| FAQ/Help |
| Calendar |
| Search |
| Today's Posts |
02-26-2010, 10:43 PM
|
#1 | |||
|
||||
|
Magnate
|
looking for any info on peoples experiences there, if they went there and that is where diagnosed with MS or any other dx?? If they thought worth it.... info on best way after getting referred there to make sure they plan to check me out totally!!
just any advice, experiences to share etc would be sooo appreciated. For any that do not know me, I am undx... have had MS like sxs starting back 10 yrs ago.... numbness/tingling pain, eventually bad enough went on neurontin, balance issues, weakness in right side, right eye blurriness... had many testing done around my small town area... just thinking I need a real place to overall check me out...tired of limbo... and just feeling like terrible... hugsss and thanks, sarah
__________________
. KEEP SMILING, LIFE IS TOO SHORT TO WEAR A FROWN!! . |
|||
|
 Reply With Quote
|
|
|
Similar Threads
|
||||
| Thread | Forum | |||
| Mayo clinic, here I come! | Myasthenia Gravis | |||
| Mayo Clinic | Parkinson's Disease | |||
| Mayo Clinic experience | Peripheral Neuropathy | |||
| Mayo Clinic | Traumatic Brain Injury and Post Concussion Syndrome | |||
| Mayo Clinic | Parkinson's Disease | |||
anyone experience Mayo clinic in Rochester,MN
Threaded Mode