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My wife and I are very adventurous sexually and are keen to try attending swingers parties…

By Disability, Lifestyle, Mik Scarlet, My story, The Love Lounge One Comment

James, Milton-Keynes

“My wife and I are very adventurous sexually and are keen to try attending swingers parties. However, I have MS and am a wheelchair user. Can I expect the swinging scene to be equipped to deal with and accepting of my disability?”

Mik

While I haven’t ventured onto the swinging scene, I have many friends who have. I do know that from my contact with them that disability is not really an issue. To be honest I kept finding myself being told that I would “enjoy” myself on that scene as many of them have a tick list, or a list of things they want to try.

Sex with a disabled person is high on that list apparently, so if you don’t mind that idea then it might be fun. I would check out your local scene and see if you like the people, which I would imagine is pretty important if you intend to sleep with them! Of course some people might be arse holes, but that is life. I should say that please go it into with your eyes open. I know many relationships that have been torn apart by trying swinging.

It may sound fun, but will either of you be able to cope if one partner is more popular than another? Jealousy can kill a successful relationship, and while it is a not fashionable emotion I personally feel it is part of really being in love. Having said that, I also know couples who have a great time and swear it has brought them closer together. So if you really fancy it, go for it. Trust me, as far I as I understand having a disability is not bar to swinging your socks off!

My spina bifida means that my body looks different to everybody else’s…

By Lifestyle, Mik Scarlet, My story, The Love Lounge No Comments

Kelly, Bournemouth – “My spina bifida means that my body looks different to everybody elses. I’m almost too anxious about it now to go clothes shopping and try them on in the changing rooms. How can I get some confidence?”

Mik – To me this issue is one of the biggest that many disabled people have to contend with. However much we might outwardly appear confident, and claim to be proud of our impairments, we live in a society that is obsessed with perfection and let’s face it, we are only human. We cannot help but be influenced by this growing need to be beautiful and perfect, and measure ourselves against the images that fill our media. It is a remarklable person, disabled or not, who is not touched by the dream of being perfect. I know that when I was a teenager, back in the early 80’s, I found myself so sure of my unattractiveness due to my disability that I developed an eating disorder. Even today what I see in the mirror and what I understand everyone else sees is very different. However, I will give you the advice I try to give myself every time I find myself looking at the mirror and seeing a monster, fuck em! You are the most perfect you ever. OK, you may not fit the stereotype of what beauty or perfection is, but who say that is right? Mostly a bunch or fat man who work in the press, or aging women in the fashion industry whose obsession with youth is driven by their fears over the passing of time. Disabled people wear their strength and individuality on the design of their bodies, like an amazing work of art. We challenge society to see what biology can actually achieve, and how robust the human form can be. Don’t let the non-disabled world make you feel less because you do not look like they do. It’s them who should feel inferior. So from now on when you get up, look in that mirror and know you see beauty and perfection. Your own totally individual form that no other person can achieve. Be proud of that, and if anyone dares to challenge it then they can go f**k themselves. As for finding clothes, I always advise find a style that works for you. Fashion is our enemy, as trends change so quickly. Instead experiment with style until you find one that fits.. and stick to it. Sure you can follow fashion, but make sure you model it to suit the style you have created. I used to wear loads of leather, not only as it looked great but because it was hard wearing and made me look like an injured biker. The alternative scene has always been less judgemental that the mainstream crowd and so I found my outrageous clothes allowed me to become part of scene who didn’t seem to care if I was disabled, or sky-blue pink!. So best bet, scan the fashion mags plus books on the history of fashion. Find a look you like and that you think will work, and THEN go shopping. With a look in mind, you are already half way there. And if you find a shop without a changing room, remember the Equality Act demands that they have one. So get shouting…. “I know my rights!” If you need any styling tips, drop me a mail, maybe with a pic or two, and I’ll see if I can help. Believe it or not, I actually studied fashion as a overly trendy new romantic youth so I do know what I’m on about!

I haven’t been on a date in well over a year and am finding it increasingly hard to meet women…

By Lifestyle, Mik Scarlet, My story, The Love Lounge No Comments

Peter, Bath – “I haven’t been on a date in well over a year and am finding it increasingly hard to meet women and get out of the house because of the pain of my early onset osteoporosis. How can I get myself motivated and out the house?”

Mik – Dear Peter, I also know the joys of chronic pain and how debilitating it can be. I have tried everything to fight it, both conventional and alternative, and I might suggest trying Mindfullness. It’s a meditation technique thatmight sound a but hippy dippy, but I have found it really works. Not only as a method of counteracting the pain but also to give you back some feeling of control. That feeling of being the captain of you own ship is the thing that will help with motivation, so it really important to get the ball rolling. Ask your GP or at your pain clinic about Mindfullness and for advice on controlling your pain. If you aren’t being seen by a pain clinic, that must be top of your list. Even before you start out on the road of finding methods of fighting your pain I would suggest allowing yourself to feel down, ill and angry. We always get told to keep your chin up and other such arse, but until you have felt real chronic pain it is difficult to understand. While it can stop you from doing anything, and I know in my past I have spent years lying on my sofa unable to sleep for days wishing I would just pass out to have some release, I would advise you to start small. Little trips out, doing things you really enjoy. Imagine it is like a little baby, trying to learn to walk. You make short trips, not pushing yourself too hard, and then build up to longer and longer ventures into the outside world. It’s a balance between reclaiming your life from your pain and not making it worse. But you will win. If for no other reason that you eventually get used to it. However try to get your medical team to understand how bad the pain is and get them to do something for you, as it can be controlled. I have my daily pain medicine, and then something stronger for break through. With the Mindfullness to help me when it gets really bad or when I know I need to spend days at work, I have a full arsenal to fight and defeat pain. With the right help you can too, and then you control it and not it you. Once you reach this point you will look back to now and see how far you have come. Trust me, it is possible. Good luck, and if you need any more help please get in touch.

My longterm girlfriend and I are separating but she is the only person who knows how to deal with my disability

By Lifestyle, Mik Scarlet, The Love Lounge No Comments

Melissa, London – “My longterm girlfriend and I are separating but she is the only person who knows how to deal with my disability and I have become very reliant on her. I am paralysed from the waist down, a wheelchair user and am scared of facing life without the aid of my partner and the prospect of not meeting somebody so understanding. How can I cope?”

Mik – Hi Melissa, as someone who is also paralysed like you, and who had a very similar experience in my past, I can only say do not be scared. I know that I felt I may never find another love when the relationship in question ended, especially as they supported me so much. However in truth it gave me the push I needed to become truly independent, and so I was able to form better and more fulfilling relationships. I am now happily married to someone who has cared for me during some very dark times, and supports me in my daily life but as I had created an independent life for myself before we got together we both know she helps me through love and not sympathy or any other negative reason. I should also say it is vital you do develop independence as you may open yourself up to bad relationships based on your belief that no one else would assist you. I had one of those, and I was brainwashed to believe that so I ended up being bled dry financially. My advice would be contact social services and work with them to put a fullcare package in place for you. Also use what may seem as a negative time to discover exactly how much you are capable of on your own. I know as I discovered how independent I could be it changed my life. Trust me, it might seem scary right now, but it will get better and you will find that this might be the beginning of a fantastic new chapter in your life.

I live in a group home and I really want a double bed… Help!

By Lifestyle, The Love Lounge 2 Comments

Firstly, is there anyone else in your group home with a double bed?

YES – Go to that person and ask them how they got the double bed, particularly the exact person who approved it. Then go to the person who has the power to approve a double bed and make a note of the resident’s top tips about how they were successful.

But if NO and you are the first person to ask for a double bed, ask the staff who has the power to approve a double bed. Now it is time for some preparation before you meet them.

Next, imagine stepping into the shoes of the general manager of your home and picture that you have a resident asking for a double bed.

Since this is the first time this has happened, imagine the questions they will ask and especially  the things that might make them say yes or no. For example, some questions that spring to my mind: Are they scared a resident could be taken advantage of by a staff member? Is there not enough space in the home as you will need a private room?

Also, does the company that runs the home have any policies on the rights of residents?

Would it help to have someone in the meeting to support you like your best friend or the girlfriend/boyfriend who will be sleeping with you in the double bed? Perhaps they can help you prepare your arguments?

Finally, you should call Enhance the UK as they can give you supporting evidence of residents in care homes with double beds.

Good Luck! With good preparation you might be surprised at how quickly you have a double bed to  Enhance your sex life!

When I was in hospital in my own room and my wife and I asked for some “private time,” it was really easy. They just gave me a “do not disturb” sign and we used a single bed for sex.

I was impressed by how accommodating and not squeamish they were, but not all homes will have the same open attitude soEnhance the UK can advise you on your rights.

I love my partner but they treat me like I’m a patient, it’s driving me nuts!

By Lifestyle, The Love Lounge One Comment

Firstly, the people who love us are programmed to look after us if we get sick, but sometimes this can go too far. If this happens, it is up to you to step in and make some clear new rules.

Changing how your partner treats you starts with changing how you expect to be to be treated.

Let’s be honest, being in hospital and having nurses do everything for you at the touch of a button can actually be quite a nice experience. One that you can easily get used to, especially if you have trouble doing some things for yourself because of your illness. There is even a point where we completely forget how to do things for ourselves, this is called institutionalisation.

I know I secretly quite enjoyed having nurses wait on me hand and foot, and then when I went home I unconsciously treated my wife like a nurse asking her to do almost everything for me. This made us both uncomfortable.

If you act like a patient sometimes your partner will react by taking up the role as nurse and treating you as a helpless hospital patient. It is a situation where it takes two to tango which means you have the power to change things quickly.

Acting like a helpless patient is NOT sexy, but the situation can be fixed relatively quickly and easily. First, as with most problems looking for a solution, you need to talk about some new rules.

We talked and agreed the cast iron rule. That she should assume I can do X myself and I will only ever ask for help if I can’t do it.

This new rule turned out to be quite empowering as I didn’t realise how I was sometimes actually deliberately making myself helpless in order to get help!

I got lazy and institutionalised in hospital to the point where I expected help all the time with everything.

So, if your partner is treating you like a patient it might mean you have unconsciously taken the habit of being nursed like one at home. We are programmed by millions of years of evolution to take the most efficient day-to-day route to living and being waited on hand and foot is easier than doing everything ourselves.

But it has a severe side effect that our partner will end us treating us differently, yet this can be avoided simply by:

Having a conversation with your partner and make it clear you don’t like being treated like a patient in a hospital and that they should only help you if you ask for it.

Firstly, the people who love us are programmed to look after us if we get sick, but sometimes this can go too far. If this happens, it is up to you to step in and make some clear new rules.

Changing how your partner treats you starts with changing how you expect to be to be treated.

Let’s be honest, being in hospital and having nurses do everything for you at the touch of a button can actually be quite a nice experience. One that you can easily get used to, especially if you have trouble doing some things for yourself because of your illness. There is even a point where we completely forget how to do things for ourselves, this is called institutionalisation.

I know I secretly quite enjoyed having nurses wait on me hand and foot, and then when I went home I unconsciously treated my wife like a nurse asking her to do almost everything for me. This made us both uncomfortable.

If you act like a patient sometimes your partner will react by taking up the role as nurse and treating you as a helpless hospital patient. It is a situation where it takes two to tango which means you have the power to change things quickly.

Acting like a helpless patient is NOT sexy, but the situation can be fixed relatively quickly and easily. First, as with most problems looking for a solution, you need to talk about some new rules.

We talked and agreed the cast iron rule. That she should assume I can do X myself and I will only ever ask for help if I can’t do it.

This new rule turned out to be quite empowering as I didn’t realise how I was sometimes actually deliberately making myself helpless in order to get help!

I got lazy and institutionalised in hospital to the point where I expected help all the time with everything.

So, if your partner is treating you like a patient it might mean you have unconsciously taken the habit of being nursed like one at home. We are programmed by millions of years of evolution to take the most efficient day-to-day route to living and being waited on hand and foot is easier than doing everything ourselves.

But it has a severe side effect that our partner will end us treating us differently, yet this can be avoided simply by:

Step 1: Have a conversation with your partner and make it clear you don’t like being treated like a patient in a hospital and that they should only help you if you ask for it.

Step 2: Start to act like the independent survivor you are and try to do everything that you can, yourself.

Step 3: Strictly enforce these new rules and refuse help from your partner unless you asked.

Take these three steps and you will be surprised how quickly your partner will start testing you like a normal human being again!

Start to act like the independent survivor you are and try to do everything that you can, yourself.

Step Three: Strictly enforce these new rules and refuse help from your partner unless you asked.

Take these three steps and you will be surprised how quickly your partner will start testing you like a normal human being again!

I love my partner but I’m scared of hurting them now they’re sick…

By Lifestyle, The Love Lounge No Comments

If you love your partner, one of your first instincts is to keep them safe and to be afraid of hurting them is perfectly natural.

But a crucial part of helping your partner recover is learning to risk hurting them during sex. Remember, we are not talking skydiving! Sex usually takes place in a very safe pace like a bedroom in your home but done the right way you can take safe risks almost anywhere. We all take risks every day. Crossing the road is risking death and even more dangerous is driving in a car, which is statistically more likely to kill you than serving as a soldier in a war zone like Afghanistan!

But you still drive and you still cross the road. The point is, everyday we take calculated risks. We calculate risks vs returns so you now must learn to take the same sort of calculated risks during sex. Sometimes something might hurt a little, or even a lot, but you must learn from that and try again. If you let fear rule your sex life it will die.

Talk to your partner about this right away, I can guarantee most of the fear is in your head and you will probably find a little risk is well worth the return of sex and connection. So bite the bullet and get talking!

There is also a simple solution taken from the world of BDSM – bondage. Use special words for the traffic light or a safe word system:

Green= Yes (More)

Orange= This is getting close to my limits (Slow Down)

Red= Stop right now

You don’t literally need to use green, orange and red. Instead you can use whatever words you like, meaning that sex play can continue uninterrupted without jarring the mood with “stop that” or “don’t do that.” You can even say “no” and mean “yes,” safe knowing your partner will stop when you use the right safe word. With this system of communication you can risk hurting someone while being completely safe in the knowledge that they are in control.

You can take the risks that help make sex hot while keeping the safety that you naturally want for your partner.

I really want to date but I don’t know when to mention the ‘D’ word…

By Disability, Lifestyle, The Love Lounge One Comment

Actions speak louder than words. You don’t even need to mention the D word to actually go on a date!
Step One: Select something exciting that you’d like to do with your beau.

Why? Studies show that when we spend time with people in adrenaline heightened situations we find them more attractive, and they will find us more attractive too. This will give you the chance to go on an “invisible date.” You know it’s a date but they don’t! For them, you just had a fun time out together. For you, it is the first step in getting to know them better and deciding if you want to take this relationship further and into the bedroom.

From there you can just keep getting to know them with more “invisible dates.” When you are clear you want to take things further, go in for a snog. After the first kiss it is clearly time to start using the D word and not long after that you can graduate to calling them your boyfriend/girlfriend!

Caroline Dempsey

I started escorting about 15 years ago… (Blog 4) by Caroline Dempsey

By Disability, Lifestyle, The Love Lounge No Comments

Caroline Dempsey

Within my work, I meet the most wonderful, open, honest, people.  At the end of the day, all most human beings want is to be held, loved, to feel safe and to be part of a relationship. That relationship can mean with others, or a wonderful life journey with oneself. At some point, we embark on learning about ourselves and others and for this self-development, we often look for a helping hand from a friend or loved one. I am privileged to have been contacted by a beautiful man who is on a journey to re-discover his connection with intimacy; with himself and with his partner, whom he loves very much indeed. Together we’ll carefully explore, until making honouring and delicious love with his wife becomes the norm once again.

His first step wasn’t easy, though and he has very kindly written his story to share here:

 

 

“Lacking confidence, self esteem, not wanting to make a fool of myself, not to let myself or others down, I guess these are the feelings I have. This could cover a multitude of things, but for me at this moment in time, it’s sex.

It’s not a recent thing either. It’s been building, I guess, for the past few years. But, after a lot of soul searching, I thought it was time I did something about it; for myself and for my relationship. The hardest part is admitting to one’s self that there is something wrong. After that, it’s trying to fathom what the best way is to tackle it. I did quite a bit of surfing the net, seeing if there were others out there that may be in the same boat, trying to see if there was somebody out there who could help.

I’m a T5 paraplegic (paralysed from the chest down). Had my accident in the mid 80’s and now I’m in my mid 40’s. I’m pretty active and fit, have a good job and a wonderful family. Really, things are pretty good, my partner and I are very close. We have been through a lot in the 10-plus years we’ve been together and are stronger as a couple for it. The only downside is our love life, and now for fear of losing so much, I’ve decided to act.

I had my accident just at the time I was beginning to find out all about girls, so that initially set me back. Although I had had some sexual experience, it was certainly very limited. However, I wasn’t a bad looking lad, had a bit of a gift of the gab and so had my fair share of girlfriends in my late teens and early 20s. I was very sexual and enjoyed every part of lovemaking and my girlfriends also seemed to enjoy it as well. During these early relationships I wasn’t bothered that I didn’t climax and it never seemed to be an issue to others either. Although I was told at the spinal unit that there’d be no problem with me having kids, I didn’t think I would ever climax and wasn’t sure what feeling I was looking for and what to expect. Prior to my accident I masturbated quite a lot, so I knew the plumbing had worked at some point. I had tried masturbating a few times in the early years after my accident, but don’t think I ever got close.

This all changed one Saturday morning with a girl who’d I’d been dating for quite a few months. We were having a nice time, messing about as you do. I’d asked her to climb on me, I was just lying flat on the bed, but this time she faced away from me, straddling me. I’m not sure why, but for some reason this seemed to really hit my spot, a feeling I’d not had before. I think the fact that we were both relaxed yet very aroused also helped. Anyway, I did manage to climax, though to be honest, I wasn’t completely sure!! I can just remember an unbelievable surge through my body, lightness in my head and then a feeling of total bliss, almost as if a great weight had been lifted from me. I felt so relaxed, it was amazing.

This now was the problem, because I had experienced this, I wanted it more. However, it soon became apparent that it wasn’t going to work every time, and although frustrating, not the end of the world. We tried a few positions and the one that worked best for me at the time was me lying on the bed with my feet on the floor, my backside just on the edge of the bed, then my partner standing over me, with her back to me. This had the greatest success, but by no means 100%.

My next girlfriend is now my current partner. In the early years of our relationship we had a very active sex life. I do remember her asking me quite early in our relationship specifically ‘can you have children,’ to which I replied ‘yes’. We also adopted this position for me and again occasionally I would climax. After a couple of years we decided to try for a family, and this is where I feel my current situation manifested itself.

As is normal now, nature takes over so it’s all a case of timing. I now had the added pressure of ‘performing’ on cue. Typically, with the added pressure and all that goes with it, more usual than not I wouldn’t reach orgasm. There’s the usual ‘oh, it doesn’t matter, hopefully next time,’ but of course this doesn’t help things, and I became more frustrated and basically stopped enjoying any of the process. There it is, ‘process,’ that’s what lovemaking had become!

So, after a couple of years trying naturally, we went down the route of IVF. At first all seemed ok, although I had to have sperm surgically removed, which isn’t a great issue, but it would have been nice to have been able to do it ‘myself’ so to speak. We had eggs fertilised, placed back to where they should be, all looked very good but they never would ‘stick’ there. We had all sorts of tests, but to no avail. Nobody knew why we weren’t conceiving, which probably was the hardest fact. Again, this went on for a couple of years. Physically and emotionally it is destroying, but we came through it and as a couple were much stronger for it. I know a lot of couples who have not made it through this process, but I feel very proud that we have.

Still wanting a family, we decided to look at adoption. Again, it’s another process, more bureaucratic this time, but still a long process. There’s a lot of questions asked, some very personal, including ‘how’s your sex life?’ to which we replied ‘perfect!’ We both knew this was a lie, but I guess that’s what people do, it’s hard to admit.  However, the outcome for us has been fantastic and we feel we have the perfect family!

During all this time though our sex life began to dwindle. For me there seemed no enjoyment. I felt as if I had that passion, drive, beaten out of me, and I didn’t feel anything coming back the other way either. We kiss and cuddle, hold each other, but at the moment that’s as far as it goes. We occasionally speak to each other about it, but it doesn’t come up very often and we seem to soon move off the subject.

During the IVF it was suggested I bought a ‘penile vibrator’ by Ferticare, specifically produced to assist spinal injured guys to climax. So I did. Unlike some other sex toys, this looks very medical, even the colour of it makes it look like a piece of medical equipment, rather than something you’d want to use in the bedroom. Because of this, I have never used it with anybody else, it has always been when I’m on my own, and when I first had it, it was just used to ‘clear the pipes’ so to speak. It was never sexual, just a piece of equipment I used. However, it did do what it was meant to do, but again, it’s far from 100% and it can take quite a while. For years it sat in the back of a draw and was never used; I had no urge to use it. I’m not sure what changed, maybe I was feeling a little aroused, may be even bored at home alone one evening about 18 months ago, but I decided to get it out.

Well, it may have been because it had been a while, it didn’t take me long, but I achieved an orgasm, and I must admit it was a fantastic feeling. It still didn’t feel particularly sexual, almost dirty as if I shouldn’t have done it, but there was certainly that release that I had felt the first time I had climaxed all those years back. After that I began to use it more often, only when I got the chance and was on my own and knew I wouldn’t be interrupted. I guess it was about once a month, may be twice. The more I used it, the more sexual it became, the more I enjoyed it. However, I didn’t always climax and sometimes it took a long time if I did manage to. When I didn’t, I felt quite low and I remember how I felt before when I didn’t perform ‘on cue’. I get so close, but can’t quite get over the top. I feel as if there’s another ‘button’ to press, something that would just make it happen that little bit easier. I know that until I can find that, I can’t see me using this vibrator with my partner.  When I do orgasm, it is so body evoking, so explosive that I want to share this, I want her to see me enjoy it for what it should be. I know my climaxing isn’t the be all and end all and there is more to it, but I just want to have the confidence that if we do go that far, I get the outcome that I want, and I know she would want it to.

What I really want is to be able to is to climax during lovemaking; is it too much to ask? Right now I want to find that elusive position, the special technique that will allow this, but in a loving, passionate, lustful way with my partner. I want to share that moment I climax with her. Is this the quest for my ‘Holy Grail?’

As I said at the beginning, I want to find my confidence again, confidence in myself, my ability to turn my partner on. I know that I can’t go in all guns blazing, it’s been too long. But I also don’t want to go in all ‘fingers and thumbs’ and put her off and go into this whole cycle again. I know this will divide opinion, but I feel as if I can approach this as I did when I trained for sport. I had a coach that would help me, make me better, help my technique, show me what to do, pass on their experience, allow me to practice, to take what I had and give me the best opportunity of fulfilling my goal.

So, after much deliberation, I decided to make contact with somebody who I hoped would be able to help me. I wasn’t too hopeful, mainly because I wasn’t sure what I wanted, or if indeed it was something I could find help for. Again, I did as much research and reading as I could and I eventually summoned the courage to contact Caroline Dempsey. She let me have her email address so I could write down my concerns, feelings and what I would dearly like to happen, and to see if she thought she could help me. So I did, I think it’s easier to write down those initial feelings, and sent it off to her.

Soon I’d got a reply and it was with great relief when I read what she’d written. She was so very understanding and I immediately felt as if she understood my predicament, and suggested that she could indeed offer to help me.

So, we met for a coffee and I was able to explain more, it was nice to be able to talk to somebody. My feeling from the email was enhanced, and after some initial nervousness and trepidation, I now feel as if I have found somebody to help me. It is still very early, we have only met once and exchanged further emails, but I am hoping that there will be a successful outcome. My greatest feeling is that she understands what I want and is willing to help me, and it is this that has helped me get over the feeling of guilt that I should even be doing this, but I feel as if I had to, for me, my partner and my family.

I hope soon to be able to bring you the next episode on this journey of discovery and I would dearly like to think that I can help others out there in a similar situation and I also look forward to hearing from other people and how they have tackled such issues, as I do believe I’m not a lone voice.”

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