Category Archives: poo

Bollocks to the salad…

Is what I thought a couple of weeks ago when I decided to try and lose a couple of pounds for my impending holiday.

A bit of background, the last couple of months at work have been hectic to say the least, I have probably been away more than I have been at home and have basically been living out of a hotel (does a Travelodge count as a hotel?!) and a suitcase. It’s really, really hard to maintain a healthy lifestyle  when you are away so much, I really do try but sometimes the urge to give into the wine or the chocolate after a long arsed day is too much.

With only a few weeks until my holiday I decided to take action and up the health and fitness regime to shift those additional pounds that crept on. I was still working away lots and before I knew it I had 17 days to go. I can do this I thought, I will just give up everything that is nice and fun and tasty until I go away, it’s easy, I can eat mainly salad and veg and not drink wine for 17 days. I lasted 5 days, (go me!) until my sister text to say they were having Pimms in the garden and I was invited! And then I just thought, bollocks to the salad, I cannot be arsed to keep depriving myself because I am 2-3 pounds heavier than I want to be.

In the few days before the lure of the Pimms, I was miserable, I was hungry and felt tired and cranky. I just couldn’t do it to myself anymore. I’m bored of feeling bad about myself because I had potatoes for dinner or a sandwich instead of a salad for lunch. I am bored of feeling like a rabbit because all I seem to do is crunch bloody crunch all day long. I am tired of exercising iron clad willpower when it comes to not eating a biscuit or a piece of chocolate (I am still waiting for that will power to come to the surface in the face of wine!). I am fed up of trying to haul myself out of bed every morning to spend an hour in the gym and feeling guilty when I don’t.

Don’t get me wrong, I live a healthy lifestyle and enjoy doing so, I want to give my body nourishment and strengthen it so it can deal with life’s curve-balls. But I don’t want to live a life of restriction that never includes a chocolate hobnob again.

I do not want to saute my broccoli, I don’t even know what sauteing is – isn’t it just a fancy word for frying?? I don’t want to eat kale and cous cous for lunch or to have to marinade my chicken for 4 hours for it to be tasty. That is why Marks and Spencer exists – so people like me can throw our veg in the microwave. I don’t like avocado and even if I did I wouldn’t want it for breakfast, I don’t want to snack on 5 almonds or take my Tupperware dish everywhere I go. So I said bollocks to it and decided that I would try to feel OK with the little extra padding and be happy instead. And weirdly enough, when  you stop stressing about food and let go a little bit your body rewards you with feeling better. I think my mum describes it perfectly –  I asked her what she had for her dinner one night and she replied with “a shit boring salad, I might just have fish and chips”!! Don’t get me wrong, I am not going to dive head first into a vat of donuts (no matter how much I want to) but I am just going to try and relax a little, maybe try thinking about my body in a positive manner instead of hating it. After all, it kept me alive during the most grueling of times and it now keeps me healthy, so I really ought to be grateful to it.

Tomorrow is the day I go away to sunny Crete and you know what, rather than stressing over my body not being the same as it was when I went away last year, I am going to enjoy the fact that I am able to go on holiday, that I can travel, that I can feel the sun on my face and make more memories with Mike, you know the important stuff. It’s a long process, trying to come to terms with your body, especially when you have an Ostomy, but I am going to really try. I have naturally ordered  champagne for my outward flight tomorrow and I may just raise a glass to my shit boring salad!!

 

Salad 2

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Oops! 

Oops, it’s been totally ages since I last blogged and yet I never meant to go this long. I wish I was one of those people that blogged regularly, but I also wish I was one of those people that got up at 6am to work out, or one of those people that didn’t like wine (do they exist?) or one of those people that ate broccoli for breakfast (wtf?)  but somethings are just never going to happen! 

  

I always get inspiration when I’m driving in my car or some other such inconvenient place and by the time I can write it down I forget! But I’m sitting here on the sofa, whilst Mike watches footie (not for the first time) so decided to ‘be productive’. There are lots of things I could write about and I will ( in a few months or so ;-)!) but I thought I would start with being able to help people. 

I want to and will, talk about clothes with an ostomy (short version, wear whatever the hell you like), travel ( it’s fine, do it), exercise (if you’re so inclined, that too is ok) food ( trial and error but give it all a go within reason). I’ll go into more detail in other posts. 

Those that know me/read my blog/follow my Facebook page know that I work for Beating Bowel Cancer Charity. It keeps me incredibly busy but I love it. April is Bowel cancer awareness month and during this time we hold a ‘patient day’ where we invite people affected to a free event. They can meet other people in similar situations, talk to nurses, attend seminars, visit the stands and just generally meet staff and supporters. It’s a great day and people seem to really love it. What’s great is being able to talk to people who also have an ostomy, some have colostomies, some have ileostomys, some don’t have a stoma anymore but did. It’s really lovely to have people come up to me and ask me about mine and ask me questions. Some people I have spoken to over Twitter and was able to meet in person and share stories.

I love that I can work for a charity and have empathy and can share my positive experiences with people going through a really tough time. But I also benefit, I also get to meet people with ostomies and hear their experiences and so many of them are incredibly upbeat, despite having to face some of the toughest times of their lives. 

I am always happy for people to approach me and ask me questions and advice and I will always be honest. I have no issue with anyone, stoma or not, asking me questions about mine. I find it far easier to be open and hope my experiences can help others. 

So, this is just to say the blog is back in action, and between 6am gym sessions and breakfasts of broccoli 😂 I shall be posting a bit more regularly!  

 

Then and now…..

Today is the 4th anniversary of my stoma and of course it’s a day I will never forget so I think it is appropriate to mark the occasion. It was the day that would change my life for ever

Sometimes, the truth of it is that having a stoma does get me down now and then. It is hard for friends and family to understand (as great and supportive as they are) as they just see me as being healthy now and that is all that matters. But, despite the positives, having a stoma is bound to have an effect on how you feel, your body image and the problems that can come with it. But, rather than talk about being down, I figured why not compare my life to pre-bag and post-bag and see the difference?

Now, I am not saying that some of the things I have now I wouldn’t have had anyway, but a major life change can cause you to reassess your life and for things to change in ways you never though possible! So here goes…..

Pre_bag (during my Ulcerative Colitis days and before 2011)

  • I had an incredibly stressful job that took up a lot of my time, didn’t allow for me to look after myself physically or mentally and I worked a lot of hours.
  • I was unfit, exercising was off the table when one wrong move could cause me to poo myself, plus the general exhaustion from being unwell made it difficult.
  • I ate what I was able to not what was necessarily healthy.
  • I was on a concoction of strong medication, painkillers and was self-administering twice daily enemas (how glamorous!).
  • Relationships were tricky and let’s just say I didn’t always make the best choice, so I was either single or in a not so great romantic liaison.
  • Travelling/going to social occasions (e.g. concerts) was a minefield and far too stressful due to the constant worry of an accessible toilet.
  • I lived in a rented flat
  • I drove an old car
  • I didn’t have pets
  • I hadn’t been on a holiday since 2009 and didn’t have many weekends/days away

Fast forward to post-bag (and after 2011) and this is what I have

(A few pics of me now)

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  • A job that I love, where I work from home and travel around the South East, I get the best of both worlds, there is a good work/life balance and because it’s a bowel cancer charity I can offer my experiences as well as fight for a very worthy cause.
  • I am so much fitter than I have ever been. This year I have managed to run a sub 60 minute 10k and a sub 30 minute 5k, plus I have been lifting weights since January and the amount I can lift has increased. Working out has become a part of my daily life and I feel so much better for it (my body has had some nice changes too – bonus!).
  • I eat whatever I want to, but am choosing to eat healthily and I have never felt so good, with so much energy. In fact, I never thought I would see the day, but I have almost gone off pizza, unfortunately the same can’t be said for my wine habit 😉
  • I don’t take any medication at all, apart from the odd Alka Seltzer after a night out ;). Or the occasional ibuprofen for normal niggles.
  • I have an amazing boyfriend, we had only been on a handful dates when I was taken into hospital, but he stuck around and 4 years later we are still together. We have a lot of fun, respect each other, make time for each other, he looks after me and I look after him and it is a GREAT relationship.
  • I have had holidays (yay) and weekends away, spa days/weekends, concerts, theatres, parties, girlie holidays, day trips and so on and I couldn’t be more appreciative. In fact I am off on holiday next week and I can’t wait.
  • I now live in a house with my boyfriend Mike and we have another property we rent out.
  • I have a nice new car.
  • I have two very cute and very mischievous kitties.

Of course my wonderful friends and family haven’t changed and have been there through it all which I am most grateful for.

So, it really helps to look at all the good stuff and what I have been able to achieve, things that once were so difficult or seemed impossible are now just part of my life. If you are going through a hard time or having to face something difficult, just remember, as much as life can change for the worse in a blink of an eye it can always change for the better just as quickly.

So, happy anniversary to me and the stoma that not only gave my life back but improved it too.

 

Cheers!

Life change

Certain events ( and of course the impending New Year) have brought question to my mind about friendships and what they really mean. Some of us have loads of friends, big groups of them, friends for every occasion and in every corner of the globe. Some of us have just one group of friends, friends that were formed at School or University and have stayed with us. And some of us have a few select friends or friend that come and go as life changes.
What matters is not the number of friends you have but the meaning of those friendships. In the days of social media it’s all about ‘friends’, ‘fans’ and ‘followers’ that I think it is easy to forget what true friendship really means. It’s easy to post a status and get ‘100 likes’ or several positive/sympathetic/advising/inquisitive (delete as appropriate) comments that our egos are fed and we feel popular (or unpopular when a status only gets 1 like, if you’re lucky!) But it isn’t necessarily a good thing, who knows if the comments are genuine or for show and we shouldn’t get fooled or measure our worth on social media ‘friends’.
A lot of people agree a true friend is someone you may not see or speak to for months, but when you get together it is like you have never been apart, or you know they would be there for you in an instant if you needed them. My friend Lisa is exactly one of these types of friends. We’ve known each other since we were 2 and have always been friends. I think it is easy to remain friends with people because they have just always been in your life regardless of if they should really be there or not. But Lisa needs to be in my life, I can’t imagine not having her there! We hardly see each other, yet we live round the corner from one another, we are always saying we should catch up, yet neither of us makes the effort! I guess we are both a little lazy and maybe we just take for granted that we will just be there. But I would rather have someone like Lisa in my life than a dozen acquaintances that I didn’t feel secure with. When I was ill in hospital , Lisa was always there, even though we hadn’t seen each other for ages, she helped me clean my teeth when Mike was coming to see me, she brought me jelly babies round when she knew I needed to eat them (I promise that is genuine!) and we gossiped over our love of strong Ribena!
When we were younger, we used to see each other every weekend until we both got bored and said we didn’t want to spend as much time with each other, neither of us got annoyed, we just somehow knew it was needed. Approximately 3 years later, I went on holiday to France with her and parents, even though we hadn’t spent much of the previous years together but it was like we hadn’t been apart!
When you have a debilitating and often invisible illness it can be incredibly isolating, you don’t always tell people you have it and many people just don’t understand. It is not their fault but people cannot understand that you are actually really ill, yet managing to hold down a job and function day to day. They don’t understand when you don’t want to or can’t go out, or that you are not being lazy you just really, really need to sleep. It is also hard to form friendships or even keep them when you are so consumed with ill health, it sometimes seems as though you are being selfish or self-centred but actually it is self-preservation and just trying to get through the days the best way you can.
So for me, having been through what I have been through, the friends I have are more precious to me as they are the ones that have been there with me, have seen the tough days and know what I went through.
They are the girls of the world, like Hayley, who kept my job going for me and has been in my life since, Ivana, who despite losing her own mum in 2010 whilst I was in hospital, never stopped being there for me, endless hospital and home visits to see me & far too many M&S biscuits! Plus not forgetting the girls who I have a great time with (the Butlins babes to name a few!) who completely understand about my ostomy bag and still listen to me talk about it even though they have heard it 1000 times!
Then possibly the most precious of all (apart from Mum of course!) is the lasting friendship I have with my sister. No-one can possibly replace that bond that close sisters have, no-one is ever the same and the best times in life are those spent with her. It would have been very easy not to have made other friendships as at times it felt like we didn’t need anyone else but each other. But those other friendships, whether friends with Leanne first or friends with me first, have just enhanced our times together and given us more precious memories. It’s a bit of a shame as we don’t spend as much time together as we used to and I miss that more than anything. We used to phone & text each other constantly, see each other every weekend and were always out together and that doesn’t happen as much these days and I miss it. But, we both have boyfriends and full time jobs and we live in different towns (this is much worse than you can imagine) so things change, but one thing that will never change is that we will always be best friends.
To me, it doesn’t matter how many friends you have (and I am sorry to the friends I have not mentioned, you are not forgotten) but what those friends mean. It is ok to have friends that you know wouldn’t really be there for you or that you know may not be in your life for ever, but for now they make a good Friday night drinking buddy, or love knitting as much as you do, or can get you a discount at Karen Millen!
But if you have just one or two friends that you genuinely know would drop everything for you and be to you in a heartbeat if your life got turned upside down, then you are richer and more fulfilled than anyone! And I am lucky and blessed because I do have those friends and a bonus friend in my sister and not many people can say they have a bonus friend!

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The important things in life……

Over the last couple of months, there has been lots going on in my life and yet I still seemed to have had writers block and not been able to come up with a post, despite always saying I would definitely write weekly! But certain things have taken place this week and it has made me think and given me some inspiration for my blog.

There was a lot of negative press over Black Friday and people pushing and shoving and shouting over reduced price TV’s and I had to wonder, when did we all become so materialistic? I have made no secret of my love of shopping, but I simply cannot be bothered to attempt going out into a bull ring full of aggressive shoppers determined to snap up a bargain. I cannot say that I have not been guilty by the tempting pull of the material stuff, I mean I am still searching for the perfect travelling outfit (It’s nearly there, but must consist of comfort yet class and glamour) and I keep finding the next item I simply must have. But, I do not let it consume me.

There are people in life that would be happy with a safe home, running water and food on the table and want for nothing more, the last thing on their mind would be a bargain TV. Yet we seem to forget this. I work in a job where I am surrounded by sadness, it is hard to work for a cancer charity and not feel it. Because we are still a small charity, we often get involved on a personal level, this is really nice as people fundraising for us can see how much we appreciate it, however, it also means being affected on a daily basis by the complete sadness that comes with people suffering from cancer.

Because of this, I am constantly appreciating what I have in life and being grateful for waking up each day and feeling healthy. But I also know, first hand, what it feels like to feel you are not going to make it and I also know how quickly life can change. I never in a million years ever thought I would have to wear a bag or have a permanent stoma. That was never part of my life plan and certainly not something I would ever have chosen. I know that in an instant, life can change so dramatically it will never be the same again. We take simple things for granted, like having an unblemished stomach, all of our limbs in tact or a body that can help us to live each day, we never expect to have these things change. And as much as people may admire my grit when it comes to living with a bag, I bet each one of them will be feeling so glad it is not them.

Just yesterday I was out with Mike, my sister, her boyfriend and some friends, we were in a pub when I realised I need to empty my bag but the worst happened and I felt like it had leaked. Upon a visit to the toilet it had leaked, now not wanting to go into too much detail, it was very watery, which made it near on impossible to deal with. Fortunately, I have a wonderful sister who came to my rescue and helped me and we got me sorted. I was determined it wouldn’t ruin the rest of my evening and carried on. Yes I got upset but that’s natural. Unfortunately, a bag leak knocks your confidence but you cannot let it stop you getting on with your life, there are worse things that can happen. I have always been honest about how I actually appreciate my bag as it gave me life back, but at times like yesterday I can really hate my bag and feel a bit down that I have it. But I will never feel sorry for myself because, I am alive. I also have so much to be thankful for, a nice home, a good job, lovely friends, an amazing family and a great boyfriend, sometimes I have to pinch myself that life is treating me this well. But as I said earlier, it is so important to appreciate every moment as it can so easily be snatched away, hopefully it won’t but it’s still better to be grateful.

I remember being in hospital before my operation and feeling so dreadfully ill that I actually thought I was dying (In a way I was, the op saved me), and I also remember feeling at peace with it, I always assumed if you were dying through illness it would be really distressing but there was something peaceful and accepting about it. However, all I cared about and all that mattered was knowing I had love in my life and just hoping my family knew how much I love them. There were no regrets, no ‘I wish I had…’ it was all about my loved ones. Nothing material even crossed my mind. Although, I do also remember thinking it would have been nice if I had managed to get in one last glass of champagne (well, this is me!). Fortunately I lived to tell the tale and got to drink  my champagne, so I can’t hate my bag, despite the leaks. But I can also appreciate that when all is said and done, all that will matter are your loved ones.

So whatever you are doing, make sure you give your loved ones a big hug tonight, appreciate everything you have and be thankful you get to wake up tomorrow and enjoy life all over again.

Thankful

 

Woooo I did it!

That was the 10K run on Sunday, where Mike and I ran for Beating Bowel Cancer in the Run to the Beat event in Wembley. It was our second 10k of the year, which in itself is shocking, as I never even thought I would do one, let alone 2 but it was a good goal to work towards. Now, I certainly wasn’t as fit or in as good shape as I was for our Bupa 10k, the training kind of fell by the wayside over Summer as I preferred to drink bubbly in the garden than go out and exercise, but I was pretty confident I could run the course.

That was until we received the race pack only to find out the course had some hilly parts, I was actually relying on a nice flat course thinking this would get me round quicker, but nope, wonderful hills awaited us. But still, I thought I could still run the 10k with hills, if a little slower.

On the Friday and Saturday before race day I had been to Surrey for work, so lots of travelling and walking (you can see the excuses forming!) and no time for short training runs. On race day, we were up at 5.30am to ensure we could get to Wembley in time. A quick banana and some water en route and we’re raring to go. A quick toilet stop for me (all Portaloos) only to discover my bag had leaked, this is a fairly rare occurrence, stoma appliances are pretty good and tend to be quite hardy. However, every now and then a leak happens and you just have to deal with it as best you can. Always having a change of bags and a clean pair of knickers on your person is usually a good idea (a clean pair of knickers is never a bad idea even if you don’t have a stoma, that and a toothbrush, you just never know!). Fortunately I had caught the leak before it got too bad and had a change of bag. Changing my bag in a Portaloo toilet is not something I wish to experience again, not particularly easy but I managed. I think it affected me psychologically though and something seemed to switch mentally despite my positive pep talk to myself. I also had a foot injury from a run the week before but was determined to run anyway as it didn’t feel that bad.

So, the race starts and we’re away, Mike is in a different group to me (the faster ones!) so I know he is well away before I have started. I did the first 1k ok, as it was all downhill and then it all just went horribly wrong. I had a stitch, I had to stop at 5k for first aid because my toes were covered in blood, I would like to be dramatic and say it was a huge gash in my toes caused by fast running but it was just a tiny cut that bled a lot! Then after that point it seemed to be all uphill, horrible steep mountains which just felt impossible. But I hobbled, jogged & walked and eventually got round. Perhaps if someone had yelled that there was a bottle of champagne at the finish line I may have got a sprint on, but it was just a few cheerers trying to encourage us slow ones (it’s a bit embarrassing) across the finish line. But at least I can say ‘Wooooo I did it!’

Mike did incredibly well, me, not so good, but I was determined to finish the course no matter what. I actually hated every minute of it but I think I may do it again next year, just to improve my time (which won’t be hard) and because it will also seem like a good idea at the time.

You will be relieved to hear that the champagne came out upon arriving home, followed by a very delicious burger, so all was not lost. Now, I have 7 weeks until the next 10K, and I am DETERMINED to do this one well!

homer

The dating game………..Part 1

The dating game is a tricky one and especially hard when you have something that makes you feel ‘less normal’, like an ostomy bag. I see quite often people asking the question about dating and when is it right to tell someone you have a bag or are suffering with an IBD such as Colitis or Crohns. The truth is that there is no right time, it is all down to individual circumstances and what feels okay for you.

I really won’t recount all of my dating stories as it may take an age and whilst I love to tell them, I am not sure my boyfriend Mike will want to read it in all its detail! Whatever our situation, we all have the horror dating stories and have all been through the mill when single but who would be without them? They are great to recount over a glass of wine with the girls, they hold funny memories and also make you realise what you don’t want out of a relationship! For example, there was the guy I dated who was a bit like eeyore, his chat wasn’t exactly lively and everything had a bit of a depressing tone to it, apparently he had a great time though as he wanted to see me again – I dread to think what he would’ve been like on a down day! Then the time I went on a date with a guy who worked at the gym I attended, after I told him I didn’t see the relationship progressing, he never spoke to me again – bit awkward when I would bump into him there, I thought I was taking the mature approach. Then there are the dates that should never turn into second dates but somehow do as you find yourself agreeing to it and then running out of excuses to use! I think my worst date was with a guy who was ever so persistent so I thought I would give him the benefit of the doubt and go out with him. Oh, it was awful, he was so boring and I really had no interest in him, as we were stood chatting I was practically sitting in the plant pot to get away from him. To get out of the date I said I was meeting my parents in a bar, he didn’t mind, he came with me (why??) so eventually I told him I had to meet friends at a different bar, this was so I could go home without him realising, however, said bar was in opposite direction to my home and he watched me go so I had to walk down to the pub anyway all by myself!

dates

So anyway, I digress but as you can see there have been some bad dates but there have also been some great ones along the way! But when it came to relationships (pre-Ostomy), telling them about my colitis was never something that featured, after all it was part of me but it didn’t define me and I saw no reason to tell them in the early stages. Sometimes I would be forced into it, such as being hospitalized 3 months into a relationship, kind of forces your hand a bit! As anyone with an IBD will know, mornings are the worst – it is like an explosion, anyone outside your bathroom may think there was a thunderstorm going on whilst trumpets play! It is horrendous. So trying to deal with that in a new relationship is awful, us girls do not like our men to think we use the toilet at the start of relationships, even going for a wee can be difficult, after all, what if they hear us and realise we are humans and not the non-toilet goddesses we have portrayed? Don’t even get me started on blowing my nose too! Having a poo is something we certainly don’t do in a new relationship, we will wait until we get home, or perhaps use a pub toilet if desperate (public places aren’t great but better than the boyfriends house) and as we exit, having been longer than may be appropriate for just a wee, we can use the excuse that we were on the phone! Men do not have this problem, someone I know (no names, she knows who she is) had a boyfriend, who gaily went off the toilet, newspaper in hand, and this was at the start of the relationship!! Bet men don’t agonise about when and where to go – they just go, and some are proud of the fact!

So, this situation is 100 times worse when you have IBD, there is no holding it in, no waiting until you get home, you need to go and you need to go now or there will be blood on the floor (and sometimes more).I have been in a relationship where there the toilet and bathroom are one room, this is the best situation – you can turn on the shower, poo in peace, safe in the knowledge he will be thinking you just have really long showers (actually, I am not sure a man would sit there and think about that), or run the tap if you have already showered to disguise any noise. Sometimes it just becomes easier to tell a person you have this condition and what can happen, it’s an embarrassing tale to tell as we are all a bit shy when it comes to talk of poo but it makes it easier for yourself in the long run.

I have a wonderful boyfriend called Mike, he is handsome, kind, loving and all other sorts of nice things and we have been together just over 3 years. Three years ago was my worst ever flare that led to my month long hospital stay which ended in my emergency surgery and my bag. I didn’t tell Mike about my Colitis until date 3, (dates 1 & 2 consisted of me barely eating and just praying that my intestines behaved). Mike mentioned about staying the night at some point, but given that I was in an awful flare I just couldn’t bear the thought of staying over at someone’s house. I decided to be honest with him rather than try and make excuses as to why sleepovers (separate bedrooms of course) were out of the question for the foreseeable future. It was a good job I did as a week later I was really, really ill and my whole nightmare began. We had a few dates in hospital, obviously I am such hot stuff in my moo cow pyjamas, attached to a drip or two with ever shrinking boobs and sticky up hair that Mike just couldn’t resist the lure of seeing me 😉 But as is to be expected, starting and maintaining a relationship whilst in hospital/recovering is difficult, so we kept in touch but nothing really happened for a couple of months.
So I was left in a situation of being ‘back on the market’ but now I had an ostomy bag to contend with, I also wasn’t sure if things were finished with Mike and I as I still felt it had potential, and I was sure once he saw me out of my pyjamas he might realise I was much better! I wasn’t going to stop myself from maybe meeting someone else but I also wanted to decide how I felt about things with Mike so I needed to give myself time. After a period of recovery, I was ready to hit the town again and so my sister and I would get glammed up and off we’d go. Then there came a point where Mike and I were seeing each other, but it was all very casual, you could say it was ‘complicated’ as Facebook would refer to it. I didn’t want to be unfaithful but then again didn’t know if I had anything to be unfaithful about. Honestly, life is far easier if you’re just honest and ask questions, but why would we be truthful and open when we can weave a complicated scenario for ourselves?! Anyway, back to dating, men may have chatted me up or made advances, shall we say, and this is going to sound awful but I would tell them I had an Ostomy bag thinking it would put them off and you know what – not once did it ever put a guy off, in fact the response would usually be ‘it doesn’t matter’ or ‘oh, so how does that work then?’, definitely not the responses I was expecting and so different avoidance tactics had to be employed!

I am not saying that some people wouldn’t be put off by it, I have not experienced that, and of course, if they were they weren’t worth it in the first place but it is not something you should worry about hiding. Don’t let it define you, have a date or two before telling them, but if it happened to come up naturally earlier on, then fine. It is whatever you are comfortable with. It’s a scary thought; after all, there is a natural feeling of thinking you could be setting yourself up for rejection, but better to find out early on. If someone is put off by it, it is a reflection on them not you, and that is true with dating anyone, illness or not. Mike has never really known me without the bag and it doesn’t bother him one bit, we are both used to it now.

And if I was single I would still go out with as much determination and gusto as before, the bag wouldn’t stop me at all, it hasn’t stopped me in any other area so why that one? Whatever your situation, if you are single, embrace it, enjoy it – even the bad dates, take them as experience, something to giggle about, but know that you are fabulous and someone else will think so too. And really, be honest, tell them you’re not interested even if they end up never talking to you again – it’s easier in the long run!

fish