Dear Hubby….

Dear Hubby,

I woke up this morning wondering how we got here.  If we had known on this day all those years ago what was in store, I wonder if you..or I…would have turned up at Chelsea Registrar’s office?Scan0023

But we did, and here we are, having weathered the storms, the unexpected, the joys and some dark times.  Back then it was just going to be us and your beloved Lotus 7, having been told that babies were not likely when I was diagnosed with polycystic ovary syndrome aged 20.  The first storm – for you at least – was the realisation, soon after we bought our flat in Fulham, that we couldn’t afford the parking space to go with it! So the first Lotus 7 had to be sold as leaving it on the road – even the posh road to Bishop’s Park and the Palace that we overlooked – was not going to happen.  Scan0025

Of course at this time we had no idea about Ehlers Danlos Syndrome – had never heard of it – we just knew I had a host of problems and had already undergone major back surgery and was very bendy. Life in London was great, wasn’t it?  I don’t think that brand new kitchen was cooked in very often as we dined out down the Kings Road or in Fulham most nights.  But all good things come to an end, and you began craving another sports car(!) so the hunt was on to move out of London.  Soon after the move to our first house came another joy in the shape of a second Lotus 7. But within months came probably our biggest unexpected piece of news….I went to the GP for a once over before starting a new job, feeling generally unwell – and came out 3 months pregnant whilst taking HRT.  Hmmm….that little 2 seater didn’t last long either.

There has been redundancy; more babies – including the tummy bug that didn’t go….oops! your little girl…..3 caesarians & increasing back pain; another house move to the same road as your in laws(!); hideous working hours for us both, including 6 day weeks and night shifts; increasing migraines; more dislocations; IBS; school choices; more back pain and finally on the eve of Obama’s first term in office – the straw that broke this nurse’s back!  Then a career lost – permanently.

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And 2 becomes..5

We are quite a few years on and many more major surgeries to add to the list.  Not forgetting the Ehlers Danlos Syndrome diagnosis – for me and the kids.  A life threatening illness for one of our parents and then your own health taking the full brunt of all our traumas. That was a scary time for us all to watch you disintegrate.

But…..we are here still standing – you at least! Me – I spend more time on the ground these days (laugh everyone!).  The kids had to grow up fast and have all turned out to be pretty bright (not sure where that came from), independent & resourceful – so long as we’re not talking about tidiness and cleaning!!  We have had to accept that I need you to officially be my “carer” – which I still hate – as my health declines, and this has been hard for us both having worked and earned from the age of 18.

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Look what arrived today!

But…..with a bit of juggling, fantastic parents and wonderful friends we are doing ok, aren’t we?  No we haven’t any money for holidays, and we worry about being unable to help the kids out financially, but this has led to our young adults working and earning – be it paper rounds, babysitting or writing websites! We are spending more time together as a family, you are enjoying setting up your own small venture and taking on a role at the kids’ old primary school, which has been the making of you. Who would have thought it a couple of years ago!  You never – or rarely – complain about me and I do know that on those really bad days, when the pain flares and I can’t settle, or the black dog (not Sam!) surfaces I can be awful to live with.  Plus there are the endless trips to hospitals across London and the different specialists to keep track of.

Neither of us signed up for this, but then you never know what is round the corner. In a funny sort of way maybe life is actually more fulfilling now.  We certainly both have almost encyclopaedic knowledge of Ehlers Danlos Syndrome and all that goes with it!

So back to the beginning…..it was a pretty dreary day and actually raining when we walked out as Mr & Mrs (at least I did prevent you walking me over the road to Stamford Park!) 25 years ago.  But today has been a bright, beautiful autumn day – Happy Silver Wedding Anniversary, hubby!Scan0024

love Claire x

Dear Hubby

Brilliant blog posts on HonestMum.com

Monday Magic – Inspiring Blogs for You!

October is here! Autumn, the nights drawing in, the beautiful colours outside, digging out the winter warmers, Strictly Come Dancing (huge fan here!) and Halloween…..not quite such a big thing here in the UK as for some of my virtual pals across the pond, but it is growing!  It also brings a special anniversary in our house tomorrow….more of that to come!Monday Magic - Inspiring Blogs for You!

If you saw my post yesterday, you will already know that I haven’t been too well this last week as my autonomic nervous system went into melt down…..causing severe dysautonomia with me unable to stand up, fainting, ear pain (anyone else get this?) and severe brain fog.  Unfortunately this coincided with a call from Ofsted for the school where I am a governor for an inspection that we have been expecting and wanting for some time.  Whilst I managed to get to the school the evening before to meet with the head, the chair and my co-vice chair, I became so aware of the effects of brain fog as I couldn’t recall any recent figures or information that may be necessary for the inspection.  Of course stress often exacerbates illness symptoms – whether chronic or otherwise – and as a bit of a worrier/internaliser (typical of EDS anxiety) I struggled more than usual to sleep and then on the morning of the “big day” I was unable to even sit up without snow vision and nausea. Great – just when I needed to use my brain, which was once OK despite what my kids may say, it was full of enormous balls of cotton wool and opiate sized holes.  My colleagues were of course just fine without me…..but once again I am left with that feeling that I have let other people down.  The loss of clarity and independence drives me bananas!9c1efbf4cd9c5c62d212584a665278e1

So once I was able to read a computer screen again – the light can make the visual disturbance so much worse – I have spent some hours over the weekend looking for some more great blog posts for you.  I am mindful that not everyone who follows my ramblings has a chronic illness, so this week I have found a mixture of posts from cookery to a podcast.

I have my coffee in my hand, so I invite you to sit down and join me for a virtual cuppa whilst enjoying reading some fantastic posts.

https://cookandenjoyrecipes.wordpress.com/2017/09/30/caashifas-apple-crumble/

https://blondewritemore.com/2017/10/01/how-to-survive-blogging-with-a-small-following-sundayblogshare-blogs-bloggers/

https://orianasnotes.com/2017/09/28/5-monthly-favorites-september/

https://www.beecontentyoga.com/aqua-yoga-for-arthritis-research/

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Image from BeeContentYoga Blog

https://upbeatliving.net/12-tips-chronic-pain-care-despite-changing-laws/

https://makinglol.com/is-blogging-right-for-you/

https://lifeofstones.com/index.php/2017/09/22/how-changing-your-mindset-can-improve-your-life/

https://cityskippergal.com/2017/10/02/klosterman-welcomes-pink-in-october/

https://poisoninlethaldoses.wordpress.com/2017/10/02/follow-your-gut-because-it-doesnt-lie/

https://makeitultrapsychology.wordpress.com/2017/10/01/negative-core-beliefs-podcast/

Please remember to comment, share, like and make a blogger’s day!

Claire x

 

Fainting for my Motability Chariot

Fainting in the car showroom wasn’t something that I had thought would be a part of my week!  We had a phone call to say that my Motability car would be arriving and it has felt like the whole process has happened so fast.  Not so long ago I was still convinced that I would be deemed too “fit” to qualify.Fainting for my Motability Chariot (2)

 

It is a shame really that the “passing out” wasn’t due to excitement, but rather a POTSIE dysautonomic response!  My symptoms are always worse in the morning from the time I get up to mid morning – my cardiologist said having laid down all night (sometimes) the body is then put under immense stress from gravity and “baggy” blood vessels to keep circulating oxygenated blood to the whole body on standing. So the system concentrates on the major organs in the abdomen, blood rushes down away from the head, pools in the hands & feet – and I feel extremely dizzy or faint. Yes, out cold! So a 9.30 appointment was never going to be great – but add in stormy weather, bright fluorescent lighting and a hot showroom and Bingo! you have the makings of a “dysautonomic nervous system” episode. Sounds grander than it feels!!

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Image from a range of products available at http://stickmancommunications.co.uk/

Anyway, the salesman came back to his desk to find me with my head back, shoes off, feet up, grey and clammy. Not my best look…..but precisely the reason that I have been awarded the enhanced rate benefit. Of course add in the dislocations, pain etc…..all adds up to me getting a brand new car and not being able to drive it! So disappointing. My mum and hubby are the named drivers on the inclusive insurance – no, the student engineer isn’t old enough, much to his disgust – and I I grudgingly accept that passing out behind the wheel or pulling an arm out of socket whilst turning the steering wheel, probably isn’t the safest way to get from A to B.

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Grey really is not my best look! Post faint…

Busman’s holiday for hubby taking a car handover and the student engineer had the bluetooth wireless phone/stereo system programmed before we had even started the engine….great except he has no understanding of why I can’t pick it up in the same “on the spectrum” way that he does.  The ride feels smoother and hopefully this will be a huge benefit for my back pain, but I haven’t been well enough to go back in it this week.  Female hormones always exacerbate my symptoms and I have had several days when I have been unable to sit upright – another post for another time!  But I’m upright today and so writing a very speedy post having missed out all week.

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My Chariot!

Thank you Motability for a fantastic scheme that has allowed me to have a car to house me – comfortably I hope – my wheelchair, shopping and a dog!

Week in Review – #BlogTour Updates and a HUGE Thank you #SundayBlogShare

Look out for Shelley’s #BlogTour visiting us here at PainPals next Sunday!

shelleywilson72's avatarShelley Wilson Author

Wow, what a whirlwind week! My new non-fiction book came out on the 22nd September and has received great feedback from early readers.

HIMMTS cover KINDLE

I decided to put together a blog tour for the new release and was delighted with the response from the blogging community.

Just in case you’ve missed any of the blog stops over the last few days then panic not, you’ll find all the links you need below.

Please do spare a moment to pop along and support the incredible hosts who work so hard to promote authors and fellow bloggers, done on their own time but with a passion for sharing the book love.

Over to my tour hosts:

Friday 22nd – The tour began with a guest blog and excerpt for the delightful Cathy at Between the Lines Book Blog – https://betweenthelinesbookblog.com/2017/09/22/guestpost-extract-how-i-motivated-myself-to-succeed-by-shelleywilson72-selfhelp-fridayreads/

21768061_10155517036825056_3470477224825889128_nSaturday 23rd – My host for today was the lovely…

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Monday Magic – Inspiring Blogs for You!

Welcome to another week and to some more great blog posts!  It has been a busy week in our household and some of you might have seen my post about moving one son home and the other off to university.  Funny how Duncan and I have both woken up with splitting headaches this morning…..the only extra comment today on the move to Nottingham, is how can a supposedly bright young man arrive in his room at university and have not packed a single pen in his luggage??

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We have also celebrated my daughter’s birthday this week and we did wonder what we were letting ourselves in for when we agreed that she and her friends could have an evening at home….pizza, popcorn, films.  Eleven girls, aged 15 & 16, on a school night – how hard could it possibly be?  Actually it was easy….but extremely loud!  The girls restored my faith in teen friendships, having heard about various fallings out in girls’ groups and bitching recently. My girl is always very concerned about her friends and tends to be the problem solver in the group, quietly trying to keep the status quo between the more vocal characters.  There have been some subtle changes in the group dynamics recently, but I can honestly say that this particular group is kind and caring.  They had made her a wonderful “Pride striped” birthday cake and arrived with a personalised balloon.  Long may it continue.File_000

 

Last night I watched the opening of the Invictus Games in Canada, and yet again I was unable to stop the tears.  How can we not be moved by these service men & women from across the globe, who have been so badly physically and mentally injured serving, yet have pulled themselves back from the brink to represent their countries again? A very different theatre undoubtedly, but the courage, strength and sheer bloody mindedness is inspirational. It does make me wonder what I have to complain about…..am I trying hard enough….but it is all relative.  However I was inspired to get some physio done in next door’s gym this morning! Monday Magic - Inspiring Blogs for You!

So whilst we are on subject of inspiration, I hope that you will enjoy this selection blog posts that I have put together this week…..a mixture of chronic illness, motivation and even preparing your own coconut oil (the photos on this post are fanatastic!).  So time to get that drink, sit down and enjoy!

https://motivatemenow.co.uk/2017/09/18/how-to-create-a-more-fulfilling-future-blog-series/

https://blondieaka.wordpress.com/2017/03/24/how-to-make-your-own-coconut-oil/

http://thedailymanic.com/manage-life-change-future-unknown/

http://xofaith.com/3-epic-reduce-stress/

https://www.mymeenalife.com/surprising-things-diagnosed-with-lupus/

http://alifewellred.com/3-ridiculously-easy-ways-save-money-holiday-season/

http://coffeeheartmind.com/meet-ivy/

http://mini2z.com/after-the-storm/

https://alifelessphysical.com/2017/09/24/perfect-presents-for-people-with-chronic-pain/

http://www.jennavon.com/?p=584

Please comment, like & share these posts, and support your fellow bloggers,

Claire x8

The Stresses of going to University for a Chronically Sick Mum!

I did it!  I survived the week in which the eldest child moved home and the middle one left.  Of course I have to point out that these are not sweet little children any more, but big, hairy men of 21 and 18 who have gathered the clutter of young adult life.

The eldest decided that it will be more cost effective to live at home for his fourth and final year, after paying the high costs of central London living for the past three years.  At the moment I am undecided who is going to find his return home hardest, him or us! His sister was distraught to find he was coming back – she thought that she would be free of both brothers….not one going and one returning!  Her plans to spread the art studio into his bedroom have been thwarted.  He has lived with the bright lights for three years, with only himself to consider (well, and the odd flatmate), whilst we have got used to having a spare room, a varied diet and no concerns about what time he is rolling out of London’s night spots, because out of sight out of mind, right?!

Stresses of Uni

He has already created havoc by deciding to decorate his room before moving back into it – but this has involved emptying said room onto the landing and then moving his flat contents back into the house, which are of course in the hall!  We cannot move for cases and computers and furniture.  So when son number two should have been packing up ready for his imminent departure do you think we could find empty cases?  Actually I don’t know why I am saying “we” as it was very much “I” – if it had all been left to him I’m not sure he would be there now!

This morning on waking with pain and fatigue running through everything, yes even my teeth, I concluded that this going off and coming back from university is pretty stressful.  “But it’s not even you, Mum!” each boy will shout at me, with no understanding that for me the decision to use up all my physical and mental resources, or spoons as we chronic community say, to ensure they are safe and sorted is a no brainer.  The journey from south London to Nottingham was hideous on Friday – there was an accident on the motorway needing an air ambulance, a huge detour and then arrival in the city at rush hour.  The B&B that I had booked, whilst fantastic in that we had a self contained flatlet, proved to be on a nightmare hill and in a huge Victorian house…and you guessed it our apartment was in the basement.  Not for the physically challenged – I needed my wheels by the time we got there – and also not for those trying to adjust to a brand new pair of varifocal specs.  So our arrival in Nottingham saw hubby in his new specs (he has never worn glasses before) trying to help me with my completely dead leg and back pain down a set of wet steps, whilst asking “Are these steps tilting to the side? I think they are at a funny angle”. NO!! It is your brain trying to adjust to new specs, but you are about to drop me…..

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Anyway we deposited the politics student (more nervous than he would admit) to his new home yesterday morning and spent a couple of hours on the very hilly, but very beautiful University of Nottingham campus.  At lunchtime the canteens and coffee shops were full of anxious looking parents and equally anxious, but embarrassed IMG_1385

new students – my son commented that no one had managed to break free of the parents yet! Charming!! The funny thing is that it seems like only yesterday that my parents were dropping me at the nurses’ home where I would live for several years, and I can still remember that feeling of panic that I wouldn’t know who to talk to or where to go.  So it was with some relief that, having told our boy to leave his door open so that he could say hello to flat mates, he informed his brother over messenger last night that he was in the pub with his flatmates.

I can’t believe I am saying this, and I expect I will contradict myself over the next 3 years, but the pain, gastric problems, increased POTS symptoms and body consuming fatigue today, have all been worth it to hear him say “Mum, I can’t talk now, I’m going to the bar with new friends”!

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Don’t tell him, but I’m actually a very proud mum!

#ThrowBack Thursday – Searching for Happiness – Happiness is a Choice

This post was put up for Throw Back Thursday by Scale It Simple and it really got me thinking.  With the emphasis being placed on mindfulness and yet more in the press (UK) this week about mental health issues in teens – apparently a quarter of teen girls have experienced depression by the age of 14 – maybe we have forgotten how to be happy.

Let me wet your appetite…..

Searching for Happiness – Happiness is a Choice

Human beings are such interesting creatures. We are the only creatures that place personal “happiness” above safety and health.

For thousands of years, humans have walked this earth like nomads of the soul, searching for happiness.

Happiness is this way. No, this way. If you do this you will be happy. No, wait, this is what really makes you happy.

Did you hear about this car? This job? This brand? If you look like this you will be happy forever. If only I was younger I would be happier, if only I was older.

Humans roam all corners of the earth searching high and low for happiness. What makes one happy today will not do the job tomorrow and what makes you happy doesn’t do the trick for me.

So how do we find it? Where is happiness?

What if happiness can’t be found at all, what if in all this searching we are just confusing ourselves and wasting our time?

What if happiness is just a choice?

Want to read more?  Follow this link for the rest of a fab article!

Copy-of-Copy-of-Why-I-Switched-to-All-Natural-Beauty-Productshttp://scaleitsimple.com/2016/07/21/searching-for-happiness-happiness-is-a-choice/

Monday Magic – Inspiring Blogs for You!

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I am shattered today, PainPals and those pals not in pain!  Saturday was the day for the big reunion – that is 3 decades – 30 years since we left school.  I’m not quite sure which timescale sounds better!  How did that time pass so quickly? I remember my grandma telling me to value every day as the older you get the faster the time flies…but as a youngster I never took any notice.  Put together a group of people, some who haven’t seen each other for said 30 years, but who grew up together during those important teenage years….and it will feel like yesterday.  Similar theme to last week!

I was worried on Saturday morning for 2 reasons – firstly would anyone turn up and secondly I was feeling extremely POTSIE with the shakes and snow vision and forgot to take my midodrine pills with mine!  But on the up side about 20 people turned up over the course of the day/evening….and whilst I spent the first part of the day in my wheelchair the adrenalin seemed to kick in and I was able to stand for periods in the pub, sent out for my pills (good old Duncan) and was still in the pub for dinner in the evening.  It is amazing how you can push yourself when you need to and when you want to.  I find that it is about picking the occasions wisely to use your spoons, as it isn’t possible to live like this every day when a chronic illness is your constant companion.

The feedback has been fantastic – we had a great day renewing old friendships, reminiscing (being thrown out of choir, altering the wording on the carol service leaflet, sending Valentine cards, hockey, rowing, detentions for pranks…..the teachers) but also learning how everyone’s lives have moved on.  We had doctors, a headmistress, lawyers, an acupuncturist, a sports coach, a teacher, a horticulturist, an entrepreneur….the list goes on. Families have grown..and shrunk. Life goes on!

Class of 87 pic
Class of 87

So whilst I have had to sit back due to a self imposed inability to stand, I have found some new blog posts for you.  This week we have blogging posts, a yummy looking recipe site, a musical tribute and the feelings encountered when a pet is found to be very sick.  I am delighted to report that my list of blogs I have shared here has grown to 230 and many of these have been featured several times.  What a wonderful community you are!

Hope you have a cuppa in your hand, an hour to sit back and the enthusiasm to enjoy and explore these fantastic blogs.

https://www.disabledgo.com/blog/2017/09/activists-plan-day-long-musical-tribute-to-radical-and-brilliant-robert-dellar/#.Wb7PB7KGPIU

http://www.youcanalwaysstartnow.com/2017/09/11/is-the-universe-pushing-your-buttons-deal-with-it/

http://www.blessingmanifesting.com/2017/09/self-care-awareness-month.html/

http://riverandquill.com/2017/09/identity-theft.html/

https://beinglydia.com/2017/09/17/what-finding-out-my-dog-is-sick-has-taught-me/

http://www.livingnaturaltoday.com/2017/09/heart-goes-texas/

http://raisingzebras.weebly.com/blog/brain-mri-and-the-wheelchair-arrives

https://starbrightcooking.com/21-tips-classic-comfort-cooking/

http://www.strugglingwithserendipity.com/blog/accepting-harvard

http://www.angiecruise.com/what-i-learned-in-my-first-year-of-blogging/

Please, please share, pin, like, comment to let our bloggers know that you have enjoyed and value their writing. Have a lovely week!

Claire x

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Picture from Struggling with Serendipity blog

 

My first forays with Motability

A little while ago I mentioned my face to face medical review for my Personal Independence Payment and I had convinced myself that my standard rate would be reduced to nothing.  I was geared up to go to panel and fight my corner, sitting here awaiting that dreaded brown envelope.  When it did flop through the letterbox, I couldn’t even open it, I felt that sick!  Duncan did the honours…..and I was stunned and delighted in equal measure to find that I have been awarded the enhanced rate for both mobility and care needs.Motability Forays

Of course I should be on this rate as my health has deteriorated so much in the last couple of years, with Ehlers Danlos zebras galloping at full pelt through my life.  But the system is such that the applicant is made to feel they need to prove that they can’t jump through those hoops the DWP want us to.  Anyway it has taken a couple of weeks to sink in, and to investigate the benefits to using the Motability Scheme  – “The Motability Scheme enables disabled people to get mobile by exchanging their mobility allowance to lease a new car, scooter or powered wheelchair“. Last week Duncan suggested a trip to Peterborough – which initially didn’t thrill me – but it was actually to a Motability show….again probably not my first choice for a day out!  But I arranged the impromptu visit to our friends that I wrote about on Monday Magic, and this would mean only driving one way on the day so off we went.

I must explain that Duncan used to work in the motor trade, so our car has always just turned up, sometimes been sold, often changed at a minute’s notice, but I have never really had anything to do with choosing a car.  Of course this time our needs are very different and actually it was very helpful having many of the manufacturers who take part in the scheme under one roof.  The volunteers for the Motability charity couldn’t have been more helpful and there were plenty of them handing out goody bags full of useful information.

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The exhibitors included motor manufacturers, mobility scooters & electric wheelchairs, and companies who adapt the vehicles to your needs.  We were able to book a test drive – although only in one vehicle as slots were limited and had been booked up by lunchtime.  For us the real value was trying the vehicles for size without trudging from one showroom to another, and I have to admit that I hadn’t realized just how difficult it would be to find a car boot that would accommodate the wheelchair alongside shopping bags for those retail therapy moments, or a dog!

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Boot mounted wheelchair/scooter lift in action

The MPV type vehicles that don’t require a large down payment just did not give us enough boot space, and we actually could not fit the wheelchair into one jeep  – it is important to remember that this car is not yours, it is effectively a leasing agreement albeit an excellent one, so long as you don’t spend out too much in the first place as the car is handed back after 3 years.

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Ramp adaptation for wheelchairs & scooters

However the sky is the limit and if you want to put down a large payment intitially, it is possible to have a plush car with all the trimmings – all down to personal taste & finance.IMG_20170909_133122830

Having said this, we discovered that there are some excellent deals with some requiring little or no down payment for a really great car.  The show definitely helped us to understand what we didn’t want/need and has ultimately this week helped us to choose and order a car that fits my needs on the scheme.  With my back problems and the spinal cord stimulator, the seat position and shape is the most important thing – particularly the headrest.  The electrode in my back which helps to control my chronic pain is very positional, so I only have to have a headrest in a car or the cinema push my neck forward, and Bang! the scs might IMG_20170909_133108400just as well be turned off as I can no longer feel it.

Sadly the downside is that when my new shiny, estate car (yes, an estate that accommodates my wheels, my shopping and the dog!) arrives, I currently can’t drive it!

 

Little post script……I saw a couple of great looking electric scooters too.  My fave was the Genny, but at £16k it is just not going to happen; but I wonder if any of you out there have this nifty little number – the Go Chair ?IMG_20170909_161956070_HDR

Visible Scars

Those invisible scars can be the hardest to heal….remarkable post from Ruby on Throwback Thursday.

a Ruky'z Life's avatarA Ruky'z Life!

I never thought about visible scars being a blessing…

I think sometimes people look at me and think I’m too weird, too silly, too immature, or too reckless. But I think to have visible scars, people also think, “Wow she went through some trauma… Wow, she can laugh the way she does after going through all that? It’s surprising she can still smile the way she does… Oh, that makes sense now.”

Sometimes having visible scars justify my actions… sometimes…

Being a trauma survivor is what makes me a part of who I am. Having visible scars lets people know I’m a survivor without having to tell them.

Some people don’t have that luxury. The luxury of having someone look at them and know they are a survivor. There are a few who don’t have visible scars. Countless survivors went through a trauma that no one knows about because they…

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