Physical Therapy

So since I've been diagnosed with SPS I've been in and out of physical therapy. First I was at a hospital's outpatient center. When I started it was crazy! I was pushed to to the limits. The pt and ot there at first made me cry because they wanted me to do better. So I did... I tried and tried my best, but my legs where just not responding not knowing I had what I did. Any ways I was there for a year or more which the end result ended with me walking, but it wasn't walking walking I looked like I was drunk sometimes. Whatever they got me walking right!

Finally after being diagnosed my neuro wanted me to go back, so I did to the same place but only for a while. Six months at the most I went before my doctor told me to take a break. I was fine not going because it was painful, although I had fun! The pt Chris would just make things fun while my ot would come up with the funniest thing sometimes.

Now after this last episode I've been place at a different physical therapy center. The physical therapist there is understand a bit more I'm guessing more because now they know what it is that I have and she actually looked in to it. Not just jumped in to figure our why it was that I wasn't walking. I enjoy it and hope I keep progressing because since I've been here in January I've started walking semi normal which is a big deal for me at least lol. Oh not to mention they helped me get a cool wheelchair where I can actually push myself not like the old lump of 50 pounds. lol.

Comments

Weekly check up

So was made it to my physical therapy this morning knowing that right afterwards I had my check up with nurse practitioner, but when I got there they decided it would be best to see her before that way she could see how the new medication was affecting me if it was. Either way we went she decided to start me back on tizanadine every 2 hours, occupational therapy, aquatic therapy, and message therapy. HA there is only so much that can be done in three day I guess we are going to have to find a way to stay either longer or figure out a way to make it all the things I've got to do. Now I've got to see her every week for a check up until my doctor appointment with my neuro. YAY! Well not really if you didn't catch my sarcasm... I've got this crazy idea that maybe I need a break. I need to spend a lot of time on my homework and studies, and staying in San Antonio doing all these things keeps me away from all of it. I constantly have to explain to my teachers why my assignmen...

Stiff Person Syndrome T-shirts

I'm Hi guys here is where you can place your Stiff Person Syndrome T-shirt order. Thank you for helping raise awareness that way we can be SEEN and HEARD about this RARE disease. It might just be the push to get help we need to get doctors understand it better, and maybe start doing more research for all of us! Each T-shirt is $20.00 I'm using the flat rate boxes to make is easier to sort out and fast to get them out to those who order. So for 1 T-shirt it's $5.80 extra for shipping, because only one of them fits. Anything more then 1 T-shirt is $12.35 and with here you order as many T-shirts as you like. These prices are only for the U.S. people placing orders anyone who want one from another country can email my person account at vanessa.rmz.88@gmail.com If a mistake is made in the order please return the T-shirt and I'll give you a full refund on your shipping and send you the right T-shirt. Also read about make whatever kind of donation...

Stiff Person Syndrome Awareness!

My friends with SPS raising AWARENESS! MY friends without SPS raising awareness! And Me...

The Good the Bad of my Life With Stiff Person Syndrome

Search This Blog