Maintenance dose symptoms and conditions

Prednisone has messed up my head. I had Bells Palsy (which is paralysis of one half of the face) and can be very scary. I have had some depression before but this stuff made me fall off the face of the earth. I went from someone in control and quite happy to the absolute pits. The depression was quite severe and sudden and I had no ability to stop the downward spiral. It has played havoc with my life. In its defense, it cleared the Bell's Palsy up very quickly but the grief it has caused me through my altered mind state wasn't worth it. Insomnia (eg - no sleep for 6 nights straight) was a trigger and then the mood swings took over and then bang....full blown depression and an inability to focus, work properly or function. I am now on the road to recovery but it has been a pretty turbulent 2 months. Be very careful with this drug....very, very careful.

I have been taking Lamictal for just three weeks. The most troublesome side effect for me has been nasal congestion and the inability to smell or taste anything. Has anyone experienced this and found relief after reaching the maintenance dose after the starter pack?
Is there anyone who has found relief from this in any way? I'm not sure I can tolerate not being able to breathe and am hoping that it goes away soon.

My 30+ year run with Prednisone
My experience began back in the 1980s when I took 2 aspirin for a headache one day and landed in the hospital with difficulty breathing. I was diagnosed with Chronic Asthma Triad (Aspirin Sensitivity, Sinus Polyps, and Asthma). My doctors (Allergist & ENT) prescribed Prednisone to help with the asthma and control sinus swelling in does ranging from low 15mg up to 80mg per day with weening off periods lasting weeks to months. Over the next 9 years I underwent 12 sinus surgeries ultimately obliterating all of my sinus cavities. Chronic asthma continues today and I have now developed additional lung disease I was followed at UCSC Medical Center in San Francisco after being diagnosed with Bronchiolitis Oblitersans, at which time I was fully disabled, unable to work at all for almost 2 years. This was the most difficult period in my life.
Over the years dealing with chronic sinus disease and controlling my lung and airway diseases I have made many trips to the ER and experienced many hospitalizations. I have not been off of Prednisone since this all began. With so many doses of steroids both by IV and by mouth with tapers in doses ranging from 120md daily (by mouth) to a low maintenance dose of 5mg per day. Believe me when I say that I know the side effects of this dug all to well. Initially I experienced bloating in the face and body, a rash that still remains today. I have developed significant bone density loss and now experience joint pain full time. From a mental side effects stand point I am in a state of fluctuating brain fog, memory loss, and confusion. At times I get baffled easily. I continue to experience mild to severe mood swings.
I am currently working full time with great difficulty and at this time taking 40mg of Prednisone daily to control my difficulty breathing and severe shortness of breath.
Of all the side effects it is my memory loss that has been the biggest impact on my ability to work and communicate clearly, I am having difficulties performing at work and at home. I had no idea this medication could have such an impact on daily living.
The bottom line? Prednisone truly is a two edged sword, on one hand a wonder drug and on the other a destroyer of mind and body.

Hi! I am a 36 year old female and have been on this HORRIBLE HORRIBLE drug (prednisone) for 2 1/2 years now..... Hopkins doctors still arent sure exactly what i have. My immune system is attacking my liver so to speak. My body is basically looking at my liver like it doesnt belong and is attacking it with large multiple lesions that is eating it away... the good thing is that it hasnt interupted the functioning of it yet but is leaving horrible scar tissue. I have been in and out of the hospital 13 times, have had just about every test imangable, 12 liver biopsies and they STILL have NO clue! They are leaning towards Church Straus desease and Wegners but the weird thing is i have half symptoms of both. The first year they had me on 80 mgs of prednisone a day which had seemed to put me in remission for about 4 months and then they came back even worse so i was put back on the prednisone, 80 mgs a day AGAIN along with 100 cc's of Methotrexate, another not so nice drug... i had EVERY SINGLE BAD SIDE EFFECT OF BOTH DRUGS!! This second time around was ALOT WORSE for some reason!!! My body DID NOT LIKE IT!! Nausea, hair loss, moon face, gained 40 pounds (and i was in great shape, worked out, i am 5'4 and was 110 pds!), EVERYTHING was swollen, legs, ankles, arms, neck, face, had the camel hump, fingers and especially my belly!!! UGH!!! Have bone, muscle, and SEVERE joint pain! Kaliedescope vision, dry eyes and then had mucus discharge (kindof like pinkeye), headaches, intestinal problems.... VERY CONSTIPATED and then the opposite!!! I literally felt as if i had turned into a man in my behind!!! Sorry to be so gross but thats how bad it was!!! Jaw problems, teeth and gums as well, skin sensitivity and have little bumps all over my skin (kindof like tiny little moles), itchy, broke out with acne and pretty much NEVER had more than 1 pimple a month, had facial hair (VERY DISGUSTING!!!! HAD IT WAXED EVERY WEEK!!!!) and then on top of all of that the swelling of my liver not to mention the PAIN! I was recently in the hospital again with 12 new lesions, pneumonia, and 104 fever. My doctors said the Methotrexate was the cause and i was having a bad reaction to it so they now have me on 100mgs per day of Azathiroprine. I am now finally down to a maintenance dose of 5 mgs of prednisone cause my body was starting to reject that as well. I thank god that i am now down to that dose!!!! It as only been 2 wks and the withdrawl symptoms are horrible worse then they were but i know what is to come =) loosing all this fluid and all of the HORRIBLE side effects i listed above. I will have to be on the maintenance dose of 5mgs the rest of my life and can live with that cause when my body gets back to somewhat normal i wont even notice that im on this CRAP!! I will be on the high dose of Azathiroprine for a few years and then on a maintenance dose of that as well for the rest of my life to keep whatever this is that i have under control.... the scary thing is is that they arent even sure that all of these meds will even work...... im a guinea pig..... The only thing that i am on out of all 25 pills/meds that i take everyday that works is my pain meds. Oh and i also forgot to mention that i had to be put on some "HEAD CASE" medication (thats what i call it =) ) for depression. Its a low dose but it does seem to help... I am terrified of what the future holds but continue to be strong and have an amazing support team... my fiance and family =) I dont even want to think about how i would be without them. I go back on the 25th of this month for my MRI so please who ever reads this keep me in your prayers as for all of you are in mine. I feel for each and everyone of you that has to endure this horrible drug everyday and i hope that everything works out you. =)

Sue =)