Posted on my blog at http://www.oberata.com on 1/11/10
More Friction Writing by me, courtesy of Lupus. Enjoy more laughs at my expense, you lushes!
With all due respect to John Fogerty, the Old Man isnít Down The Road. Heís actually right here, roasting weenies in my living room.
No. Thatís way too cute. Indulge me a writerís do-over, because I hate this son-of-a-bitch.
Itís more like Terminator 2 Ė remember? Ė when that slick, non-Arnold,
My migraines seem to be getting more intense and more frequent, I don't know how much more I can take? They have been absolutely dibilitating! I was once again a patron of the ER last night. The Dr. of which I know pretty well is a very caring and understanding person. Blessing I know!!! I told him I felt like I could see, hear and feel my pulse all over my body. I told him to put his hands on my fore head and feel my pulse, he did and he felt it. He said that the blood vesels were dialated which
Originally Posted by wrightrs
Over Christmas I developed a rash on my chest and stomach. It burned like fire. So I called my rheumy. I started calling at 8:30, because that is when they open. There was no answer for 2 hrs. When I finally got though I had to leave a message. When they finely called back they told me to call my PCP. I didn't like it at all. So I call my PCP. They told me to call my rheumy. I told them I already did. They told me if it's a lupus rash I need to see the rheumy. So I called back and told them what
I went to the rhuematologist today and i have been on methotrexate for 12 weeks now and because of the pain i am still having in my joints he increased the dosage and the pharmacy called and said that if i do not have cancer it is no longer covered they all ready turned me down for cell ceph so what do you do. Bonita