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FRECKLES-AND-ALL.COM

Freckles & All

A blog about appreciating the little and lovely things in life while recovering from chronic fatigue syndrome / CFS / M.E.

http://www.freckles-and-all.com/

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44.1●●●●0292
Fa●●●●●●●●●●@gmail.com

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Faye Savory

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59 l●●●●bost

Isle●●●●ewis , Westernisles, Hs2 9ns

United Kingdom

44.1●●●●0292
Fa●●●●●●●●●●@gmail.com

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Freckles & All | freckles-and-all.com Reviews
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A blog about appreciating the little and lovely things in life while recovering from chronic fatigue syndrome / CFS / M.E.
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Freckles & All | freckles-and-all.com Reviews

https://freckles-and-all.com

A blog about appreciating the little and lovely things in life while recovering from chronic fatigue syndrome / CFS / M.E.

LINKS TO THIS WEBSITE

katharineandme.blogspot.com katharineandme.blogspot.com

Katharine and M.E.: February 2014

http://katharineandme.blogspot.com/2014_02_01_archive.html

Saturday, 22 February 2014. A while ago I came across Voices from the Shadows. A film “born of desperation” made by the mother and brother of a severe ME sufferer. It tells the true stories of several ME patients and the injustices and abuse they and their families have been subjected to. An introduction. Today, in the twenty-first century. From the Sam and M.E. blog. So, while I may not be big enough, powerful enough (or, indeed, healthy enough) to change the world and its opinion of my illness, I can.

katharineandme.blogspot.com katharineandme.blogspot.com

Katharine and M.E.: On a life-long love of reading

http://katharineandme.blogspot.com/2015/03/on-life-long-love-of-reading.html

Thursday, 5 March 2015. On a life-long love of reading. We all spend our lives telling them - about this, about that, about people. Some stories are so good we wish they'd never end. They're so gripping that we'll go without sleep just to see a little bit more. Some stories bring us laughter and sometimes they bring us tears. But isn't that what a great story does? It makes you feel. Stories that are so powerful, they really are with us forever. To being unable to pick up a book, let alone read it. M...

going-slowly.blogspot.com going-slowly.blogspot.com

going slowly: good reads

http://going-slowly.blogspot.com/p/good-reads.html

Katharine and M.E. ME myself and I. Subscribe to: Posts (Atom). Simple template. Powered by Blogger.

katyfletcher.blogspot.com katyfletcher.blogspot.com

Katy Fletcher.: February 2015

http://katyfletcher.blogspot.com/2015_02_01_archive.html

Thursday, 26 February 2015. New week. New Techniques - Part Two. P e w t e r . ]. This the first time I've ever worked with pewter and I absolutely loved it! The block of solid metal quickly melts under the heat of the blowtorch and can then be poured into a mold. Not a great photo (its very dark in that corner of the workshop! Continuing on with the same domed shape I enlisted the help of my tutor Ed to help make a wooden press mould to press sheet metal into. This requires lots of precise calculati...

merussia.wordpress.com merussia.wordpress.com

Блоги/Blogs — merussia

https://merussia.wordpress.com/blogs

Миалгический энцефаломиелит, или синдром хронической усталости: знание — шаг к пониманию. About/Обо мне и сайте. Благотворительные организации, сайты про МЭ/More useful links (charity, science and so on). 8212; не только потрясающие развёрнутые тексты и материалы про МЭ/СХУ, симптомы и жизнь с этим заболеванием, но и множество рецептов натуральной еды, которая в чём-то помогает справляться с болезнью. ME, Myself and I. 8212; Здесь, пожалуй, одно из самых полных описаний жизни с МЭ/СХУ. Начиная с 2012...

nicolemmorgan.blogspot.com nicolemmorgan.blogspot.com

Nicole Morgan: February 2015

http://nicolemmorgan.blogspot.com/2015_02_01_archive.html

Saturday, 28 February 2015. Online Support With A Chronic Illness - Rare Disease Day. This post is about something thats very important to me. It's also rare disease day today so it fits in nicely. You may not all be aware but I have 3 chronic illnesses called Ehlers Danlos Syndrome. And ME/Chronic Fatigue Syndrome. Ps I'm no way encouraging you to self diagnose, if someones suggested an illness to you never assume you have it until a medical professional has diagnosed you). Follow me on Blog Lovin' here.

katharineandme.blogspot.com katharineandme.blogspot.com

Katharine and M.E.: February 2015

http://katharineandme.blogspot.com/2015_02_01_archive.html

Friday, 20 February 2015. Mum, Helen and Heather walk 26.5 miles for ME Research UK! It's less than 6 months since my birthday fundraiser and I have more. Very exciting fundraising news! This time, though, I'm not doing anything myself because. My Mum, her best friend Helen, and my best friend Heather (who is also Helen's daughter) are walking 26 and a half miles in one day - all in the aid of ME Research UK. As part of the Bath Beat. And getting electrocuted by electric fences amongst other obstacles!

katharineandme.blogspot.com katharineandme.blogspot.com

Katharine and M.E.: August 2015

http://katharineandme.blogspot.com/2015_08_01_archive.html

Thursday, 13 August 2015. Things have been quiet around here for quite a while. Thankfully, this isn't due to a deterioration in my health; I've just been working on other projects (such as writing an article for ME Awareness Week for my university's student newspaper. And writing a chapter for an anthology on the unique lived experience of childhood ME). This post has been languishing in my 'drafts' folder for over a year. I feel now is the perfect time to rediscover it. Thing in the world. In the words...

katharineandme.blogspot.com katharineandme.blogspot.com

Katharine and M.E.: March 2015

http://katharineandme.blogspot.com/2015_03_01_archive.html

Thursday, 19 March 2015. I'm worth more than £50. This morning there was a discussion on The Wright Stuff, on Channel 5, entitled "Is the NHS failing M.E. sufferers? It featured the CEO of Action for M.E., Sonya Chowdhury, and Graeme Bloom, who has M.E. While I expected to be left feeling very angry and upset (as I usually am whenever M.E. is mis. Aside from a rather unfortunate remark from Nadine Dorries that "97% of young people with ME/cfs recover" ( if only this were true! How is this right? Firstly,...

katharineandme.blogspot.com katharineandme.blogspot.com

Katharine and M.E.: December 2014

http://katharineandme.blogspot.com/2014_12_01_archive.html

Monday, 29 December 2014. What 2014 taught me. Frosty mornings follow wintry nights; sunsets greet us eagerly in the mid-afternoon chill. The year hurtles unwaveringly towards its dignified end, taking its final, icy breaths as we wait patiently, hoping to discover better things on the next page. The year has passed by in a flash of light and dark, highs and lows, hopes and fears; it seems like an eternity has flown by since I said hello to 2014. Uncertainty is the refuge of hope". Never be afraid to rai...

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Freckles & All

Shop and Donate to the M.E. Association. Thursday, 16 July 2015. Starting a Business Interview on Fibro Geek BearHugs. My interview about starting BearHugs is up on the lovely Donna's blog Fibro Geek. Find out a bit about my new venture and read the full interview here. There will be a proper update coming soon when I have the time/energy. In the meantime, you can find BearHugs at. My website, www.bearhugsgifts.com, is also on its way very soon. Or come and say hello on Facebook ( here. Read Part 1 here.

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