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All the best URLs were gone

All the best URLs were gone. Invisible Illness Awareness Week 2015 – part one. October 3, 2015. First of all, a nice tidy list of my illnesses and what they mean:. Chronic migraines – this mostly speaks for itself, but chronic migraines are diagnosed when an individual experiences migraines and associated symptoms (such as photophobia, nausea and dizziness) for more than 8-15 days a month. My migraines are thankfully significantly less frequent now due to medication. These are only my “main” ...I’m...

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All the best URLs were gone | allthebesturlsweregone.wordpress.com Reviews
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All the best URLs were gone. Invisible Illness Awareness Week 2015 – part one. October 3, 2015. First of all, a nice tidy list of my illnesses and what they mean:. Chronic migraines – this mostly speaks for itself, but chronic migraines are diagnosed when an individual experiences migraines and associated symptoms (such as photophobia, nausea and dizziness) for more than 8-15 days a month. My migraines are thankfully significantly less frequent now due to medication. These are only my “main” ...I’m...
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All the best URLs were gone | allthebesturlsweregone.wordpress.com Reviews

https://allthebesturlsweregone.wordpress.com

All the best URLs were gone. Invisible Illness Awareness Week 2015 – part one. October 3, 2015. First of all, a nice tidy list of my illnesses and what they mean:. Chronic migraines – this mostly speaks for itself, but chronic migraines are diagnosed when an individual experiences migraines and associated symptoms (such as photophobia, nausea and dizziness) for more than 8-15 days a month. My migraines are thankfully significantly less frequent now due to medication. These are only my “main” ...I’m...

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freyaprevett | All the best URLs were gone

https://allthebesturlsweregone.wordpress.com/author/freyaprevett

All the best URLs were gone. Invisible Illness Awareness Week 2015 – part one. October 3, 2015. First of all, a nice tidy list of my illnesses and what they mean:. Chronic migraines – this mostly speaks for itself, but chronic migraines are diagnosed when an individual experiences migraines and associated symptoms (such as photophobia, nausea and dizziness) for more than 8-15 days a month. My migraines are thankfully significantly less frequent now due to medication. These are only my “main” ...I’m...

2

On “Letting Your Disability Define You” and other such things | All the best URLs were gone

https://allthebesturlsweregone.wordpress.com/2015/08/21/on-letting-your-disability-define-you

All the best URLs were gone. On “Letting Your Disability Define You” and other such things. August 21, 2015. Chances are, if you’ve been on the internet for any amount of time, you will have seen pictures like this:. What a fighter, what a beacon of hope for humanity! I see this phrase used an awful lot around disability. “Oh, she’s deaf, but she doesn’t let it define her! 8221; “The only way to truly have a good life is to not let your disability define you! Leave a Reply Cancel reply. You are commentin...

3

Letting Go Of “Normal” | All the best URLs were gone

https://allthebesturlsweregone.wordpress.com/2015/07/23/letting-go-of-normal

All the best URLs were gone. Letting Go Of “Normal”. July 23, 2015. Be like everyone else – but be yourself! 8230; The list goes on. And despite the fact that the world is gradually becoming more accepting, standing out or being different in today’s society is scary as. I’ve never felt normal. Ever. And over the years, some of this has begun to make more sense. But until very recently, I felt. PS sorry for not updating in over three months I am horrifically unreliable). Leave a Reply Cancel reply. Blog a...

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About | All the best URLs were gone

https://allthebesturlsweregone.wordpress.com/about

All the best URLs were gone. Freya England. 17. Disabled. Queer. Lover of all things soft. Probably hungry. Welcome to my blog (whatever the heck it is). Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out. You are commenting using your Twitter account. ( Log Out. You are commenting using your Facebook account. ( Log Out. Notify me of new comments via email.

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The Glass Box | All the best URLs were gone

https://allthebesturlsweregone.wordpress.com/2015/04/19/the-glass-box

All the best URLs were gone. April 19, 2015. In which I make bad mental health analogies and attempt to organise my thoughts into vaguely coherent sentences. Imagine you’re maybe ten or eleven, and just going about your daily life as normal. Going to school with hardly any issues, having fun with your friends, all the standard stuff. Then one day, someone comes along with a glass box, herds you into it, then locks the door. At first, you’re confused. What is this box? Where did it come from? There is no ...

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lifewithseveremeandrandomotherthings.wordpress.com lifewithseveremeandrandomotherthings.wordpress.com

Accepting Chronic Illness, not giving in – just accepting that life will be different! | lifewithseveremeandotherrandomthings

https://lifewithseveremeandrandomotherthings.wordpress.com/2015/01/09/accepting-chronic-illness-not-giving-in-just-accepting-that-life-will-be-different

ME, living with Severe M.E and other random things. Follow lifewithseveremeandotherrandomthings on WordPress.com. Accepting Chronic Illness, not giving in – just accepting that life will be different! In many cases the people who you would have assumed would be there to help and support you should you ever become ill aren’t there for you and are often dismissive of the fact that you are ill or that there’s actually anything wrong with you at all. Loneliness, and acceptance. I think there’s a simila...

lifewithseveremeandrandomotherthings.wordpress.com lifewithseveremeandrandomotherthings.wordpress.com

How can others understand if we don’t understand each other? | lifewithseveremeandotherrandomthings

https://lifewithseveremeandrandomotherthings.wordpress.com/2015/01/28/how-can-others-understand-if-we-dont-understand-each-other

ME, living with Severe M.E and other random things. Follow lifewithseveremeandotherrandomthings on WordPress.com. How can others understand if we don’t understand each other? Do we as severely affected patients ever stop to think about someone with mild/moderate ME and how their lives are affected? Also if some people mildly affected don’t realise how severe ME can be why don’t those of us severely affected tell them? If you constantly had periods of being able to do things hoping your health was improvi...

lifewithseveremeandrandomotherthings.wordpress.com lifewithseveremeandrandomotherthings.wordpress.com

Getting an M.E Diagnosis…..and how others react! | lifewithseveremeandotherrandomthings

https://lifewithseveremeandrandomotherthings.wordpress.com/2014/12/21/getting-an-m-e-diagnosis-and-how-others-react

ME, living with Severe M.E and other random things. Follow lifewithseveremeandotherrandomthings on WordPress.com. Getting an M.E Diagnosis….and how others react! Finally you make an appointment with the doctor to discuss what has been going on and talk about all the symptoms you have noticed. The doctor records what you’ve said and tells you that they will do some tests to see what is going on. And doctors know all about illness and how to cure them or at least treat them! Sadly, where M.E is concern...

lifewithseveremeandrandomotherthings.wordpress.com lifewithseveremeandrandomotherthings.wordpress.com

December | 2014 | lifewithseveremeandotherrandomthings

https://lifewithseveremeandrandomotherthings.wordpress.com/2014/12

ME, living with Severe M.E and other random things. Follow lifewithseveremeandotherrandomthings on WordPress.com. Getting an M.E Diagnosis….and how others react! Finally you make an appointment with the doctor to discuss what has been going on and talk about all the symptoms you have noticed. The doctor records what you’ve said and tells you that they will do some tests to see what is going on. And doctors know all about illness and how to cure them or at least treat them! Sadly, where M.E is concern...

lifewithseveremeandrandomotherthings.wordpress.com lifewithseveremeandrandomotherthings.wordpress.com

About | lifewithseveremeandotherrandomthings

https://lifewithseveremeandrandomotherthings.wordpress.com/about

ME, living with Severe M.E and other random things. Follow lifewithseveremeandotherrandomthings on WordPress.com. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out. You are commenting using your Twitter account. ( Log Out. You are commenting using your Facebook account. ( Log Out. You are commenting using your Google account. ( Log Out. My Color Is Lyme.

lifewithseveremeandrandomotherthings.wordpress.com lifewithseveremeandrandomotherthings.wordpress.com

What M.E is, and what it’s not! | lifewithseveremeandotherrandomthings

https://lifewithseveremeandrandomotherthings.wordpress.com/2014/12/16/what-m-e-is-and-what-its-not

ME, living with Severe M.E and other random things. Follow lifewithseveremeandotherrandomthings on WordPress.com. What M.E is, and what it’s not! Sadly many people have little to no knowledge about the illness which sadly includes many medical professionals! ME affects every bodily system and symptoms can include;. Cognitive dysfunction (often referred to as brain fog),. Post Exertional Malaise (a worsening of symptoms after activity). Sensitivities to noise, light and chemicals. Sore and swollen glands.

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January | 2015 | lifewithseveremeandotherrandomthings

https://lifewithseveremeandrandomotherthings.wordpress.com/2015/01

ME, living with Severe M.E and other random things. Follow lifewithseveremeandotherrandomthings on WordPress.com. How can others understand if we don’t understand each other? Do we as severely affected patients ever stop to think about someone with mild/moderate ME and how their lives are affected? Also if some people mildly affected don’t realise how severe ME can be why don’t those of us severely affected tell them? If you constantly had periods of being able to do things hoping your health was improvi...

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aineemac | lifewithseveremeandotherrandomthings

https://lifewithseveremeandrandomotherthings.wordpress.com/author/aineemac

ME, living with Severe M.E and other random things. Follow lifewithseveremeandotherrandomthings on WordPress.com. Https:/ lifewithseveremeandrandomotherthings.wordpress.com. How can others understand if we don’t understand each other? Do we as severely affected patients ever stop to think about someone with mild/moderate ME and how their lives are affected? Also if some people mildly affected don’t realise how severe ME can be why don’t those of us severely affected tell them? If you constantly had perio...

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All the best URLs were gone

All the best URLs were gone. Invisible Illness Awareness Week 2015 – part one. October 3, 2015. First of all, a nice tidy list of my illnesses and what they mean:. Chronic migraines – this mostly speaks for itself, but chronic migraines are diagnosed when an individual experiences migraines and associated symptoms (such as photophobia, nausea and dizziness) for more than 8-15 days a month. My migraines are thankfully significantly less frequent now due to medication. These are only my “main” ...I’m...

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