stories meaction.net

ME Stories Share your experiences living with Myalgic Encephalomyelitis and Chronic Fatigue Syndrome

Share your experiences living with Myalgic Encephalomyelitis and Chronic Fatigue Syndrome. March 27, 2016. I first saw a GP for post-exertional malaise about 6 months after my symptoms started following a nasty virus. She told me it was probably the menopause despite me having no other symptoms of this and. Read more . They told me to do some exercise. March 27, 2016. Read more . December 3, 2015. Read more . Tale of an Invisible Illness. December 2, 2015. Read more . November 11, 2015. Im still und.
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OVERVIEW

The web site stories.meaction.net currently has an average traffic ranking of zero (the lower the more users). We have analyzed nineteen pages inside the domain stories.meaction.net and found twenty-two websites interfacing with stories.meaction.net. There is one social communication sites retained by this website.
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19
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22
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1

STORIES.MEACTION.NET TRAFFIC

The web site stories.meaction.net has seen varying quantities of traffic for the whole of the year.
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LINKS TO WEBSITE

MEAction Fighting for health equality for Myalgic Encephalomyelitis and Chronic Fatigue Syndrome

A global health network for people with Myalgic Encephalomyelitis, also known as chronic fatigue syndrome. Here are some of our many community projects. Time For Unrest is a global impact campaign designed to strengthen the growing movement advocating for more recognition, education, research, and funding around ME. Jen Brea presents at TED in June of 2017.

WHAT DOES STORIES.MEACTION.NET LOOK LIKE?

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STORIES.MEACTION.NET SERVER

Our crawlers observed that a lone page on stories.meaction.net took one thousand one hundred and eighty-eight milliseconds to load. Our web crawlers could not find a SSL certificate, so therefore our web crawlers consider stories.meaction.net not secure.
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1.188 sec
SSL
NOT SECURE
IP
104.196.144.96

SERVER SOFTWARE AND ENCODING

We revealed that this website is employing the nginx server.

HTML TITLE

ME Stories Share your experiences living with Myalgic Encephalomyelitis and Chronic Fatigue Syndrome

DESCRIPTION

Share your experiences living with Myalgic Encephalomyelitis and Chronic Fatigue Syndrome. March 27, 2016. I first saw a GP for post-exertional malaise about 6 months after my symptoms started following a nasty virus. She told me it was probably the menopause despite me having no other symptoms of this and. Read more . They told me to do some exercise. March 27, 2016. Read more . December 3, 2015. Read more . Tale of an Invisible Illness. December 2, 2015. Read more . November 11, 2015. Im still und.

PARSED CONTENT

The web site stories.meaction.net has the following on the web site, "Share your experiences living with Myalgic Encephalomyelitis and Chronic Fatigue Syndrome." I noticed that the webpage also said " I first saw a GP for post-exertional malaise about 6 months after my symptoms started following a nasty virus." They also said " She told me it was probably the menopause despite me having no other symptoms of this and. They told me to do some exercise. Tale of an Invisible Illness."

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