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IV therapy

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Hello everyone, my name is

I'm a newbie to this list and have decided to jump in and get my feet

wet.

I was diagnosed with Reiters Syndrome about 5 years ago and have been on

the AP for almost 4 years now.

Initially I went through the usual treatments, Prednizone,

Sulphasalazine, Methotrexate, Plaquinil, Sandimue, and a host of others,

with little success.

Once I was introduced to the AP, I improved dramatically. My arthritis

retreated from my jaw, neck, back, hips, knees, and made a last stand in

my feet, where it has remained, entrenched for about 2.5 years.

I moved to Vancouver about 2 years ago and was unable to continue with

my periodic IV treatments. The new Dr.s here did not believe that the IV

Clindamyacin therapy was necessary to the treatment. After insistng,

they agreed to prescribe oral Clindamyacin as a substitute.

I'm currently on Doxycycline (200 mg/day) and Indomethacin (100 mg/day)

as well as Misoprostol (400mg/day). Every three months I would shock my

system with 1800 mg of Clindamyacin per day for 5 days.

I have noticed over the past 8 to 12 months that my arthritis has slowly

been seeking out its old haunts in my body and has discovered a few new

places to infest.

I am pushing to re-instate the IV therapy hoping that it will subdue

this new arthritis attack.

Does anyone know of any studies or articles that validate the IV

treatment for Reactive arthritis?

Any comments, opinions, or suggestions are welcome.

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