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Jenny Helen
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42 followers
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The effect of brainfog
This was written in mid May, but I decided not to put it up whilst the  ' ME from another perspective '  series was going on, there were a lot of posts going up at that time and it seemed out of place. Since this was written my brainfog has been worse, but ...
The effect of brainfog
The effect of brainfog
jennyhelenmyspoonielife.blogspot.com
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Why I'm going to Breakaspear Hospital
I was sure that I had written a blog post about this before, and kept it safely in my drafts section, but have now realised that I've just thought a lot about talking about this on my blog! I first became aware of Breakspear hospital just under a year ago w...
Why I'm going to Breakaspear Hospital
Why I'm going to Breakaspear Hospital
jennyhelenmyspoonielife.blogspot.com
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Lizzy's perspective: Her journey with ME
This post is part of the ' ME from another perspective ' series which I am running to contribute towards ME awareness this year. I have known Lizzy for about 6 years, when we met we were both severely affected school aged sufferers of ME. Since then I have ...
Lizzy's perspective: Her journey with ME
Lizzy's perspective: Her journey with ME
jennyhelenmyspoonielife.blogspot.com
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Kat's perspective: The unique challenges faced by young adults and children with ME
This post is part of the ' ME from another perspective ' series which I am running to contribute towards ME awareness this year. Last year Kat kindly wrote a guest blog post called How ME has changed my life . I am so glad to have her back again, to write a...
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Deanna's perspective: 10 things she wishes she'd known when she first got ME
This post is part of the ' ME from another perspective ' series which I am running to contribute towards ME awareness this year. Deanna is back with a second blog post about the things she wishes she'd known when she first got ill. Some of these things are ...
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Tasha's perspective: Denial
This post is part of the ' ME from another perspective ' series which I am running to contribute towards ME awareness this year. I was overwhelmed by how much Tasha's experiences resonated with me, ME is so often denied by society, but also ourselves. Comin...
Tasha's perspective: Denial
Tasha's perspective: Denial
jennyhelenmyspoonielife.blogspot.com
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Ellie's perspective: Getting a handle on ME
This post is part of the ' ME from another perspective ' series which I am running to contribute towards ME awareness this year. Ellie and I have realised that went to the same university. Ellie was diagnosed while she was at uni, and I had my diagnosis bef...
Ellie's perspective: Getting a handle on ME
Ellie's perspective: Getting a handle on ME
jennyhelenmyspoonielife.blogspot.com
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The Power of Sigma, A Campaign by Change for M.E.
This week I saw a really powerful campaign talking about the emotional affect that stigma can have on ME patents. It is honestly one of the best ME campaigns I have ever seen, which is why I have decided to share it with you with permission of course! Livin...
The Power of Sigma, A Campaign by Change for M.E.
The Power of Sigma, A Campaign by Change for M.E.
jennyhelenmyspoonielife.blogspot.com
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Hannah's Perspective: The 10 unexpected blessings of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome
This post is part of the ' ME from another perspective ' series which I am running to contribute towards ME awareness this year. As I have got to know Hannah, I have been blown away by her positivity and enthusiasm for life. It therefore was no surprise whe...
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Deanna's perspective: How she got ill
This post is part of the ' ME from another perspective ' series which I am running to contribute towards ME awareness this year. Deanna has written two posts for this series. The first post tells the story of how she got ill, and explains how she has reache...
Deanna's perspective: How she got ill
Deanna's perspective: How she got ill
jennyhelenmyspoonielife.blogspot.com
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