Docto symptoms and conditions

I have been getting the cortisone shots on and off for about a year now, basically, whenever my ankle flares up. I had one earlier today (or yesterday as it may be), and now here I am at 2:45 am, deathly tired, but with my mind so active I cannot sleep. I noticed the same thing after an injection a couple of weeks ago. I can't believe I never noticed it before. I have always had the woozy/loopy feeling afterward, afraid to drive home, but thankful I live less than a mile from the doctor's office. This is usually followed by a day of nausea and other side effects. It's weird, though. The websites with info on this drug don't talk about the nausea, the dizziness, the "feeling out of it", the headaches. Only that the pain is worse before it is better (definitely true!). But do the docs not know about this or are they just turning a blind eye? I keep reading that such side effects aren't possible because cortisone occurs naturally in the body. But the stuff they are injecting us with is not produced by ur bodies. It is synthetic, and being that we are not producing the dose naturally, it is very likely overload. So, how can there not be side effects?

Had injection 2 pm today immediately had head spins like I was off my face (I am a 45 yo mum so no drugs here) heart racing very dizzy and hearing was distorted. Told doctor he was not concerned. I have had injections before and have experienced the burning skin sensation rashes and tummy aches and cramps. I try to hold off for months on getting another but the pain in my shoulder is so bad I have to eventually. ATM my shoulder pain has intensified 10 fold although eventually I will be pain free in a week or so this should last up to 3 months. I will be able to sleep better which I desperately need as I shift work and have a young family.

I am in month 4 of a 4 month Lupron shot that my doctor gave to prepare for surgery. I was told I might get hot flashes, loss of libido, increased urinary symptoms for a few weeks. No one said anything and there was absolutely nothing in all the drug leaflets they gave me that would have prepared me for the the horror story that my life was about to become. As if having cancer was not bad enough.Since day 2 I have suffered so many bad side effects that I have lost count. The worst is insomnia and nothing has helped including high doses of Ambien. They suggested Lunesta but my health insurance company balked and even if they had said yes, my co-payment would be unaffordable. This stuff is more expensive than gold. I am exhausted all the time. I have terrible memory problems that are so bad that I can be talking to some I know really well and not remember their name. I am unable to concentrate on anything, my mood swings are unbelievable, I feel mentally disoriented and dissociated all the time, high blood pressure, racing pulse, high blood sugar, hot flashes, raging night sweats, dizziness, bad balance. The side effects that I can handle include nausea, headaches, diarrhea, joint and muscle pain. I am supposed to be on Lupron for 2 years. The only difference I see with my Lupron experience and others here is that my gender is MALE and I have early stage prostate cancer. Being male, my other serious Lupron side effect is complete impotence which is going to go on for a long while due to the radiation. I had radioactive seed implants into my prostate gland done a week ago and I have to follow this with 5 weeks of beam radiation. Lupron seems to be an equal opportunity drug. Lupron has messed me up so badly that for the past 5 weeks I have been off work on disability status with no chance of going back for at least a month and my Dr thinks that may be optimistic. No one seems to know how long it will take to get back to some kind of normal. I just could not function at work and ended up in my doctors office having a complete emotional meltdown. I would caution anyone, male or female, to consider Lupron very carefully before having it.