I am an Undergraduate Student who has Reflex Sympathetic Dystrophy and embraces the Vegan lifestyle. Reflex Sympathetic Dystrophy is a Chronic Neurological Condition that I hope and pray there will be a cure to one day. Until then I live my life to the fullest, embrassing the life the Good Lord has given me.

Showing posts with label Rechargable. Show all posts
Showing posts with label Rechargable. Show all posts

Saturday, August 28, 2010

Surgery Update

Wednesday was my Spinal Cord Stimulator Battery Revison. I was schedueled to go in around 3 in the afternoon. I had recieved a call from my Dr's office letting me know that I was able to come in earlier since the person who was suppose to have surgery before me cancelled or their surgery was cancelled. This of course excited me since I had to fast starting midnight the night before and I was hungrey and thristy since I wasnt aloud to drink anything either except tiny sips for pills.

Everything with the surgery went well. It was around 7 or so that evening that I got released. My side was hurting but it was still a bit numb from the numbing shots I was given. The day after the surgery when the shots really wore off I was hurting. I was hurting because of the post-op pain, my battery is working wonderfully. My boyfriend came over that night which helped alot. Im not one to lay in bed day in and day out so when Im forced to due to surgery pain I get bored fast. Im not a fan of movies since I know I can be doing something else and more productive. I made a stake of movies next to my bed and well, they havent been watched. J and I finally figured out how to use the Movies on Demand feature and watched a movie the first night he came over. He came over again yesterday and since I was still hurting a good bit we hung out around the house. I did end up venturing out to get a bite to eat which made my day.

Like I mentioned a bit earlier in this post my new battery is working amazingly well. I am so happy I got the re-chargable battery vs the 3-5 yr battery. Now that I have this new battery I can tell that mine was dying and Im not scared to turn it up to get the relief I need. I have noticed that I have recovered faster from this surgery than anyother one including the revision I have done last summer. I think its because of being Vegan and eating more health oriented type of foods. I have been making sure to get more protein during this time since Im healing from surgery.

Monday, August 23, 2010

Pre-Op Tests and Rechargable SCS Battery

Hello All!

I hope you are all liking the new design of my blog. I was creative one night and instead of pulling out all of my scrapbook supplies I came on here and did a new blog design.

I had my Pre-Operative tests done today and surgery is a go on Wednesday. It is not scheduled till around 3:15 in the afternoon so I know that I am going to be pretty hungry by the time they knock me out. I always tend to believe that the fasting and IV are the worst parts of procedures. My body just cant go without food that long and getting an IV well that's another story.

I am excited though that I will be getting the rechargeable Spinal Cord Stimulator Battery so that I wont have to be going through this for at least 10 yrs or so (last how long the battery is suppose to last). I will have to charge it at least once a month or more depending on how much voltage I use but that is worth it to me not to be having to go through this every few years. The battery I have in now was suppose to last 3-5 years and Ive had it less than 3. It will be officially 3 years in December but my Dr and nurses are surprised how quick it went.

I was explaining to J (my boyfriend of 2 months) about RSD and the SCS and he was curious just like everyone is when they first here about it. I have been blessed though with a boyfriend who has taken the time to ask me questions and understand that there are somethings I am not able to do but just because I have RSD doesn't mean I cant be an active participant in life. I think we all need to keep in mind if you or a loved one has a chronic illness / chronic pain doesn't mean their voice shouldn't be heard or they cant participate in activities. We love to have fun just like everyone else.

For those who are about to be getting the SCS and would like to contact me please feel free to. It was the best decision I made and I still love the SCS today. It has helped me gain my life back and there was no way I could have done that without it. I don't feel like I "gave into it" or "settled" for it. Its an amazing piece of technology that people with Chronic Pain have been given access to.

Healing Thoughts to All!


Email:
erikkaberry@yahoo.com