Battling to Sleep with Ehlers-Danlos Syndrome

Battling to Sleep with Ehlers-Danlos Syndrome

In my next life I shall be a cat who sleeps anywhere.

In my next life I shall be a cat who sleeps anywhere.

I was settling down to go to sleep the other night, and putting my joints in the right positions – and it made me think about how much effort I have to go to at night to get it right.  Most people jump into bed, lay in whatever their favourite comfortable position is and go to sleep.  But for me, a lot of thought has to go into it, and it still often goes horribly wrong!

First of all it’s all about placement.  I have to make sure no joints have too much pressure on them – particularly my hips, knees and shoulders.   Sometimes it’s a no-win situation, for example I have to sleep on my side, and if I lay with my shoulder underneath me then the pain builds.  However, if I pull my shoulder forward to take the pressure off – it’s likely to subluxate or go into spasm.

Many of my joints have to be bent – particularly my elbows and knees, otherwise they will lock in hyperextension (this is when the joint goes past its normal range of movement) and ‘freezes’ in place.  When this happens I have to warm the joint up, and then slowly, and very painfully force it out of hyperextension and fold it back into position.  It will usually throb with pain sometime after this.

However, other joints must not be bent, including wrists, and fingers, otherwise oddly they too will freeze in this position.  Last night I ended up in a lot of pain because in my sleep the top joint of one of my fingers had bent.  The pain in just that one tiny joint woke me up and kept me awake for some time!

Most importantly – with any joint, they cannot get left in the same position for too long, or I’ll be in for a world of pain in the morning.  So I have to wake up regularly to turn over, and move each joint in turn.  Often a joint gets locked up – usually one of my hips – and I have to turn over and try and drag it over with me which is more difficult than it sounds.

In addition, as anyone that knows me will have seen and heard – I’m always having to crack my neck.  This continues throughout the night – with the pressure in the joint building up until it wakes me, and I have to crack it all out which you can’t do very well lying down.

Sometimes trying to solve one issue causes another.  For example putting a cushion between my knees help eases my lower back pain slightly.  However, on day three of using this cushion I get absolutely horrendous hip pain that leaves me unable to walk.

No matter how carefully I try and keep in the right positions, my fidgeting continues into my sleep and that causes a lot of problems.  I cannot sleep on my back, at all – but sometimes this happens, and in return I wake up screaming with burning nerve pain shooting down my leg.  I also frequently get cramps, or muscle spasms that make me jump awake.

This is just a normal night – often I have an injury, or a flare up in a specific joint that throws everything out.

So you wonder why I’m tired?  People with Ehlers-Danlos Syndrome struggle to get into the final REM restorative stages of sleep.  We also tend to wake up naturally hundreds of times a night.  On top of that, I suffer from insomnia – and often don’t get to sleep at all until 6:00am – 7:00am.

So no, I don’t do mornings.

Fellow EDSers – do you relate?

Finding Support with Fellow Sufferers

Finding Support with Fellow Sufferers

Credit to Puiu Adriana Mirabela

Credit to Puiu Adriana Mirabela

Today I went to a Chronic Pain support group.  I love going, it’s quite a great feeling being in a room full of people who know exactly what you’re going through.  Sadly it usually clashes with a work day, so I’m not able to go.  We spend the time just talking about our current issues – sharing things that have worked for us, having a bit of a vent and quite often having a laugh at ourselves.

Speaking of work, things came to a head when I went to see my GP recently and explained how low and stressed I was feeling.  She then said she wanted me to have a break from work, and signed me off for a month.  She also referred me back to the chronic pain clinic at the local hospital to see if they can try something new, and decided to put me on Prozac, to see if I can kick this depression.

Work took it in their usual way.  I have an occupational health assessment tomorrow, which they asked me to have when I joined the company.  I’m quite nervous about it, but will see how it goes.

I’ve been trying to think of something new to do a fundraising event for Fair Access to Colchester.  The group has no money, and I desperately want to advertise and do lots of other things that cost money.  I’ve run some pamper days for a village hall charity before, and I wanted to do something different.

At the same time, I was trying to arrange a craft themed meeting for Fair Access.  I have found lots of disabled people are into crafts, and that’s how I got into them myself really – by looking for a hobby that could distract me from the pain.   I suddenly realised the craft theme could work on a larger scale – by getting a large hall, and having lots of different crafters in giving small lessons.  For example someone would come in a pay a small fee to make a bracelet, or a card, or paint something.  That way people get to do something fun and try out something they may not have done before.  It’s expensive starting a new hobby, and you want to make sure you’ll like it before you spend money.

I thought I could have some tables selling crafts, some children’s stuff and maybe a raffle or something.