Psoriasis symptoms and conditions

Im 25 years old. After my daughter was born in November 2008, I decided on the Mirena because Im terrible at remembering to take pills. So, Ive had it for about 9 months, maybe 10. I just recently started getting acne excessively bad. I thought I was pregnant again and I had to get back on my Pro-Active. I also started getting this really dry, gross spots on my head and they itched SO bad. I went to the dermatologist and she diagnosed me with Psoriasis. But, after reading all the side-effects, it makes me wonder if its caused from this birth control. I have spoken to my husband and he told me to have it taken out. Did I mention that I can't lose ANY weight. Which makes me feel like crap! But thats another paragraph. Anyways, Im really glad this website is on here because it really give me the insight on real people who are going through the same side effects as me!

Well, I just had my mirena IUD taken out last week. I had wanted to take it out pretty much since I got it in a year and a half ago. It was the second one that I had. The first I got put in when I was 17 due to a heavy period, and I could not use birth control because I suffered with depression on it. At that time I did not associate changes in myself with the IUD because they happened gradually. I lost all sexual appetite which I had believed was because I was ending a relationship at the time and I was uninterested. I began getting acne, which worsened in the colder months, so I did not associate it with the IUD. I had mood swings and was tired a lot. I associated this with stress from being a teenager and in being in school. Two and half years into having my first IUD I met my husband. My sex drive had come back, my my acne continued, and the pimple would get really inflamed and tender. My psoriasis never seemed to fully clear up either. My tiredness and moods continued, and I also became extremely emotional often. I just thought that this is who I was because I had got the IUD so young!
SO when the 5 years on the old IUD was up I thought I should get another one. With the new one my acne persisted, I lost my sex drive again and I now would be dry all the time, whether I was turned on or not. I just couldn't stop but thinking that it was the IUD. So i got in taken out finally after we got married. I didn't want to be a pregnant bride. It has been a few weeks, and my acne has pretty much cleared up, I am wet all the time, and I want to have sex. My psoriasis is also much much much better. I still feel tired sometimes, but I hope that will ease as well.
If it doesn't feel right to you, get it taken out. What is the point of being in a birth control if you don't want to have sex anyways!!! good luck everyone.

Thank God for this site. I have been trying to figure out for the last year what is wrong with me! I have had such unexplainable depression and mood swings for so long and I never would have thought to attribute it to Mirena. Thank all of you ladies for posting on this site and diagnosing me, because obviously none of my doctors are qualified to do it! Everyone I have seen has done nothing but brush it off. I also had an US done the other day and they found a cyst on my ovary. My psoriasis (which I have only had a few small spots on my scalp my entire life) has flared up tremendously all over my body. I have lost all motivation to do anything and have nearly ruined all of my relationships with family and friends due to my laziness, depression, and mood swings. I will hate having a period again, but as I keep reading all of your posts I realize that having a period will be a blessing compared to dealing with all of this. I am making an appt on Monday to have it removed! Thanks so much ladies!

wow I thought that everyone really enjoyed the Mirena I know that i do. I actually do not get a period at all just thee occasional spot here an there. I Never got half the side effects that everyone else has gotten on this page..lol so I am thinking that this is another "Med" that has different side effects for everyone boy am I sure thankful that i didn't read some of the articles in this site or I would have never got it!!!! I am 22 a mother of two and my husband and I wanted to wait for a while to have another. Since the Pill didn't do its job and thats how I got baby girl #2 so I turned to the Mirena. Other then the uncomfortable insertion I was fine I bled for a few weeks after I had it put in but I absolutely love it. i have had mine for about a year..In fact a year next month and I AM NOT HAVING MINE REMOVED...lol I just have to say to everyone out there you cant be sure what its like till you give it a try...

hello friends, I had the Mirena put in 08/08 and shortly there after started feeling depressed, moody and tired and started shedding my hair. Lost my mom about 2 months later so I chalked these symptoms up to that. then I got scalp psoriasis, and have no family history of psoriasis period, even though it is supposed to be genetic. I finally found this sight 3 months ago, and had it removed promptly. Wanted to let you all know I am feeling a lot more normal now. The only thing that is not going away is the scalp psoriasis and the hair shedding......I swear I am going bald. Can anyone tell me when their hair stopped falling out and/or if anyone else has had psoriasis with this beast as well? Thank you and good luck to everyone who has this.

Return of my sense of smell that had mysteriously been lost almost 10 years earlier! I had a small dry patch at the outer edge of my left eye that just wouldn't go away. My husband has psoriasis and uses MG217 Ointment with success so I tried a very small amount on the area at night for a couple of weeks. Smell returned off and on. I didn't make the connection until I stopped using it and my sense of smell diminished...only to return when I used it again in the same way. I have had a few days beginning January 1, 2009 when I have had a complete, accurate sense of smell. Wow!

I am on two 500 mg doses of cephalexin daily to help heal a bug bite..Still waiting for the biopsy to come back. Doctor suggested could be a brown spider bite. Definitely want to stop the skin deterioration and get the wound from where the bite was removed healed but the itching started on day 3 on my stomach and has now spread to entire torso, back, insides of arms and legs. I have tried aveeno baths, benadryl (knocks me out) and eucerin itch-relief. Today I coated my entire body with 1% hydrocortisone with little relief. HELP - I am scratching to the point of bleeding and now that I have read these other comments will NOT take another one of these pills. Any other OTC relief anyone has found?

I was prescribed 750 mg Levaquin for 7 days for a bacterial skin infection that I got under my breasts from inverse psoriasis. I took one pill and it hit me like a ton of bricks. I was up all night long with feelings of dread and like I was on a bad acid trip. The next day, I was so exhausted, I could barely even lift my head off the pillow and literally slept all day. The day after that I was going through withdrawal-like symptoms and my husband finally took me to the ER. The nurse practitioner there told me she NEVER prescribes Levaquin because she sees so many patients coming into the ER who are experiencing horrible side effects. I quit taking it obviously but am still feeling shaky and weak. Also, today, both of my feet started feeling like they were asleep with the pins and needles feeling. Also, I have TMJ and my jaw is aching as well. All of this for a little skin infection that the doctor didn't even examine. He just got the results of the cultures back but didn't actually see the infection to determine if it actually needed something so strong. I am taking Keflex now which isn't near as bad and is helping just fine. The difference is the cost. I'm sure the doc got a huge kickback for prescribing the higher-cost Levaquin. I will not be seeing him again. All doctors are interested in is prescribing drugs. They don't ever try a natural means of healing which I do not understand. I am so frustrated...I hope this crap gets out of my system soon!!!

I'm 15 years old and i've been taking prednisone for a few months, and from what i've read i'm on a really high dose. i was diagnosed with rheumatoid arthritis and another autoimmune disorder concerning my muscles at the same time. my doctor told me prednisone was my only choice; it was either that or i would lose the ability to walk. he told me there'd be side effects, but i had no idea it'd turn out like this or i would have fought harder for another course of action. i started out on 30mg twice a day, and since then was weaned down to 20mg twice a day and now i'm down to 30mg once a day. i've been looking up a bunch of information trying to figure out if there's a way to lessen the side effects or any hope at all that they will get better. apparently there isn't much. after reading a bunch of these stories i gotta say i'm not feeling great about this. i totally understand everything everyone is going through. i'm sure you can imagine what it's like being smack in the middle of high school with a huge puffy face, acne so bad on my face, chest, back, neck, and shoulders that wearing a bra could put me in tears, and mood swings so bad i've lost friends over it. everyone knows how brutal high school can be, where appearance and attitude are everything. and i try to tell my doctor about it and he literally looks at me like i'm a whiny teenager and says "you're just going to have to deal with it." and people like my mom and my closest friends don't get it either. nobody understands how beyond frustrating it is. i'll get into the worst moods and not have a reason for it, but i'll stay angry for hours or burst into tears over someone looking at me the wrong way. it'll get to the point where i have to isolate myself from other people because the abrubt mood changes get so bad. as bad as i hate to admit it, the pain from the arthritis is gone now and supposedly my muscles are doing better too. developing arthritis caused me to have to quit cheerleading, something i've loved doing for 6 years, because the pain got to the point where i couldn't get my arms above my head or bend my knees. however, i'd almost rather deal with the horrible joint pain than deal with the side effects of prednisone. if your doctor gives you and alternative method, take it. i've always been confident in the way i look and really outgoing and happy and now i sometimes catch myself thinking about suicide. that's shocking to me because i've got so much going for me, but this medicine makes me miserable. and when i complain about it, anyone i'm talking to just looks at me like i'm being a cry baby. my mom does too, she'll say things like "you just have to do this. i know it's not what you want but to be honest i'm sick of hearing you bitch about it."
i feel a little better knowing other people feel the same way - like nobody gets whats going on with them. the prednisone does give me days of really great euphoria and days when i feel like i could run a marathon, but waking up in the morning to the acne and huge face puts me to tears every day. i have to pee all the time, usually getting up at 2 or 3 am. i don't sleep well anymore and i do sweat all the time. which also sucks being a teenage girl. i'm always hungry, and when i eat i never feel full so i don't know when to stop. my neck and face have put on so much weight that when people see me in the halls or out and about they ask me what happened. mind you these are people i don't talk to, just ones i know from classes or whatever. and it's pretty bad when teenage boys i've never really talked to ask what happened to your face. kind of a blow to the ego, or whatever is left of it at this point.
i'd like to know if, as my dosage gets lowered, the side effects will diminish and when i'm off the prednisone completely if they will disappear altogether. any help there?
or if there is any way to help the acne or puffy face

my doctor just put me on something called methotrexate or something like that to help wean me off the prednisone, and does anyone know what those side effects will do? or if they'll affect the prednisone side effects?
i'm constantly obsessing over gaining weight and what my skin looks like and what i eat and how heavy my face feels and the occasional pressure in my eyes to the point where i just want to be put out of my misery.
and after reading other people's stories i really don't understand why this drug is still given out as freely as it is. but maybe all doctors are like mine, they just don't get it.
best of luck to anyone who's on prednisone, my heart goes out to you; i'm right there with you
sorry this became like a book it wasn't meant to be this long

I suffered with huge patches of psoriasis on both elbows which continued to grow larger and larger for years. Numerous treatments of various creams and light therapy had absolutely no positive results on my problem. Then I found a doctor who injected some small amounts of Kenalog directly into the layers of my psoriasis, and FINALLY the psoriasis disappeared completely. It was a MIRACLE for me! My patches of psoriasis now normally remain in remission for about two years. When I notice them to slightly reappear, I got get another Kenalog injection to clear it up for another couple of years. I have never had any side effects with this procedure except for positive ones! My self image has improved, and I can now wear short sleeve shirts without anyone asking me "what's wrong with your elbows?". I think it's the best thing!

very effective, no problems, even though I have psoriasis and I am sensitive to many drugs and other chemicals and foods.

i must tell you that I had a kenalog shot in my hip 10days ago to try to relieve a terrible case of psoriasis on my fingers that not only was hideous to look at but i couldn't pick anything up without my hands my fingers cracking oe bleeding. in these ten days the psoriasis has totally cleared up but I do have a severe metallic aftertaste in my mouth. No other severe side effects as of yet.

Ok so...I started taking Loestrin 24 almost a year ago and I can't really complain too much. I've had a few pregnancy scares because of missed periods but they were just that- missed periods. And there's nothing wrong missing a period or two imo :D
About two weeks ago I ran out and couldn't refill so I neglected to take any pills for a week, figuring I would just pick back up when I could. I've since started taking them regularly again but in those two weeks my personality changed sooo much. In an attempt to describe myself I'd say I was...confused and depressed, for no real reason. My stomach was so messed up I don't even want to share the details. And the strangest thing... I've noticed two VERY SMALL spots (one on my upper thigh and one on my butt) that are slightly red and drier than the skin around it. I'm positive it's not an STD but I'm concerned nonetheless.
In conclusion, I'm gonna take my pills regularly from now on.

But seriously if anyone else has gotten weird small spots of dry skin, plz respond cause it's definitely worrying me a little.

No question, Cymbalta caused me to have psoriasis of my nails and on my feet. My nails started looking funny and ridged a few weeks after taking the Cymbalta, and I could not get the callouses off my feet to save my life, and they were so itchy and flaky. I took it for about 6 months and the psoriasis got worse and worse, I had a few spots in other places on my body but they were small. I switched off the Cymbalta and immediately my nails started growing back normally and the callouses and dry spots on my feet and elbows went away.

I received my first shot on Kenalog three weeks ago, for a bulging disc in L5, and it took me from a 8 out of 10 pain scale, to a 2. After two weeks , I received my second shot, and now I feel about 98% better. As an added bonus, my Psoriasis of 15 years, that no Doctor could seem to control, has all but disappeared! Also a severe pain in my r/foot under 2nd tow area, has completely gone away, after 10 years of misery! I also am seeing my two toenails, and one fingernail restoring themselves to normal again(the nails had fallen off years ago, like a fungus, but it was not fungus). My dermatologist told me it had no cure and that I would have to deal with it! Kenalog benefits have FAR outweighed the negative effects so far... I have lost about 5lbs in 3 weeks, and anxiety is a mild issue, as is mild night sweats, but for me, this is a small price to pay for pain relief that was making my life miserable!

This post is directed to anyone who has contacted me regarding a possible class action lawsuit, which I was trying to initiate, as stated in my Oct 17th, 2008 post.
After contacting as many as 10 law firms, from NY to San Francisco, I have virtually "thrown in the towel". In essence, what they are saying is, this will be too expensive to litigate. The pharmaceutical companies have "teams" of lawyers, and I believe they are reluctant to go up against them.
I find it diabolical that this drug Kenalog is causing so much suffering, some emotional, some esthetic and some, like myself, sheer physical pain...but nothing can be done about it.
For all of you who have emailed me and I was unable to return your ems, I apologize....but I have been waiting to hear something positive feedback to relay. Unfortunately, that was not the case. If anything does develop I have stored your information and will get back to you. I would hope you would do the same.

Took Lisinopril for several years but recently changed to a different medicine due to a very severe cough. Also noticed that shortly after stopping Lisinopril my problems with psoriasis has just about cleared up completely.

I started the Nuvaring 2 1/2 weeks ago. Within the first week and a half I broke out in a horrible rash on my hips and thighs. My doctor said that it is not a side effect of the ring but I have never had sensitive skin or been allergic to anything. She did prescribe me a topical to apply twice daily. By the end of the second week the rash has spread to everywhere except my face, hands and feet. On my chest it looks almost like a heat rash but everywhere else is painful red bumps. I guess as a birth control it is working because my boyfriend will not go anywhere near me. Has anyone else had this problem and know how to treat it. I have made my way through Benadryl creams, the medicated cream prescribed to me, oatmeal baths. Please help me!!! I am so irritable and crabby but I am sure it is because I have not slept in two weeks because I cannot stop scratching myself.

Has anyone experienced multiple pulmonary emboli (blood clots in the lungs)?

Has anyone suffered severe dandruff and itchy scalp, to the point of distraction like???

I just today took my very first dose of Lisinopril of 10mg. My b/p has been very high and this is my first attempt at reducing it. I also have had chronic case of Psoriasis for 20 years. I am obviously nervous how this drug will affect my Psoriasis as any one who has it knows how difficult it is to control. I will make a point of posting here weekly to report any impact on my psoriasis and any additional side effects.

Coughing, eye pain and aggravated psoriasis!
My doctor recently took my off Lisinopril as it was causing me constant coughing. I have been off this medicine for about 2 weeks and the cough is gone. Also I noticed how GREATLY improved my psoriasis has gotten since stopping Lisinopril. In general I feel a lot better since I stopped this medicine and cannot tell you how happy it has made me to see such an improvement with the psoriasis.

I have been on atenolol for 6+ years. I am soo tired all the time. My symptoms are hair loss, weight gain, muscle pain,loss of memory, no creativity, no sex drive. I always feel so blah! I would like to find an alternative so I can live again.

I have been taking Lisinopril for 11 months. I've had psoriasis for 18 years and never did I have an outbreak on my face until the past month! After reading and doing research I've found that Lisinopril can cause outbreaks. After reading all these blogs I realized I am not crazy! I though all my symptoms like dizziness,shortness of breath and muscle aches were all in my head. I want to reach out to those that have suffered with psoriasis like I have never to take this pill! It had truly ruined my holidays and is putting my job on the line because I do not want to be seen like this.

I started on Advair on January 14, 2008. Soon after that I developed
dermatitis on my legs which I was treated for and it went away.
Shortly thereafter, on occasion, my legs would itch so badly at times that I though I would have to SCRATCH!!!!!! FOREVER!!!!!!! Not a good situation. It is now a year later. I resorted to using a Psoriasis cream and with Benadryl , knock on wood, I have been two days without itching. Keeping my fingers crossed. The Advair has really helped with my asthma, but I'm wondering if
anyone has had this side effect?