This is nothing to do with beauty regimes.
This is all about conserving spoons and energy.
I drew inspiration from Courtney Carver's Be More With Less mini-mission on Habit-Stacking.
I find that a regular routine trains my body to know what's expected of it, and this is a routine I've been working with for around a couple of weeks now, and it helps to set me up for the day.
Times are variable depending on what I'm doing that day, but I'm going to tell you about a typical work-day morning here. The whole routine takes around 90 minutes for me to complete:
Alarm: 5.30 am: Two days a week I have to be at work for 7am, so I need to give myself ample time to fit my habit stack in, and 90 minutes seems to be about right.
Yoga: This really helps my joints loosen up in the morning, which is beneficial for my physical job of lifting, shifting and stacking shelves. I then do some gentle neck stretching exercises. This whole sequence takes around ten minutes.
Meditation: Since I have started meditating I've found it to be really beneficial. I started with a 5 minute session, and have gradually worked it up over the past couple of weeks to a ten minute session. The longer sessions happen in the evening, but in the mornings I have time to fit in 5 minutes of quiet contemplation. I sit on two pillows with my back propped against the end of my bed as it would take far too much energy for me to sit up straight unaided this early in the morning!
Food, water, and supplements: Time for breakfast! Usually some toast with jam or spoonie energy bars (recipe coming soon, all being well!) along with yogurt and fruit sweetener (honey alternative). I also make sure to drink around 500mls of water as it kick starts my hydration for the day, which is essential for keeping my fibromyalgia symptoms in check. I also take my daily dose of three supplements.
Teeth: I went through a period in my life as well where I had neither the energy or inclination to even lift a toothbrush to my mouth, but now I brush, floss and mouthwash every day, and I make time for it twice daily.
Wash hair & get dressed: Unfortunately my hair is something that will not behave unless it is washed daily! Whilst my straighteners are heating up I get dressed for work and "put my face on" to make myself presentable for the lovely customers that day ;)
Then it's off to work I go!
A daily routine, as well as pacing, is a huge part of my life now, as it's enabling me to maintain an consistent level of energy without getting into a boom and bust cycle.
What sorts of things do you do to get yourself ready for the day? Do you have any spoon-conserving tips you'd like to share? Tell me in the comments or tweet me @JayHell83, I love to hear positive, inspiring stories from the spoonie community.
Look out in the near future for a post about my evening/bedtime routine!
J x
DISCLAIMER: The information provided here is NOT medical advice, If you think you have ME/CFS or are worried about your symptoms, please speak to a trusted physician :)
Showing posts with label pacing. Show all posts
Showing posts with label pacing. Show all posts
Tuesday, 25 March 2014
My Morning (Spoonie) Routine
Labels:
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mecfs,
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Tuesday, 31 December 2013
New Year 2014: Looking Ahead and Leaving The Past in The Past
The past few weeks I've been thinking a lot about how much my health has improved over the last 18 months, and how I've continued to learn to manage my symptoms to keep me "on a level" as it were. This involves pacing, eating right and getting good sleep. Finding balance out lives is something we all strive to do, whether or not we are "spoonies". I have come to the conclusion that I don't want my symptoms to define me anymore. Yes, they will always be there, but I want to get out and live my life, I'll be 31 in January and I feel like I am missing out on life experiences, however small. I have a list of things I want to do and places I want to visit, and I also plan to step out of my comfort zone a bit more in 2014 and confront my social anxiety, whilst also being kind to myself and not overdoing it.
So what does all this mean for this blog? I want to share more of my daily "spoonie" life with you, and stop getting bogged down with lengthy posts about how chronic my illness is. I tweeted a picture the other night of my "weekly cook-up" which is an exercise I do about once a week to make sure my freezer is stocked up with easy to prepare food. I don't have energy to waste on doing this daily, so I do it in a batch.
So I could make a little post about that. Practical stuff, knowledge and tips that I can pass on. Basically what I intended this blog to be about in the first place.
I'm rambling. What I'm trying to say is that, whilst I will always have my symptoms, they don't define who I am, and they shouldn't for you either. We are all human underneath, and we are more than just our illnesses.
I will continue to refer to myself as a "spoonie" but only in the correct context. I will continue to pace, eat mindfully and keep good sleep hygiene, just as someone who has asthma continues to use their inhaler-as a tool to manage symptoms. Nothing more dramatic than that.
This is my life and this is who I am, and I intend to embrace that in 2014.
Happy New Year everybody!
So what does all this mean for this blog? I want to share more of my daily "spoonie" life with you, and stop getting bogged down with lengthy posts about how chronic my illness is. I tweeted a picture the other night of my "weekly cook-up" which is an exercise I do about once a week to make sure my freezer is stocked up with easy to prepare food. I don't have energy to waste on doing this daily, so I do it in a batch.
So I could make a little post about that. Practical stuff, knowledge and tips that I can pass on. Basically what I intended this blog to be about in the first place.
I'm rambling. What I'm trying to say is that, whilst I will always have my symptoms, they don't define who I am, and they shouldn't for you either. We are all human underneath, and we are more than just our illnesses.
I will continue to refer to myself as a "spoonie" but only in the correct context. I will continue to pace, eat mindfully and keep good sleep hygiene, just as someone who has asthma continues to use their inhaler-as a tool to manage symptoms. Nothing more dramatic than that.
This is my life and this is who I am, and I intend to embrace that in 2014.
Happy New Year everybody!
Labels:
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Thursday, 6 December 2012
CFS Progress Review: One Year On...
A
year ago today I phoned in sick to work and didn't go back for seven
months. Reading back over my blog posts the time seems to have flown
by. I am going to try and condense the last 12 months into a concise
blog post that sums up the best and worst of the last year.
Starting
with my 2012 Manifesto in January:
- Look
at how I can change aspects of my lifestyle to benefit my physical
and emotional health
Make time to develop my art, craft and vintage business(es!)
- One
Thing At A Time
Stop doing what I think others/society/”they” want me to do and start doing what makes ME happy and healthy.
February: Starting simply with nutrition and diet I adopted the practise of drinking four pints of filtered water a day. Recently I have lapsed with this, and the process of re-reading my posts has reminded me how important it is, so I am back on the water wagon again! A frozen lemon wedge adds a lovely cool zing too! I quickly realised my cow's milk intolerance had returned from childhood, and as we know, CFS has lots of links with candida, thrush and yeast infections so I discovered I was intolerant to yeast too.
I started doing my food shopping online. This gave me back a sense of independence whilst also enabling me to conserve energy. I think this simple idea is one of the best inventions of recent times, and I am so grateful to the friendly Sainsbury's drivers-I never had any problems with my orders and would highly recommend the service.
I quickly realised that my energy levels were directly related to the food I was eating. I now focus on natural foods, minimal animal products, and freshly cooked produce whenever possible; although if I am having a low energy day I do not berate myself for putting a frozen pizza in the oven, and I do allow myself treats, but my body will not hesitate to tell me if I am not eating well!
Fascinating fact: In February, a “good day” meant I could do 45 minutes of light activity before I had to lie down and rest completely for 15 minutes. Incredible to think that I went from that, to presently working four 4 hour shifts per week!
March: By March I was beginning to feel better, but I knew the key to a great recovery was PACING. I cannot stress this enough. I hated the idea at first, and even though I had read loads and loads about it, I still wasn't sure. But I gave it a go, and started making notes of every little thing I did throughout the day, what time I did it and for how long. This gave me a really clear idea of how I was proportioning my time, how productive I was being and where I could conserve energy by doing something called “switching/pacing” (give it a Google!)
As well as being productive throughout the day, I knew I had to address my sleep hygiene and my bedtime routine. I downloaded some relaxation mp3's, which I still use (they're amazing), and made sure I kept a regular bedtime and waking routine. I was getting to the point where I could be up and dressed for 9am, even though I might not do anything the rest of the day!
I was also able to incorporate a bit more exercise into my daily activities, even if it was just walking outside for a few minutes. Not only was this a huge step physically, it was also a huge mountain to climb for me within the psychological aspect of my recovery. I hated going outside as I feared people would see me and think I was “skiving” from work, as to all intents and purposes I looked well (as we know this happens with ME/CFS), even though I still felt physically and mentally exhausted the majority of the time. But getting out and about, even for short periods, helped boost my confidence and lessen my depressive symptoms massively.
April
& May:
“When
you have ME/CFS the last thing you need is pressure. Pressure creates
stress, and stress exacerbates ME/CFS.”
By
April I was cycling 2 minutes a day on my exercise bike, and getting
out for 6 minute walks when I felt up to it.
I was keeping up with all the goals I had set myself so far, like
drinking plenty of water, getting healthy, natural foods inside me,
pacing, and having a good sleep routine. In May I began my course of
CBT. Re-reading my blog posts now I can see that around this period
of time, my writing became much more cohesive, upbeat and positive. I
really couldn't recognise myself in the tone of the early posts.
June: In
June I saw my GP for the last time, as she declared me fit for work!
I had actually asked her to do this as I had been feeling much much
better for quite a while, and was actually now beginning to get
frustrated sitting at home all day. I wanted something to do. I
wanted my life to begin again.
I
came up with a three-point manifesto to take me through the coming
months:
Maintain
a good state of health by applying all knowledge learned within the
past twelve months.
Steadily
increase working hours up to sixteen per week, using phased return.
Enjoy
creative pursuits and other hobbies to enhance physical and mental
well-being.
A
couple of weeks before I returned to work, my beloved feathered
friend, Jimmy the budgie, passed away. I was so sad to lose him, but
I somehow knew that he
knew he had helped me through the most difficult time of my life. He
was a fluffy old bird, and it was time for him to go. I will never
forget his amusing chattering, singing and squawking! He now
regularly sends a whole menagerie of different birds to my back
garden where they feast on nuts, seeds and fat balls!
July
& August: As
I was back at work, I wanted to make sure I kept my immune system
topped up. To this day (touch wood) I have not yet caught one cold or
bug that's gone round at work, while colleagues have been smothered!
I am obviously feeding and treating my body correctly now.
I
decided to go vegetarian for a month, and this increased my energy
levels noticeably. I do eat meat now, but I eat generally with a much
more mindful approach, and really think about what I am consuming and
why.
I
finished my course of CBT in August, my therapist was extremely happy
with the improvements I had made. I review everything monthly now,
just to refresh where I am at emotionally, and to notice if there is
anything in my life I am finding difficult. I can then go back and
apply the CBT principles to help me overcome this.
September:
Time
for another manifesto:
1) I am single and I embrace this freedom and independence
2) I have no interest in having children and this is fine
3) Some people might see my job as "boring" or "dead end", but I find it fulfilling and challenging
4) I am happy for making art to be my hobby or second income, I much prefer this than striving to achieve in an over-saturated industry
5) Taking time to relax and take care of myself is just as important as wanting to actively achieve any goal I may set myself
2) I have no interest in having children and this is fine
3) Some people might see my job as "boring" or "dead end", but I find it fulfilling and challenging
4) I am happy for making art to be my hobby or second income, I much prefer this than striving to achieve in an over-saturated industry
5) Taking time to relax and take care of myself is just as important as wanting to actively achieve any goal I may set myself
I believe that full recovery from ME/CFS is not possible until
you accept that your lifestyle and every aspect of it must change.
You must want this change, be ready for it physically and
emotionally, and be happy with it.
October
& November: By
now I seem to have developed a new rhythm in my life. One which is
beneficial and fulfilling to my mental and physical health. I try to
apply mindfulness to my daily activities, be they at work or at home,
and be more self-aware. I listen to my body more by applying
meditation techniques, and communicate with my body and my self. I
have only recently started being creative again, and creating art
that I really really like, instead of striving to appeal to the
masses. I look forward with enthusiasm to my free time, as I have
lots of exciting projects that I am in the midst of. I really enjoy
cooking healthy meals and searching out new recipes, and I enjoy
getting out in the fresh air and power walking-recently I walked 5k
in under an hour!
December: So
here I am, one year on. I hate getting philosophical or sentimental,
especially when I know I am publishing this for the entire internet
to read! But this time last year I had a raging sore throat, a cold
that wouldn't go, and was so physically tired I had to drag myself up
the stairs on all fours to use the bathroom. I was in a very very
very black place come 23rd
December, and was searching for all sorts of things on the internet
that one should never have to read. I wouldn't wish what I have been
through in the past 12 months on anyone, anywhere, ever, and I think
it's high time the authorities concerned started taking this illness
much more seriously.
If
my blog has helped only one person change one thing about their
ME/CFS affected life that improves it, then I have done what I set
out to do 12 months ago.
I
wish everyone who is suffering to whatever degree, the very best for
the future. If you know of anyone who has this illness please don't
laugh it off or make light of it, be there for the person and help
them if you can.
Thank
you all so very much for reading.
This
blog post is written in memory of my amazing Grandma, Bernadette
Mawdsley,
who
passed away peacefully in her sleep on Thursday 22nd
November at the grand old age of 90.
Rest
in Peace Grandma, night night your God Bless xxx
Labels:
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Saturday, 17 November 2012
Runner vs. Chronic Fatigue Syndrome
| I take no credit whatsoever for this image. I found it on Pinterest |
If you keep up with my recovery progress on Twitter, you will know I regularly log my fitness progress on the website Walk Jog Run. I have been power walking for a couple of months now, and by following the training plans on their website, I have been able to pace myself and can now walk 5k in under an hour! Then something really unexpected happened-the guys from Walk Jog Run wanted to feature me as Runner Of The Week! Click the link to see my interview with them entitled "Runner vs. Chronic Fatigue Syndrome" where I talk about my CFS recovery and how getting out in the fresh air has really helped my progress.
Labels:
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Showing posts with label pacing. Show all posts
Showing posts with label pacing. Show all posts
Tuesday, 25 March 2014
My Morning (Spoonie) Routine
This is nothing to do with beauty regimes.
This is all about conserving spoons and energy.
I drew inspiration from Courtney Carver's Be More With Less mini-mission on Habit-Stacking.
I find that a regular routine trains my body to know what's expected of it, and this is a routine I've been working with for around a couple of weeks now, and it helps to set me up for the day.
Times are variable depending on what I'm doing that day, but I'm going to tell you about a typical work-day morning here. The whole routine takes around 90 minutes for me to complete:
Alarm: 5.30 am: Two days a week I have to be at work for 7am, so I need to give myself ample time to fit my habit stack in, and 90 minutes seems to be about right.
Yoga: This really helps my joints loosen up in the morning, which is beneficial for my physical job of lifting, shifting and stacking shelves. I then do some gentle neck stretching exercises. This whole sequence takes around ten minutes.
Meditation: Since I have started meditating I've found it to be really beneficial. I started with a 5 minute session, and have gradually worked it up over the past couple of weeks to a ten minute session. The longer sessions happen in the evening, but in the mornings I have time to fit in 5 minutes of quiet contemplation. I sit on two pillows with my back propped against the end of my bed as it would take far too much energy for me to sit up straight unaided this early in the morning!
Food, water, and supplements: Time for breakfast! Usually some toast with jam or spoonie energy bars (recipe coming soon, all being well!) along with yogurt and fruit sweetener (honey alternative). I also make sure to drink around 500mls of water as it kick starts my hydration for the day, which is essential for keeping my fibromyalgia symptoms in check. I also take my daily dose of three supplements.
Teeth: I went through a period in my life as well where I had neither the energy or inclination to even lift a toothbrush to my mouth, but now I brush, floss and mouthwash every day, and I make time for it twice daily.
Wash hair & get dressed: Unfortunately my hair is something that will not behave unless it is washed daily! Whilst my straighteners are heating up I get dressed for work and "put my face on" to make myself presentable for the lovely customers that day ;)
Then it's off to work I go!
A daily routine, as well as pacing, is a huge part of my life now, as it's enabling me to maintain an consistent level of energy without getting into a boom and bust cycle.
What sorts of things do you do to get yourself ready for the day? Do you have any spoon-conserving tips you'd like to share? Tell me in the comments or tweet me @JayHell83, I love to hear positive, inspiring stories from the spoonie community.
Look out in the near future for a post about my evening/bedtime routine!
J x
This is all about conserving spoons and energy.
I drew inspiration from Courtney Carver's Be More With Less mini-mission on Habit-Stacking.
I find that a regular routine trains my body to know what's expected of it, and this is a routine I've been working with for around a couple of weeks now, and it helps to set me up for the day.
Times are variable depending on what I'm doing that day, but I'm going to tell you about a typical work-day morning here. The whole routine takes around 90 minutes for me to complete:
Alarm: 5.30 am: Two days a week I have to be at work for 7am, so I need to give myself ample time to fit my habit stack in, and 90 minutes seems to be about right.
Yoga: This really helps my joints loosen up in the morning, which is beneficial for my physical job of lifting, shifting and stacking shelves. I then do some gentle neck stretching exercises. This whole sequence takes around ten minutes.
Meditation: Since I have started meditating I've found it to be really beneficial. I started with a 5 minute session, and have gradually worked it up over the past couple of weeks to a ten minute session. The longer sessions happen in the evening, but in the mornings I have time to fit in 5 minutes of quiet contemplation. I sit on two pillows with my back propped against the end of my bed as it would take far too much energy for me to sit up straight unaided this early in the morning!
Food, water, and supplements: Time for breakfast! Usually some toast with jam or spoonie energy bars (recipe coming soon, all being well!) along with yogurt and fruit sweetener (honey alternative). I also make sure to drink around 500mls of water as it kick starts my hydration for the day, which is essential for keeping my fibromyalgia symptoms in check. I also take my daily dose of three supplements.
Teeth: I went through a period in my life as well where I had neither the energy or inclination to even lift a toothbrush to my mouth, but now I brush, floss and mouthwash every day, and I make time for it twice daily.
Wash hair & get dressed: Unfortunately my hair is something that will not behave unless it is washed daily! Whilst my straighteners are heating up I get dressed for work and "put my face on" to make myself presentable for the lovely customers that day ;)
Then it's off to work I go!
A daily routine, as well as pacing, is a huge part of my life now, as it's enabling me to maintain an consistent level of energy without getting into a boom and bust cycle.
What sorts of things do you do to get yourself ready for the day? Do you have any spoon-conserving tips you'd like to share? Tell me in the comments or tweet me @JayHell83, I love to hear positive, inspiring stories from the spoonie community.
Look out in the near future for a post about my evening/bedtime routine!
J x
Labels:
daily routine,
life,
mecfs,
morning routine,
pacing,
recovery,
spoonie
Tuesday, 31 December 2013
New Year 2014: Looking Ahead and Leaving The Past in The Past
The past few weeks I've been thinking a lot about how much my health has improved over the last 18 months, and how I've continued to learn to manage my symptoms to keep me "on a level" as it were. This involves pacing, eating right and getting good sleep. Finding balance out lives is something we all strive to do, whether or not we are "spoonies". I have come to the conclusion that I don't want my symptoms to define me anymore. Yes, they will always be there, but I want to get out and live my life, I'll be 31 in January and I feel like I am missing out on life experiences, however small. I have a list of things I want to do and places I want to visit, and I also plan to step out of my comfort zone a bit more in 2014 and confront my social anxiety, whilst also being kind to myself and not overdoing it.
So what does all this mean for this blog? I want to share more of my daily "spoonie" life with you, and stop getting bogged down with lengthy posts about how chronic my illness is. I tweeted a picture the other night of my "weekly cook-up" which is an exercise I do about once a week to make sure my freezer is stocked up with easy to prepare food. I don't have energy to waste on doing this daily, so I do it in a batch.
So I could make a little post about that. Practical stuff, knowledge and tips that I can pass on. Basically what I intended this blog to be about in the first place.
I'm rambling. What I'm trying to say is that, whilst I will always have my symptoms, they don't define who I am, and they shouldn't for you either. We are all human underneath, and we are more than just our illnesses.
I will continue to refer to myself as a "spoonie" but only in the correct context. I will continue to pace, eat mindfully and keep good sleep hygiene, just as someone who has asthma continues to use their inhaler-as a tool to manage symptoms. Nothing more dramatic than that.
This is my life and this is who I am, and I intend to embrace that in 2014.
Happy New Year everybody!
So what does all this mean for this blog? I want to share more of my daily "spoonie" life with you, and stop getting bogged down with lengthy posts about how chronic my illness is. I tweeted a picture the other night of my "weekly cook-up" which is an exercise I do about once a week to make sure my freezer is stocked up with easy to prepare food. I don't have energy to waste on doing this daily, so I do it in a batch.
So I could make a little post about that. Practical stuff, knowledge and tips that I can pass on. Basically what I intended this blog to be about in the first place.
I'm rambling. What I'm trying to say is that, whilst I will always have my symptoms, they don't define who I am, and they shouldn't for you either. We are all human underneath, and we are more than just our illnesses.
I will continue to refer to myself as a "spoonie" but only in the correct context. I will continue to pace, eat mindfully and keep good sleep hygiene, just as someone who has asthma continues to use their inhaler-as a tool to manage symptoms. Nothing more dramatic than that.
This is my life and this is who I am, and I intend to embrace that in 2014.
Happy New Year everybody!
Labels:
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anxiety,
cfs,
cfsme,
chronic fatigue syndrome,
chronic illness,
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fibromyalgia,
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inspiring story,
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optimism,
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Thursday, 6 December 2012
CFS Progress Review: One Year On...
A
year ago today I phoned in sick to work and didn't go back for seven
months. Reading back over my blog posts the time seems to have flown
by. I am going to try and condense the last 12 months into a concise
blog post that sums up the best and worst of the last year.
Starting
with my 2012 Manifesto in January:
- Look
at how I can change aspects of my lifestyle to benefit my physical
and emotional health
Make time to develop my art, craft and vintage business(es!)
- One
Thing At A Time
Stop doing what I think others/society/”they” want me to do and start doing what makes ME happy and healthy.
February: Starting simply with nutrition and diet I adopted the practise of drinking four pints of filtered water a day. Recently I have lapsed with this, and the process of re-reading my posts has reminded me how important it is, so I am back on the water wagon again! A frozen lemon wedge adds a lovely cool zing too! I quickly realised my cow's milk intolerance had returned from childhood, and as we know, CFS has lots of links with candida, thrush and yeast infections so I discovered I was intolerant to yeast too.
I started doing my food shopping online. This gave me back a sense of independence whilst also enabling me to conserve energy. I think this simple idea is one of the best inventions of recent times, and I am so grateful to the friendly Sainsbury's drivers-I never had any problems with my orders and would highly recommend the service.
I quickly realised that my energy levels were directly related to the food I was eating. I now focus on natural foods, minimal animal products, and freshly cooked produce whenever possible; although if I am having a low energy day I do not berate myself for putting a frozen pizza in the oven, and I do allow myself treats, but my body will not hesitate to tell me if I am not eating well!
Fascinating fact: In February, a “good day” meant I could do 45 minutes of light activity before I had to lie down and rest completely for 15 minutes. Incredible to think that I went from that, to presently working four 4 hour shifts per week!
March: By March I was beginning to feel better, but I knew the key to a great recovery was PACING. I cannot stress this enough. I hated the idea at first, and even though I had read loads and loads about it, I still wasn't sure. But I gave it a go, and started making notes of every little thing I did throughout the day, what time I did it and for how long. This gave me a really clear idea of how I was proportioning my time, how productive I was being and where I could conserve energy by doing something called “switching/pacing” (give it a Google!)
As well as being productive throughout the day, I knew I had to address my sleep hygiene and my bedtime routine. I downloaded some relaxation mp3's, which I still use (they're amazing), and made sure I kept a regular bedtime and waking routine. I was getting to the point where I could be up and dressed for 9am, even though I might not do anything the rest of the day!
I was also able to incorporate a bit more exercise into my daily activities, even if it was just walking outside for a few minutes. Not only was this a huge step physically, it was also a huge mountain to climb for me within the psychological aspect of my recovery. I hated going outside as I feared people would see me and think I was “skiving” from work, as to all intents and purposes I looked well (as we know this happens with ME/CFS), even though I still felt physically and mentally exhausted the majority of the time. But getting out and about, even for short periods, helped boost my confidence and lessen my depressive symptoms massively.
April
& May:
“When
you have ME/CFS the last thing you need is pressure. Pressure creates
stress, and stress exacerbates ME/CFS.”
By
April I was cycling 2 minutes a day on my exercise bike, and getting
out for 6 minute walks when I felt up to it.
I was keeping up with all the goals I had set myself so far, like
drinking plenty of water, getting healthy, natural foods inside me,
pacing, and having a good sleep routine. In May I began my course of
CBT. Re-reading my blog posts now I can see that around this period
of time, my writing became much more cohesive, upbeat and positive. I
really couldn't recognise myself in the tone of the early posts.
June: In
June I saw my GP for the last time, as she declared me fit for work!
I had actually asked her to do this as I had been feeling much much
better for quite a while, and was actually now beginning to get
frustrated sitting at home all day. I wanted something to do. I
wanted my life to begin again.
I
came up with a three-point manifesto to take me through the coming
months:
Maintain
a good state of health by applying all knowledge learned within the
past twelve months.
Steadily
increase working hours up to sixteen per week, using phased return.
Enjoy
creative pursuits and other hobbies to enhance physical and mental
well-being.
A
couple of weeks before I returned to work, my beloved feathered
friend, Jimmy the budgie, passed away. I was so sad to lose him, but
I somehow knew that he
knew he had helped me through the most difficult time of my life. He
was a fluffy old bird, and it was time for him to go. I will never
forget his amusing chattering, singing and squawking! He now
regularly sends a whole menagerie of different birds to my back
garden where they feast on nuts, seeds and fat balls!
July
& August: As
I was back at work, I wanted to make sure I kept my immune system
topped up. To this day (touch wood) I have not yet caught one cold or
bug that's gone round at work, while colleagues have been smothered!
I am obviously feeding and treating my body correctly now.
I
decided to go vegetarian for a month, and this increased my energy
levels noticeably. I do eat meat now, but I eat generally with a much
more mindful approach, and really think about what I am consuming and
why.
I
finished my course of CBT in August, my therapist was extremely happy
with the improvements I had made. I review everything monthly now,
just to refresh where I am at emotionally, and to notice if there is
anything in my life I am finding difficult. I can then go back and
apply the CBT principles to help me overcome this.
September:
Time
for another manifesto:
1) I am single and I embrace this freedom and independence
2) I have no interest in having children and this is fine
3) Some people might see my job as "boring" or "dead end", but I find it fulfilling and challenging
4) I am happy for making art to be my hobby or second income, I much prefer this than striving to achieve in an over-saturated industry
5) Taking time to relax and take care of myself is just as important as wanting to actively achieve any goal I may set myself
2) I have no interest in having children and this is fine
3) Some people might see my job as "boring" or "dead end", but I find it fulfilling and challenging
4) I am happy for making art to be my hobby or second income, I much prefer this than striving to achieve in an over-saturated industry
5) Taking time to relax and take care of myself is just as important as wanting to actively achieve any goal I may set myself
I believe that full recovery from ME/CFS is not possible until
you accept that your lifestyle and every aspect of it must change.
You must want this change, be ready for it physically and
emotionally, and be happy with it.
October
& November: By
now I seem to have developed a new rhythm in my life. One which is
beneficial and fulfilling to my mental and physical health. I try to
apply mindfulness to my daily activities, be they at work or at home,
and be more self-aware. I listen to my body more by applying
meditation techniques, and communicate with my body and my self. I
have only recently started being creative again, and creating art
that I really really like, instead of striving to appeal to the
masses. I look forward with enthusiasm to my free time, as I have
lots of exciting projects that I am in the midst of. I really enjoy
cooking healthy meals and searching out new recipes, and I enjoy
getting out in the fresh air and power walking-recently I walked 5k
in under an hour!
December: So
here I am, one year on. I hate getting philosophical or sentimental,
especially when I know I am publishing this for the entire internet
to read! But this time last year I had a raging sore throat, a cold
that wouldn't go, and was so physically tired I had to drag myself up
the stairs on all fours to use the bathroom. I was in a very very
very black place come 23rd
December, and was searching for all sorts of things on the internet
that one should never have to read. I wouldn't wish what I have been
through in the past 12 months on anyone, anywhere, ever, and I think
it's high time the authorities concerned started taking this illness
much more seriously.
If
my blog has helped only one person change one thing about their
ME/CFS affected life that improves it, then I have done what I set
out to do 12 months ago.
I
wish everyone who is suffering to whatever degree, the very best for
the future. If you know of anyone who has this illness please don't
laugh it off or make light of it, be there for the person and help
them if you can.
Thank
you all so very much for reading.
This
blog post is written in memory of my amazing Grandma, Bernadette
Mawdsley,
who
passed away peacefully in her sleep on Thursday 22nd
November at the grand old age of 90.
Rest
in Peace Grandma, night night your God Bless xxx
Labels:
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Saturday, 17 November 2012
Runner vs. Chronic Fatigue Syndrome
| I take no credit whatsoever for this image. I found it on Pinterest |
If you keep up with my recovery progress on Twitter, you will know I regularly log my fitness progress on the website Walk Jog Run. I have been power walking for a couple of months now, and by following the training plans on their website, I have been able to pace myself and can now walk 5k in under an hour! Then something really unexpected happened-the guys from Walk Jog Run wanted to feature me as Runner Of The Week! Click the link to see my interview with them entitled "Runner vs. Chronic Fatigue Syndrome" where I talk about my CFS recovery and how getting out in the fresh air has really helped my progress.
Labels:
cfs,
cfsme,
chronic fatigue syndrome,
exercise,
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