So yesterday I had two appointments one was in Silver Spring, MD and the other in Bethlehem, PA.
I left my house before 6 am and did not make my appointment in Silver Spring due to horrible traffic on the Beltway. I got there 45 minutes late which they worked me into the schedule since I called and told them I was having issues. I am extremely lucky to have doctors that are so understanding.
So besides being extremely frustrated from traffic, being that I already have all of these crazy problems... it just adds to my severe pain. The surgeon was pleased with my EMG results from last week, because the function of muscles and nerves in my left leg are normal. What is not normal however are the sensory nerves that are in my groin area, where I always have pain. So we discussed what options were out there for a long-term solution to getting myself out of this pain. That lead us to where the doctor was expecting to go which is a nerve decompression.
Of course it is not normal to want to have to get cut open again, but in this case I want to be out of pain so bad that I will take making it worse to get better. That is what happened with my surgery in September so I have a good outlook on this even though it is an extra stress to my life right now in the busiest part of my work year. I have scheduled the surgery for April 9th and will have a long recovery. The good news is that the doctor does want me exercising, I can continue walking on the treadmill and I am to add swimming two times a week as well. He wants me to strengthen my body as much as I can, even though I am not allowed to lift or do anything too strenuous.
I was warned in advance that the surgery will be invasive and it will be painful, I am to expect a lot of pain after and that my physical therapy after will also be difficult.
Then I had the drive to Bethlehem, which was long and miserable. I had the worst case of road rage ever as I was worried I would be late to my appointment, I made it just in time which was good. In the mean time I had an issue with work and I had to find a Starbucks to get the internet. I was just stressed in every way possible.
At my second appointment of the day, I talked with the doctor and we altered some of my medications to try and help in the mean time, which makes me feel kind of foggy today (it probably doesn't help much that I did not sleep well and then hit the gym at 5 am). The doctor feels that he thinks that having this surgery will help calm everything else down as it is so painful right now. So I will continue getting treatments as well in the mean time.
I then talked with my doctor on how hard this is to try and talk to people about, because I just don't feel that people fully understand how miserable this feeling really is. He said that is extremely common from his patients and that it is something hard to explain and for people to understand. He once again told me however that this is something that is more common that we think when it comes to the IC and the issues within the pelvic floor (I have other issues going on as well, see the surgery remarks above).
I wish it was easier to talk about and for people to truly understand the pain that this causes. This will be my 3rd surgery in a year's time.
Right now I need to focus on everything else I have going on and in the mean time just try and make sure I am taking care of myself.
This blog details my diagnosis of IC and severe chronic pelvic pain. Thoughts outlined here are my own and these experiences are how I am coping with and learning to live with my diagnosis.
Showing posts with label doctors. Show all posts
Showing posts with label doctors. Show all posts
Thursday, January 31, 2013
Wednesday, October 17, 2012
What a week
Well my bi-weekly doctors appointment was today. I got my shots and instillation and took the 2 hour drive there and back. The doctor was also nice enough to help me out with an antibiotic for the super sinus infection that happened to strike at me today.
Some days I really wonder... I mean that is truly the last thing that I need, to get sick. With an event in three weeks and helping out with political campaigns things have been super crazy.
I am going to try and get a good nights sleep and take care of myself.
I am looking forward to tomorrow though. Apparently there is a program that Zoup has called Zoup to the Rescue and two of my friends in Colorado put my name in to possibly get this great gift. So it works out great that I am sick and getting wonderful soup delivered to my workplace tomorrow morning. So a shout out thank you to Jason and Abby Bryant.
Some days I really wonder... I mean that is truly the last thing that I need, to get sick. With an event in three weeks and helping out with political campaigns things have been super crazy.
I am going to try and get a good nights sleep and take care of myself.
I am looking forward to tomorrow though. Apparently there is a program that Zoup has called Zoup to the Rescue and two of my friends in Colorado put my name in to possibly get this great gift. So it works out great that I am sick and getting wonderful soup delivered to my workplace tomorrow morning. So a shout out thank you to Jason and Abby Bryant.
Saturday, September 1, 2012
In honor of IC Month
I thought it might be interesting to share a few facts that affect my everyday life living with IC:
- I go to the bathroom what seems like all the time.
- I have to base the clothing I wear depending on how I feel.
- I don't think anyone fully understands what it feels like to have this problem unless they have it.
- I denied for a long time that I had IC, because I had the test done and it came back negative. However, I have learned that in 10% of people with IC can take the test with negative results, apparently I really am special.
- IC and bladder problems effect more women in this country than most would think, however many women do not seek treatment.
- The multitude of problems I have... took me months to be able to talk about without crying.
If you think you have a problem, do some research, there are some great websites out there and talk to your doctor. One thing I have learned through this process is not to be afraid to say or ask whatever you may think while you are at the doctor.
You yourself are the best advocate for YOU! Read here for more information on IC.
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