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“I’m a single mum and I suffer chronic pain and spinal problems…”

By Emily Yates, Mik Scarlet, The Love Lounge No Comments
 Hello there,I’ve just read an article about your organisation and wondered if you could help me. I’m a single mum and I suffer chronic pain and spinal problems and things are hard. The pains debilitating and I’m very lonely. Is there any service you can offer me, put me in touch with likewise people with disabilities. I’m not sure if this is something you offer.
Kindest regards, Rachael

 

 Hi Rachael, many thanks for writing in to us at the Love Lounge.
Sorry to hear of your struggles, but great that you’ve written in to us, and you’re wanting things to change.
Pain is such a tough thing to deal with, and for us to give advice on, as it really does differ for everyone! If it’s really debilitating and affecting your life so severely, I’d suggest having a chat with your doctor to see if anything else can be done. In terms of getting yourself out there and kicking that loneliness into touch, what really works for several people I know is planning ahead – having dates in the diary to look forward to, and being able to factor in ‘rest days’ or even ‘rest hours’ into your day so that these dates in the diary (hopefully) end up being events you can attend and enjoy without too much pain or worry.  When there isn’t anything huge to look forward to, could your friends come to you instead of meeting you for coffee in town, just so you can socialise and still be in control if pain really strikes?
It’d be great to know more about you – do you use any mobility equipment to get around, and can certain friends or family members be at hand to accompany you on a girly shopping afternoon, or take single mum pressures off you when you need some ‘me’ time, even if that’s relaxing in front of the TV?!
In terms of dating, I’d recommend boosting your confidence a little by taking some lovely photos of yourself, writing up a positive profile about what you enjoy, and trying online dating.  It’ll get conversations going, you can do it from the comfort of your own home and, you never know, these online conversations might turn into dates for your diary! 🙂
If they do, please let me know! There’s lots of equipment out there that can also help with chronic pain in the bedroom….
Wishing you lots of luck,
Emily x

 

Hi Rachel,
I know how you feel, as I experience high levels of pain. It is something that can get in the way of every part of life, especially intimacy. It’s tough to feel sexy when just being touched hurts. However, I must say that sex is also a fantastic method of pain relief, so don’t think that being in pain will stop you from being intimate with someone. I have found that sex alleviates pain, and this can last for some time. Not always but some times.
On the dating front, I must admit I’m way out of touch with dating in today’s world. I’ve been married for ten years, to the woman I’ve been with for twenty. But I have always lived with pain, ever since my spine collapsed and so know how it can make you feel you might not be the catch of the year. Don’t let that thought colour the way you act. The right person will be supportive, but I found along the way to finding the right person that even a few wrong ones are understanding around pain. They might have been wrong for other reasons but most people seem to understand that pain might make you feel off now and then.
The whole online dating scene is alien to me, but if you fancy trying old school dating try finding activities you enjoy. Then when you are doing them socialise and et voila, you may find Mr Right. I met my wife like this, and it allowed us to stay together as we have so much in common. Emily’s advice around building schedules that allow you to recover is vital. It’s how I have built a successful life. I work, or party or whatever, and then I book some time off to recover. I’m writing this from my sofa, after returning from a holiday. I even book time off to recover from holidays! This is the best technique for beginning to get out now and then. Arrange something that you really fancy doing, do it, and then give yourself the time to recover… and never knock yourself for needing this time. Your health is vital and you should never feel bad for needing recovery time. As you go out more, your confidence will grow. Sure they’ll be knock backs, times when the pain wins out, but you will be in control, not the pain.
Another technique I tried which changed my life was mindfulness. This meditation technique sounded far to hippy dippy for me, but as you know sometimes pain can get so bad you’d try anything. It set me free! Ask your GP to see if they run Mindfulness for pain in your area. It allows you to develop a different relationship with your pain and when it gets bad you can use it to lessen it’s impact. Can’t sing it’s praises too highly. Mik.

“I can’t help thinking that any move that is made on me is a bit of a joke or a dare…”

By Emily Yates, Lifestyle, The Love Lounge No Comments

To the Love Lounge,

My name’s Alex, I’m 26 and a wheelchair user.  I’m really lucky – whenever I go out loads of girls come up and chat to me and they’re really interested in me.  I know that I’m reasonably good looking, but I can’t help thinking that any move that is made on me is a bit of a joke or a dare?  It’s always in the back of my mind when someone pretty is chatting to me, and it needs to stop. Please help!

Hi Alex,

What an interesting post, thanks so much for sharing this with us.  The answer to this is simple, but I don’t know whether it will give you the solution you’re looking for.  Basically, society has made us feel that, as disabled people, we are less attractive and our bodies are ‘broken’ – nowehere near sexy or desirable!  It’s a really tough cycle to rebel against, but these girls that are coming up to you obviously think you’re sexy AND desirable!!  The trick is to focus on your assets rather than your wheelchair.  You’ve said it yourself – you’re good looking, I’m sure you can make great conversation and crack a joke or two.  This is so much more important to many people than whether you’re standing or sitting. And even then, if you do get the odd joke or dare approach, who’s attitude needs to change? It certainly isn’t yours 🙂

Best of luck in your journey to love,
Em x

“Will sex hurt with my Cerebral Palsy?”

By Emily Yates, Lifestyle, The Love Lounge No Comments

Dear Emily,

My boyfriend and I have been together for a while now, and it’s time for us to go the next step and have sex. I have cerebral palsy, affecting my arms and legs, and I’m terrified that I don’t know what to do, whether it will hurt, and whether it’ll be good for both of us.  Do you have any advice for me please?

Thanks,
Katie.

Hi Katie,

Thanks so much for writing in.  This is something that is a real worry for many people, and it was for me, too! I also have CP, so can hopefully give you some good advice.  Firstly, it’s great that you and your boyfriend are in a stable relationship and are ready to move to the next stage, but my first bit of advice is that you should talk about what’s going to be your first time.  It shouldn’t be the elephant in the room!! Hopefully chatting about sex and knowing that your boyfriend loves you and won’t ever intend to hurt you or make you feel uncomfortable should put you at ease.  Is your boyfriend disabled too, or able-bodied? Is this also going to be his first time? This will obviously affect how you talk about certain positions and the logisitics of ‘doing it’.  In terms of ‘knowing what to do’, talking frankly to family members really helped me.  I was really honest with my sister, mum and auntie, and spoke to them about my worries.  They all told me about positions and movements that they thought would be the easiest and least painful for me, but to be honest, you and your fella should be comfortable enough with each other to talk through everything and willing to change positions at any moment if they aren’t working out for you.  Communication is the key.  The first time probsbly won’t be red hot fireball passionate sex, but that will come once you’ve found your ‘rhythm’. In terms of pain, the more you relax and communicate, the less it will hurt.  If it does hurt, it’s simple: stop, talk, and try something different.  The worst thing you can do is keep going in the hopes it’ll get better!  If you’re confident and comfortable going into it, I’m sure it’ll be really great for you both.  If it isn’t, you can always try something new next time! Good Luck 🙂

Em x

“How useful can I expect disabled dating sites to be?”

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

Hello Emily,

First of all I think it’s a great campaign as disability and
relationships need to be open with increased awareness. I am 25 with mild
CP I enjoy skiing and going to the gym. I am slightly addicted to spin
classes! I have a small group on friends who all have girlfriends and
are slowly getting married. I have tried a number of speed dating
events including silent dating, blindfolded dating and online dating.
I have been honest about my disability in my profile, and have
received 0 messages I gave wrote about 50 I am not surprised by this.
I am wondering if you have any advice on where to meet women who would
be willing to overlook my slightly different walking gate? I am
finding it hard to accept people’s negative views and narrow
mindedness. I have been tempted to sign up to these dating agencies :
one has been used on the undateables on channel 4. Have you heard any
reviews of there usefulness? I have given up on online dating and the
use of tinder as they are so image focused. I look forward to hearing
from you.
Kind regards,
Peter.

Hi Peter,
Apologies for the delay in replying – this one is tough as, unfortunately, we live in a very image conscious society ESPECIALLY when it comes to dating!!!
Great that you have so many interests and you’re getting yourself out there and doing what you love; that’s half of the battle!  Are you involved in any groups or classes that relate to your skiing or love of fitness? This is often a great way to meet people as there’s a mutual interest to focus on straight away.  What else are you interested in? Travel? Music? Volunteering? These are all great ways to meet people too!  I play wheelchair basketball, and made some amazing friends through that (and even had a couple of relationships….) Have you thought about joining a club near you?
I’m afraid I can’t comment on the usefulness of any particular dating sites, but I will say that you’re much more likely to be successful in your search for love if it is your personality that shines through first, rather than just the way you look/walk.
There’s been many ways that disabled people have played the game of online dating, many have even experimented to see how many responses they get when their disability isn’t photographed or mentioned on their profile at all.  I’m not suggesting you do this, but it is an option!
Maybe online dating just isn’t for you.  And that’s fine! But someone, somewhere will be for you, you’ve just got to keep trying (however tedious and lonely that can seem at times).

Let me know if you want to chat some more; I can even introduce you to your local Wheelchair Basketball team if you’re interested?
Hope this helps, and good luck!
Emily x

 

Jennie Williams

Disability and dating faux pas

By Disability, Lifestyle, The Love Lounge No Comments

My name is Jennie Williams, I am the Director and Founder of user led disability charity Enhance the UK, and ​​I have degenerative hearing loss​. My hearing loss is believed to be linked to a heart condition I have called long QT, which is otherwise​ known as sudden death syndrome.

For communicating, I wear two hearing aids which I rely on a lot. I am also an extremely good lip reader and sign up to​ British ​Sign​ Language (BSL)​ Level Three​. But, really, ​how many people do you know that sign? Within the hearing world, BSL is not much use to me at all.

​People tend to get very confused about what hard of hearing actually means. They tend to associate it with old people, so I often get people saying to me, “oh, yeah, my nan wears a hearing aid, we shout at her. I think she has selected hearing…chuckle chuckle.” I would be a very rich woman if I had a pound for every time I heard that, and yep, I mean ‘heard that’ because I can still hear things.

Sometimes, I can be in a room full of wheelchair users at a conference, for example, and I am the most able bodied person there. I am moving tables and chairs, assisting people to the loo if needed and then speakers will start up on the stage and, all of a sudden, I am the most disabled person in the room.
I normally can’t hear speakers clearly and often in these circumstances, the hearing loop (if they have one) doesn’t work or I can’t understand the BSL interpreter (again if they have one) as they are too fast and BSL is not my first language. So I sit, try really hard to lip read, take a painkiller as I know the dreaded ‘hearing headache’ will come on and try my best to keep up. It is hard work trying to lip read and, believe me, I don’t know any hard of hearing people who have ‘selected hearing.’ It depends on someone’s tone, how tired you are, your tinnitus (ringing in your ears) and how you feel that day.

So​ how do I approach telling people about my​ disability?
​When I am at work, I am very assertive most of the time. I have to be. I am a campaigner and a disability awareness trainer – that’s what I do. I tell people from the off that I am hard of hearing and for them to please look at me when they are speaking to me or to keep their hands away from their mouths. I even tell them when I need an eye break. ​When I am in a social situation, however, things can be very difficult and different for for me.
I tend to just struggle on a lot of the time, laugh when everyone else is laughing, strain to keep up and, even worse still, I apologise. Why is that? I guess I don’t want to embarrass people and make them feel like they are not including me. I often feel like I am being annoying when I keep asking what is being said and, frankly, it becomes boring for me as well. So the answer to the question is not an easy one, it depends on which Jennie you are in the room with.

​A lot of the time when you say to someone, ‘sorry,’ (I always start with a sorry, how very British of me, “Sorry but I am deafened could you turn and face me please,”) that person will more often than not appear to be somewhat embarrassed, say sorry as well and then shuffle around slightly and try to work it all out in their heads. A classic example of Scope’s ‘End the Awkward’ campaign. You see, I don’t seem as though I am hard of hearing, I have a hearing voice as I was born hearing, I am a good lip reader and you can’t see my aids as my hair is in a bob.

Now it is not all bad being hard of hearing. I fear I have painted a very negative picture so far. Would I change my hearing loss and and my disability? The answer is no, not because that is the PC thing to say and I am ‘owning my disability,’ I am saying it because that is how I feel. I believe I have an empathy, understanding and frankly unstoppable passion to support people who have communication impairments.
This is why I started up the charity Enhance the UK and do the work I do. I know so many cool​, talented​, fun people who are ​disabled, and of course some who are not. I truly believe that I would not have Enhance the UK in my life, and all that goes along with it, if I did not have my hearing loss.

So let’s talk about my favourite subject before it gets too deep. Dating!​
​There can be some real​ perks of dating someone​ with ​a​ hearing impairment, we can get you into the theatre for free or cheap, same with the train, and a lot of us can lip read conversations that you were never meant to know about from quite a way off and get all the gossip. Winning!

​Dating someone with hearing loss can be hard and somewhat awkward at times, for all the social reasons I talked about before. Not to mention when you are getting down to things and having a good old snog, the last thing you want is your bloody hearing aids whistling every time the hot man (in my mind he is always hot) puts his fingers through your hair. And then your aids end up flying out of your ears, then the floor and the dog runs in and eats one of them. That is a true story, killed the moment I can tell you.

​Let me tell you about one of my​ favourite, and also most awkward, dates.
​I was single, living in London and looking for a boyfriend, so I did what all single Londoners do – I joined a dating site. I started chatting to this guy who looked cute and we had a bit of banter via email. ​We soon arranged to meet up as I was not one for chatting online for too long. We met on the South Bank and as I walked out the tube, I was greeted by the cute detective that I had been speaking to. He even looked like his photos, result!

We went onto one of the boats on the river and had a drink. We chatted about work as you do. I may or may not have been twisting my hair and trying to make my lips look all pouty and thinking to myself, ‘I really fancy this guy.’ So, I went to take out my lip gloss and out fell both of my hearing aid batteries at the same time. They are really small and so this guy, who I named Gov as he was a detective and I thought it was funny, said to me, “what on earth do they power?” I then explained my hearing loss and he replied by saying, “why do deaf people do this?” Cut to him waving his hands in the air and scrunching his face up with the tongue in his bottom lip making weird groaning sounds. Oh dear.
I was thinking about throwing my drink in his face but that would have been childish, and a waste of a drink, so I explained about British Sign Language and the culture behind it. I don’t think he got it at all but he was embarrassed and didn’t know what to say, so he offered to take me for a ride on his massive motor bike (not a euphemism) around London and then buy me dinner. I am very shallow.

Next favourite subject…sex.
​Sex is great, we all love having sex but it can be a little awkward sometimes if you are hard of hearing and someone is trying to whisper sweet nothings in your ear. You can mishear totally which results in jumping up, turning on the lights and saying, “you want to do what to me?!” Again, true story and I won’t tell you what I thought he was saying to me.

Having sex with someone who is also deaf or hard of hearing can be hilarious. When I was younger I was having a fling with someone who was deaf and we always had to have sex by the door just in case his old’s came in, or we would put towels down​ against the door to try and block it from being opened, but always having one eye open just in case. Real romance.

So, back to the slightly more serious stuff. I started the campaign Undressing Disability three years ago.
I believe that ​having a disability can be a very isolating experience. As well as physical barriers, there is still a huge amount of prejudice towards disability amongst the general public
Undressing Disability is about challenging the misconceptions that create this unbalance and ensuring that better access to sexual health, sexual awareness and sex education is granted to disabled people. We provide a safe place in The Love Lounge for people to write in and discuss their problems and, in short, know they are not alone.

If people want to be sexually active they should be. I think there is this massive misconception that sex workers and disability go hand in hand. In some cases they might, but this should be a choice not the only option that people, men mainly, have. Most people I know and talk to want a loving relationship and want to feel loved and to love. Everyone has the right to have human touch, even if it is not sex as we know it. Any sense of intimacy between two people who care about one another is so important. Even if it’s a one night stand, but it is your choice, that’s also important. Lets face it, most of us have not only slept with people we ‘love.’ We all want to be found attractive and sexual relationships are the most natural thing in the world.

Sadly, Scope’s new research shows that that only 5% of people who aren’t disabled have ever asked out, or been on a date with, a disabled person. Am i surprised by this? No, of course I am not. Am I motivated to keep pushing the campaign until these statistics change? You bet I am.​

The Love Lounge

Thank You, Lovehoney

By Disability, Lifestyle, The Love Lounge One Comment

Enhance the UK would like to say a massive THANK YOU to Lovehoney, the sexual happiness people, for their very generous donation of £10,000 to The Love Lounge.

The Love Lounge is a safe online environment where disabled users and their families can confidentially ask any questions concerning sex, relationships and disability to our panel of disabled ‘non-expert experts.’ They are Emily Yates, an accessible travel writer for ‘Rough Guide’ and Mik Scarlet, a prominent disability activist and TV personality.

We initially approached Lovehoney for sponsorship, as they seemed to be just the kind of organisation we wanted to align ourselves with, especially for this specific project. They are a sophisticated lingerie and sex toy online retailer and community who champion a varied, enjoyable and safe sex life.

Lovehoney are a conscientious company, recognising and valuing issues close to Enhance the UK’s heart. They are committed to regularly donating to national and local charities, as well as running the world’s only sex toy recycling scheme!

Now by providing us with this donation, which far exceeded our wishes, Lovehoney are emphasising the importance of intimate relationships for all. We will now be able to continue maintenance on our website and spread the work of The Love Lounge to potential new users around the country and beyond.

Thank You again, Lovehoney. Your money will go on to support physically disabled and sensory impaired people and their families seek help for the sensitive and important issues affecting them concerning sex, relationships and disability.

“My daughter is 18 and has been blind from birth…”

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

Tim: “My daughter is 18 and has been blind from birth. She goes to college in our local area and is generally quite independent all round. My wife tells me that now, she has started seeing a boy in her year at college. Part of me is happy but a big part is being protective father, especially because of her blindness. Should I just let her be a normal teenager?”

Mik: “Hi Tim, Arh the joys of fatherhood. Especially if you have daughters! It’s all worry worry worry! But lets face it Tim, you’d be worried whether of not your daughter was visually impaired. It’s your job, you’re a dad!

I hope you know the answer to your question at heart. It’s let her fly. She is an adult now, and is carving her place in the world. Part of that will be dating, no matter how much it hurts you inside. It’s time to face up to the fact that your little girl is growing up, and be proud of how well she is doing.

This is a red letter day really and proof of how well you have raised her. She is obviously a confident, independent adult who is having no issues with getting out there and building a life for herself. Don’t worry about her impairment, or what might happens with those pesky boys. Just support her, and wait to see if she needs a shoulder to cry on… if those aforementioned pesky boys do what teenage boys do and act like fools.

Don’t envy you though. I dread to think what I’d be like if I was a Dad!”

 

“Should I brave using my arm prosthetic on the first date?”

By Lifestyle, Mik Scarlet, The Love Lounge No Comments

Michelle: “Hey guys, I have recently started internet dating since after Christmas and had a lot of interest on my profile, which is flattering! However, I only have one arm after losing it in a motorbiking accident in my teens. I usually only wear a shoulder prosthetic and skip my arm prosthetic as it can be a real pain – but should I brave it when going on the first few dates to avoid any awkwardness? What are your thoughts? Thanks x”

Mik: “Hi Michelle,
I am a big fan of being up front, so I would go as you best feel comfortable. If you don’t feel yourself when wearing your prosthetic then that might get in the way of the date. To me if anyone isn’t keen on you because of your impairment then you’ve been saved from wasting time on a looser.

I had a mate at school who lost her arm at an early age and she never wore a prosthetic. She also never had any issues with guys. Her confidence was really attractive to us guys. Most of the men I know would much prefer someone who was happy with who they were than someone trying to be something they are not.

So I think my advice would be ‘Be proud and leave the prosthetic at home.’
Good luck and have a great time!”

“I have cerebral palsy and can count my sexual experiences on the fingers of one hand.”

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

“You invite people to share their stories of sexuality.
I have cerebral palsy and can count my sexual experiences on the fingers of one hand. A psychiatrist once tried telling me this was because I was sexually deviant. I did not argue, but I felt he was mistaken and that he had no basis for advising me because he was not disabled and had not had any experience remotely related to disability.I would genuinely like to know how much you relate to this experience and its point of view. Thank you very much indeed.​” – James

Emily – “Hi James, many thanks for writing in.
From one with CP to another, I can absolutely relate to your story.Seeing as ‘deviant’ really means ‘differing from the norm,’ we’re probably all sexual deviants in our own ways, and this should in no way be seen as a negative thing.  The problem is, the psychiatrist that you spoke to definitely displayed it negatively!

As I don’t know the psychiatrist, I can’t tell you whether he was capable of advising you or not, but what is coming through loud and clear is that fact that he seemed to give you little option to define for yourself what you sexually ‘were’ or ‘were not’.  And that’s a problem that plagues society as a whole.
For example, society (in general) sees fewer sexual experiences as something to be ashamed of, society (in general) sees disability as an asexual concept, and these are the things that we are desperately trying to change.

In short, I sincerely hope that experiences like yours become fewer and more far between.  Do write back in if you’d like any advice on any other aspect of disability, sex or relationships. Wishing you a lovely festive season, Emily x”

Mik – “Argh James, the old “you’re deviant due to your disability” line eh? It is true that many non-disabled people seem to find the things that disabled people sometime need to, or want to, do disconcerting. They like to say it is because they consider what ever fantasy or sexual predilection we admit to as being kinky, but I really think it is because they are uneasy with us wanting to not have sex but enjoy it. Those in the medical and social professionals can be the worst, as they really think they understand disabled people as they have learned about us during their training. It takes a really skilled and rounded “expert” to be able to explore their own feelings around disability and sexuality, and to come out the other end being able to admit that we have all the same wants, dreams, desires and even fetishes as any non-disabled person might do. I would say never let anyone tell you are deviant, unless you are into some really weird shit.

 I have had the exact same experience just on a much more public scale. In the mid 90’s I was a well known TV presenter. I also sang in a rock band and we played on the fetish scene a lot. The Daily Mail ran a story “outing” me for being into kinky sex, yet only a year earlier the News Of The World ran a story with the headline of Wheelie Sexy, claiming they had found this new disabled sex symbol singer and presenter. What it seems is that if you appear sexual as a disabled person that’s fine, but if you actually have sex and know what you might want out of sex then that’s just sick. It taught me that the wider public really do find the subject of disability and sex frightening and confusing, but then they are a repressed bunch mostly.
As well as being freaked out if disabled people express an interest in experimenting with sex, many people find the fact that we might need to try different stuff due to our specific physical needs equally troubling. I have written several articles on how many of the techniques used by disabled people to enable them to have sex would be of benefit to the wider non-disabled community but they are only ever featured in speciality magazines. The mainstream press find the whole idea of us teaching them something to bizarre to accept.
Without knowing what exactly it was that caused you to be called a deviant, all I can say is if you really are into fetishism or any other left field sexual activity, why try visiting a local fetish club. It’s one of the few places where people accept you as a sexual entity, and you might find someone that thinks what you are into is perfect match for them.
I should also like to say that only being able to count your sexual partners on one hand is not a bad thing. I don’t know how old you are but until I was nearly 30 I could have done the same with fingers to spare. Even today I could only use both hands and I was a famous TV presenter. It’s not the quantity that matters, but the quality. I’d much rather have a few great nights to remember than a succession of crap shags.”

“I have Muscular Dystrophy and my girlfriend has Cerebral Palsy…”

By Emily Yates, My story, The Love Lounge No Comments

“I have muscular dystrophy and my girlfriend has cerebral palsy. We’ve been together 7 months and we need advice as to moving forward and getting more intimate. We both have severe disability and limited movement.” – Richard

Hi Richard,

Great to hear from you and many thanks for contacting the Love Lounge.  Finding intimacy that works can undoubtedly be more difficult when you and your partner both have a disability, but certainly not impossible! I have Cerebral Palsy myself and I am currently with an able-bodied partner, but I have had very fulfilling sexual relationships with other disabled partners too.

The biggest and best bit of advice I can give to you regarding taking steps forward in terms of intimacy is… talk to each other.  Finding out what works and what doesnt with sex is always going to be a method of trial and error.  When you are trying different positions, for example, make sure that you are both always communicating with each other to confirm you’re both happy, comfortable and enjoying what’s going on.

A wonderfully intimate relationship does not have to include penetrative sex either.  I’ve had some amazing sex without having intercourse.  Get comfortable laying with each other and telling each other what feels good and what you’d like to try.  Certain sex toys might make things really enjoyable whilst also allowing you both to be comfortable and not too physically active too soon.  Funnily enough, I’ve just been told about a voice-controlled vibrator that might help those with limited movement.  See what you think!http://www.honour.co.uk/silicone-voice-activated-vibrator-amy.php#long-description

Additionally, to help make certain positions more comfortable, check out Liberator ramps and wedges (a little on the pricey side, so they might just give you a bit of inspiration of similar products you could use at home) http://www.liberator.com/wedge-ramp-combo.html

Really hope this helps.  Please let me know how you get on and if you need anymore specific advice, just shout! 🙂

Emily x

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