| FAQ/Help |
| Calendar |
| Search |
| Today's Posts |
04-24-2012, 12:18 AM
|
#1 | ||
|
|||
|
Member
|
How did you all figure out what kind of PN you actually have? Was it hard to find out?
Also, do you think l would have a better diagnosis of my PN if l visited a special PN clinic in the US? So far here l am having blood test, urine test and not sure at this stage if l should have a cat scan of my chest and other parts of the body, not sure hwy yet. Did any of you need x-ray or cat scan? The neurologist said they are very bad for our health and should be avoided. Sue |
||
|
 Reply With Quote
|
| Thread Tools | |
| Display Modes | |
|
|
Similar Threads
|
||||
| Thread | Forum | |||
| What Type of TOS Do I Have? | Thoracic Outlet Syndrome | |||
| What type of doctors to see to confirm diagnosis in New Jersey? | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
| Diagnosis Parkinson's Disease: You Are Not Alone Video Diagnosis Parkinson's Diseas | Parkinson's Disease | |||
| Not convinced of my diagnosis of CRPS Type II | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
| Fibromyalgia Syndrome: Presentation, Diagnosis, and Differential Diagnosis | Fibromyalgia and Chronic Fatigue | |||
Diagnosis of the type of PN?
Threaded Mode