Walking Post-DBS: Still Working On It
You can see from the video that I still have to work on my walking.
Walking Post-DBS: Still Working On It Read More »
You can see from the video that I still have to work on my walking.
Walking Post-DBS: Still Working On It Read More »
There’s a new addition to my drugs list, but the game for you is to figure out what’s missing. (See answer below.)
New Medication List + Quiz Read More »
Soon after I got Deep Brain Stimulation, my walking ability was terrific. But over the months since then, it’s gotten worse. You can see the before and after
Something’s Wrong with My Walking Read More »
******** The above image says it all. Before I had Deep Brain Stimulation (DBS), every day I was taking 10.5 pills of carbidopa-levodopa (Sinemet) – the main drug to
How Am I Doing? 6th Update Read More »
******** That iPod-like thing you see in this picture is actually the gismo my husband uses to modify (usually that means “increase”) the electrical current that my Deep Brain Stimulator
How Am I Doing? 5th Update Read More »
My husband and I started taking daily walks. Each day we walk longer and longer distances.
How Am I Doing? 4th Update Read More »
********** I can smell again! Like most Parkies, I lost the ability to smell anything soon after I was diagnosed. But my olfactory powers returned last night, and are still
How Am I Doing? 3rd Update Read More »
********** Almost two weeks have passed since the doctors at Mount Sinai turned on the batteries for my Deep Brain Stimulation setup. How am I doing? Check it out: I
How Am I Doing? 2nd Update Read More »
It’s been five days since the medical staff at Mount Sinai turned on the current in my DBS system. In general, the time since then has been OK. For the
I’m about to undergo three procedures to surgically install Deep Brain Stimulation (DBS) wires in my head and a battery pack in my chest.
Heads Up! It’s Time for Deep Brain Surgery! Read More »