Tag Archive for: stoma

Struggling with a swollen stoma in the heat

Sorry it’s been a couple of weeks since my last post! We’re having such an amazing time in Australia that I haven’t had the time or energy. It has been non stop in exploring, visiting family and generally just having an amazing time!

My stoma and bag have been doing ok but the last few days I have been struggling. My stoma swells in the heat and when I’m exerting myself, I don’t want to miss a thing so I’ve been snorkelling, swimming, walking and doing everything I can. The problem is that my bag has to fit snugly around my stoma and so when I cut it to fit my swollen stoma, as the swelling decreases it leaves a gap and that gets the acidic output on my skin so I’m left with a Red raw ring of skin.

If I cut my bag to fit my normal sized stoma, when it then swells, my bag cuts into the edge of my stoma. It is now ridged, bleeding and very tender.

I’m in catch 22! If anyone has any advice it would be greatly appreciated. I have texted my stoma nurse for help and I have arranged a clinic visit for when I’m back in the Uk. We fly home on Tuesday, I can’t believe it’s been almost 6 weeks!!

Apart from the issue my stoma and bag have been entire dealable. I’m really glad we came traveling and would recommend anyone with a stoma to not be put off by the idea of travel.

This trip would have been impossible during a flare up. My bag meant I have had a trip of a lifetime and been able to enjoy things I never thought I would.

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Love Sam xx

UPDATE – I spoke to my stoma nurse who suggested using a donut (a sticky , mouldable ring) around my stoma before I put my bag on. This didn’t solve all the problems, but it definitely helped!!

When in doubt call your super stoma nurse!!!! Xxx

2013 – what a year!

This year has been filled with highs and lows. I got sick, lived in an amazing house, held our Cleastonbury festival, laughed a lot, cried quite a bit, had my colon removed, got an ileostomy bag, had some big disappointments but also some fantastic highs, I have visited Vietnam and I’m ending the year in Sydney with my big sis!

I’ve faced my biggest challenges this year, two weeks in hospital, IV steroids, moon face, mood swings, pain, fear and the ‘decision’ – I had a subtotal colectomy with an end ileostomy and spent the last four months living with an ileostomy bag.

sam cleasby ulcerative colitis ibd ileostomy surgery

It has been one of the hardest years of my life, there were times when I felt so low, that life was unfair and that I didnt want to have to deal with all this.  But through the support of my friends and family I got through it.  I founded this blog as a cathartic way to express my feelings while I was on this rollercoaster ride and was amazed that so many of you read it.  Over 30,000 views since I started!!!!

ulcerative colitis surgery ibd ileostomy hospital

As tough as this year has been, I have come through stronger and with a sense of what I want from life.  Im more adventurous and open to change, I want to make the most of every second, Im braver than I thought and stronger than I seem.

colectomy scar ulcerative colitis

I am covered in battle scars that remind me of what I have been through, Im not ashamed of them nor do I feel the need to hide them or cover them up.  I wear my ileostomy bag with pride as it is a symbol of wellness for me.  Before my operation my life was ruled by the toilet, my quality of life was suffering and I just couldnt see a happy future.  Now my bag lets me lead a better life.

stoma ileostomy photo shoot woman beauty ibd surgery ostomy

Im travelling at the moment, I am been to Vietnam and Im in Australia now.  This is something I couldnt dream of doing before as the fear of having a flare up would have ruined it all.  In the last 3 weeks I have been swimming, snorkelling, rode a bicycle around a Vietnamese island, travelled over 12,000 miles, hiked through Aussie bush and LIVED.

vietnam bicycle ulcerative colitis ibd warrior ileostomy ostomy stoma adventure life travel

2013 has made me realise that who you are is not what your life throws at you, but how you choose to deal with it.

ibd warrior inner strength confidence ostomy ileostomy bag

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woman with stoma ileostomy ostomy stoma images

sunbathing with an ileostomy stoma ostomy travel holidays bikini swimwear

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So that was 2013, lets see what 2014 brings!

Happy New Year to you all!

Love Sam xx

Illness and Ileostomies

Last night I started with a stomach bug, I felt queasy and then the output from my stoma turned to water. My bag was filling extremely quickly, I was emptying once or twice an hour and I felt awful.

I had a google and thought I’d try some Imodium (loperamide) to deal with the very watery output from my Ileostomy. I went to bed after puking with a hot water bottle and feeling sorry for myself. I had stomach pain and felt awful. I was a little worried that it could be a blockage, but from dr google I realised that even if it were, the best things to do were drink hot drinks, massage my stomach and try different positions to sit and lay.

I woke this morning after a really restless night feeling terrible. Still awful diarrhoea, nausea and stomach pains. But worse than all that was my mood. I just felt so down, like this was a setback in my recovery. I don’t think I’m generally one to feel sorry for myself but today I’ve been such a Debbie Downer…

eeyores gloomy place

I hate feeling sick. I’d rather have pain that nausea, that queasy feeling is the thing that drops me to my knees. So today the nausea teamed with tiredness, a leaky bag, soreness and pain has made me a proper mardy arse!

I try to keep chipper through all this but this has knocked me, I’m feeling low and fed up. Tonight we were meant to be having a few friends over, a bonfire, fireworks, good food and sparklers! Instead we had to cancel and Timm had taken the kids to the local bonfire, so I’m sat at home listening to other people’s fireworks feeling pretty sorry for myself.

feeling ill and miserable

The plan is Imodium, plenty of fluids and rest. I’m hoping it will be over soon and I’ll be feeling better. Sometimes we need to go to bed with a hot ribena, a hot water bottle and have a little pity party.

And so I’ll do that, and then pick myself up, shake off the grumpiness and smile…

Sam xx

Stoma and Ileostomy photoshoot

When surgery became a possibility I did what we all do these days and googled it… THAT was a mistake (seriously don’t google stomas, you’ll give yourself nightmares!!)

Many images are medical, none are particularly flattering, most are terrifying.

Since having my subtotal colectomy and ileostomy I have realised that neither is anywhere near as frightening as I thought they would be.  My bag is barely noticeable and my stoma is kind of cute to be honest!

I had two separate emails from women recently, one saying she had a stoma and an ileostomy a few years ago and didn’t leave the house for six months till she had the takedown surgery.  And another from a woman due to have surgery who spoke of her fears of being ‘ugly’ and ‘disgusting’.  Both emails broke my heart.  I feel so sad that this life saving operation has such a bad reputation when it comes to looks and self esteem.

I understand the feelings.  When I first had my surgery I was to scared to look at my stoma.  The thought of my intestines being on the outside horrified me and from the images I had seen online, I believed my femininity and any form of attractiveness would have been removed along with my diseased bowel.

Since then I have been googling A LOT – I wanted to find some powerful, beautiful images of women with ileostomy or colostomy bags and stomas to share on this blog.  I struggled…. There are some model shoots for stoma products that I found cheesy.  There are plenty of medical photos and quite a few selfies!

So I decided that as I live with a photographer and Im not really a wallflower that I may as well do a photo shoot to show off my bag and stoma and hopefully to create a series of photos that show femininity, sexuality, creativity and beauty.

I would LOVE your feedback as Im feeling quite nervous about putting these out there…  I wanted to show others the true face of stomas and ileostomies.  Im obviously not a model, Im a normal size 16 woman with wobbly bits and stretch marks.

I have a stoma and I wear an ileostomy bag but they are such a small part of what I am.  I hope this can inspire others who have had or are due to have the surgery.  Your body is awesome.  This surgery saves lives and that little bit of intestine doesn’t change who you are – be proud, be confident and be amazing.

Love Sam xx

All photography is by the awesome Timm Cleasby of The Picture Foundry.

stoma ileostomy photo shoot woman beauty

stoma ileostomy photo shoot woman beauty

stoma ileostomy photo shoot woman beauty

stoma ileostomy photo shoot woman beauty

stoma ileostomy photo shoot woman beauty

stoma ileostomy photo shoot woman beauty

stoma ileostomy photo shoot woman beauty

stoma ileostomy photo shoot woman beauty

stoma ileostomy photo shoot woman beauty

stoma ileostomy photo shoot woman beauty

stoma ileostomy photo shoot woman beauty

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stoma ileostomy femininity black and white photography creative shoot

stoma ileostomy femininity black and white photography creative shoot

stoma ileostomy femininity black and white

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ileostomy and stoma photo shoot black and white female woman with ileostomy bag

ileostomy and stoma photo shoot black and white female woman with ileostomy bag

Update

Sorry I have been away from the blog for a week or so, the downside to feeling better and stronger is that you have to start doing all the things you were doing before illness!! I am back to work, which to be honest feels GREAT.  I run a photography company called The Picture Foundry with my husband and getting back on track feels really good.

sam cleasby

I am driving again (AT LAST!!!!) I felt really isolated and out of control not being able to drive for so long.  We live out in the sticks and have no buses, we don’t even have pavements – so being literally back in the driving seat is a big move forward to me feeling like myself again.  Im also back into the grind of housework and the like.  That bit I could do without!!

All this has meant that I haven’t had time to update the blog, so I am very sorry and I promise to try and be a better blog keeper!  You can always take a peek over at The Picture Foundry’s blog to see what we are up to.

Ive been getting some fab comments this week though about the blog – it still surprises me how many of you are reading.  Thank you!!

One comment that made me laugh…

‘I love reading your blog! Its just like that 50 shades of Grey!!’

‘Ermmmm are you sure you are reading the right one?!!’

‘Ohh I mean I just can’t put it down, I read it as soon as I get in from work!’

 

I have also had quite a few comments from people who want me to write more about life affirmation, positivity and how to improve your life.  That seems like a big thing to do, but Im willing to give it a shot, so look out for some new posts soon.

In other news, I have been asked to speak at an International Women’s Day event in Barnsley next year.  It’s such an honour to be asked and though I am nervous, Im definitely going to do it… Id better get planning!

I still feel a little in shock about the events of the last two months, sometimes I can’t quite believe that it all happened.  Physically I am healing really well, though I still feel tired easily and Im not back to 100% – I am feeling almost back to normal.  I have eventually found what seems like the right ostomy bag for me.  I was having a lot of issues with leaking and the flange not sticking properly (Its ok, you are allowed to laugh at the word ‘flange’) but after trying out a few different products I have found the DanSac diamond shaped one piece is working brilliantly for me!

I had a bit of a tummy bug last week and had diarrhoea (how can you tell? asked a lot of people – it was like water and there was a lot of it!) and so decided to try the marshmallow trick that was mentioned in hospital.  Apparently a few marshmallows really slow down the output and can stop you getting dehydrated.  I found these bad boys!! The BIGGEST marshmallows I have ever seen!!

mega marshmallows

I attended a Stoma Open day last week.  My friend said they should rebrand it as the Ideal Stoma Show – y’know sex it up a bit! Anyway, it was good to see the different companies and products but if Im honest I found the whole thing quite difficult.  Id say I was one of the youngest people there by a good few years.  Most were over 65 and so the event was aimed at that age range.  It made me feel a bit out of place.  Stall holders seemed to assume I was a carer and didn’t interact with me as they were the other folk visiting.  The thing is, I KNOW that there are a lot of people with stomas through IBD in the 20s to 40s, so it just made me wonder, where are they? Do they just not want to attend these events? Is it because they don’t need them or because they seem so keyed to older patients?

If you have a stoma I would love to know if you attend events like these and if not why not?  If you do, then let me know your experiences of them.

Love Sam xx

My stoma

I’ve been a bit shy about sharing a photograph of my stoma. It’s a bit like showing someone your bum hole!! But I know how much it helped me to see other people’s stomas before I had my surgery, so here it is!

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It may not be pretty but it has changed my life. Because of my stoma I no longer have pain, diarrhoea or bleeding. I am off all medication for the first time in ten years and I’m learning to live a new life!

Thank you stoma!!

Sam xx

Is the media too embarrassed to talk about poo?

If you read my blog or know me at all, you will know I talk a lot about poo… Some may say I talk shit, but we’ll overlook that!  I started the blog as I wanted to stop poo being a taboo, to talk about Ulcerative Colitis and IBD.  Over 180,000 people in the UK have either Crohns or Colitis yet it is not something discussed very often.  Now I have my stoma, I talk a lot about Ostomies and what its like to have a bag.  Over 100,000 people in the UK have some type of ostomy, yet again as a nation we just don’t discuss it.

Since starting the blog I have been shocked at the amount of readers I have, in September alone I had over 13,000 views of the site.  I receive so many emails, messages and comments about the site and all have been very positive.  I am delighted, if not a little shocked, at how popular the blog has become.  When I share my blog on Facebook and twitter, many friends share it with their friends.  This is lovely and very much appreciated, it really means a lot.

So I thought it would be good to get the blog out to a wider audience.  I tweeted, messaged and emailed a lot of people in the public eye including several magazines and though the feedback I have is good, no one seems to want to publicise the blog or the subject of poo.  It leaves me wondering why this is?  My viewing figures show that people want to read about the subject so why are people in the public eye so shy of promoting health awareness when it comes to poo?  Is it embarrassment? Or do they think that the general public don’t want to read about poo?

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Everyone poops

I emailed a LOT of magazines including a journalist who sent a PR request out for ‘women in their 30s who started an inspiring blog this year about a life changing event’.  It seemed perfect!  But though the journalist thought my story was interesting and inspiring, it wasn’t right for the magazine.

Now I don’t want to seem big headed, and I really don’t expect every journalist in the land to raise their hands in awe and think my story is the best thing ever!! But it does surprise me that no one seems to want to cover the subject.  I have asked a number of people who I know, who are in the public eye if they would share the blog on Facebook or twitter and Im not getting anywhere with that either.

I *know* that poo is a taboo subject with some people, but when hundreds of thousands of people in the UK are suffering from the same diseases or living with a stoma, I just want to speak openly and honestly about it.  When you have these things it can feel very lonely and its easy to feel isolated so it was so important to me to get out in the open and start talking.  What I have gone through and what Im still going through is rubbish, but it shouldn’t be embarrassing to discuss it.  Yes, I had a disease that involved my arse and spent ten years with diarrhoea.  Yes, I now have a stoma, I wear an ileostomy bag.  At times I struggle with these things, but talking about it just makes things easier.  I do not need the media to promote the idea that this is embarrassing or not to be spoken about.

poo taboo

Or even worse, promoting ostomies as something disgusting and horrific.  The Cincinnatti Police department recently started an initiative to lower the gun crime rate by showing teenagers photographs of people with colostomy bags to show the possible affects of being shot.  “You’re not killed, but you’re walking around with a colostomy bag and that’s just not the way to get a girl’s attention by limping down Warsaw Avenue with a colostomy bag,” said Lt. Joe Richardson.

Well fuck you Lt. Richardson, I guarantee you that my stoma doesn’t stop me getting attention from the opposite sex. My stoma doesn’t take away my sexuality. I’d rather date someone with a stoma than someone who is ignorant.

Their message was that having a bag is the most unattractive thing that could happen to you. A news report actually said the police showed teens “gruesome photos of people with colostomy bags” It promotes the thoughts that if you have a stoma, you are unattractive, smelly and you should be ashamed of the fact. Myths like these arise because of campaigns like the Cincinnati Police Departments. By portraying an ostomy as a tragic and gruesome way to live out the rest of your life, it continues the stigma surrounding stomas and discourages people with ostomies from speaking about their condition without shame publicly.

Where are the stories of inspiration? Where are the stories of people feeling beautiful, empowered and proud? Having a stoma means you were in a situation that meant this drastic, life altering surgery was your best chance of having a life without pain. For many it is emergency surgery done to save lives. I think people who have been through this deserve to be celebrated not shamed or ignored.

Obviously it would be lovely for people to share my story and my blog, but if you don’t want to do that – share someone else’s, or just don’t be afraid to discuss poo and illness. One thing that many people have told me is that after reading and discussing or sharing my blog, they learnt that someone they know has IBD or a stoma. It surprises me that once you start talking then others feel comfortable enough to share their experiences too.

After I started this blog I got an email from my cousin who told me that he too has ulcerative colitis. He lives quite far away from me and I don’t see him often but I couldn’t believe a family member had the same disease as me and we didn’t know about it! That no one in our families had spoken about it and connected that we had the same thing!

I had a person come up to me in the street and say ‘Sam!!! I have a bad ass too!!!!’ The power of blogging, eh?!!

I write this blog as I want to share my experiences to help others and to get people talking. Please help me do that by sharing this post and letting me know if it helps you or someone you know.

Many thanks

Sam xx

Feeling emotional – Stoma and Ileostomy worries

I am still recovering well, physically my strength is returning though I still feel very tired.  Im able to do more now, cooking and cleaning and have developed a terrible nesting instinct!  Honestly its like I am 9 months pregnant, I have an urge to rearrange all the rooms, organise and declutter the world!  This means my house is now worse than it was before as there are piles and stacks of ‘stuff’ everywhere!

I think now that I am recovering physically that my mind is working overtime and mentally I am struggling.  Im over thinking things and at times just feeling really sad.  Im sad that my life revolves  around this bag.  I spend so many hours a day in cleaning, emptying, changing, washing, worrying… I have never been the sort of person who spends hours getting ready so it feels odd to spend so much time on myself.

I spoke to a friend yesterday about the blog and how so many people had told me that it was helping them, and I was worried about posting about the bad days as I wanted it to be about positivity.  She told me that she didn’t think my blog was about positivity, it was about honesty.  And being honest is talking about the downs as well as the ups.  She also reminded me that a blog that was always hyper happy comes across as smug!! So I thought Id write a bit today about how Im feeling.

My sleeping patterns are still all over the place, some nights I sleep well, others the insomnia kicks in and I just can’t sleep at all.  Im also getting up once or twice in the night to empty my bag.  A friend told me that our minds get into habits and it will take time to break those habits.  From June till the end of September I was on Prednisolone and the meds made me be unable to sleep and so for all that time I was taking sleeping tablets.  So I know that its going to take time for my mind and body to readjust to sleeping without any drugs in my system.

But in the middle of the night, when everyone else is sleeping and the house is silent, I sit and overthink… These thoughts tend not to be positive ones.  I feel sorry for myself, a big pity party in my honour.  I sat the other night at 4am weeping at the loss of my ‘normal’ life.  Mourning the loss of a life that didn’t involve wearing an ileostomy bag and having to (literally) deal with shit every day.  I sat there wishing I could rewind time and go back to before my operation.  I cried about how my body looks and feels, that Im weak and tired and that I have the scar and this stoma, this weird looking thing on my stomach that spews waste and I have no control over it.  I feel sad that feeling unattractive affects how I feel around my husband.  I feel devastated that my kids still avoid cuddling me as they don’t like the stoma and are worried about hurting me.  I feel scared that the course of my life has changed so drastically and that it won’t ever be the same again.

When the sun comes up it also lightens my worries, its a lot easier to be upbeat during the day.  I talk to Timm a lot and to my friend Caroline, I know I can talk to them openly and honestly and I know that talking helps.  The old saying of a problem shared is a problem halved is so true.  Im not asking for an answer or a solution to the problems, but saying them out loud makes me feel that I can overcome them and that I have support.

At times when Im not feeling down I can look at things logically, I know that when I want to rewind my life or want my ‘normal’ life back, that actually before the op I was ill.  I was so sick, my bowel was ruling my life.  I was going to the toilet 10-15 times a day and bleeding constantly.  I was one the highest doses of meds and wasn’t responding at all.  If I hadn’t had the surgery I believe I would still be in hospital, I would have had to go onto drugs like Infliximab that carry such awful side effects.

I know that this surgery and my annoying little stoma has saved my life, though it is difficult, it has set me on a road to recovery, a road to a new life without pain, without bleeding and without medication.  Though I still feel that I spend a lot of time emptying and changing my bags, I have to remind myself that before the surgery I sometimes lost control of my bowels.  That was the most humiliating and devastating part of my Ulcerative Colitis.  Now I don’t have that worry!  Before the surgery I was in pain pretty much all the time, now I have no pain.  Before, I was bleeding so much from my bum that at times I had to wear a pad, now I have no bleeding at all.

talking through problems

I have a few friends who are going through really tough times at the minute, all in totally different ways but equally tough.  It makes me think about life and the challenges we face during our lives.  When I was younger and Id read about someone facing illness or the death of a loved one, I’d think ‘how do they cope?!!’ – I now realise that there isn’t an alternative to ‘coping’ – Coping is just putting one foot in front of the other, taking each day at a time and accepting that sometimes life is shit, things happen that are not fair, that situations feel so huge and overwhelming that all you can do is sit and weep.

Sitting and weeping is a necessary process, we need to express our pain and let out our frustrations.  Then we get up, brush ourselves off and keep going.  I think it is so important to have people to talk to, this blog is cathartic for me, I feel that writing all my feelings here allows me to release them. Talking is key, whether it is a partner, family, friends or a councillor.  I think if we can talk things through and be open about our feelings it really helps.  Giving a voice to your worries takes the power away from them.  We all know that we can take a concern and make it bigger and badder in our heads than it really is, speaking about them with someone you trust deflates the worry and I swear it will make you feel better!

99 problems

Its not about ‘getting over’ a tough time, its about learning to live with it and that is what I will do, I will accept the bad days and sometimes Ill sit and weep, but I will keep going and learn to live with my stoma.

 

Love Sam xx

 

A day of firsts…

A day of firsts and not all good ones Im afraid.

The day started at 4am when I woke to find my bag had somewhat exploded…  Im thinking making it three weeks before having a full blown blast out is good though, yes? Poor old Timm was woken up and helped sort me out and get me in the shower whilst he did a full bed strip and got some washing on.  I know this is gross, but it’s life for someone with a stoma so I thought it was important to share.  Basically my bag was completely filled with air and so all output was forced out of the sides of the flange (best word ever)… Not a good start to the day.

Anyway this morning my lovely friend Caroline took me into Sheffield for a bit of shopping.  Its the first time I have been out without Timm in a month so it was a little nerve racking but lovely, we went to the Forum for brunch and it was just so nice to be out as a ‘normal’ person.  We chatted, shopped and were generally just a bit giddy.  Ive not had enough giddiness in my life for the past few weeks so it was fantastic to have some time with my friend.

We did have a bit of a laugh when I was explaining to Caroline about ‘phantom rectum’ which is where despite the fact that I have no colon and nothing is connected, I sometimes feel that I need a poo… This is known as a phantom rectum – As I was giggling about the funny name, her response was “Well it does have a ring to it!” Cue hilarity…

Then comes my next first.  I went to the loo and realised I had some leakage on my bag, so I came out and used the disabled loo and my radar key for the first time! I also had to do a clean up and put a new flange and bag on in a public toilet! A bit terrifying as so far Im used to taking my time and doing it in my bedroom.  But I managed it and was just really glad I had my full pack up of products with me.  It really made me realise the importance of being able to use the disabled toilets.  I need the space, but more importantly the use of the basin in the cubicle.  Also the importance of having a spare set of everything I need to do a change.

stoma products

I got a travel bag from Fittleworth who are my delivery company for all my ostomy supplies.  Its not the most fashionable thing in the world but it keeps everything together and was a lifesaver today.  The only thing is that its quite big and so I need a large handbag to fit it in.  I have a couple of larger bags but thought it was VERY IMPORTANT that I had another… Right?? I bought this beauty today from one of my favourite shops Within Reason by The Bombay Satchel Company.

bombay satchel company bag

 

Coming home from our few hours out, I could barely keep my eyes open.  I can’t believe how exhausted I feel after doing so little.  Its a reminder that my body is still mending and healing and though I have more energy now, I really need to make sure I don’t push myself too hard.

So Im off for a nap now to recover from a hard day drinking tea, eating and shopping!!

Love Sam xx