A few things have happened and caught my attention lately that have made me think about relationships.

I have recently been given a new status.  That of being disabled.  A word which I hate with a passion as I think I am very able thank you very much.  I just need help here and there with a few things.  This recent status change has led to lots of form filling and lots of questions.  All of which focus on the negative.  What I CAN’T do.  Which totally goes against the grain of my mindset as I prefer to focus on what I CAN do.  Can I get dressed without help?  Yes, as long as life can cope with me in clothes without buttons or zips, or even if pyjamas were acceptable in coffee shops.  Can I cook without help?  Yes, although the scars on my hand tell me I probably should really stay away from hot things.  Can I use my insulin pump without help?  Yes, but it takes me five times as long and I regularly manage to empty a vial of insulin over the kitchen floor.  So maybe I do need a bit of help to make life a little bit safer and easier.  Step up to the mark Mr E!

Me and Mr E married in September 2009.  The left side of my face dropped in December 2009 and there began years of problems resulting in my diagnosis of aggressive RRMS (Relapsing Remitting Multiple Sclerosis) which is the main reason for my ‘disabled’ status.  Poor Mr E did not sign up for this!  But he has stood by me and learned to step in when it’s needed and to help out.  Which leads me to the question, at what point does your partner become your carer?  A lot of these forms have asked me who my carer is.  I always reply that I don’t have one, just a very supportive husband.  But should I get some help in the house and in the kitchen?  Would that allow Mr E to remain a husband without the added responsibility, or burden, of being a carer too?

A recent tweetchat was about ‘diabetes and dating’ which made me very thankful to be in a relationship!  Dating is a minefield!  Let alone with any disability or LTC (Long Term Condition).  When I was single I never thought that men would look at me twice, I think they would now, but only to try to work out if I was drunk or not!  Hidden disabilities are so difficult.  I either look drunk or clumsy.  Although to be fair, I may actually be drunk…  How do you date with these added issues?  Do you pretend they aren’t happening?   Do you explain things straight away?  Do you set your date a test and monitor his or her reaction when you whip your blood testing meter out?  This week I read a tweet asking if there were any dating sites for those with disabilities or LTC’s.  Why should there be a separate one?  Perhaps because most ‘normal’ people just don’t get it.  Those of us in relationships or who are of a certain age (I’m not divulging mine but my son calls me a fossil) are more chilled and offer advice like ‘find the one who accepts you as you are’.  Easier said than done.  You have to get through all the awkwardness first and to kiss a fair few frogs before you find ‘the one’.

It’s not just relationships with partners that I’ve been thinking about.  In March I will be going to the PWD conference where I will be meeting lots of twitter folk.  I ‘met’ these twitter folk when I was fairly well and a lot have followed my progress through the tricky terrain of diagnosis and treatment.  To be able to last the whole day, I may have to use my wheelchair.  Will that chair change how people relate to me?  Will people see past it and realise I am still ditzy Jules…with wheels?  I think they will as they know my story.  But what about old friends?  If they see me in my chair will things change?  Will they be too embarrassed to ask about it?  Will they not be interested and not ask for fear of being bored?  Will they assume I don’t want to be part of ‘girls night’ anymore?  Will they just say ‘nice wheels’ and carry on as before?

I think that sometimes it is best not to think too much about these things.  Relationships are two-way.  If I am worrying about reactions etc, those reactions will be based on the signals I’m giving off.  I need to accept help and be grateful for it.  Although I feel like a burden and a let down to Mr E, should he ever be in my position, I would of course stand by him and support and help him.    Relationships are tricky at the best of times.  Accepting ourselves and our situation, whatever that may be, is the first step.


Author: julesedwards1

I want to use this blog to relate some of my experiences, mainly revolving around Diabetes, MS and depression. I don't have any medical background and I don't seek to tell anyone what to do. In this life i have learned that there is no right or wrong way to do anything. All I offer is my own experiences in the hope that it will make me understand myself better and maybe help you, the reader, if you recognise things in my life that are maybe happening in yours. You are not alone :-)

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