Our Weekend Wanderings, Week Eight!

Last weekend began on a Friday, because I couldn't let some awesome artwork pass by, without giving it a mention. I have to admit, it wasn't the most exciting weekend, as I somehow managed to injure my leg, doing absolutely nothing and haven't been able to walk on it since. It's really been annoying me. If I get a painful injury, I want an exciting story to go with it. At the very least, I want to have done something to earn it. No fair! We did manage a couple of trips out, though,and Jade did very well after being dispatched to Lush for emergency bath bombs! 

Living With Thoracic Outlet Syndrome. A Guest Post by Chloe

In our occasional series, Hidden Illnesses, we invite guests to talk about the illnesses that effect them, particularly those that aren't obvious on the outside. We hope to help sufferers and their families learn about the conditions and what they can do to help. Today, Chloe, from Life Unexpected, talks about the little known condition Thoracic Outlet Syndrome and how it has affected her life. Life Unexpected is a family lifestyle blog that follows a millennial mum. With posts about world travel, life with a toddler, general parenting and life as a working mum. 

Wear Yellow for Microcephaly Awareness Day on 30th September!!

Our Hidden Illness series continues, with this post from Sarah.

Tomorrow will be a very special day for me and my family. The 30th of September is Microcephaly Awareness Day. "What's Microcephaly?" I hear you say. Well Microcephaly is a neurological disorder that means the circumference of the head is smaller than it normally should be because the brain has not developed properly or has slowed or even halted growth. Micro means small and cephaly means head. Microcephaly affects 2-2.5% of the population, which actually makes it more common than Autism!

Living with ME - A Guest Post by Catherine

Today in our occasional series Hidden Illnesses, Catherine has joined us, to talk about ME which is a long-term (chronic), fluctuating, neurological condition that causes symptoms affecting many body systems, more commonly the nervous and immune systems. ME affects an estimated 250,000 people in the UK, and around 17 million people worldwide, but many people know little about it. The message, as always is; just because you can't see it, that doesn't mean it isn't causing massive problems for the sufferer. Read on to find out more and perhaps help someone you know with this horrible condition. 

Living With a Back Condition

I'm contributing my own post to our Hidden Illness series today. Something I've been wondering about doing for a while. A lot of the subjects I blog about begin with the same thought; 'Do other people feel this way?' I started this blog because I wanted to offer support to other parents by not being perfect. Because, to be a parent, you don't have to be perfect, you just have to try. You won't always get it right, but you do your best, and your children exist safe in the knowledge that you love them enough to always give them your all, even if sometimes it's a bit wonky or soggy in the middle...

Find Me Face Down on the Floor Behind the Sofa. A Narcoleptic’s Tale.

Our 'hidden illness' series continues with an amazingly insightful and frank post from my fabulous friend Rebecca on Narcolepsy.

If you ask somebody who is ill what the worst thing is about an illness, you will find pain is probably at the top. Followed closely by lethargy or exhaustion. So we know tiredness is awful yet we fail to recognise as a disability. This blog article for The Parent Game is to help you understand the rather odd life cycle of a narcoleptic. Please try and stay awake!

Living with Asthma from a Young Age - How to Help

This guest post is written by my daughter Jade, who would like to tell you about her experiences as an Asthma sufferer. She was first diagnosed at the age of 2 and has lots of advice to help young people cope with asthma, based on her own experience. If you know a young asthma sufferer, you might find this post helpful, because no one knows this illness better than someone who has battled it for 20 years. Asthma is dangerous and prolific and it costs lives. Many people are affected by it and the charity Asthma UK is campaigning for Change to improve the lives of the millions of sufferers in this country. Please click the links to find out how you can help. Over to Jade, who I'd like to thank for writing such a lovely post!

Living with MS, Lorna's Story

I have a lovely friend called Lorna, who I have known for a number of years. I am constantly in awe of her, since she is the sort of mum other mums are jealous of. She bakes amazing cakes, she is super-organised, holds down a demanding job and even finds time to be a fantastic Beaver Scout leader! She is amazing. However, one thing you may not notice about Lorna is that she has a Multiple Sclerosis, a serious medical condition that can effect all kinds of areas of function within the body. She has kindly agreed to spend a little time telling you more about it. Her words a truly inspirational and I may just love her a little bit more after reading them! 

Family Life with Sensory Processing Disorder (Guest Post)

There follows a guest post from my lovely friend Emma, who has kindly agreed to write, in her own words, about her experience of a condition that affects up to one in twenty children, to varying degrees. I think she's amazing and I hope her story will encourage other families facing similar challenges.