Psoriasis :: Hydroxychloroquine - Cheeks Looked Red And Swollen
May 18, 2016
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.
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.
View 9 Replies
Advertisement
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 Replies
Ok so is it normal if it comes out? I'm 19+3. I'm not sure if this is what it is. I went pee and wiped and it looked like green snot. Should I be worried?
View 5 Replies
I've been diagnosed with rosacea.
My cheeks sometimes get very red and hot.
Didn't like the cream they gave me. I've recently been using caneston cream
Which seems to be helping. (At moment) I rub a little on my cheeks each day.
It's just my whole face complexion, it's blotchy and horrible.
Find myself having to wear foundation. I'm not a person that wears make up everyday.
Is there anything else that may help out there? I
View 2 Replies
I am from India.I have been suffering with pimples for more than 8 years.I have consulted so many doctors but all my attempts were futile. I am getting pretty much depressed and losing all my confidence.
My condition is getting worse. Now I have small lumps with fluid(Not pus) on my right cheek(lower cheek) and I have been getting them on the same spot frequently and periodically and they are painful and I have pimples on my left cheek too and they are normal.
View 6 Replies
Omg my but cheeks are sore. Why?
View 5 Replies
I received a "VIP" dance at a strip club where a stripper shoved my face in between her but cheeks. My mouth was open and my tongue did get out. She was wearing a gstring, and i'm concerned about any STD risks. this lasted for quite awhile. I was drunk and on top of feeling genuinely embarrassed (and ashamed), I am concerned. I haven't noticed anything that looks like a symptom.
View 1 Replies
Anyone else experiencing shooting pains down one of their butt cheeks? It's starting to happen more often and at longer durations after sitting on a hard surface too long. Definitely painful! I'm 29 weeks tomorrow.
View 4 Replies
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.
View 1 Replies
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?
View 2 Replies
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 Replies
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.
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.
View 2 Replies
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.
View 1 Replies
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 Replies
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 Replies
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
Not taking anything is now causing deformity in my joints and tissue inflammation so an important decision.
View 3 Replies
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
View 38 Replies
I just picked up my first Lyme prescription and was surprised to see two antibiotics, Doxycycline & Hydroxychloroquine. I'm not sure if I am supposed to take this together or the doxy first and THEN the hydroxy when I finish that.
Obviously, I can wait until the morn and call my doc, but I'd love to get started tonight. Anyone know if these are usually prescribed together for Lyme?
View 2 Replies
Doe anyone know anything about this med or have taken it?? Have gone from 15 mgs of pred to 10 to 7.5 mgs since December when I was diagnosed with pmr. 7.5 was not cutting it and dropped it back to 10mgs and also started me on hydroxychloroquine. The hope is to get off of the pred all together. I'm taking both meds for now until my next appt. in July. Has anyone had experience on this med?
View 21 Replies
I was diagnosed with OA in my lumbar & cervical spine 10+ years ago although it has not caused me any severe problems. I am now in a new state & under the care of a new rheumatologist. She has diagnosed me with Sjogren's & also "probable lupus" (I have many of the symptoms but nothing has shown up in blood tests as of yet.)
Over the past few months my knuckles have gotten bigger so that I cannot put on rings or remove my wedding band. My fingers also swell, & there are some nodules on the knuckles of 2 fingers up near the fingernails. My rheumatologist told me I now have RA.
I have been taking prednisone bursts every now & then to help with my problems. I have also taken it for several weeks at a time, either 10 mg/day or 5 mg/day. Most recently I had been taking 5 mg/day but it was not helping me. I asked at my last appointment about bumping it up to 10 mg/day again, but she is not wanting to do that. I don't know if its just this state I'm living in or what, but every medical professional I see tells me that taking prednisone long term is not good ... yet I know of people elsewhere who have been taking it for many years.
Three weeks ago my rheumatologist asked me to try hydroxychloroquine while I tapered off the prednisone. Not long after I started taking this medication, I noticed I was having ringing in my ears. I really didn't pay much attention to it ... figured it was just some fluke thing. I never had ringing in my ears prior to starting the hydroxychloroquine. As time went on the ringing got worse. I checked the side effect sheet that came with the medication & ringing in the ears was listed as an "unlikely but serious side effect" & it was noted that if this occurred I should "notify my doctor immediately."
I called my dermatologist's office & unfortunately her nurse took the call. This nurse seems to feel that she is a doctor. She has given me incorrect instructions in the past regarding medication. When I told her what was happening, she told me to stop taking the hydroxychloroquine for one week, then to start taking it again ... "just to see that there's nothing else that could be causing the ringing."
If the ringing hadn't been happening prior to me taking the medication, & it stopped immediately after I stopped taking it, then why do I need to start taking the medication again? Again, this ringing is described as an "unlikely but serious side effect." I am concerned that starting to take it again may result in irreparable harm to my hearing.
Am I just being silly/overcautious? Has anyone had this experience or a similar one?
View 5 Replies
What can I do while I wait to see what medication is going to help me. Predisone and hydroxychloroquine 200 mg
View 1 Replies
