When I was diagnosed with Emotionally Unstable Personality Disorder earlier this year, I learnt it was the same as Borderline Personality Disorder (BPD). The psychiatrist said it was quite unusual to be in a long term relationship as I had been married for 12 years. I think he meant that as a compliment, but I wasn’t sure if he was actually questioning the stability of my relationship.
When I got home I instantly googled it. I think we all tend to google our lives in the digital times we find ourselves in, we’re prone to believe the answer to every question is a click away. I soon found we were known for “Intense & Unstable” relationships according to the Mind website. Every booklet or website I looked at said it was virtually impossible to maintain a relationship with some with BPD. We were described as needy, manipulative & difficult, so basically keep away. As I looked back over my 35 years, I could identify where so many relationships had gone wrong. Not all, but many friends & family found it difficult to be around me. I need to be someone’s world, & when I’m not I instantly assume they hate me. It’s Black & White Thinking, love or hate, I don’t see grey!
I am so lucky to still have my best friend, from when I was just 11 years old, 25 years & still going strong having spent last weekend with both of our families in Peebles, on the Scottish Borders. How has she put up with me? You’d have to ask her, but I’m so grateful she has.
I was fortunate to meet my now husband when I was 19 & looking back I can now see the signs in our relationship too. I was constantly trying to end the relationship to see if he cared, but he never gave up on me, even when I’d given up on myself. We’ve had our ups & downs, like I said I’m needy, but he doesn’t give into that & never has. He lives in the here & now, & sometimes he has to drag me back here when I’m off on my anxious journey & living 3 weeks, months or even years in the future. He makes me laugh, all the time & for me that helps so much. I wish I could laugh myself better, & we both wish every day that this wasn’t a condition I had, but I do. He loves & supports me as I do him. He doesn’t always understand, he still gets frustrated, but he tries to be supportive. He orders me books to help build my confidence with the condition, he cooks for me because he knows I won’t eat anything if he doesn’t, he sometimes finds excuses for me to have to get up & go out just so I’ve done it. He is honest with me & however hard that is to hear at times, it means I trust him, something everyone with BPD struggles with. He understands when I need to be on my own & he’s also learning to know when I shouldn’t be on my own. He can see signs of my deterioration before I do.
I have to work hard too. I had to learn he wasn’t my carer, not to take him for granted, make sure he gets time away with his friends. I also had to lower my expectations from the fairytale fantasy that had to be perfect. I had to realise that laying around all day feeling sorry for myself wasn’t good for me & I had to learn to listen to him.
Together we nursed his dad & my mum through their battles with cancer, which is also something that has cemented our relationship. And it was hard, but it means we have empathy for each other & another bond. Our two daughters also bring us closer every day.
So it’s not a dead end. Your condition doesn’t define you, you do. Don’t believe what you read, listen & learn & change how you react. You need honesty, love, support & humour, a lot of humour!
So is it easy, no! Do I still get paranoid & needy, yes! Do I still frustrate him when I lie around in bed, yes. Is he going to leave me? Honestly I’ll never know, but I’m learning to live more in the moment & enjoy it. When we get time with just the two of us I used to ruin these by trying to make them perfect. Now I just enjoy them & this weekend we’re off to London.
This blog was published by the Huff Post last week first.
I enjoyed learning a lot more about you, your condition, your life and everything about you. You are not defined by your mental illness. And I am so glad you can see that.
Keep the positivity going. People like you who are positive and know life has its ups and downs, regardless, help me in my recovery.
Thank you for this post. I needed to read something like this. 🙂
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Thank you so much Fazia, that means a lot. We’re not defined by it so I’m glad you agree. X
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You are welcome. Anytime.
I know what it feels like to feel down or have a bad day. I suffer from social anxiety, general anxiety disorder and mild form of depression. So it can be hard at times to see the positive in everything.
PS. And it is Faiza by the way not fazia.
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Awww thank you Faiza. My typing is shocking. Your support means a lot x
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No worries. I love supporting other bloggers and it makes me smile to read or hear that what I say ,means a lot to them. Including yourself.
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It’s so true. I’ve got some evenings free this week & I can’t to catch up with all my favourite bloggers!
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