Injections For Psoriasis
Mar 30, 2016
I was diagnosed with lupus and then psoriasis around 3 years ago. Having tried various creams that did nothing, I was put on ciclosporin which helped because this time last year I could hardly walk. However, it affected kidney/liver so despite trying a lower dose I was take off it. I was then put on Fumaderm and the same thing happened! My Nephrologist took me off. I am now back on Acitretin which helps but does not control it. My Dermo wants to go for injections - has anyone else had any experience of this? I understand it is a last ditch thing partially because of the cost and it has to be done in the hospital. I am nearly 78 years. I am very worried about potential side affects - I do not know name of injection because i am waiting for the appointment and the paperwork.
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Should I notify the doctor ahead of time that I have Psoriasis in my groin area? I am wondering if it would stop the procedure from happening?
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I got the chickenpox 6 months ago for the first time at the age of 21. I have Psoriasis but they were dormant until the chicken pox, it took me near enough 6 months and still ongoing, to get rid of them by UV Treatment. Now my brother has chicken pox, and i was wondering if can i get them again within 6 months of the last time ?
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I've had Psoriasis ever since I was 3. I have tried numerous treatments, mostly creams, most of them being steroids and some herbal. I had been able to control it using those for quite a while, up until now that is.
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I was encouraged to be in the sunlight by my GP but being in the UK that is really hard, the Summer we've just had wasn't much of a summer either. When it is sunny I can't go out wearing shorts or short sleeves due to how bad it is.
I am about to start my second year in college and it has gotten much worse over summer. Nobody would guess I suffered from Psoriasis from a distance from the way I dress but I fear I won't be able to hide it much longer, over summer it started spreading to my hands and steroids can't get rid of it, touching my keyboard hurts my hand, I can't wash the dishes and I have to keep hiding my hand from people.
I am currently studying Computing at College, hoping to study Computer Science at Uni, this problem has already affected my social life, at times I even skipped school because of how bad it got. Due to the stress I have started losing a lot of hair, it was great just a few months ago - stress is a killer! If I can't even touch the keyboard how on earth will I pass?
I spoke to my GP about Phototherapy about 3 weeks ago and I've had no contact at all from them or the Dermatology clinic. Many people link Psoriasis to stress and I try to stay happy but the problem is that the moment you see it, what it is doing it, how it is affecting your present and future it gets too much.
Balding itself doesn't worry me too much but the fact that I have Psoriasis on my scalp would just make me want to hide in my room, some of it is quite visible already. I have used various shampoos and although they tend to stop the build up of flakes the redness itself doesn't go away.
We all know that kids my age aren't exactly mature and don't deal with these things well so I wanted to know your advice as to how I should deal with this.
I just want to get through this year of college and perhaps take a gap year before finally going to Uni. I don't know how long the Photo-therapy will take but I wanted to know if I was allowed to ask my GP for help with my hair loss and with the Psoriasis on my hands. The redness on my scalp is so visible so if I can keep my hair at least I will be able to hide it, the pain I get from using my hands sometime even puts me off from doing work.
I have tried keeping my hands moisturised and it helps, albeit a little but do you think my GP would prescribe me Propecia? If it stops the balding for the duration of college I will be happy, once it is over I will stop the treatment and shave my head as I believe that fresh air and more access to sunlight will help the Psoriasis on my head.
I have Spor/Arth. and have been treated for over thirty years.
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Almost every joint has been affected over the years,operations to hands,toes and knees.
Diagenic stopped after 20 years which put my body into shock,now taking Tramacet for the pain.
A major problem now is pain generating in the neck and into my entire head and into my ears nose and face.
I can feel small lumps under the skin and the head pain is severe.
Also heavy sweating from the neck.
I also have a heart condition,thyroid dysfunction Chronic fatigue syndrome.and kidney problems.
There is a number of medication I cannot take because of the other
conditions I have.
I have had acupuncture,physio,and steroid injections but the head pain is so severe even to the touch.
I have a concern and not sure if i am at risk of hiv transmission through oral sex. I receive oral sex from a massage worker for around 10 mins and ejaculated outside her mouth. One thing to mention that i have 2 months old penile psoriasis on the head of my penis. Can some expert assess my risk?
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I was prescribed the above about two months ago. About two weeks after starting it my cheeks looked red and swollen and I had an itchy rash under my chin. Stopped taking it and it all cleared up in the following two weeks.
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the Rheumy nurse has told me to try it again to make sure it was the cause. Thing is, I've had Sjogrens for about 20 years with the usual dryness, but I cope with eye drops and vaginal lubrication and HRT cream. Apart from the odd tummy troubles, I'm thankfully not in pain and lead a pretty normal life.
i'm not at all sure if taking hydroxychloroquine is worth it for me, as I dread it damaging my eyesight. My Specialist seems to think it may help with my poor sense of taste and smell, which would be great as it's depressing.
I'm 40 years old, mum to 2 girls 16 & 11. I just been diagnosed with psoriatic arthritis and I'm so scared and confused, I'm looking for people in the same boat to help me understand what I'm going through. I have suffered with scalp psoriasis for about 10 years. For about a year I had the odd pain here and there, but nothing I thought was worth going to the doctors about, but 6 months ago my knee started to hurt more regularly but I still put it down to getting old. One night I woke up in excruciating pain on my knee, could not move it at all, took a couple of hours with a bag of frozen peas to ease the pain and after taking painkillers the pain went and I carried on with my life. Just under 2 months ago that same pain came back but not just my knee, my shoulder, my elbow and my neck were affected too. I felt like I was paralysed by pain and had to be practically carried to the GP. That was the first time I ever heard of PA...I didn't even know it existed. My GP suspected it and sent me to loads of blood tests, and prescribed a load of tablets. A week later the pain was not easing so back to the GP and this time he gave me stronger co codamol and the pain started to get better. Another week and the blood tests results came back and showed inflammation, very low vit D and folic acid, so GP gave me supplements and decided to give me a 3 vial steroid injection, which he was hopeful could relieve me of pain for a month, while I was being referred to the rheumatologist. I was pain free for 3 days and then it came back with a vengeance. Back on the co codamol and naproxen but the pain was easing just a bit, I couldn't sleep as I any position made something hurt. GP asked for an urgent referral, but that got lost and despite me trying to get things moving, nothing was happening fast enough so I went private, got an appointment within 2 days and a diagnosis. I started methotrexate 2 weeks ago, which makes me very sick and diarrhoea for 3 days, then it settles. Still on co codamol for pain as I refused the steroids the rheumy wanted to prescribe. My life has been turned upside down, almost every day I wake up with different joints hurting. I feel like the pain is eating me away, it's so disheartening when I can't even prepare my child's lunch box because my hands won't allow it. I work through an agency and they are on the verge of getting rid of me because I have taken the odd day off when the pain is just too much. I have been on anti depressants for years and I feel my depression getting worse, I don't want to leave the house or see anyone because I feel so so low. Will it ever get better?
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I have been to the hospital today. I have been treated for psoriatic arthritis for about 5 years. My consultant says that as I have tried everything else, without success I now have to decide whether to have Enbrel. I am a bit concerned about the side effects especially increased chance of infection. While I was on methotrexate I had quite a few infections including shingles.Also not keen on giving myself injections
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Not taking anything is now causing deformity in my joints and tissue inflammation so an important decision.
Is anyone taking Hydroxychloroquine for PA? I got it on prescription from my rheumatologist yesterday. Reading a few forums,and user reviews of insomnia,nightmares,stomach upsets rashes,to name just a few of the side effects. Is the treatment worth it for all the side effects?
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despite using strong painkillers, oxycodone-both long lasting plus short acting plus amitriptyline for sleep plus topical ointment, I cannot get on top of the pain or swelling. I started Stelara in December after DMARDs, Enbrel & Humira failing. I'm also on 7.5mg Prednisone daily. I can't cope much longer, this flare started in November. I suppose I should be grateful that my skin is clear but the pain in my joints is horrendous. My knees, hands and wrists are so swollen. Mobility is crap, I'm virtually crawling to get upstairs, getting dressed is so difficult and painful. I'm seeing OT in 2 weeks plus my rheumatologist on 8th March, also I'm seeing another rheumatologist in may for 2nd opinion because I'm not convinced my current one is expert in PsA. I've been going to hydrotherapy for a few weeks and am going to continue as a paying client because it's been good for me mentally and I don't want to sit around waiting to become completely immobilised. My knees are like melons today, should I rest, elevate or what? Sorry for negativity but I've just about had enough
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On Thursday I had my meningitis C vaccine in my left arm, and diphtheria, polio and tetanus in the other. I've been feeling a bit off since.
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Basically- my arms hurt(which I know was to be expected) but they hurt more than everyone else's seemed to...
Then on Friday I completely lost my appetite, I just didn't want to eat at all, I felt like crying all day(not out of pain though?) I had a really bad headache, my arms still hurt...mainly the meningitis arm, I felt exhausted, all throughout the day, especially in lessons, and I was really irritable and moody towards a few people then today I've been feeling a bit better, although I think the vaccine gave a me a cold? My voice at the moment is husky and I'm worried I'll lose it...
Is it normal for those vaccines to make me feel like this? If so, what can I do about it?
I had my operation 3 months ago when a fibroid was removed from my womb .. I have had 6 months of zoladex injections prior to my operation. I bleed 2 weeks after my operation .. which felt like a period and then 3 weeks later I again had some heavy bleeding .. nothing as bad as it use to be .. My concern is I haven't had a period since and it's been around 4-5 weeks..does it take time for your body to settle down after 6 months of zoladex injections.
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I'm getting some period like pain but nothing..I had a scan recently my womb is fine normal in fact but he did notice my ovaries was full of eggs..he said there bursting but your brain is not acknowledging it..He mentioned PCOS which freaked me out..to be honest my periods were never really irregular before the fibroid problem..I did come in a week later or early or a day later or early but never months..I don't have access hair or acne..I don't think I could handle another period problem..
My husband suffers from Hay Fever quite badly. He takes one Hay Fever tablet in the morning and then another at night. He then has his nasal spray which he takes everyday as well as eye drops to stop them from itching.
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Also to help keep the pollen off his skin he will take 3-4 showers a day.
I have tried to convince him to at least try the Hay Fever injection but he says it is too dangerous and can cause heart problems.
The fact that he doses his system up on the tablets, sprays and eye drops everyday can't be healthy either!
Does anyone know of where I can find information to try and convince my husband that what he is doing isn't that great for him either?
Anyone have experience with SI joint injections?
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I have been dealing with pain (from nagging to disabling) for almost a year. A year ago, the pain slowly progressed to the point that any position was uncomfortable...sitting, standing, walking, sleeping was impossible (for some reason the pain seems worst at night). At that point, I called my spine surgeon (had a lumbar burst fracture 5 years ago so already had a doctor ), but the first available appointment was a month out...I scheduled the appointment and went to the ER after not sleeping any more than an hour or two for several weeks in a row due to pain. They gave me a Toradol injection, muscle relaxers, and Vicodin. I went home thinking that I would finally sleep...WRONG! All those drugs did nothing to stop the pain! I struggled through the next few weeks until my appointment. My doctor's first guess was a disc problem due to my history; however, MRI showed healthy discs and fracture site looking as good as a burst fracture can After a few more tests, he diagnosed me with an SI joint problem and put me on Relafen for 6 weeks to control inflammation. After 3 weeks, I did see improvement...The pain returned to the "annoying" level. Since that time, the pain has been up and down...Always there, not always awful, but sometimes miserable for weeks at a time. I had a foot/ankle reconstruction in November and had a HUGE flair up after that...I realized that I really had an issue when my back pain was keeping me awake at night, not the heel bone that had been sawed into three chunks! I was hoping this problem would just disappear as mysteriously as it began; but, unfortunately, it looks like it's here to stay. My doctor has recommended an SI joint injection as the next step.
Has anyone had success with SI joint injections? My typical symptoms are left side lower back, hip, and thigh pain from just annoying to feeling like my bones are disintegrating...that's the best description I can come up with I also have a lot of muscle soreness in those areas.
How was the "injection experience?" I've had cortisone injections in my foot before, and they were not pleasant...So, I'm definitely not excited about this. I have a high pain tolerance and have dealt with a lot of medical procedures, but something about someone sticking a big needle in my back doesn't give me a warm, fuzzy feeling.
Did you have increased pain for a few days following the injection? After the ones in my foot, I had fairly severe pain for several days...I think they called it a cortisone flair.
Has anyone heard of b12 injections to get off Cymbalta? I have been on for 3 years and can't get off this drug. The withdrawal is horrible. the spins, sweats and other stuff is a killer. I am down to my last 30mg pill and will try to take some of the stuff out like suggested but does anyone have any vitamin help on this?? I am going to read the the B12 epidemic book but have yet to hear of anyone that this has helped.
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my son was diagnosed with B12 a year ago he got the 6 booster jabs last September he had been getting sore heads that were lasting up to 8 weeks his joints ache his shoulders and neck are really sore he was getting ear infections had 10 in last 6 months pins and needles in his hands and feet he is sleeping about 15 to 18 hours a day they started to give him 3 monthly jabs and after 6 month put him on monthly also done a blood test went back to get his second monthly jab but said his b12 levels were normal so put him back to 3 monthly but he could hardly get out of bed they have now put him back to monthly jabs which are only lasting a week if that asked if they could be given weekly the doctor said he would not be happy giving the jabs sooner he got his last jab on the 17 sep and its only lasted till yesterday the are treating him for chronic migraines and now telling me they think it is ME I am sick getting put of by doctors as my son has no life now and i was wondering if I could give him tablets in between jobs because when he first gets his b12 jabs the symptoms all disappear and he gets a week of feeling a lot better but they won't listen
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Did my first methotrexate injection on Tuesday. Seem to have had a splitting headache ever since. Do not know if coincidence or side effect. If side effect any tips?
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I am due to have cortisone injections on 7th November but am feeling a bit anxious about it.
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Since 3 yo I have had pain in my back and up until I was 12 they said that it was growing pains! they then said I had wear and tear at l3/4 and suffered everyday since but been a pain I know that's there but didn't stop me I just grit my teeth and get on! Every few years I have a flare up of it and knocks me for a few weeks then back to usual bearable pains!
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April 2013 woken to numbness /tingling legs and feet 3 days later horrendous back pain and it hasn't left since! Been 15 month of living hell! I've tried pt many many times over the years and always made my pains worse! I've eventually seen PM who said they will do facet joint injections in July however I am due to fly on holiday 5wks later! I can't imagine coping on holiday being the way I am atm however if I get worse then I won't be able to go!
Anybody had facet joint injections? Any good for you ? All experience welcome please
I was taken 300mg X2 daily pregabalin (lyrica). 250mg x 3 naproxen daily and 30mg oxycodone 2x daily they have cramped my meds to now 50mg x2 lyrica, 60mg x1 duloxetine and 30 mg X2 oxycodone! All the meds do is take the edge of the pain but if having a flare up then nothing helps!
I have to use crutches constantly just can't walk without at least one because it causes to much pain in my lumber,hips, groin and my legs sometimes give way!
The things I have been diagnosed with are, ddd, spondylosis, osteoarthritis, fibromyalgia. (They said I have loss if disc height and osteophytes too)
Has anyone breastfeeding had facet joint injection i've been told by 1 surgeon i can feed after 2 days another said 2 weeks and another not to feed again anyone any ideas which is right.
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