bluesea
New member
- Joined
- Sep 1, 2012
- Messages
- 7
- Reason
- Learn about ALS
- Country
- US
- State
- CA
- City
- Los Angeles
Hey guys,
PLS has been on my radar for a while. it's the ONLY condition that corresponds with many of my symptoms. i'm 4 years in. 100 tests (a conservative guess), dozens of doctors and several misdiagnoses. For the past many months, i've put finding a diagnoses on hold. began to matter less what it was called and i needed to focus exclusively on pain treatment. even though i was being treated for pain, my pain was not by a very long shot being managed. i spent a good deal of the last 3 years laying on my back incapacitated by pain. i'm with a different PM doc now outside my HMO and seeing some promising results (knock wood).
i look forward to being part of this forum.
PLS has been on my radar for a while. it's the ONLY condition that corresponds with many of my symptoms. i'm 4 years in. 100 tests (a conservative guess), dozens of doctors and several misdiagnoses. For the past many months, i've put finding a diagnoses on hold. began to matter less what it was called and i needed to focus exclusively on pain treatment. even though i was being treated for pain, my pain was not by a very long shot being managed. i spent a good deal of the last 3 years laying on my back incapacitated by pain. i'm with a different PM doc now outside my HMO and seeing some promising results (knock wood).
i look forward to being part of this forum.