Pulmanologist symptoms and conditions

Ok here's my story with Prednisone. Let me first give you a little back ground info on me. Born with a VSD, that was repaired at 8 months of age, only after developing severe pneumonia. Was fine as a child growing up until at 18 i developed asthma. i am 29 now and have been on and off prednisone during that time. During that time however I have always been on a metered dosage pack that has always tapered usually within 5 days with no side effects.

Now lets talk present day with me. First off I went in back in early Sept. for what I thought was just a sinus infection, turns out my lungs were so tight, i was immediately put on 80 mg for 5 days straight, and you guessed it no tapering. Those 5 days were the worst five days of my life. I have SVT- taychcardia and the med made it worst, I was running around like I was on Speed or something. Also, I had started to urinate like crazy. Headaches, nausea, muscle pain as well as joint pain. i can not walk without feeling as though my knees, and ankles are going to break. Also, i am not as foccused as I usually am. Ever since that faithfully day in September I have been on this stuff. it has already been 2 months and im on 40mg now. And I cannot sleep at all at night and during the day now i crash once it seems like the prednisone starts wearing off. its horrible. I am going to go see the Pulmanologist Monday hopefully he will have some answers, and Im dreading him telling me i may have COPD, from a protien defiency(sorry for spelling, this med is messing with my thought process). Any who, i cant just stop taking it, i have been warned about that. something has to give or my body may give up.

hope this helps.

this med is good if used correctly but i agree Doctors need to fully warn patients before hand of all possible side effects.

My 5 1/2 year old son began taking 4mg Singulair in the p.m. and an inhaler (asmanex) in the a.m. We were still having trouble controlling the asthma and his Sing dose was raised to 5mg. & within 1 week of the increase he began having terrible facial tics and aggravated behavior (defiant, poor listening, easily frustrated and angered) The tics were in the form of opening and closing his mouth, as if you were trying to clear your clogged ears after a plane flight. This caused him much pain in his jaws and facial muscles, so he would tic and then cry as he was in pain. This ramped up his anxiety and it made the ticking worse. He has been off of all asthma medication (cold turkey) for 5 full days. He has episodes where the tics happen for 10 min -1/2 hr, other times during the day it is one here and one there. He does not want to leave the house to do anything, even his favorite activities. Thank god I found this site (and others like it), as I got some answers and some hope. We went to see my cousin this week who is a neurologist and he never heard of the correlation of Singulair and neurologic side effects like these. He said that (hopefully) the medication side effects will cycle through and resolve the ticking and behavioral changes. If not we are probably looking at a Tic Disorder which is in the Tourettes Family.He put my son on a very low dose of Klonopin to mellow out his anxiety and help reduce the tics, but has only been on it for 1 1/2 days and it usually takes a wk or 2 for full absorption and results.I have since sent him and my pediatrician and allergist links to this site and others. I think that I see some improvement in my son, yesterday I thought he did better and my husband thought it was a worse day, I think we have totally lost our perspective and objectivity on this. If anyone out there has a time frame on when they saw significant recovery and positive changes I would love to hear from you. This is a total nightmare and if it is this drug, someone is going to pay. My prayers go out to all who are going thru this.

I was just placed on Cellecept last week- 500 Mg 4 times a day-
for my autoimmune muscular myopathy- I was a body builder 6 months ago- now I can barely make it across the Target parking lot.
I am sure the myopathy is Statin induced as I was on Lipitor-)rather than Prednisone as my doctor said less side effects.
He said I should see improvement in about 6 weeks- is any body taking Cellcept for autoimmune disease?
Thank you.
PS; So far- side effects seem to be weakness- more shakiness-