Just a "zebra" trying my best to live life to the fullest with EDS and POTS...and loving the ride.

Posts Tagged ‘Benefit Concert 2015’

Five For Friday 12/12/14

Written by Katie. Posted in Five For Friday

Life has been going at a crazy pace, but I guess, better late than never…

1. Medical Stuff:

  • 1 Day of PT. I have been having increasing headaches, which I suspect is from some neck instability. My PT did a lot of cranial work, which is an incredible help with decreasing the amount and severity of headaches. It may be time for more prolotherapy.
  • 2 Days of Home Rehab.
  • I saw Larry on Friday. The focus of our appointment was my ribs…I had about 5 out so he put them back in place, and also helped me figure out how to schedule the echo that Dr. Grubb ordered for me. It’s that time again. I was told every 2-3 years, an EDS’r needs their heart checked; mainly for mitral valve prolapse.

Five For Friday 11/21/14

Written by Katie. Posted in Five For Friday

1. Medical Stuff:

  • I had a better week. Especially with sleep, and therefore keeping symptoms at bay. Hoping this continues, and feeling grateful for better days.
  • 2 Days of Home Rehab.
  • I saw Larry on Tuesday. He put my ribs back into place and did cranial OMM on me.
  • I saw Dr. Rosen (shrink) after Larry on Tuesday. We discussed my recent med adjustments, and the best ways to cope through this flare. We came up a with a log I will be keeping for now, with information about each day (flares, no flares, where I am at in my cycle, medication info, how I feel, any differences to note, etc…)
  • I spent a lonnnnnggggg, but very worthwhile day in Toledo on Thursday seeing Dr. Grubb for POTS. I will try and blog about my appointment later.

Five For Friday 10/31/14

Written by Katie. Posted in Five For Friday

1. Medical Stuff:

  • I had to cancel PT on Monday. I felt sick after school, and was worried about driving.
  • 2 Days of Home Rehab.
  • I saw my shrink on Tuesday. It was a needed appointment to talk meds, and figure out how to cope with this latest flare. Love him.
  • I still had a week of struggling with POTS, and therefore sleep. I started a new med, and am really, really, REALLY looking forward to feeling like my body is somewhat cooperating with me again.