Thin skin symptoms and conditions

I'm sitting here in tears reading all of your posts because I've also been on prednisone and have horrible side effects. I was diagnosed with metastatic breast cancer in my lungs in June of 2002 and, after starting at 60 mg/day then, I have been on 20 mg/day for years now. The very first posting that I read mentioned problems with the femur bone. Besides all of the other problems associated with this devastating drug, in December, 2007, I broke a bone in my left foot with no known cause for it. Then I started experiencing pain standing or walking in my left leg and was diagnosed with a fractured femur bone and after several months of trying to get it to heal (including an ultrasonic bone healing system), it just kept getting worse until an orthopedic surgeon recommended that I have a 16 inch rod put into my leg which I did and it ended up to be one of the worst decisions that I have ever made. After experiencing all of the prednisone side effects for almost seven years including depression, severe fatigue, weight gain, moon face, thin skin, cataract surgery on both eyes, hump on my back, mood swings, etc., the pain and suffering that were caused by that operation brought me to seriously consider suicide. I was also diagnosed with chemical neuropathy in both of my legs also which makes my legs so weak that I have to crawl up any steps and have trouble just standing. I actually have an appointment for this evening to have an x-ray done to see what is wrong with my knees and did not realize that this also is yet another side effect. I never make it through the night without waking up in pain and getting a pain pill and then getting up in the morning is almost unbearable with that "burning" pain. I am now on Cymbalta for depression, Xanax for anxiety, Percocet for pain, and of course 20 mg of Prednisone. I was told that I would have to remain on Prednisone for the rest of my life because of the lung scarring and COPD. After reading all of your comments, I have decided that I would rather put up with any breathing problems (and I don't even know how slight they may be at this point) than to remain on the Prednisone. I have tried weaning off several times but get so fatigued that I can't move and that's dropping one mg every week. I'm affected by the decrease but it gets out of hand when I get to 14 mg and I get so frustrated and depressed at not being able to do anything that I just go back up to the 20 mg/day. If you have been able to wean off of it, would you please let me know how you did it and what you had to go through? I'm 65 years old now but I have two wonderful granddaughters (ages 4 and 6) who I can't do any normal "Grammy" things with anymore at this point and I have to change this condition for them and for me. Obviously, the doctors don't recognize the severity of the drug because they just keep prescribing it and out of a regular doctor, an oncologist, an orthopedic surgeon and a neurologist, they can't seem to get together to come up with a solution. I have to say that I haven't considered suicide lately but I do wish that I would just die and be out of this pain. My family and definitely my granddaughters and wanting to see them grow up are the only things that keep me going. There are probably things that I'm forgetting but I'm sure that one of you have covered it in our posting. Although my family is so supportive, no one and I really mean not one of them, realizes knows what we all go through because of this drug. How could they know that something that is supposed to help you could cause these problems? My life is a living hell, all because a pulmonary doctor prescribed prednisone seven years ago and I trusted him to only do what was right without informing me of what was to come. I more than sympathasize with all of you. I sincerely appreciate the time that you took to post to this site and so thankful to know now that this knee pain is not something new that I have but another side effect of the prednisone. I wouldn't have known that if it wasn't for this site because I'd be willing to bet that after I would have had this x-ray done, one of my doctors would have just prescribed another medication to take. Please feel free to contact me directly with any comments or especially any help that you can give me. I know that all of you are going through the same thing so if I can do anything for you, even just listen and understand, please contact me also. Sometimes that's the only thing that people can do is to listen and someone who is in the same situation can always understand. I'm here for anyone who needs a hug for the day.

Been taking this for the past ten years and it is the only thing that allows my skin to quickly recover from eczema. Eczema started at age 22. After my first injection I felt more powerful than Darth Vader and noticed an increase in energy and stamina. A few weeks later, a crash begins and I feel the side effect of lethargy. Consistently, after each Kenalog shot, my skin will develop several pimples around my buttocks area and sometimes on my back after a month or two. I would prefer never to use Kenalog, but it has been the only thing that relieves the patches of skin that become red and flaky due to stress, lack of sleep, and a poor diet. Ultimately, I did develop 'hypercutia' which is a skin condition which allows my dermis to bleed more easily. After stopping the Kenalog injections for a few years, my entire dermis still remains thin and more vulnerable to bleeding. I make my living as an actor and it is part of the reason i still rely on Kenalog whenever an audition comes up and I need to show my body. The pimples eventually become little scars, which eventually become little darker spots on my body. I still believe that in spite of all the side effects, it is worth it if you make your living as an actor or model.

I have been on the med for 4 yrs now (I think). 300 mg/day. At times, especially during the winter I get cold hands & feet where they become numb (& tingly from med. I assume). Fingers may turn white. I have thin skin in those areas (can see veins, redness). I wear double layers of clothes during winter/some spring & I live in Missouri (during the day, sleep). Still have tingling some in toes & fingers, ringing in the ears, memory & word loss, little stuttering/thought process before speaking, dry mouth. Fatigue - but I am a busy person. Stomach issues - constipation (but I also don't eat very well). Anxiety - Welbution generic the whole time I have been on this. Weight loss has been nice. After reading a lot of your comments I am wondering if it is time to get off of the medicine & see how I feel

Hey all. I have had asthmatic bronchitis for about 6-7 weeks now and I have never had asthma or bronchitis before. It started off as a normal flu for 3 days with fever. Then when the flu went away, I started having trouble breathing and shortness of breath. It felt like I ran a marathon walking to the bathroom. I never had that before. The doctor told me it was bronchitis. All tests were fine. I was taking azithromycin (took 3 paks of them) and that was the only thing that made me feel normal, but it did not get rid of the infection. Then I was placed on cipro and steroids. Now I'm not on any antibiotics. I'm taking prednisone and just started the advair inhaler. I was having asthma attacks that I never had before. Very scary. Did anyone have asthmatic bronchitis before??? What did you do to get over it and how long??? Please help!!!

I am recently out of the hosp after 9 days with COPD exas, pneumonia, flu. I have been on heavy antibiotics, steroids--home now for 1st time with oxygen---I feel GREAT.First time in years I feel like I have a life to live. Like a veil has been lifted. I'm scared for this feeling to go away--what is it? the steroids?? the oxygen?? Whatever it is I need to know so I can fight for it and stop just waiting to die.

I have been on prednisone continuously now for 15 years. I was put on it in March of 1995 for a lung condition called chronic eosinophilic pneumonia. I was 122 pounds when I first started prednisone. Now 15 years later I am 197 pounds. I am 35 years old with osteoporosis. I have dealt with depression, terrible headaches, stomach ulcers, hormonal imbalance, hair loss, swollen feet and ankles, I now wear glasses when I didn't before, I have thin skin now that looks older than my 35 years, I deal with night sweats, and in the summer out in the heat my very round moon face turns red as a beet. But, no one can get me off the prednisone. I have seen many specialists, and within 1-2 days of starting to wean past 10mg I get so sick I have to be hospitalized, I literally can't breathe or live without it. I hate this stuff and what its done to me, but I have no choice but to take it or I will die. Doctors have tried alternate medications, nothing but prednisone works. If there is ANYONE who has had to be on it as long as I have or have had success in getting off it after being on it for so long, I would love to hear from you.

I have experienced, avascular necrosis of both hips (resulting in total hip replacements) and avn of both solder (this time it resulted in partial shoulder replacements) Not to mention as everyone else has the thin skin, the weight gain. I have been on prednisone for 8 years - it is part of my immune suppressant cocktail that I take everyday. I have been on 4mg for approximately 5 years. It's very hard to lose the extra weight, the moon face lessens after a time but it is hard to tell because of the weight gain.

I've been on Topamax for 3 years for migraine and it works most of the time. I am currently having a hard time with the usual side effects of memory loss, hair loss, word recall problems, coldness, depression, no sex drive, and am developing a cough. BUT I had a side effect that has not been mentioned when I first started taking it (25 mg in am and pm -- I'm now on 50mg in am and pm).
For about 2 weeks, I would get in my car to go to work and miss my turns because they would cognitively come up too soon (this is after 15 years of going to work the same way everyday). I had to be extremely conscious of my surroundings when I drove or I'd miss all my normal turns. I got lost in my own neighborhood once going home. At work, I'd get up from my desk to go to a co-worker's desk and arrive there amazing fast to my mind. I was experiencing time/space/distance distortion. It became fascinating to me, but it passed.

Being weaned from Methylpred, for the third time in 1 1/2 yrs. VERY bad side effects from losing weight, to siezures, thin skin,lots of bruising, mood swings, depression, anxiety, shaking. Now that I have been decreased once more, from 42mg daily, to 12 mg, my stomach is enlarging by the day! My body and face are thin, (size 4) however, my waist is now 35" and my lower abdomen is 39". I am totally uncomfortable. I work out daily, watch my caloric intake, but each day my clothes get tighter. Any ideas? Is this normal. Can I hope to get my flat stomach? I was placed on mega doses of steroids, when it was rhought I had Polymyositis. Had leg biopsy---inconclusive, however, steroids seemed to lower CPK numbers after several months. Now Neurologist believes steroids are causing numbers to raise, and weaken my muscles. Yuck! Thanks for any help JN

Paper-thin skin on arms, hair falling out by the handfuls, clotting problems with the slightest scrape on my arms, bruising on my legs. Going to go back to Advair 250/50 and see if these problems go away.

My 15 y.o. daughter has has first hand experience with weight gain on Advair. About 6 years ago at about 9 y.o., she gained 20 lbs in 6 months - and it started happening exactly when she started the drug. She was very active (swim team, gymnastics, etc) and did not overeat. It is very frustrating that both her pediatrician and her asthma/allergy specialist deny that her small dose of Advair is to blame.

For some reason, and I have talked to others that this has happened to, switching to Singulair did not help her with the weight problem. Seems the people who are hypersensitive to inhaled steroids are also sensitive to Singulair. Concerned about her rapid weight gain, and because she was always so thin, I took her to an endocrinologist to rule out any other problems. After a lot of bloodwork, he concluded that he could not rule out that it was a side effect of the Advair and/or Singulair, and that they may have elevated her blood sugar. I have read tons and tons of postings on the internet about children & adults rapidly gaining weight from inhaled corticosteroids (i.e. Flovent, Advair), along with the round face, bloated stomach, stretch marks, thin skin, easy bruising, etc. but nobody ever says what happens after stopping any of these drugs. Do people ever go back to normal? Do kids look like themselves again? Do any of the side effects disappear?

She is now 15 y.o. and cannot reverse her weight gain no matter what (30 lbs overweight). The last 2 years, she has only been on a small dose of Pulmicort (a different class of corticosteroid even safe to take when pregnant) since she has mild persistent asthma, and allergy shots have helped trememdously. My husband and I have been looking for 6 years now on how to avoid our daughter's weight gain with asthma drugs. If you run into any info., please let us know. Any experiences or info would be greatly appreciated. Thanks!

Been on Prednisone for 3 years now for ulcerative colitis. At first tolerated the drug quite well. But after a few months started to gain weight, acne. After 3 years of yo-yoing between large and low doses, each increase in dose made me feel worse. I am now at a state of osteopenia and of extreme tiredness and brain fog. I see 80yo with more energy than I. I cant walk up 10 sets of stairs without feeling tired out. I need to sleep 3-5 hours a day just in order to function. As mentioned before brain fog is amazingly bad. I'm a scientific researcher which can no longer work.

Prednisone has introduced to me what panic attacks are, mood swings, joint pain and swelling, extreme muscle fatigue and wasting, blurry vision, in habitual eating habits, depression.

This drug has ruined my life. I would have preferred having surgery to remove the colon and going to the toilet 10 times a day rather than not living as brain fog and tiredness that makes my life a dream-state nightmare.

I have asthmatic bronchitis. In June 2006 I came down with an infection in my lungs, which also set off my asthma. Between the two I was hospitalized and put on 240 mg of intravenous Prednisone and the antibiotic Levaquin. I was cured of the infection and was able breathe normally again but it took a great toll on my body It took me 3 months to taper off of the Prednisone and almost a whole year to feel myself. I was a strong, physically active person before this happened to me and I have not gotten my energy level and endurance back to what I was before I was sick. When I was released from the hospital I went from 160 mg of intravenous Prednisone to 80 mg of pill Prednisone. That step down was too severe and I went through intense joint and muscle pain in my body that it woke me from a sound sleep in the middle of the night. I luckily had an old Vicodin that I took which only made the pain bearable. I should have upped the Prednisone to make it go away but I wanted off. This pain lasted one week with each day getting less. The side effects I experienced from then on were so plentiful that I almost can't remember them all. The physical problems were, thin skin that bruised or ripped and bled profusely with the slightest bump, blurred vision, sensitivity to light, muscle cramps in my legs and hands, sleeplessness, dry mouth and frequent urination. My stomach bloated and got stretch marks. I didn't have any before that. The muscles in my thighs and upper arms atrophied so bad that I could not walk up stairs w/o using my arms to help. My arms were also very weak and I got hemorrhoids; another muscle that was affected. I had a bad case of the drops. I couldn't hold on to anything and broke many glasses. I got moon face that took a couple of weeks to go away after I was off the Prednisone. Because I was on such high doses, my hair died and stopped growing. About 40% of it fell out in one month. It took 6 months to grow back and it all grew back curly. On January 30, 2008 my bronchial tubes closed again due to a sinus infection. Again I was hospitalized with 240 mg of intravenous Prednisone and Levaquin. This time I responded much better, because I jumped on the infection/asthma instead of waiting. I stepped down from 240 to 180 to 90 to 60 and decrease 5 mg a day until I was off. This time I did no lose my hair land did not get hemorrhoids. The other physical effects were pretty much the same but much less severe. However, this time the emotional effects of Prednisone were much worse than last time. I was not a nice person. I was short tempered and argumentative and even had to stop myself from resorting to violence a couple of times. That is definitely not who I am. Prednisone stops your adrenal glands from working and adrenaline is you chemical way of coping with stress. I have been off of the Prednisone for one week and still find it hard to cope with the slightest controversy. My brain is still in a fog and I get confused easily. I cannot handle too many questions at once and forget things. My face is still round. Both times, I have found it the hardest dealing with the Prednisone at the very end and even after I finished taking it. I think it builds up and even though the chemical is suppose to be out of your body in 24 hours, it's effects stay a lot longer. I thought I knew what to expect but the second time was different again. It is a horrible drug but my trade off was breathing. Sometimes I think, that if I have to go through this a few more times, the side effects will kill me before the asthma. I wish all you Prednisone users loads of luck and stay positive.

I have been taking Advair 500/50 for about two years ( I am now 60 years old,) to help control my allergy related asthma (that only presented itself when I had to take steroid eye drops for glaucoma.) While I had the hoarseness, dry mouth and occasional mouth sores, they seemed livable compared to uncontrolled asthma.

One morning about a month ago, when I was taking my normal AM puff, I suddenly felt as though a giant sledge hammer banged down on my head - pounding me into the floor - almost losing consciousness. Then, I experienced pounding, racing heart that felt as though it might jump out of my chest. I turned white and gray - my family and I thought I was having a heart attack.

I was terrified to take another puff - thinking it might be my last. Two days went by, when, I decided to experiment by taking a very light puff, barely taking any into my lungs. (I had been further scared by warning about suddenly going off steroids.) My doctor was out of the country and no one wanted the liability of advising me.

One hesitant puff of Advair caused the exact same pounding - heart jumping and racing reaction. I decided right then that I did not need further evidence to "pound into my head" that Advair was now toxic for me.

The odd thing is that my doctor seems to discount my experience by saying I am the only person this has ever happened to (implying there must be something wrong with me!) When I asked about the dangers and appropriate process for suddenly stopping steroids, she pooh-poohed my concern saying there are no side effects from inhalers with steroids. (Several nurses recently told me that was not necessarily true. Who knows what to believe!)

I have stopped Spiriva and Advair and have scheduled an appointment with a doctor and nurse practitioner who use diet, exercise and nutritional supplements to help treat asthma. A friend has gone to them for several years and is now off all asthma medication, has lost about 50 pounds, has improved health and looks 10 years younger! I can only hope this works for me!

I am also writing Advair manufacturer with my experience;copies to FDA. I can only wonder if there are others as 'rare' as me? If so, let it be known. thanks

I

I take 10mg Lipitor every day, I broke out with dark red itchyskin eruptions on ankle,stomach, and hip thin skin over eruption when it peels off there a large open ulcer like sore, takes many weeks to completely heal! Been to a dermatologist wanted to do biopsy on sores to see what it is, I have been taking lipitor for about 3 years. Never had out breaks like this before going on lipitor. Went off lipitor for about a month outbreaks stopped! Went back on lipitor outbreaks started again, anyone else had similar eruptions?

Hello,
I doubt if this is a new side effect but it really is getting on my nerves. Besides the moon face I have very thin skin and huge red marks on my arms. With the slightest touch they will break open and bleed. I almost fainted today because one started bleeding and it must made me sick to see it there was so much blood.
I haven't had pred in a while but am on cortef, 20mg a day.
Does anyone know if the side effects would go away if I were to reduse my dosage? I have been trying to but left with no energy when I do.
any advise would be appreciated.
Vicki

My 12 y.o. daughter has has first hand experience with weight gain on Advair. About 3 years ago, she gained 20 lbs in 6 months - and it started happening exactly when she started the drug. She was very active (swim team, gymnastics, etc) and did not overeat. It is very frustrating that both her pediatrician and her asthma/allergy specialist deny that her small dose of advair is to blame. For some reason, and I have talked to others that this has happened to, switching to Singulair did not help her with the weight problem. Seems the people who are hypersensitive to inhaled steroids are also sensitive to Singulair.

Concerned about her weight, and because she was always so thin, I took her to an endocrinologist to rule out any other problems. After a lot of bloodwork, he concluded that he could not rule out that it was a side effect of the Advair, and that it may have elevated her blood sugar.

I have read tons and tons of postings on the internet about children & adults rapidly gaining weight from inhaled corticosteroids (i.e. Flovent, Advair), along with the round face, bloated stomach, stretch marks, thin skin, easy bruising, etc. but nobody ever says what happens after stopping any of these drugs. Do people ever go back to normal? Do kids look like themselves again? Do any of the side effects disappear? She's been off the Advair for about 6 months now (uses albuterol as needed) but cannot reverse her weight gain no matter what!

My husband and I have been looking for 3 years now on how to avoid our daughter's weight gain with asthma drugs. If you run into any info., please let us know. Any experiences or info would be greatly appreciated. Thanks!

I've been off Advair for almost 6 weeks now. Use Albuterol as needed. Had been on Advair for 2 years. Breathing was wonderful.

Red/purple bruising on arms and tissue thin skin was major problem. Applying Retin A (Trentoin) twice daily has helped to rebuild the collagen. Still bruise, but not nearly as much.

Has anyone had problems with infections? Mainly staff. I have had to go on antibiotics almost constantly the last 2 years. Seems my immune system can't handle anything anymore.

Going to try a detox diet and try to get all these chemicals out of my system.

The purple-red bruising I've had along with the thinning skin is ecchymoses - which is listed as a possible side effect affecting 3% or so. Been off Advair 9 days and have had to use Albuterol maybe once daily.
Blood pressure is going down, also.
Going to tackle the 20 lb. weight gain next.
Hoping to see if this ecchymose will go away in the next month.

I have been on Advair 500/50 for 2 years taking 1 puff twice daily. I have had these side effects:

weight gain
dry skin
itchy skin
pain in muscles and joints, mostly legs
thin skin on arms
bleeding problems/ clotting disorder
rapid heart beat
thinning hair
difficulty sleeping
thirsty throughout the night
dental problems
water retention
heartburn
I hate taking this drug but it does help keep my COPD(emphysema) under control. I get depressed at times due the side effects of this drug and the impact it has on my life and how I feel about myself. I often think of just stopping the drug and seeing how I feel but I am afraid to.

Mood swings, upset stomach, WEIGHT GAIN (50+LBS!!), forgetfullness, paranoia,hallucinations, feeling invincible, muscle weakness, high blood sugar, high blood pressure, thin skin, fatigue, not caring about anything, talking a lot, feeling hot all the time, excessive sweating resulting in body odor, not liking things that fly( I was especially freaked out by bugs and birds) lack of tactfullness, I'll add more when I think of them.... and heres the clincher......

one day when I was driving on the highway, I was suddenly convinced my car's engine was on fire.

I had a kenalog injection in Sep of 2003 in my upper arm for an allergic rash. Two months later an indent appeared and gradually got worse until March 2004. Now in June, some of the muscle is growing back (its was just thin skin a bones for a while!). The fat doesn't appear to be growing back and the skin is scarred and discolored. I noticed some acne around it for a while and some dark hairs have grown around it (a few shades darker than my arm hair). I think that I will always have some small scarring and deformation, but at last it is healing! No doctors could tell me anything..just to wait it out.
Also for a few months after the shot (5 months) I had periods with horrible cramps that were only about 20 days apart. I don't know if that was related, but I am back to normal now.

I have been on pred for 2 years off and on for Temporal Arteritis that the doctors at long last have decided that I don't have. They started me out on 60 mm and now they are taking me off at 1mm every other week. I am down to 11mm now. I have experienced all the side effects except the acne and problems with periods. I gained 40 pounds and have such bad pains in my lower back that I can't stay on my feet for long. And I'm always hungry though I try to control it. My main withdrawal symptom is extreme itching from my neck to my wrists and thighs. especially where there is any pressure on the body such as waist bands etc. I tried to get off it once but it was at a faster rate and that is when the itching started. I will gladly put up with the itching as long as I can get off this "Satans curse" of a medicine. I also have jerking in my hands and a general feeling of shakiness. I was glad to read that someone else had painful sensitive teeth I didn't know it was connected to the pred. I too wonder if I will be able to lose all this weight after I'm off the pred. I do know that the moon face goes away because it did the one time I came off the pred then had to get back on it. I also have weakness in my thighs and arms. and my arms are always getting big ugly bruises or torn skin on them to the point that I have to wear long sleeves in hot weather.feel free to email me with your story. Especially if you are off of it so I can have some idea what might happen to me

I experience insomnia, fatigue, snoring due to increased neck fat, moon face, painful abdominal bloating, 10 lb weight gain, increasing blurred vision, purple rash on stomach, thin skin and easy brusing,hair loss, facial hair growth, night and day sweating. I started to decrease prednisone 2 1/2 mgs. per week alternate days in early December. Everything was going well and I could see slow improvement in my condition until mid February. Since then I have had more weakness in my hands, arms legs, and increased blurred vision. Since I may have to be on a low? dose of prednisone for a long time I have some questions.
1. How low a dose is necessary for side effects to diminish?
2. Does all your hair fall out to necessitate a wig? When does it start to grow back.
3. Does the weight go back to normal without dieting? Does your shape go back to pre prednisone?
4. Will the weakness, control, and pre prednisone vision come back to allow normal functioning?

Weight Gain especially in abdomen, neck and shoulders

Thin skin with reddy purple bruises

Difficulty sleeping

Muscular weakness

Excellent control of Asthma symptoms