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 ?
View 1 RepliesI had chicken pox in February and after a few weeks they went but I still have one on my chest and its sore, what can I do?
View 1 RepliesI 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.
View 1 RepliesShould 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?
View 2 RepliesI'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.
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.
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?
View 10 RepliesI 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.
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?
View 32 RepliesI 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
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?
View 2 Repliesdespite 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
View 38 RepliesIve just caught it off my two young daughters (who both still have it). I paid to have a private jab £125 to vaccinate me against chicken pox as soon as my girls developed it. Anyway, a week later i felt very tired, spent all of wednesday in bed, temperature of 37.9c, went work on thursday, hot and sweaty (thinking it was the jab), friday, got up feeling rough, covered in spots (jab was too late).
Id say i had about 1-2 thousand spots, my head was one red carpet. My body, back, arms, and tops of my legs are all covered, tho not as dense. My doctor gave me a sick note for two weeks (but thats only after i told him i didnt want to self cert). But thats all he gave me. No pills, lotion, nothing.
Anyway, most days have been spent in bed with brief periods with the screaming girls. My wife has been wonderful, coping with it all, just giving me space and making sure i drink!
Oddly, the big spots have got bigger and the small ones seem to be retreating, but it just looks like really bad acne. I have also found that the areas i didnt put calmine lotion on are much more comfortable and a lot less inflamed... I left my chest alone altogether and ive hardly noticed it.
Wish id never put any on my face and head.
Im taking lemsip twice a day and any old painkillers i can find before i go bed.
I cannot see that i will be in any shape to go work in 10 days, not unless they start scabbing over soon.
I spent the first few days really worrying about the scars i may get on my face, now i couldnt care less, i just want it over asap, i want to be able to eat without pain, sit, lie down, blink without feeling the huge blisters on my eylids touching, pick things up without the blisters on my fingers screaming.
Other than that im starting to feel ok, im going to go round the house later and remove all the mirrors.
My advice, only put calomine lotion on if you need to, keep cool - avoid sweating if poss. And avoid reading stuff on the internet, this site is the exception, i want to hear from someone on day 14...
I have just come back from the Dr. and told it 'may' be CP. On Sunday (2 days ago), I noticed two spots and thought they may be bites. Thought nothing of it, but on Monday, these spots turned into 6 different blisters around the same area. I have been given calamine lotion.
It doesn't help that, as I going through my menopause, I get the odd flush (which of course could be temperature change re: CP)
I have been generally feeling unwell, but we had a hectic few days a couple of weeks ago for a big event at work and put it down to that, along with the change of weather.
It also doesn't help that I take medication for blood pressure and therefore, the odd headache may be due to that, or it may be due to CP.
I caught this awful chicken pox from my daughter who has now fully recovered,i saw my first spot on sat,so took myself to the gp first thing monday and he gave me Acyclovir which i started taking right away,i'm abit worried as he told me it should have been started with in the first 24 hours for the full effect,but my spots didn't start showing until monday ,i only had the two prior to that would it still work? now i'm covered in them and i feel like crap,has anyone gone through this if so how was it and how long did it last for?
View 4 RepliesI was wondering if it's safe for me to be around my 13 week pregnant friend as one of my other friends child has chicken pox? And I've spent alot of time with him this week?
View 3 Repliesi wanna know if a child has chicken pox he can take bath and he can go to sea ?
View 6 RepliesAm i right in thinking that there is a injection available for chickenpox.
View 5 Repliesi had chicken pox 2 months ago, and the marks is still on my skin and im trying so hard to get rid of it but their not going away.do you know anything or anyway on how to get rid of chicken pox mark?
View 2 RepliesMy son has terrible chicken Pox, he has it everywhere & so aggressive too!! tried virasoothe which helped, now using Poxclin which seems much better!
I'm I'm unsure if I should keep my 6month old away from others in case she has it but it hasn't come out yet?
can anyone advise?
I had a kind of risky encounter about 7 months ago. I used the oraquick test at 1 month, 3 months (twice) and 6.5 months. All came back negative. Can I rely on these results as being accurate and not a false negative?
View 7 Replies