Guest guest Posted February 3, 2011 Report Share Posted February 3, 2011 Heya guys... It has been a rough 6 months.. first with the full blown worst flares that I've had in over 15 years started off my summer.. I had 2 more in the fall.. RD suspected Enbrel wasn't doing it's job so we finally got switched to Humira and within just a few days after my first dose my blood pressure went sky high. I think I told yall about all this. I was sick all during Christmas and New Years. I took 2 doses of Humira and my blood pressure continued to stay high.. as in 190/145.. Had to go to the ER 3 times ordered by my family doc for CT scans since I was having bad headaches with it and blurry vision. Fortunately the CT scans were always normal. Now that the humira is completely out of my system my BP is back to my normal range which is usually around 105/70. So I'm back on Enbrel. We are hoping that I just had a bad batch back in the summer. Took my first shot last week so far my joints are doing good. Im still on prednisone but I'm down to 7.5 mg per day... Will go to 5mg next week then hopefully to 2.5 two weeks after that then hopefully be off of it. I'm totally bummed that they took Darvocet off the market. It always seemed to work well for mild to moderate pain for me, with less potential for addiction than hydrocodone which is what I'm taking now. But during my flares I was having to take oxycodone then demerol. And 60mg of pred for a week. I went about 3 weeks with no pred but flared again so we did 60 again and cut it slowly. I have a hard time with prednisone... It really, really makes me , well irritable is not even the word, more like fly into a rage at the drop of a hate... And my anxiety went from a 1 to 100 ! My family doc put me on xanax.. it takes the edge off but I still feel some anxiety but I'm getting better. My face is so round.. I haven't gained any weight though. I was too sick to have an appetite so that's sorta good in a way because I need to lose about 50 lbs that I've gained over the past 2 years. I'm having one of my insomnia nights again and of course pred sure doesn't help that. I usually take ambien most of the time t works but sometimes it doesn't work at all. Xanax doesn't make me sleepy at all either. Just like most narcotics .. they actually keep me awake.. So that's my update in a nutshell.. Can't believe I will be 40 years old in a week. Was thinking today that more than half of my life I have has Stlll's. Had it for 22 years this fall. Wow where has the time gone. Seeing my orthopedic surgeon for my 2 year check up for my last hip replacement. I think everything is going okay with it. I'm just paranoid a bit that I'm gonna catch staph again from someone so I tend to avoid most people and stay home alot. I've been dating someone for a couple of months. He's a nice guy but I've got to get over my issues with intimacy. I have a difficult time with that cause all I can think about is germs on your skin, ever since the infectious disease doctor told me most people are carrying staph but those with good immune systems have no problems , but for us on the biologics it becomes a problem even simple hugging if I have a cut or something, which for some reason I seem to always have some little scratch and Im running to wash it and then put polysporin on it. My Boyfriend doesn't really understand but I said look 'I've had MRSA twice in my hips and it was pure hell both times. And the scary things was I was fine one day and the next day the area around my scar ( I was 2 months post op) began to hurt and by that evening I had a pone the size of a tennis ball and I was in surgery the next morning. Sometimes I wonder if I suffer from PTSD from all these surgeries since each one always had bad complications and sometimes the pain was excruciating post-op , especially the last. I've been thinking about seeing a counselor to try to help me deal with my phobia I've developed about staph and other germs and having another surgery cause I know in a few years I will need another revision , my first thr, the stem part has been in since 93 so that's almost 18 years and it's the not the metal type so the life expectancy for it was 15-25 years... And for many years when I was in remission I was very active with it and they say they wear out a bit quicker the more impact you put them through... Well... that's something I read years ago....so who knows that may have changed... I don't research like I used too. I'll try to post more often now that Im feeling a bit better. Love you guys! If anyone ever needs me for anything for just want to ask a question feel free to email me personally anytime for facebook me.. Jen Quote Link to comment Share on other sites More sharing options...
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