Hello - Joined tonight. I have Psoriatic Arthritis
Catage29
Member Posts: 9
Hello everyone 
I randomly decided tonight I wanted to fins a forum for people with Arthritis... so here I am.
I am 29 now but was diagnosed with Psoriatic Arthritis when I was 17. I would love to hear from anyone who has the same type of Arthritis as me or who is of a similar age.
Sometimes I feel like people (mainly some friends) don't really understand what it's like to live with Arthritis, especially the tiredness!
Would love to hear from anyone :0)
Catherine. X

I randomly decided tonight I wanted to fins a forum for people with Arthritis... so here I am.
I am 29 now but was diagnosed with Psoriatic Arthritis when I was 17. I would love to hear from anyone who has the same type of Arthritis as me or who is of a similar age.
Sometimes I feel like people (mainly some friends) don't really understand what it's like to live with Arthritis, especially the tiredness!
Would love to hear from anyone :0)
Catherine. X
0
Comments
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Hello, I have PsA (it wasn't diagnosed for nine years and went untreated for five) and the resulting joint damage has led to OA in my knees and ankles. I am older than you (I am sorry about that!) but, like everyone else on here, I know all too well the realities and difficulties of coping with this disease. I'm on meth, humira and sulph for the PsA, what are you taking? Tiredness is a constant theme on here and yes, those who don't have arthritis do struggle with understanding how it can affect one. I look forward to seeing your name here and there, and I also wish you well. DDHave you got the despatches? No, I always walk like this. Eddie Braben0
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Hey DD
Thank you for your message :0)
I'm on Methotrexate (hate it!!), and Humira too!! I sometimes take Celebrex if I need to but I've been trying to ween myself off of it.
Gosh they took a while to diagnose you!! Poor you. It took them about a year to diagnose me I guess. By that time I got a diagnoses I was unable to walk on my foot at all... was sort of walking on the side of it. The x-rays showed that I have bones missing in my foot where the Arthritis ate through it. Yuck.
Every now and again I have a flair up. Do you? I'm (touch wood) OK at the mo but if I get stressed it's terrible. I at one point couldn't turn the shower on and got stuck in the bath it was so bad. And I live on my own. In the end I just ended up laughing. What else can you do?!!
I pick up a lot of bugs nd I'm off sick loads at work. My boss actually told me I can only be ill on Friday's... my day off!!!! I couldn't believe my ears! Do you pick up bugs with it?
Chat soon hopefully,
Catherine.0 -
Hi Catherine
well that was a good 'random' thing to do
I have inflammatory arthritis not PsA, but treated very similarly so can totally empathise with you. I also have some OA in my back and neck, having had surgery on my back in the past.
I get flares too where things are really awful and even a sheet on my joints can hurt, I get a temperature and and too tired to stay awake.
I think your attitude is really great and positive! Laughing is a good medicine
I look forward to seeing you post on some of our other forums. Take a look around as see which and just join in
Love
Toni xxx0 -
Hi Catherine
Its lovely to meet you and welcome to the forum
Sorry I cant help, but you will get lots of support on here , and its amazing how good people are at coming forward with answers.
You take care and I hope to see you posting more very soon xxLove
Barbara0 -
Hello again. My meth, humira and sulph are pretty much controlling the PsA (inasmuch as my inflammatory markers are consistently less than five) but it took a good few years to get to this point and the joint damage is already done. I am reliant on crutches and have recently graduated to a rollator to help me get around better and for longer. I am waiting for new knees (I have another two years at least to go), mine are bone-on-bone through about 3/4 of both knees but I have to be 55 before I'm considered for replacements. I haven't had a flare for a while but they do crop up every now and again despite the meds. As for bugs, well, I work as a private tutor for dyslexics and am assiduous about applying hand gel to me and the clients, and I have anti-bacterial wipes for surfaces and equipment. I wash my hands as soon as I come in from the shops etc and if I do go down with something I stop the meth and humira so that my immune system can fire up to help me get better. That is what my rheumatology department have told me to do and I obey.
I was on Celebrex but my GP at the time took me off that due to the cost to him. :roll: I then phannied around with Naproxen for a while but that didn't help, so my current GP prescribed diclofenac and that has proved to be good. I take a stomach protector too when I take a short course of that. The two constants in my life are a lack of energy and pain but I am used to that and 'budget' my life accordingly! DDHave you got the despatches? No, I always walk like this. Eddie Braben0
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