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Dublin: 12 °C Wednesday 22 May, 2013

People living with psoriasis ‘avoid social situations’

World Psoriasis Day is being marked on 29 October. A new survey says that some people find psoriasis reduced their confidence over time.

Image: Jo Andre Johansen via Creative Commons

OVER 100,000 PEOPLE in Ireland live with some form of the chronic autoimmune disorder psoriasis, which presents as scaly patches of silvery or red skin.

New research launched ahead of World Psoriasis Day – which will be marked on 29 October – shows that half (48 per cent) of the people surveyed say that their “fear of what others might think” affects them more than the physical challenge of psoriasis.

The international survey showed that women (61 per cent) were more likely than men (39 per cent) to avoid social situations because of their psoriasis and over half (56 per cent) of women, as opposed to only 43 per cent of men, said that their psoriasis has led to “reduced confidence over time”.

Three-quarters (75 per cent) of respondents said they avoid situations where their psoriasis will be on view.

Under the Spotlight

Under the Spotlight is an initiative which follows people with psoriasis over time. A series of video testimonies from patients in Ireland are online at underthespotlight.ie to highlight the impact of the condition and assist those affected.

One of those featured is Theresa Tierney-Bugler, (28) from Carrigaline, Co Cork, who works as a children’s psychiatric nurse. She has had psoriasis since she was 11 years old, and said she used to hide behind long sleeve tops “so that people wouldn’t stare or make negative comments”.

While psoriasis used to define me, it’s doesn’t anymore. I’ve come to realise that sometimes people with psoriasis are more self-conscious or aware of it than other people are of the condition. The key is to learn how to manage it properly with the right treatment and supports such as the Psoriasis Association of Ireland, and dress around it, so you feel comfortable in all social situations.

Caroline Irwin, chairperson of Psoriasis Association of Ireland said:

The research shows that a quarter (25 per cent) of people living with psoriasis feel that people “treat them differently because of their condition” and 20 per cent believe they “would have more friends” if they didn’t have the condition. To those people, I would say, you are not alone. If you are feeling self-conscious, or experiencing low self- esteem, rest assured that there are supports out there. Talk to someone, a GP, friend or family member, or contact us anytime for free advice and information.

Professor Brian Kirby, consultant dermatologist at St Vincent’s University Hospital, said that doctors are aware of the physical symptoms associated with psoriasis but patients may not be sharing the psychological consequences with them, and doctors should be aware of this.

Under the Spotlight is an initiative of the International Federation of Psoriasis Associations (IFPA) and the Psoriasis Association of Ireland, and is supported by Abbott, the global health care company. The program runs in 13 countries. For more information, visit www.underthespotlight.ie.  If you think you may have psoriasis, visit your GP to find out more.

Hair

A campaign was also recently launched by Claudia Carroll, who endorsed an educational booklet on scalp psoriasis which will be available in hairdressing salons across Ireland. For more, visit www.mypsoriasis.ie.

Read: New method of monitoring skin could replace biopsies: UL study>

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Comments (64 Comments)

  • It’s a terrible thing to have, especially in such an image-focused society.

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  • Something needs to be done about the price of medication for it. I suffer from a type that only flares up around joints(elbows, knees,etc). Thankfully I don’t have an extreme case but I’m unemployed and I can’t afford the cream to treat it. It costs €95 for a tube of cream that will last just over a month plus the 50 quid to go to the doctor for the prescription . The crazy thing is, it’s made by Leo Labs here in Dublin. I lived in London a few years back and went to the doctor about it. Between the appointment,writing the prescription and buying the same cream, it cost me £7.50. You only get a discount in Ireland if your medication comes to over €120 so I stopped buying it!!

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  • What a great platform for support and education on all issues in life, well done @TheJournal

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  • I am currently doing the light treatment programme in James’s. I have been doing it for 4 weeks now and have literally only 2 more weeks left. Skin has cleared up significantly. After reading that article it is quite true. I am 21 years of age and on nights out I would be referred to ‘scabby ****’ along with ‘spotty’ and would often be asked ‘what was ‘wrong’ with me?’ I would try to pretend that this close minded comments didn’t upset me. But in reality they did. However as time went on, I have learned to accept my psoriasis and couldn’t give a fiddlers what anyone else thought.

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  • You in general get under mine… your comments are never funny or clever….

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  • I have suffered with psoriasis since childhood most recently affecting my face. I don’t remember not having it so I’m used to dealing with symptoms and trying to manage triggers. the older I get the more I’ve accepted the appearance but as recently as two weeks ago I avoided a catch up with good friends due to appearance of face!

    My main issue is how people look at it (even though people close to me say ‘you can’t see it’) with a disgusted look on their face as if I’m contagious and ask what it is when they don’t know me that well. I don’t want to be reminded in the pub after applying make up that you can still see my raw skin! This stands for any skin conditions not just psoriasis.

    That said there could be a lot worse wrong with me so I’ll put up with ignorant comments and grin and bare it!

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  • Peace and love to all my fellow itchy and scratcys! It’s an awful pain in the arse (sometimes literally) but once I came to accept that it’s part of who I am it got a little bit easier to live with! My mother had it, I have it, I just hope that that my kids don’t get it!

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  • Them comments using the funny puns are sickening…i got it 3mths ago…the pain at times is best described as a burning sensation on the sides of my legs..back and sides..my skin all over is ruined for the moment and it looks like I went on a sun holiday to Chernoble and actually laid out my towel on top of the reactor core for 2 weeks..thats how bad I look…massive shortage of dermatologists in the country…10 week waiting list crazy…I was going to go to manchester to be seen privately and no waiting list…steroid creams and gels..are a waste of money..coal tar didnt work either…as soon as i came off the Ciclosporin it came back viciously within a day and spread all over and the pain was unreal..im currently just started on uvb light treatment so i hope it goes away soon…im convinced its triggered by stress caused by recent unexpected family berevements and other things…

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  • I have psoriasis but it isn’t too bad. Constantly on my elbows and then get random patches on my legs. The price of the medicated cream is terrible. I work but still only go to get it when it gets really bad. Maybe the new deal the government has done with the pharmacutical companies will reduce the cost? Here’s hoping…..

    Reply
    • Niamh

      The problem with these Medecines is that they are uses in relatively rare medical conditions and for this reason tend to be more expensive than widely used products. I know that doesn’t help but it explains why the prices are so high.

      Reply
  • zebedee 22/10/12 #

    I’ve had this skin condition for 30 years or so. Can hit the confidence of a young person alright . I’ve learnt to live with it as I got older.
    If it flares up I find Silcock’s Base works. Only around €5 for a large tub that lasts a good while
    Smear it onto the affected areas on skin 5 mins before a shower.

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  • I have a very mild, nigh invisible psoriasis (on my scalp). I thought that was all there was to it, ubtil I started getting severe joint pain and swelling in my fingers, and was diagnosed with Psoriatic Arthropathy.

    I am not scaremongering, but it is meant to affect 30% of those with Psoriasis. So it pays to be aware of it.
    http://en.wikipedia.org/wiki/Psoriatic_arthritis

    It’s like arthritis, but not detectable using the normal arthritis tests. So please let your doctor know of your Psoriasis, if you experience any arthritis like symptoms.

    Sláinte,

    Bob

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  • Moogoo have a cream called Irritable Skin Balm. Its fantastic. Their goats milk soap and shampoos are great too. Cant recommend it enough!

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  • I suffer with it on my hands elbows, knees and scalp i tried all the creams tried the uvb treatment am now on methotrexate has worked brilliant only a few side affects

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  • Stephen Maher, washing your hair regularly with a good Aloe Vera shampoo from the health food shop really does help, and a coal tar shampoo gets rid of the build up first

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  • Your comment was the first comment you idiot!!

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  • Three members of my family suffer from this and for one it is very painful.But at least you got to make a stupid joke as first comment well done you.

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  • Gotta love the prefect specimens with their clever thought out comments.

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  • Check out The Food Hospital programme on C4. Guy on the programme got great results from their diet.

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  • I have a friend who had it bad on his face , he tried everything in the book, eventually he went on a strict diet , cut out dairy , all yeast foods and it cleared up , the majority of ailments are diet related but the doctors and specialists don’t like telling you incase they lose business and back handers from pharma companies.

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  • THIS IS REALLY LONG IF YOU DONT WANT TO READ ALL, I RECOMMEND GOING TO THE END AND READING THE LAST 2 OR 3 PARAHRAPHS.

    I’ve had this condition for the last 13 years or so. Was extremely bad at the start, so much so that the only part that was not affected is the only part that is illegal to show in public. I was literally covered head to toe.
    I tried all the prescribed creams, ointments and gels, nothing worked after about 4-6 months of not using anything,it calmed down to a level that was noticeable, but only if someone was actually looking for it. so I thought nothing of it, a few years later it flared up bad again. I decided to not have it checked by my GP but just left it ease itself. which it did after a few weeks.
    Until recently.

    I only had it on my scalp, eyebrows, nose, chin, elbows and the odd patch here and there.
    In March this year my fiance, who is Romanian, went back to Romania with our baby boy so his grandparents could meet him. while there he started to teeth and his cheeks became dry. she brought him to a doctor and hebadvised a cream called “NIDOFLOR”, which could be bought over the counter, our baby’s face was clear within a day.
    She brought home 2 tubes at a cost of ?2.50 each. fair enough they are small but you only need tiny amounts.
    In march I had a bad flare up, you could Barely see my face, within 3 days of using this cream my face was psoriasis free. I have recently started to put this on my elbows which were very bad at the start of October, I am now almost psoriasis free on my elbows aswell, the only part which I cannot treat with this cream is my scalp, obviously because of my hair.
    In short, if you ever go to Romania pick up this cream, or see can you order this online as it cannot be got here.
    That cream again is NIDOFLOR

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  • im 25 and developed guttate psorosis around 5 months ago, after a month of phototherapy it cleared up enough that its not noticeable and hopefully its gone for good, plus i got a great colour so its one plus.

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    • Hey Ciaran….i got the guttate version in july…started the phototheraphy last week..my abs are getting a nice colour like we would get by day 5 hanging around the pool in the Canaries…im sure it will clear….fingers crossed..

      Reply
  • try cortopin,it’s helped my psoriasis a bit,still flares up every now and again though but might help someone

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  • I have it and it’s horrible ,,, I’m 23 now and the older I get the worst my skin gets its not a nice ting to have .I went to do skin treatment in st.vinents hospital it worked but after few months it has come back !!!

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  • I have it on my scalp. The itching and pain is horrible. It flamed up when I was pregnant and hasn’t calmed down since. Hate going out or going to the hair dressers as someone always comments on the ‘rash’ if my hair is up to the ‘dandruff’ if my hair is down. Because its in my hair I use the Thelma shampoo which receives it for a few minutes but then flares over night. I also went to download the app but its not available up north!!! It’s awful for anyone to have.

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  • I have it on both my arms. I did a trial of the MooGoo on one arm and the newest edition to my prescribed cream on the other. The MooGoo worked only slightly better than the steroid cream. But only reduced the redness a little neither really worked enough to continue buying either again

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  • Don’t thank me only the journal comments policy and my own sense of decency stops me from telling you what i really think of your stupid comment.

    Reply
  • zebedee 22/10/12 #

    Damn auto correct…..before taking a shower.

    Reply
  • Hi everybody :) You are not alone in this world.
    I have psoriasis on my head and was using lots of different medication. Lots of them helped but then i realise they are steroids and actually were making more damages.A big story short. I decided to try an offer what I sow on Moore Lane in Dublin. There is a Chinese clinic on the corner and they had promised, that they would get rid of it. It was expensive ( I paid around 300-400 euro 3 years ago and didn’t finish the course) but have to say it helped me. And helped me a lot. I went to procedures for about month or two and then 2 years could live happily :) Now my ‘ Friend’ is back and we try to live friendly :D

    Good luck ,
    LM

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  • I’ll ask him to give me the details of the programme and meds if you want?

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  • *This comment cannot be displayed due to offensive or abusive language*

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  • I used to have scalp and nail psoriasis since the age of 10. Now 30 years later I went on a gluten and alcohol free diet for other reasons and cleared the psoriasis as a side effect. Nowhere close to easy (specifically for someone used to have a drink every evening) but worth it.
    leakygutresearch.com

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  • I used to have it but then i visited a local lady -a faith healer- who gave me 3 sweets which I think were blessed which I took at 9 day intervals..a few
    days after the last sweet it began to change colour and eventually faded
    away ..no explanation for it!!

    Reply
  • I detect you’re bit psor about my comment and I apologise.

    Reply
  • I find your comments irrashional.

    Reply
  • Thanks Norman.

    Reply

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