It doesn’t happen to people like me… World Mental Health Day

Mental health issues, they don’t affect people like me.  I’m a natural optimist, a giddy kipper who is loud, giggly and excitable.

People like me don’t get depressed. Don’t get anxiety. People like me are ok Jack.

Only it turns out that mental health issues don’t care about optimism or character.  They’re not bothered whether you’re old or young, rich or poor, working or at home.  They’re not fussed about race, sexuality, ethnicity or gender.  Mental health issues strike without prejudice.

When I was diagnosed with anxiety and depression this year, it floored me.  For a while I couldn’t accept it, feeling that some mistake had been made. I wasn’t embarrassed, I have many people in my life with a whole host of mental health issues and never judged one of them.  I felt compassion for them, I wanted to help them.  But I didn’t see myself as the sort of person with depression.

But what is that? What does that person look like?  I imagined someone in bed, crying and alone, someone who always looked sad and miserable.  A pessimist, someone who saw the glass half empty. I basically imagined Eeyore in human form.

How patronising and judgmental of me.  It goes to show that mental health issues need to be spoken about more.  I’m a left wing, feminist, socially conscious person who desires to be aware of the struggles of fellow people and who would fight for the freedoms of others.  Yet I was holding silly, preconceived ideas of what a person with mental health issues looked like.

Depression takes many forms and has many faces.  And it took me having episodes of pure anxiety to recognise it in myself.

It has been terrifying to admit my feelings and one of the toughest things I’ve had to do is to go to the doctors and open up about the scary thoughts and feelings I’ve had.  To write about it on this blog and on social media took a lot of courage, but from that I have received nothing but support, compassion and help.


If you are struggling, I beg you to speak out. I promise you that you aren’t alone and that if you can take this massive leap, things can start to get better.

There’s no shame in asking for help and the stigma of mental health issues will only continue whilst we don’t speak out about the reality of it.

For a long time, I thought that mental health issues didn’t affect people like me.  Till it did.

On World Mental Health Day, please reach out, learn more, raise awareness and hold out your hand to anyone in your life who is affected.

www.mentalhealth.org.uk/
Sam XX

18 years ago today…

I was in the Leadmill with my friend Lizzy, her boyfriend was the DJ at a new club night and she’s got us tickets.  I wasn’t going to go out but she really wanted to see her fella so I agreed. 

We went and danced and partied and I was glad I’d made the effort to go out.  She went to see her boyfriend whilst I went to the bar and as I looked up at the DJ box for her, I spied a man with long hair wildly dancing hanging off the booth whilst taking requests and was just a little bit smitten!


I recognised him as the bloke I’d seen a few weeks earlier in the same club skating in and dancing with friends. I’d wanted to speak to him then,  but bottled it.  Lizzy came down and I asked about him, she said he was called Timm and that I should come meet him. 

I know people may not believe this but I used to be so shy and unconfident and I was too embarrassed to speak to him. So she dashed off and jumped up to the box and called the immortal words “HEY! My mate fancies you!” 

I was mortified. 

He looked down and said “the one with a skin head?” She nodded. “Bring her up!”  Shyly I went and said hi and he handed me some champagne in a chipped mug. I thought it was the coolest thing ever! 


One thing led to another and 18 years and three kids later, here we are! 

Timm is my best person in the world, he makes my life happier, fuller and better and I know it sounds cliche but I genuinely love him more with each year that passes. 
I worry about him. I worry that all the stress and hardships of my illness will be too much for him.  He’s a good bloke though and I know he’d never just walk away but this makes me worry that he feels stuck with me, that I’m a burden to him. 


I worry that he has turned from my partner to my carer and that I make him unhappy.  Often people think so much about the person who is ill but their partner is expected to just cope with it all.  Timm’s had to do so much for me in the last 13 years and the past 3 years and 5 surgeries have put so much strain on him. I feel sad that the cause of his stress is me. 

Timm makes me feel like the best woman on earth, he tells me I’m beautiful even when I’m in pyjamas and unable to shower and haven’t slept for two days.  He says I’m the best even when I know I am further towards the worst.  He makes me laugh even in my darkest hours. He listens, he supports, he makes everything better. 


I thought I loved Timm when I was 18. And I did! But the depth of my love for him now at 35 is so much more than I could have ever imagined.  It’s a love that comes with time, he knows me better than anyone else in the world, there’s no facade, no fakery, nothing hidden.  

He is my everything. And though I struggle with feeling that I’m a burden to him, and worry I’m not good enough, he has my heart and always will. 

Happy Anniversary of when a skin head’s friend told you that she fancied you. 

18 years bubsy xxx 

How to not be a dick patient in hospital

I have spent a lot of time in hospital on the wards, it adds up to months and months of my life and in that time, I have seen a lot.  Mostly good stuff, but some things that set my teeth on edge!  I love our NHS, we are so lucky to have one of the best health care systems in the world that is free at the point of use.  Our NHS is run on nurses, wonderful, brilliant, hard working nurses, as well as a whole plethora of support staff, doctors and surgeons who work together to give us outstanding care.

I know it goes wrong sometimes, I have had the odd bad experience with nurses and doctors and that’s not ok.  But you know what is really bloody wrong? The amount of crap nurses have to put up with from some patients, and so I thought I would give you my guide to avoid being the patient everyone dislikes, how to not be the one who sets the staff’s teeth on edge, how to not be a dick patient in hospital.

dick3

 

Be polite.

It’s a simple one, but oh, so important.  I know you may be in pain, frightened, at your lowest ebb, but manners cost nothing.  Say please and thank you.  People are doing things for you, therefore you should thank them for their time and effort.  Need a bed pan? Don’t demand, ask nicely.  Has a member of support staff just cleaned your shit up? Say thank you!

You aren’t more important than anyone else

Your illness is important to you, but your pain and suffering is no more or less important than anyone else on the ward.  Your needs will be prioritised by someone in the know.  Don’t assume you should get attention above others.  I have seen it a million times when a patient calls your nurse away from you.  Wait your turn!

Be humble

If you are laid in bed and unable to do anything for yourself then no matter how much money is in your bank or how important your job is, you are at the bottom of the food chain, so be humble and grateful to those around you.  That woman mopping the floor is currently lapping you, so thank her.  The man making you a cup of tea is beating you in the ‘being able to get out of bed, go to work and make tea’ status, so smile and be grateful.

hospital drip stand IBD disability

 

Don’t be a dick

I know you may be in pain and feeling terrible, you are probably scared and shaken, but don’t be a dick about it.  The staff know it is hard being a patient and want to do everything to make you comfortable, they don’t deserve to be shouted at, mocked or abused.  I have heard patients loudly comment about nurse and support staff’s weight, appearance and sexuality.  Not cool.  Not cool at all.

Speak up, don’t scream out

If you are struggling, speak up.  But don’t scream out.  It can be frustrating and anger inducing to be in hospital, but don’t lay this at the feet of the people caring for you.  They are at work and doing their job, they are human and don’t deserve to be a verbal punching bag for you.

ibd hospital jpouch canula medications

Be respectful

Respect is a two way street, I have seen patients scream at nurses, call them names and then whinge that they aren’t liked and everyone ignores them.  The people caring for you are doing a tough job, give them credit for caring for you for little more than the living wage.

Think of your fellow patients

You may be at your lowest point, but it’s likely that so are the other 7 people on your ward, so think of them too.  Keep the noise down, smile at them, don’t be nosy about their private medical needs.  “So, what you had done?” is never really an ok question in my books.  If people want to talk about themselves they will, don’t pry.

sam cleasby ulcerative colitis ibd ileostomy surgery

If it’s good, say so…

If you are receiving great care, then say so, thank the person, tell them how much of a difference they are making to you.  If you feel a certain person has made your life so much easier, then let them know.  My nursing friends tell me that even in their worst nightmares of shifts, the praise and gratitude of one patient can make it all better.

 

So much is put on the behaviour and attitude of NHS staff, and rightly so.  They should have to behave in a way that is respectful, caring and professional, but us patients have our role too and we need to think of others even in our own greatest time of need.

 

Sam x

Surgery number 5

Like Mambo number 5 but with more general anaesthetic!

So if you follow me on Facebook, twitter and instagram, you may have seen that I have been under the knife again.  I have had two hernias develop since my last op in January and I was on the waiting list to get them fixed by Mr Brown but last week, out of no where, I had a huge, sharp pain in my stomach and my incisional hernia (that runs through my belly button) had popped out and got stuck.

I was sick with the pain and knew immediately that I needed help, I never go to A&E as I hate the waits and the people in the waiting rooms (I know that’s judgemental, sorry!!) But I called Timm from work and asked him to come home and take me to hospital.

incisional hernia with ostomy

I was vomiting with the pain, sweating, crying and a general mess but was seen quite quickly and taken onto a surgical assessment ward where doctors thought I would need surgery as soon as possible.  I stayed in overnight and had a CT scan as they thought that there were loops of bowel stuck through my hernia and were worried they would be damaged.  The scan showed that the hernia was very large and there was fat and tissue stuck through it but luckily no bowel.  I was very relieved as I don’t have that much left, so I can’t risk losing any more!! The other thing it showed though was that my parastomal hernia was worse than imagined and the two were almost joining up with only a centimetre between them, so surgery was the only option.

It was all such a whirlwind, the next thing I knew I was being prepped for surgery, and then I awoke in recovery!  It was a big surgery, almost 5 hours long and a lot more complicated than the doctors had first thought.  They had to open me up and pull in the muscles from the sides, remove the tissue that had been stuck and fix the two hernias with two types of mesh.  One was made from pig skin, so you can officially call me Miss Piggy!

incisional hernia with ostomy surgery

After a few days in hospital, I asked to be discharged home on Monday and have been recovering at home since then.  It has been really painful, a lot more painful than my last hernia op, than in comparison was extremely simple. I feel like a punchbag, I am pretty much bed ridden and really struggling to do much at all.  I am feeling quite emotional and sad about it all, I think it is just the shock of everything happening so quickly, it is taking a bit of time for my head to catch up with the rest of me.

It’s all a bit sudden to be honest and has thrown things up in the air as I am due to start a new job and also because I am about to fly to India in a couple of weeks and so I was in a real panic going to surgery as I had no idea how it would affect these things.  But after talking with Timm, we are on it.  To be honest, it is good timing for the job, I’m not due to start till after my hols and so it means that it is done and dusted before work starts.

Regarding India, it is a bit scary.  If this were just a holiday, I would cancel.  But we are going to our family’s home town where they are honouring my grandfather who passed away this year in a football match and commemoration where we are scattering his ashes.  It is so important to me to attend and so I am fighting through.  Doctors are backing me on this as they understand how much it means and I am under instruction to wear surgical stockings, have daily blood thinning injections and a whole list of other things to keep me healthy.  We are getting a wheelchair to help me whilst we are away and Timm, my mum and the kids are all going to help support me too.

incisional hernia with ostomy surgery staples

So the next couple of weeks is all about rest and healing.  I am doing nothing other than concentrating on my health and getting fit and ready for what I hope is the start of a new chapter in my life.  The past three years have been so difficult, with surgeries, anxiety, illness, fatigue and depression, but now I feel I am turning a new page (ALLLLLL the cliches are coming out now!) and with a surgery to fix all the hernias done, my ileostomy settling in and a new job, I hope life is going to be brighter.

 

Thank you all so much for all your love, support and care

 

You are awesome

 

Sam xx

No Coloniversary

Three years ago today, I was wheeled into theatre and had my colon removed and my first ostomy created. I’d been in hospital for weeks, and this was the end of the line after 10 years of ulcerative colitis.  At the time, I thought it would be the end of all my problems and though I was upset, distraught and terrified, I truly felt that I could start a brand new life without illness.

In the past three years, I’ve had three further surgeries, multiple hospital visits and I’m awaiting a date for my fifth and possibly sixth surgeries!
Don’t get me wrong, I don’t regret what happened. I’d had years of flare ups and illness but I don’t think I really recognised that this was just another chapter in my health story, rather than the end of it.

sam cleasby blogger ostomy ibd disability

There are so many wonderful things that have happened in the past three years, things that would have been difficult, if not impossible with my ulcerative colitis. I travelled to Vietnam and Australia, I renewed my wedding vows and I started this blog!
This place has been such a blessing, it has been my diary, a cathartic release to spew out all my feelings. It’s also let me down a new career path, three years ago I’d have never believed I’d be on TV and radio or that I’d be featured in nearly every major newspaper! I wouldn’t have thought I’d be sitting on the This Morning couch with Holly and Phil, be going to parliament, be writing for a newspaper or be in US People magazine!!

sam cleasby this morning holly willoughby Philip schofield

More than that though, I wouldn’t have believed that id have the strength to help others. To inspire and support people all over the world.  I wouldn’t have thought I’d be meeting wonderful new people who courageously share their stories with me and make me carry on writing.
Three years ago today, as I lay in the high dependency unit, tubes everywhere, I was at my lowest.  I was broken, helpless and my soul hurt.  I felt like my body was a failure, that I had become a burden to everyone around me. I felt as though the world would be better off without me.

sam cleasby blogger ostomy ibd surgery

This blog helped me through the toughest times of my life and I want to thank every single one of you for reading, commenting and supporting me.  I’ve had well over 2.5 MILLION views now, I still can’t believe that number when I say it out loud! And every single reader has a place in my heart.
Thank you for following my journey for the past three years, I hope you’ll continue to be by my side for the next three.

Love Sam xxx

Would you take part in a clinical trial? UK Ulcerative Colitis patients needed

Clinical trials are research studies that look into treatments for certain illnesses and gather information for future reference to further knowledge of those illnesses.

I am working with clinical research company, Quotient Clinical as they have a study for people with Ulcerative Colitis and are looking for participants.  The purpose of this study is to see how a study drug is taken up by the body, the drug is being developed for the treatment of pain and diarrhoea in Ulcerative Colitis patients.

People choose to take part in clinical trials for many reasons, it helps increase understanding of their condition and it may benefit others in the future.  As we know, there is no cure for Ulcerative Colitis and the current treatments can be very harsh on our bodies, I am a strong advocate for research and development of treatments and studies like this are a good way to seek out a better way to treat our symptoms and illness.

This study requires a few visits to their unit in Nottingham, firstly an initial screening appointment lasting 4 hours.  Then there is a 2 night residential stay in a unit, two further brief 30 minute visits for sampling and then a 30 minute final follow up visit.  That’s quite a lot of commitment, I know, but the group do pay £915 plus a travel allowance for your time and effort and you will have the knowledge that your participation will help future sufferers.

Studies like this aren’t for everyone, you need to think about your own personal circumstances, but for some people it will be a positive experience where they can potentially help future patients.

sam cleasby sheffield blogger disability

The NHS website give some advice on taking part in studies;

Advantages of being in a clinical trial

  • The main reason for carrying out trials is to assess whether one treatment is better than another
  • Trials are very important in helping find better treatments. By being involved in a trial, you’ll obtain information and evidence that may be helpful to you in the future, as well as helping the NHS provide people with the best possible standard of care

Disadvantages of being in a clinical trial

  • It’s possible you’ll experience unexpected side effect
  • You need to commit time to completing the study

Interested? Or know someone who might be?

The requirements are that you are aged over 18 years old, you must have been diagnosed with Ulcerative Colitis at least 4 months ago and have a BMI between 16 and 35.  You must not have taken part in a clinical trial within the past three month or donated blood in the three months before the start of trial.

There are various dates in September and October and dates are flexible

For more information, go to the Quotient Clinical website and fill in the application form or contact them on 0330 303 5000 or email 

 

clinical study ulcerative colitis

 

Love Sam xx

 

Disclaimer: This is a sponsored post. From time to time, I work with companies and groups who pay me to showcase their products or events.  This helps me fund this website and keep it running.  I only work with companies whom I believe are of interest and beneficial to my lovely readers.

Hello… It’s me!

Hello you lovely lot, it is good to be back here blogging.  Thank you for all your kind messages and support over the last few weeks, I have taken a bit of a leave of absence to get my head together and just haven’t had the energy to blog.

I opened my laptop today for the first time in a month and honestly, it took a lot to do it.  I have been feeling very low and my anxiety has been sky high.  I just felt so overwhelmed by everything that I thought it wise to avoid anything that was causing stress.

I have always used this blog as a cathartic way to deal with my emotions, writing has always been my way of dealing with the shit that goes through my head and for the first time, I just couldn’t make it happen.  But as things get every so slightly better, it feels really good to be back here.  I feel like I have come home.

So how have things been? Well, not great.

I went to see my doctor and was prescribed antidepressants to help with my low moods and anxiety and we are still trying to sort my dosage, it has been upped twice and we are working together to find the dose and medication that is right for me.  I have also been today to see the psychotherapist today to get an assessment of how they could help me, I am going to see a counsellor to try CBT and see how I get on.

This struggle with my mental health has really knocked me for six, I don’t feel like myself.  I have always been the sort of person to just power through, to be positive and be the confident, silly, loud one.  So to all of a sudden feel like I am depressed and anxious has been really difficult and frustrating.  I feel like I have been hit with a shovel.

chronic illness and mental health

Some days are better than others, and most of the time I can paint a happy face on and smile and laugh, I find it extremely difficult to open up and talk to people about how I am feeling and so I almost feel like I am acting most of the time.  I am playing the role of Normal Human Being.  Whilst inside I am ridden with sadness and anxiety.  It has been tough.

The doctors are suggesting it could be PTSD, (Post Traumatic Stress Disorder), that the last few years of multiple surgeries and illness have taken their toll and my mind is just catching up with it.  Whatever it’s title doesn’t really matter to me right now, what is important is that I have recognised how I am feeling and I have asked for help.

It is funny that whilst I sit here on my bed, typing away, the sun shining through my window and the sound of kids playing outside dancing on the wind, I can open up.  I can say how I am feeling.  Yet when I am with others, I find it so damn hard to find the words.  My throat closes and I feel sick at the thought of telling people my sad and dark thoughts.

I worry that they will worry, that it will make them sad.  I worry that this is just one more thing that makes me a burden to those closest to me.  I worry that they will be scared, that they will think I am an unfit mother.  I worry that they will not believe me, after all, my instagram and Facebook are filled with photos of me laughing, so how can I be depressed? I worry a lot.  You can probably tell.

I sometimes wonder about this label of depression, what does a depressed person look like? In my head, I imagine gaunt, hollow souls floating around a psych ward in hospital gowns and bunny slippers.  I think about someone who is crying, wailing and hurting themselves.

It turns out that my perception was so skewed, I see that depression doesn’t have a look, it doesn’t have a character, it is, like everything else in the world, so personal.  I know that on the outside I look happy, confident and strong, yet inside I feel like I am crumbling.  I am honoured that so many of you have been in touch and spoken about your own mental health issues and I want to thank every one of you for taking that time to reach out.

sam cleasby so bad ass blogger health ibd ostomy

I am working hard to feel better.  I am taking meds, I am forcing myself out of bed and into the allotment, making myself go out and see people, pushing myself to do ‘normal’ things.  This is easier some days than others, some days I can do it.  Others it takes everything I have just to get out of bed in the morning.  The effort of showering and changing out of pyjamas defeats me some days, but I am learning not to beat myself up about that.

This will take time.  And effort.  But I know that I will get there.

Thank you all for reading and supporting me and my little blog.

You are all awesome, you are all so bad ass

 

Sam xxxx

 

When you can’t breathe 

Sorry I’m not posting as much as usual right now. The thing is, I am really struggling. 
Sometimes, I can’t breathe. The tide of panic gets too high and fills my lungs. Sometimes, I feel numb. I can’t connect with people around me. Sometimes, it’s all too much. I want to hide from the world. 
Sometimes, I feel like an actress. I’m playing the role of human woman and making my actor face smile and speak. Inside I’m just watching. 
Watching my bad acting. Recognising when I spoke too loud, acted too jovial. I see the fakeness in my smiles and hear the insincerity in my laughter. 
Being with the kids helps, it makes me pull myself together and try really hard to be me. I don’t want to give them yet another thing to worry about me and so I need to just be ok, be me, be mum. 
I’m a week into meds, and to be honest I’m not feeling any better. If anything, I feel worse. I sway between manic anxiety and numbness and the guilt levels of feeling like this are sky high. 
I’m not sure any of this is making much sense, but I thought that writing it all down might help. I wish I were better at opening up to people, but I find it so difficult.  
It has shocked me to feel like this, after so many years of poor health and surgeries, I am so annoyed that now I am struggling emotionally! It’s really pissed me off, I want to be well. And healthy. And happy. So why am I screwing this up? 
Usually, I can talk sense to myself, I can assess my thoughts and feelings and reason with myself till I feel ok. I give myself therapy and thrash it out till I feel better. But this time, I can’t get to the root of it, I don’t know why I feel like this. So I’m not sure how to make myself feel better? 
What I do know, is that I should share this, that it’s ok to feel like this, I shouldn’t be ashamed. And nor should you. Thank you for all your messages, those telling me your stories of mental health and those thanking me for starting the conversation. As with the surgeries, if me talking about this can help, then it gives it reason and purpose. 
I know this is a depressing post. If you came here today for spirit lifting words or inspiration, then I apologise. I don’t have them in me today. 
Because I just can’t breathe. 

Sam xx 

Chronic Illness and mental health

I am very rarely lost for words, this blog is a stream of my internal thoughts and so I usually find it easy to empty my brain onto the page, but today I am struggling.  I am struggling because I find it really difficult to write about my own mental health.  I can share a million photos of me in my undies with my ostomy bag on show, yet when it comes to the health of inside my brain, it is tough.

I wrote recently about making the leap and asking for help and the response I got from you guys was overwhelming, so much love and support and people sharing their own mental health experiences, it made me realise that it is important to share these things along with the physical side of chronic illness.

The truth is that I am really struggling.  After 12 years of living with IBD and 4 surgeries in the past 2 1/2 years, my life has changed dramatically.  The past 3 years, things have moved quickly, surgery after surgery, change after change.  Each surgery, I thought would be my last but then problems arise and I find myself back under the knife.  I feel I haven’t had time to deal with these things, but just had to react to each event.  I think I went into survival mode.

Now, after my last surgery in January, I have 2 big hernias and know that the only treatment to get rid of them is more surgery and it has frazzled my brain.  It is the straw that broke the bad ass’s back and has crumpled me to the ground.

I went to see my GP last week to talk about it, I wound myself up all morning and was a shaking mess by the time I got there, I couldn’t breathe and felt like I would puke.  The idea of telling a stranger just how messed up the inside of my head feels right now was almost too much to bear but I did.  And she was wonderful.

She listened, questioned and encouraged.  We talked about just how huge the changes in my life had been and that it was understandable that I was having a bit of trouble in my head catching up with my body, we talked about PTSD (Post Traumatic Stress Disorder) and how the brain reacts to traumatic events.  How people with chronic illness often have issues with mental health and how society doesn’t always think about healing the mind as well as the body.

chronic illness and mental health

We talked about my feelings of having another surgery and she suggested that we try and make me feel better in my self before making a decision on hernia surgery.  Her thinking being that if I can feel better in my head, that I am better placed to decide whether to have surgery immediately or to put it off for a while.

I am on the list to see a psychotherapist, but there is a 10-12 week wait and so we decided to try some medication to help calm my anxieties and lift my mood.  I hate having to take any medication to make me ‘normal’, 12 years of taking meds every day to stop you shitting yourself does that to a person.  But I had to think seriously about what is best for me right now.  And this is it.

I don’t feel depressed.  I don’t think I do.  When I speak to friends with depression, they talk of a lack of hope, of darkness and feeling stuck in a hole.  I don’t feel that.  I feel massively anxious.  I feel panicky and distressed.  I can’t sleep for the millions of thoughts of all the bad things that could happen to me or the people I love.  I check plug sockets a lot.  I feel I can’t breathe, that something is trapped in my chest.  My heart pounds.  My throat closes.

Not all the time, there are times when I feel ok, there are times when I am fine.  When I feel that things will get better, that it will all figure itself out.

Then BANG! It hits and I can’t breathe.  I walk down the stairs and see myself falling and breaking bones, I get on the train and imagine the carnage of a derailment, I go to events and think about how I would get my family out if there were an attack.  I look at my hernias and think that I have had my fill of surgical luck and what if, this time, I die.  I panic when Timm goes out, visualising the policemen coming to the door to tell me he has been in an accident.  I think about the kids getting snatched, or hit by a car, or falling and cracking their head open on a kerb and never getting up.

And then later I am fine again.  I cook tea, I write articles, I have meetings, I go for a drink, I speak to friends.  I make plans.

Then it is there again.  Terror, fear, panic.  I sit in the garden at 3am to get some air, to overcome the stifling thoughts.  Adrenaline surges through my body, and I can’t sit in bed.  It compels me to get up and wander through the house, checking.  Checking the kids, checking plugs, checking locks.

And on and on, the cycle goes.

Well, it is time for it to stop.  And so, though I find it very hard to talk about, I am putting it out there.  The events in our life have to have an effect on our mental and emotional health, I know there is no shame in admitting this, but it is still tough.

This isn’t me, I am not a worrier or a panicky person, I am ever an optimist and think things will be fine, so it is a shock to suddenly have these thoughts and anxieties.

I know I am not the only person going through this and I just hope that in writing about it, I can help someone else to speak out and get themselves help.  I am not an expert, I have little experience in mental health, but I do know that when I have written about my physical health, that it has benefitted others, so hopefully in writing about this new hurdle, I can help someone else too.

 

Sam xx

Love Festivals, hate camping?

Love the idea of a festival but loathe the reality of sleeping in a tent, washing with baby wipes and shitting in a filthy portaloo?

You want to get yourself to Tramlines!

Tramlines festival in Sheffield is an award winning, city wide festival of live music taking place on 22nd – 24th July this year and is the perfect antidote to festival tent face.  Forget glamping, it’s all about music, glitter and ridiculousness and then getting in your own lovely bed at night!

Seriously, it’s a great idea for those of us who have disabilities or illnesses where the very idea of a festival sends chills.  Camping can be tough, camping at a festival with few facilities and acres of mud between you and your toilet can be a fucking nightmare.

Tramlines is a cracking deal for a weekend of music, at just £32 for a weekend ticket, it’s a full on bargain when you look at the cost of other festivals.  You can pay that for one gig!

reverend and the makers mark tierney tramlines

Photo: Tierney Photography

Sheffield is an amazing city for culture, music and nights out, and the awesome thing about Tramlines is that it is city wide. With a main stage at Ponderosa and second stage on Devonshire Green, you get the big festival feel and a cracking line up.  But what’s even better is the loads of little venues around the city showcasing bands, artists, film and culture.

Be sure to check out the Folk Forest in Endcliffe Park and the beautiful Sheffield Cathedral, as well as all the fringe venues around the city.

Your ticket gets you a wristband that allows you into a ton of venues and you can wander around the city and soak up the brilliant atmosphere and see bands and artists you would usually not know about.

This is a real bonus for those of us with accessibility needs. Festival sites are notoriously shit for accessibility, which can really put off people with illnesses or disabilities where they gave extra needs. Being city wide means you have a wider scope of places to visit and it’s a bit easier to check them out beforehand.

tramlines festival sheffield

Tramlines has accessible viewing platforms on the main stages and if you have a carer, they can get in for free!  There are a few Changing Places in Sheffield meaning if you or your pal needs a full access toilet, you have a choice. Check out the website here. 

The line up this year is fab, I’d highly recommend it for a weekend out whether you’re a regular festival goer or a festival virgin.  Get tickets now before they sell out.  And if you want to see my lovely son playing loud guitars, head over to see Goathead at the Leadmill on the Saturday!
I’ll see you there bad asses!!!!

Love Sam xxx

tramlines festival sheffield

tramlines festival sheffield

 

tramlines festival sheffield
Disclaimer: This is not a paid post, I’ve not received any remuneration for writing about Tramlines, but my brill hubby Timm is a festival director and so I suppose I do indirectly benefit from the festival. Even if I didn’t though, I’d still highly recommend it. Cos it’s wicked. So buy a ticket.