You're More Than Your Illness

Hello Everyone!

I made it, kind of. It’s the last day of me posting every day of the week for M.E and Fibro Awareness Week. I’m going to try post something more fun next time to counter act for all this although I’ve tried to be up beat some days. I just hope this has all helped someone or somehow and we’re all a little more educated on these chronic illnesses.

I’ve talked about mental health, raising awareness, tips for bed bound, being positive, relationships and treatments. I thought I would finish with talking about how you are not your illness, your illness does not define you and how you are a lot more than that.

Yes, you may suffer from a chronic illness like M.E and Fibro or you may know someone who does but that person is a lot more than that. Just like when someone asks what you are, meaning what do you do for a living normally, people will usually say they’re a nurse or a student or accountant, and so on. I think you’re not just your job title. For example:

I am a

Aspiring Actress

Sister

Daughter

Blogger

Massive Film Fan

Niece

Grand-daughter

Cousin

Friend

maybe even a Best Friend

Girlfriend

Sweet tooth

Photo Horder

Sarcastic

and plenty more!

But yes, I also suffer from a chronic illness or two.

The chronic illnesses don’t define who I am, its a part of me, but a very small part of me. I want to raise awareness and talk about my illness and if people have questions I’ll happily answer them but don’t just let that be all we talk about, I still have an opinion on if I thought last nights Corrie was decent or if the latest Hunger Games was my favourite in the series or not. There’s a lot more to someone than an illness and it goes for anyone, if they work in a hospital its likely they’re not gonna want to talk about it out of work much. I just want (and I think this goes for anyone like me) to feel a lot more normal than I am sometimes.

Thank you if you’ve stayed with me all week and read every post or any post I’ve done really.

I’ll be blogging a lot more from now on and not leaving it to one a month hopefully.

Take care and I’ll speak to you soon!

Natasha

xoxo

Comments

Doctors, Hospitals and No Success.

I decided I think I should explain exactly what I have been through with the doctors and hospitals including treatments. As I explained in my post 'The Past 3 Years...' this all started just over 3 years ago now. I started having flu like symptoms just after Christmas 2010 and after seeing the doctors every week I was finally tested about 5 weeks later for Glandular Fever, by this time the doctor said the virus would probably have left my system so my blood tests all came back fine. Unfortunately there was never a definite answer for this mystery illness that started these long, long years. After finally going back to college and completing my A Levels and having my 18th birthday in June 2011 I went back to the doctors after the cold, blocked nose and coughing symptoms had gone but left me still aching all over, mainly in my legs. At the beginning of August 2011 I went to the doctors AGAIN and I was sent to the 'GUM' department of the Princess Royal Hospital to be ...

My week of HELL.

Hello again! First of all I want to say thank you to any comments, messages and emails I have received since I started this blog. I didn’t think anyone would even read it. It means a lot to me the amount of support there is and that people understand M.E/CFS and Fibromyalgia even that little bit more. So first I’ll talk about the Lidocaine Infusion I had two weeks ago. Basically I sit in a chair and they hook me up to all the machines that check your heart beat etc. Then they take your blood pressure and weigh you to check everything is okay for you to go ahead with it. Then they put the cannula into your hand and add the drip which slowly for an hour and a half puts the anaesthetic into you. Then they take your blood pressure every 10 minutes whilst you just sit there (bored). After the infusion I didn’t feel any different apart from feeling dizzy. The next day I did think the pain in my arms was better which was good but my legs just seemed to get worse and worse. ...

30 Years of Mr and Mrs Spychalski

27.06.1987 - Mum and Dad's Wedding Day. On the 27th of June 1987 was Pamela Robinson and Richard Spychalski's wedding day, soon to be my Mum and Dad. I wasn’t around 30 years ago. People still say it was the best wedding they’d ever been to, that's probably because of the free bottle of vodka they placed on every table. Mum and Dad lets face it, the six years of marriage without me in it were pretty dull. I must have been the best anniversary gift you’ve ever received the day after your six year anniversary, I guess Dad was pleased he could save money on a gift that year, until he found out I was a girl and realised the small amount of money on a gift for mum is nothing compared to the money spent on a daughter for the rest of his life. You're welcome Dad. If I’m honest I don’t know how they haven’t both packed up and moved away from me, together or not, although they are on holiday together this week, without me. My Mum will be up all day and night...

Natasha Jade

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