually we are more influential than we know. C helps us decide what to have for dinner when we plan meals and when it is just me & her she gets to pick dinner. Her choice for the past few weeks (except tonight when she went fro haggis) has been salmon, boiled egg, veg and a wee dollop of mayo. This came about because I had it one night when she'd already eaten. As I have been thinking about it if I eat chocolate or MrF has a packet of crisps she will ask for them, but if just asked what she wants she will go for fruit 9 times out of 10.
So as much as I owe it to myself to eat a healthy, balanced (I'm all for the occasional treat) diet, I owe it to my daughter to show her that I make healthy choices.
Linking up with the lovely Autismmumma and #wobbleswednesday http://www.autismmumma.com/2014/01/show-me-the-veggies-wobbleswednesday/
It is not until September 21st so I have plenty of time but I have a lot to do. The challenges are actually not phasing me too much - yes they are going to be tough. However, the thought of running 5k (I know it is really not far) makes me want to cry a little.
So I am starting gradually, I will do at least 30 minutes of exercise a day. This may be anything from Insanity to a brisk walk, dancing with C (which is more of a workout than you would think, there are a lot of lifts involved) to, gulp, going for a run. But I will do it. Everyday.
Everyone struggles to get motivated to exercise, there is always something better to do, like I don't know, waiting for facebook to update. however, it is extra tough when you are already hurting, the sofa seems like a far better option. After all when you ache all over why would you want to add to it? But, really what is the alternative? Yes sitting on the sofa is and immediate relief but in the long run being fitter and stronger can only be beneficial. So, for now I will be doing my 30 mins a day, by March when I am in the habit and it is, hopefully, second nature, I will start regularly running. yes, me running. Remind me again why I am doing this?
There is no point in getting into the regular exercise habit if I do not eat right. Now overall my diet is not that bad. I don't drink alcohol, mostly drink water, cook most of our meals from scratch, watch sugar and fat intake. I'll not lie sometimes this just means watching chocolate go from packet into mouth :-)
One of the reasons I am doing this crazy race is to show C that you can do anything you set your mind to and to be a positive role model to her. It occurred to me the other day that we do a lot of moaning about advertising aimed at kids and the amount of junk that is sold solely with kids in mind. While I agree there is way too much rubbish out there marketed at kids, actually we are more influential than we know. C helps us decide what to have for dinner when we plan meals and when it is just me & her she gets to pick dinner. Her choice for the past few weeks (except tonight when she went fro haggis) has been salmon, boiled egg, veg and a wee dollop of mayo. This came about because I had it one night when she'd already eaten. As I have been thinking about it if I eat chocolate or MrF has a packet of crisps she will ask for them, but if just asked what she wants she will go for fruit 9 times out of 10.
So as much as I owe it to myself to eat a healthy, balanced (I'm all for the occasional treat) diet, I owe it to my daughter to show her that I make healthy choices.
Linking up with the lovely Autismmumma and #wobbleswednesday http://www.autismmumma.com/2014/01/show-me-the-veggies-wobbleswednesday/
Labels:
#WobblesWednesday,
diet,
EDS,
fitness,
health,
hypermobility,
Insanity,
kids,
pain,
Spartan,
workouts
Subscribe to:
Posts (Atom)