All about… me :)

For another change I thought I would talk about and show pics of me from my past.

I haven’t really given much background on myself, snippets here and there but the older I get the more I look back, I think being unwell makes you look back more often too.

I am the fifth of six children, all from the same parents no step. I have four older brothers and a sister 17 months younger than me.

Along with my parents, and the several dogs we had over the years it was a very manic, no personal space, boisterous, noisy but happy home.
Luckily we had a three story house and 100ft garden, where my parents and sister still live, so we had room to play, fight, move about without it being too crowded.

Having four older brothers did create a lot of teasing, jokes, being dared to watch scary films etc.. which I think moulded my character a lot. The traits of standing my ground, not easily scared, my humour, the standing up for myself and others.
I didn’t grow up very girly, I played football, cricket, made dens, but I still had Barbie dolls and have a memory of washing my dollies clothes and hanging them on our washing line as my Mum hung our washing.

We were not rich, or well off. We never had spare money and were lucky to have enough money to pay the bills. We grew up with no central heating, we relied on three coal fires and in a three story house you can imagine how un practical that was. In the winter it was freezing, and I mean so cold you could see your breath when in bed.

I have so many happy memories though, toasting bread in front of the fire, laying against our much loved and still missed dog Kano as I read and wrote stories. Playing cards, star wars figure games with my brothers. Playing practical jokes on each other, being teased but always knowing my brothers would and did fiercely protect us.

The one thing we always had was food. My Mum is the kind of woman who will not let you leave her home without haven eaten something or taken food with you. God knows how she managed this with so many mouths to feed, I know she went hungry many times so there would be enough food for us children.

This resulting in me being tubby.. well overweight as a child.

I matured at a very young age, physically as well as mentally. I was not a pretty child, I had big front teeth, wore glasses, was tubby, clumsy and wore baggy clothes to try to hide my chubbiness and maturing body.
This is me at 7 years old…481237_4248001119537_280510860_n

It took having my son to lose weight, which is unusual. I was 12 stone before pregnancy, 14 half stone after pregnancy and within six months was 9 stone, which over two years became 7 stone which was way too thin.
This is me at 15 on my sons 1st Birthday185858_1604570995436_1346613_n

From having my son, I changed my life around. I was a little wild before hand, never in school, hanging around with older and wrong people. I have no doubt I would not be here today if it wasn’t for having my son, I was on a slippery slope that could of only ended badly for me.

At 15 I was a Mum, working as a cleaner, in school and college. They have a brilliant school for young mothers in Bristol, where you take your children with you as you study. I have recently looked it up and it now offers 6th form and university level courses. I haven’t visited for a few years and kept meaning too, but the last two years have made me unable to do so. I plan to get in contact with the headteacher soon though. She is an amazing woman who campaigns for young mums and help any of us she can.

Some of my best years were spent in that school, I still miss those days more than I ever thought I would so many years later.

As regular readers know I suffer from Endometriosis too, the last 8 years of my life have been blighted by illness. I was not as bad then as now, and still had the silly side I do now which has helped me through a lot.
Dressed as Miss Christmas 3 years ago 487051_4126717687527_88182370_n

So that is a little bit of my early life I wanted to share with you. I hope it didn’t bore you too much 😉
All of us that are unwell, have long term illnesses, short term, any illness that impacts on us had a different life before we became unwell.

For the people who only see us as we are now, sick, stick walking, wheelchair using bed and home bound need to realise this. That we are people, just like them. We were children, teenagers, adults. With all the past, memories, feelings families, experiences that well people had and have.

We are people, not a diagnosis.

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Injection

So my patch idea helped a lil but the pain and sight is still terrible.

I resemble a pirate so much, what with my crippled leg, shoulder walk, patch and scowl.. All I need are candles in my hair and I would be Edward Teach, Black Beard the pirate, and he came from Bristol! He was born five minutes away from me.
Arrrr I be like sailing the seven cups that need washin up, the sea will ave to wait!
😉

In other non pirate related news I arranged my vitamin D injection and it’s Monday at 2pm. And the best thing is the injection goes in my arm not my bum as people kept saying! Oh yeah, no stifling inappropriate jokes for me now! ;D

I am trying anything that could help me, even if it’s just a lil bit. The injection makes the vitamin D go straight into my system and I reckon it will help. I’m to have one each month until my levels go to the ‘normal’ 75+ instead of under 10. If it helps I am happy to continue it, I’m really hoping it does. Fingers crossed and gypsy luck! 🙂

It is beyond hot here at the moment, with my pain causing me to have a constant temperature and my having to lay/sit on an electric blanket most of the day is turning me into a human sauna! I would charge people to have a sauna but they’d have to sit on my lap to get any benefit and I’m not keen on that idea. I’d be covered in their sweat too, yuck! I’d rather be poor!
🙂

My father is dropping off some of my billion of pills today, so it’ll be great to see him and have a catch up.
I’m very similar to him and we are very close. Even more so since my illnesses. He’s always there for me, for anything and that’s rare but runs through my family. I am incredibly lucky to have such support and help from my family, we are very close knit. I feel for people who don’t have this and always hope they have someone, be it a family member, friend, partner. It’s important to have someone, chronic conditions are so isolating, so emotionally difficult that being alone coping with them must be a nightmare.

I may be severely chronically unwell but I have support, laughter, help and people to talk to if I need it. As far as I’m concerned I’m extremely lucky, and I am grateful for all I have. I have far more in my life than I don’t and no matter how bad things get I hold onto that and things don’t seem that bad after all 🙂

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