Christine
DIS Legend
- Joined
- Aug 31, 1999
- Messages
- 32,552
Hi everyone!
I was diagnosed last year with posterior tibial tendonitis (really tenosynovitis) last year. Nothing has helped it. Boot, PT, massage, etc. I also have plantar fasciitis with it. But the PTT is the worst and has progessed to a flat foot deformity. I have moderate pain every night and walk like a cripple for 20 minutes every morning until it loosens up. I have not had a day without this pain since November 2018.
Last week, my doctor (podiatrist) and I decided to put me back in the boot and go as "non weight bearing" as possible in a last ditch effort to help this. He also prescribed a short course of prednisone, starting at a high dose for 3 days and the taper. Being as sensitive as I am, I couldn't take the high dose but started at half that amount. I'm on Day 4.
The good news: Overnight, my PTT pain was reduced by about 95%.
Bad news: I'm experiencing side effects as expected. Insomnia (haven't slept really at all for 3 nights). Jittery sometimes. It has flared up my rosacea (which the literature says it can do) so I'm flushing easily and my cheeks feel a little "burny." But the weird one is that my hands, mainly my fingers, itch like they are super dry. But their appearance is totally normal. They don't look any more dry than normal (and they are dry) but they feel it and they itch. It's really starting to drive me nuts.
Anyone had this?
Oh, and my doctor is on vacation this week. He is a one man office and doesn't even have a nurse. It's not a big deal, I can quit slowly without needing to talk to him but was wondering if anyone has had this and what course it took (stayed the same, got worse, etc).
I was diagnosed last year with posterior tibial tendonitis (really tenosynovitis) last year. Nothing has helped it. Boot, PT, massage, etc. I also have plantar fasciitis with it. But the PTT is the worst and has progessed to a flat foot deformity. I have moderate pain every night and walk like a cripple for 20 minutes every morning until it loosens up. I have not had a day without this pain since November 2018.
Last week, my doctor (podiatrist) and I decided to put me back in the boot and go as "non weight bearing" as possible in a last ditch effort to help this. He also prescribed a short course of prednisone, starting at a high dose for 3 days and the taper. Being as sensitive as I am, I couldn't take the high dose but started at half that amount. I'm on Day 4.
The good news: Overnight, my PTT pain was reduced by about 95%.
Bad news: I'm experiencing side effects as expected. Insomnia (haven't slept really at all for 3 nights). Jittery sometimes. It has flared up my rosacea (which the literature says it can do) so I'm flushing easily and my cheeks feel a little "burny." But the weird one is that my hands, mainly my fingers, itch like they are super dry. But their appearance is totally normal. They don't look any more dry than normal (and they are dry) but they feel it and they itch. It's really starting to drive me nuts.
Anyone had this?
Oh, and my doctor is on vacation this week. He is a one man office and doesn't even have a nurse. It's not a big deal, I can quit slowly without needing to talk to him but was wondering if anyone has had this and what course it took (stayed the same, got worse, etc).