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Patients Psoriatic arthritis
How do you manage your daily pain with PA?
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rita_portsmouth
rita_portsmouth
Last activity on 26/01/2023 at 06:00
Joined in 2019
8 comments posted | 1 in the Psoriatic arthritis Forum
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I really feel better now I've moved to a gluten-free and lactose-free diet, one year ago. I'm still in pain but I feel there has been change in a good way.
p.adden
p.adden
Last activity on 01/10/2024 at 11:49
Joined in 2019
7 comments posted | 5 in the Psoriatic arthritis Forum
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I have tried all the drugs with NO effect I don't know where to look
DebsBowman
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DebsBowman
Last activity on 13/06/2024 at 11:46
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10 comments posted | 2 in the Psoriatic arthritis Forum
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I suffer this day in day out it goes so bad some time I find it so hard to do any thing some day just getting up put me in so much pain on I'm on strong pain killers and there no longer working I getting to the point where standing is just to much to cope with the pain is so bad it make me cry and I get so low I thinking of just ending it all I can't live with it I nead a brack from it suffering pain day in day out and night time is worsened I can sleep so I'm have to get up every 2 hours or so has I can only lay on one side and the pain gets worse as I lay on it and in the end it gets so bad I have to sit up to take more pain treatment and some time I end up over loseing on then to and the pain killers as mimicked up my liver so now I suffer liver disease and my joint and beening diabetic to I some times think what the point I get pain in my side to from my liver disease is making me feel sick and I have to go to the bathroom a lot to because my liver don't work that well I get a bold up of toxin in my body to
Trudij
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Trudij
Last activity on 22/04/2022 at 17:30
Joined in 2017
30 comments posted | 3 in the Psoriatic arthritis Forum
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I'm on no treatment or any painkillers . But I'm in no more pain than I was when I was on pain killers . This disease is ruining my life I'm 50 and I feel like I'm 90 years old
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Going through different treatments at the moment but each treatment goes on for about a year and so far nothing has really helped my symptoms. Have been given different painkillers but find most do very little to help. Sleep badly so always very tired and some days so muddled cannot think straight. I definitely know when i'm having a good day in comparison to having a bad day. Only get to see the Consultant about once a year otherwise monitored by nurses who are supposed to make contact but who do not. Monitor my own blood tests as no one else seems to be doing this. Tend now to rely on over the counter pain relief as do not have a current prescription for anything else.
JosephineO
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JosephineO
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Last activity on 15/07/2024 at 09:21
Joined in 2018
989 comments posted | 6 in the Psoriatic arthritis Forum
6 of their responses were helpful to members
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@rita_portsmouth @p.adden @DebsBowman @Trudij @Dee237 Thank you all for sharing :)
What do other members try? Do you use some of the ways previously mentioned?
@magicmick @upanddown @lesjames @Darukswoman @bantam @Nicolabruce247 @phyll144 @Lynnm209 @georgelh @Sallyhr @Beaton @Marrkk @Pooks69 @Debbi28 @ColieDevoy @rita_portsmouth @coryyuen @Lynn1976 @Jolanta @Lcomg64 @Flints @freddie78 @EllieJ97 @Nicolad @Fullerdonna2 @Softcrab @suse2001
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Josephine, Community Manager
p.adden
p.adden
Last activity on 01/10/2024 at 11:49
Joined in 2019
7 comments posted | 5 in the Psoriatic arthritis Forum
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I have tried everything over the past 3 years with zero relief which intern drags you down a bit thank god I have got some good private pensions to cushion the impact of this terrible condition.
ElkePickard
ElkePickard
Last activity on 29/07/2024 at 20:09
Joined in 2018
5 comments posted | 3 in the Psoriatic arthritis Forum
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Hi All, I'm on sulfasalazine x6 daily , inject imraldi every two weeks and have just started pregabalin, the new drug does take the edge off the pain, I really struggle with the fatigue, it's so tempting to stay in bed, I have to push myself e very minute of every day, I dread to think about the future.
p.adden
p.adden
Last activity on 01/10/2024 at 11:49
Joined in 2019
7 comments posted | 5 in the Psoriatic arthritis Forum
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My advise is simple, there is no cure, and no relief from drugs, they don't work, so enjoy the rest of your life as you can, life has no boundaries so enjoy what you have in life, and if you can live it to your best.
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I myself have multiple medical conditions including Psoriatic Arthritis with gutter psoriasis in the folds of the skin mostly very red and sore. However the Psoriatic Arthritis has caused me untold pain and discomfort. Daily I have to put up with the balls of my big toes knocking on the ground however some of the other toes are going the same way, I have to wear specialized footwear. In the mix I'm a Diabetic two
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reikiboo64
@Courtney_J
Hi
Well where do I start!
I get frustrated by the constant exhaustion in my muscles. The slightest action feels like I have just done a work out to that part of my body whether it be an arm or a my legs for example.
I am aware that my disease isn't managed at all yet even though I have been diagnosed 18 months or so. It just feels like Russian Roulette with my medication as to whether I will be allowed to continue it from one blood test to the next as my liver rebells.
Everyday a new part of my body starts to creak and feel stiff and painful. To be honest it's scaring me just how quickly things are progressing. It is really getting me down. I can't walk far, self care is difficult . I'm determined to be independent so I'll struggle to succeed in the task.
I want to have the energy to get through my day as I work full time running a women's refuge which is mentally very demanding but fortunately not too physically. I'm so tired at the end of each day. It's an uncomfortable exhaustion. I also suffer from Narcolepsy diagnosed at a similar time to the arthritis, and this also gives me fatigue- I have a double whammy of fatigue.!
I am shielding at the moment so I have had a chance to rest. The first week off work I slept solidly and now I feel more rested. I confess I am anxious about becoming so exhausted again but I am determined this illness won't stop me from doing what I love.
Overall I feel distressed with it all and just want it to go away, My healing has gone to pot. I have put weight on as I can't exercise, I dread going upstairs and at times I just don't know how to deal with it.
Sorry to sound so down hearted, I just don't feel I can bring any positivity to this discussion.
x..
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reikiboo64
@Courtney_J
Hi
Well where do I start!
I get frustrated by the constant exhaustion in my muscles. The slightest action feels like I have just done a work out to that part of my body whether it be an arm or a my legs for example.
I am aware that my disease isn't managed at all yet even though I have been diagnosed 18 months or so. It just feels like Russian Roulette with my medication as to whether I will be allowed to continue it from one blood test to the next as my liver rebells.
Everyday a new part of my body starts to creak and feel stiff and painful. To be honest it's scaring me just how quickly things are progressing. It is really getting me down. I can't walk far, self care is difficult . I'm determined to be independent so I'll struggle to succeed in the task.
I want to have the energy to get through my day as I work full time running a women's refuge which is mentally very demanding but fortunately not too physically. I'm so tired at the end of each day. It's an uncomfortable exhaustion. I also suffer from Narcolepsy diagnosed at a similar time to the arthritis, and this also gives me fatigue- I have a double whammy of fatigue.!
I am shielding at the moment so I have had a chance to rest. The first week off work I slept solidly and now I feel more rested. I confess I am anxious about becoming so exhausted again but I am determined this illness won't stop me from doing what I love.
Overall I feel distressed with it all and just want it to go away, My healing has gone to pot. I have put weight on as I can't exercise, I dread going upstairs and at times I just don't know how to deal with it.
Sorry to sound so down hearted, I just don't feel I can bring any positivity to this discussion.
x..
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JosephineO
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JosephineO
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Last activity on 15/07/2024 at 09:21
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989 comments posted | 6 in the Psoriatic arthritis Forum
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Hello everyone,
Unfortunately, everyday chronic pain is a reality from many people suffering from PA. So we wanted to ask you, what do you do to manage your pain each day? Did you use any pain management applications? Any alternative medication?
Please share in the comments! :)