Living with Chronic Fatigue Syndrome/ME

My Daughter suffers with CFS this page is to share our story both as sufferer and carer, and to maybe help others feel that they are not alone

May 7th is the start of ME Awareness week, as many of you know my Daughter has been ill with this  since 2015.  Before she became ill, I had heard of ME but like many… View Post

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Wow that is another month that has flown by, I swear I blinked and missed April, so as it is now May it is time for my April Round Up. As always I will start… View Post

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Those of you who have been with me from the start of my blog, will know that when I started writing StressedMum, I had a healthy 11 year old who was just about to spend… View Post

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Today I am hosting another post from a friend and fellow Mum of a child with ME, showing a different side to how this illness can affect our children and the care they desperately need… View Post

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I have somehow managed to get to the middle of March, and realise i have not posted my February Roundup, I swear it was only the end of February a day or so ago. As… View Post

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I am hosting a guest post from a friend and a parent of a child with ME,  quite a powerful post but one that will give an insight into how much our children and those… View Post

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As you all know I have a Daughter with a chronic illness, part of her illness means walking too far or walking at all is common for us now, so we need to rely heavily… View Post

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Recently I have been like a bear with a sore head, I am constantly angry, I can be fine one minute and then just explode th next, for what might seem to be over nothing. … View Post

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We are one month down into the new year and already it is February, where did January go, so time for my monthly round up. As always I will start with C, she has had… View Post

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Regular readers will know that my Daughter C has been unwell since Christmas 2015, in March 2016 C was diagnosed with CFS/ME, you can read our first post here, where I talked about how she… View Post

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