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 life goals. Show all posts
Showing posts with label life goals. Show all posts
Sunday, 28 July 2013
My Recovery Journey over six months on...
I have decided it's time to resurrect this blog, under a slightly different theme. From now on my focus will be on blogging about how to focus on staying well after going into remission from ME/CFS, which is where I see myself now.
I have given the blog a new look, and made it easier to be viewed on phones for those of you who find it difficult to access a computer.
I have had a long time to reflect on how I want to share my knowledge and personal experience of having ME/CFS and have come up with a number of ways to do this, including making art and using Twitter as a platform for fellow spoonies to connect. You can even follow me if you want!
There will be two future posts, one telling a (very short) background story of how I came to be diagnosed with ME/CFS, and another about how I see it started. From then on I want to focus on the positives and the future, and share my tips and experiences to help others.
I hope to re-kindle some interest in this blog, more importantly, if I can help just one person that would be enough for me.
I hope to see you here again soon.
Please leave a comment if you would like to see me blog about a particular aspect of recovery and I will do my best to post something helpful :)
Labels:
cfs,
cfsme,
chronic fatigue syndrome,
chronic illness,
fibromyalgia,
fms,
hope,
inspiring story,
life goals,
me,
myalgic encephalomyletis,
optimism,
post viral fatigue,
recovering,
recovery,
wellbeing
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:
cfs,
chronic fatigue syndrome,
diet,
exercise,
fibromyalgia,
fitness,
food,
goal setting,
healthy eating,
hope,
inspiring story,
life goals,
me,
optimism,
pacing,
post viral fatigue,
recovery,
wellbeing
Friday, 28 September 2012
CFS Progress Review: September 2012
This month: Mortality, Priority and Moving Forward
Some of the readers of this blog (however few or many there may be) might laugh at me for contemplating my mortality at 29. But how many of you who are older did the same at my age?
I am single, have no desire for children, and certainly see no joy in trying to climb either a property or career ladder right now.
Although at one time in my life I did see value in some of these things.
Having M.E has changed me (for the better).
I have spent much of the last month and the last week in particular, sitting with my thoughts and moral beliefs and trying to get comfortable with them. If I found myself becoming uncomfortable, I asked myself why that was so. And (after a whole lot of soul searching) I came to some pleasing conclusions:
1) I am single and I embrace this freedom and indepence
2) I have no interest in having children
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 acheive 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 don't want to go into detail about any of these points, as they are are private and personal to me. They could be thought of as my "big" life choices/beliefs. Although I have given you a brief outline of them for a reason...
I believe that full recovery is not possible until you accept that your lifestyle and every aspect of it must change. Thinking that you want to get back to how things were before you were ill is pointless-when you think about it, how much were you enjoying or getting out of life before you were ill??? For me my life consisted of struggling to keep up with my work, my social life and spending ALL of my days off sleeping. Who wants that lifestyle back again?
However, making change is not easy, which is why I've stuggled so much emotionally the past month. Letting go of the past and embracing the future is hard work. The points listed above could well be thought of in opposite terms twelve months ago; but now they are as they are, and reading them excites me and makes me happy and content. And that, really, is all we want out of life, isn't it?
Some of the readers of this blog (however few or many there may be) might laugh at me for contemplating my mortality at 29. But how many of you who are older did the same at my age?
I am single, have no desire for children, and certainly see no joy in trying to climb either a property or career ladder right now.
Although at one time in my life I did see value in some of these things.
Having M.E has changed me (for the better).
I have spent much of the last month and the last week in particular, sitting with my thoughts and moral beliefs and trying to get comfortable with them. If I found myself becoming uncomfortable, I asked myself why that was so. And (after a whole lot of soul searching) I came to some pleasing conclusions:
1) I am single and I embrace this freedom and indepence
2) I have no interest in having children
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 acheive 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 don't want to go into detail about any of these points, as they are are private and personal to me. They could be thought of as my "big" life choices/beliefs. Although I have given you a brief outline of them for a reason...
I believe that full recovery is not possible until you accept that your lifestyle and every aspect of it must change. Thinking that you want to get back to how things were before you were ill is pointless-when you think about it, how much were you enjoying or getting out of life before you were ill??? For me my life consisted of struggling to keep up with my work, my social life and spending ALL of my days off sleeping. Who wants that lifestyle back again?
However, making change is not easy, which is why I've stuggled so much emotionally the past month. Letting go of the past and embracing the future is hard work. The points listed above could well be thought of in opposite terms twelve months ago; but now they are as they are, and reading them excites me and makes me happy and content. And that, really, is all we want out of life, isn't it?
Labels:
cfs,
cfsme,
chronic fatigue syndrome,
chronic illness,
hope,
inspiring story,
life goals,
mortality,
myalgic encephalomyletis,
optimism,
progress,
recovery,
wellbeing
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Showing posts with label life goals. Show all posts
Showing posts with label life goals. Show all posts
Sunday, 28 July 2013
My Recovery Journey over six months on...
I have decided it's time to resurrect this blog, under a slightly different theme. From now on my focus will be on blogging about how to focus on staying well after going into remission from ME/CFS, which is where I see myself now.
I have given the blog a new look, and made it easier to be viewed on phones for those of you who find it difficult to access a computer.
I have had a long time to reflect on how I want to share my knowledge and personal experience of having ME/CFS and have come up with a number of ways to do this, including making art and using Twitter as a platform for fellow spoonies to connect. You can even follow me if you want!
There will be two future posts, one telling a (very short) background story of how I came to be diagnosed with ME/CFS, and another about how I see it started. From then on I want to focus on the positives and the future, and share my tips and experiences to help others.
I hope to re-kindle some interest in this blog, more importantly, if I can help just one person that would be enough for me.
I hope to see you here again soon.
Please leave a comment if you would like to see me blog about a particular aspect of recovery and I will do my best to post something helpful :)
Labels:
cfs,
cfsme,
chronic fatigue syndrome,
chronic illness,
fibromyalgia,
fms,
hope,
inspiring story,
life goals,
me,
myalgic encephalomyletis,
optimism,
post viral fatigue,
recovering,
recovery,
wellbeing
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:
cfs,
chronic fatigue syndrome,
diet,
exercise,
fibromyalgia,
fitness,
food,
goal setting,
healthy eating,
hope,
inspiring story,
life goals,
me,
optimism,
pacing,
post viral fatigue,
recovery,
wellbeing
Friday, 28 September 2012
CFS Progress Review: September 2012
This month: Mortality, Priority and Moving Forward
Some of the readers of this blog (however few or many there may be) might laugh at me for contemplating my mortality at 29. But how many of you who are older did the same at my age?
I am single, have no desire for children, and certainly see no joy in trying to climb either a property or career ladder right now.
Although at one time in my life I did see value in some of these things.
Having M.E has changed me (for the better).
I have spent much of the last month and the last week in particular, sitting with my thoughts and moral beliefs and trying to get comfortable with them. If I found myself becoming uncomfortable, I asked myself why that was so. And (after a whole lot of soul searching) I came to some pleasing conclusions:
1) I am single and I embrace this freedom and indepence
2) I have no interest in having children
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 acheive 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 don't want to go into detail about any of these points, as they are are private and personal to me. They could be thought of as my "big" life choices/beliefs. Although I have given you a brief outline of them for a reason...
I believe that full recovery is not possible until you accept that your lifestyle and every aspect of it must change. Thinking that you want to get back to how things were before you were ill is pointless-when you think about it, how much were you enjoying or getting out of life before you were ill??? For me my life consisted of struggling to keep up with my work, my social life and spending ALL of my days off sleeping. Who wants that lifestyle back again?
However, making change is not easy, which is why I've stuggled so much emotionally the past month. Letting go of the past and embracing the future is hard work. The points listed above could well be thought of in opposite terms twelve months ago; but now they are as they are, and reading them excites me and makes me happy and content. And that, really, is all we want out of life, isn't it?
Some of the readers of this blog (however few or many there may be) might laugh at me for contemplating my mortality at 29. But how many of you who are older did the same at my age?
I am single, have no desire for children, and certainly see no joy in trying to climb either a property or career ladder right now.
Although at one time in my life I did see value in some of these things.
Having M.E has changed me (for the better).
I have spent much of the last month and the last week in particular, sitting with my thoughts and moral beliefs and trying to get comfortable with them. If I found myself becoming uncomfortable, I asked myself why that was so. And (after a whole lot of soul searching) I came to some pleasing conclusions:
1) I am single and I embrace this freedom and indepence
2) I have no interest in having children
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 acheive 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 don't want to go into detail about any of these points, as they are are private and personal to me. They could be thought of as my "big" life choices/beliefs. Although I have given you a brief outline of them for a reason...
I believe that full recovery is not possible until you accept that your lifestyle and every aspect of it must change. Thinking that you want to get back to how things were before you were ill is pointless-when you think about it, how much were you enjoying or getting out of life before you were ill??? For me my life consisted of struggling to keep up with my work, my social life and spending ALL of my days off sleeping. Who wants that lifestyle back again?
However, making change is not easy, which is why I've stuggled so much emotionally the past month. Letting go of the past and embracing the future is hard work. The points listed above could well be thought of in opposite terms twelve months ago; but now they are as they are, and reading them excites me and makes me happy and content. And that, really, is all we want out of life, isn't it?
Labels:
cfs,
cfsme,
chronic fatigue syndrome,
chronic illness,
hope,
inspiring story,
life goals,
mortality,
myalgic encephalomyletis,
optimism,
progress,
recovery,
wellbeing
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