My leg has ached for days. The only thing that I was doing that was any help was using a heating pad and taking Panadeine. The heating pad was more help because the Panadeine was making me more sleepy than anything. Sure, it is taking the edge off, but I am currently loopy from taking Panadeine earlier. It is like operating in a fog.
I saw my GP on Friday morning. Brendan came with me. He had strict instructions to make sure I stayed on topic of my leg hurting. I was in a Panadeine fog for the appointment too. So I gave my wonderful and patient GP a rambling, somewhat confusing account of my leg hurting. Then I told him I wanted some pain relief, and asked, "So, you got any questions?"
He did have questions. Did I remember injuring it? No. What kind of pain was it? That one is a bit more difficult to answer. It aches constantly like a toothache, and the joints ache like arthritis pain. He asked some other things, but I forget what they were. There was questions about it being connected to the MF. He also commented that I probably knew more about my condition than he did. That is somewhat true. I have been doing a lot of research.
He did a physical examination of my legs, and he was impressed with my flexibility. I was proud of that; all those Dana-modified yoga stretches are still doing their job. He seemed to accept that an injury had not occurred.
Then we began talking about MF and how this was probably a symptom of it. That is what I suspected from the beginning. We discusses compression stockings. (They are really expensive. Around $120 seems to be the going price.) He didn't seem to think the expense was worth it at this point, and he suggested I get something he called "Tubigrip". He also gave me a prescription for Ibuprofen 400mg to take 3 times a day. I also got a sleeping pill prescription because the pain is messing with my nighttime sleeping. He also told me to keep doing what I was doing: heating pad, resting my leg and Panadeine for breakthrough pain. He wants me to talk to my dermatologist to make sure the pain isn't a side effect of the narrow band UVB treatments.
Off to the pharmacy and I put in my scripts. When I asked about the Tubigrip, the assistant had no idea what it was either. After a brief description (that I stole from the doctor), she showed me a similar product. I am modeling the beauty of the thing in the previous post.
So far, the regime seems to be working. I am in less pain that I have been in days. I hope the pain is only a short term annoyance, and it will go away soon.
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