... and I'm admittedly a bit nervous. I had such an amazing experience with my in-home PT, I'm worried that my new outpatient PT will somehow mess with the progress I've made. Ever since my diagnosis/in the time before starting PT anew, I've continued to do my exercises at home. All of them center around my pelvic floor muscles. When I'm home alone with R, I find that I can get away with doing standing exercises most easily - no extra time needed to situate myself on a bed or on the floor. Other than standing exercises, I also do bed exercises (which, yes, all start with me lying on my back on the bed) and floor exercises (all of which start with me on hands and knees on the floor). I do the standing exercises at the kitchen sink, or really anywhere where I can balance my hands on something that's at about waist height. If anyone is interested in more information about the specifics, just comment below.
While none of the exercises are vigorous, I always feel a sense of accomplishment when I do them. Before my injury, I was a very active person: Frisbee, field hockey, running, biking - all of it. My postpartum months have definitely been the most inactive of my life to date. It's such a downer... but thankfully PT is something that helps lift my spirits, while at the same time enabling me to make physical gains, too. #staythankful!
Friday, April 22, 2016
Saturday, April 16, 2016
Doctor, Doctor, Give Me The News
After meeting with the ortho doc a few days ago, I've got some more information on my situation. Here is what I found out:
* I won't be needing surgery. Apparently, surgery to fix a pubic symphysis rupture is relatively rare, and this doctor told me that, while he has done the surgery before, he "regretted it". It can make for a faster recovery time, but it can be extremely painful and complications are possible (as with any surgery, I suppose). Also, by inserting a plate between the pubic bones, you can cause more SI joint pain... no, thanks.
* I'm going to restart physical therapy. As of my first week postpartum, I had in-home PT 2-3 times per week. We stopped after I got my diagnosis, but before I spoke with the ortho doc. While the progress was s-l-o-w, there was definite gains over the past 2 months: I went from not being able to lift my legs onto the bed, to using a leg lifter, to now being able to do it independently with minimal discomfort. During PT, I did light stretching, standing exercises, floor exercises, and bed exercises, all of which focused primarily on core strength/the SI area. I'm looking forward to getting back into it.
* I won't be wearing a binding belt. According to the doc, wearing one is hit-or-miss, as far as helping with the pain goes. I wore one for about 40 minutes during the MRI of my pelvis, and I was back to a pain level 8-9 (out of 10) for the next 48 hours. Given that info, the doc said I should skip it. He didn't need to tell me twice!
* I'll continue taking ibuprofen and a NSAID as needed for pain. I've been trying to taper (before this, I hardly EVER took OTC pain meds), but I find I need to take a full dose overnight (sleeping for even 3 hours in a row in the supine position bothers me).
* Other than PT, "patience, my dear, patience!" is the primary ingredient of my treatment plan (quote the doc). It'll take me 4-6 more months to recovery fully.
* "Recover fully" for me means back to my old-self, at 100% functionality! I was REALLY worried about asking the doc if that was even a possibility: I know from my internet research that, even years after an injury that caused PSD, people live with chronic pain. Even though I'm hesitant to set myself up for failure - to believe that I WILL get better, all the way - I need to focus on it, in order to keep my spirits afloat.
SO, there you have it. Writing here with a newborn on my hands is turning out to be trickier than planned, but I'll update as much as the little man allows (for example, right now R is sleeping in his Rock 'N Play - I'm rocking him with my foot as I type)..... and he's awake! More later.
* I won't be needing surgery. Apparently, surgery to fix a pubic symphysis rupture is relatively rare, and this doctor told me that, while he has done the surgery before, he "regretted it". It can make for a faster recovery time, but it can be extremely painful and complications are possible (as with any surgery, I suppose). Also, by inserting a plate between the pubic bones, you can cause more SI joint pain... no, thanks.
* I'm going to restart physical therapy. As of my first week postpartum, I had in-home PT 2-3 times per week. We stopped after I got my diagnosis, but before I spoke with the ortho doc. While the progress was s-l-o-w, there was definite gains over the past 2 months: I went from not being able to lift my legs onto the bed, to using a leg lifter, to now being able to do it independently with minimal discomfort. During PT, I did light stretching, standing exercises, floor exercises, and bed exercises, all of which focused primarily on core strength/the SI area. I'm looking forward to getting back into it.
* I won't be wearing a binding belt. According to the doc, wearing one is hit-or-miss, as far as helping with the pain goes. I wore one for about 40 minutes during the MRI of my pelvis, and I was back to a pain level 8-9 (out of 10) for the next 48 hours. Given that info, the doc said I should skip it. He didn't need to tell me twice!
* I'll continue taking ibuprofen and a NSAID as needed for pain. I've been trying to taper (before this, I hardly EVER took OTC pain meds), but I find I need to take a full dose overnight (sleeping for even 3 hours in a row in the supine position bothers me).
* Other than PT, "patience, my dear, patience!" is the primary ingredient of my treatment plan (quote the doc). It'll take me 4-6 more months to recovery fully.
* "Recover fully" for me means back to my old-self, at 100% functionality! I was REALLY worried about asking the doc if that was even a possibility: I know from my internet research that, even years after an injury that caused PSD, people live with chronic pain. Even though I'm hesitant to set myself up for failure - to believe that I WILL get better, all the way - I need to focus on it, in order to keep my spirits afloat.
SO, there you have it. Writing here with a newborn on my hands is turning out to be trickier than planned, but I'll update as much as the little man allows (for example, right now R is sleeping in his Rock 'N Play - I'm rocking him with my foot as I type)..... and he's awake! More later.
Monday, April 11, 2016
Hello, and Welcome
This is my first ever blog, let alone blog post. My goal is to chronicle my postpartum experience, primarily with a ruptured pubic symphysis. I've found that there isn't a lot of information out there for inquiring (aka, freaking out!!) minds, so hopefully I can compile some here. I was inspired to start this blog in part by Rowena, a fellow blogger whose blog has been a source of both information and comfort for me (check her out: http://pubicsymphysis.blogspot.com/).
I'm 8 weeks postpartum as of today, and have an appointment with an orthopedic trauma surgeon this afternoon. Hopefully we'll make a plan of attack... stay tuned.
Here are some fast facts about me, outside of my PS issues:
* I live in the state of Maine, USA - our motto is "The Way Life Should Be" for a reason!
* R is my son, and my first child - although his arrival prompted my PS rupture, he's honestly perfect. I'm a total goner for this kid.
* E is my husband - the love of my life, and a tremendous support throughout the last 2 months.
* The title of my blog is a line from the lullaby that we sing to R before bed each night. My dad used to sing it to my sisters and I, and his dad sang it to him. Somehow it seems like the right fit for this space.
* Stay Thankful is my life's motto. I have it inked on my right wrist.
All for now -
I'm 8 weeks postpartum as of today, and have an appointment with an orthopedic trauma surgeon this afternoon. Hopefully we'll make a plan of attack... stay tuned.
Here are some fast facts about me, outside of my PS issues:
* I live in the state of Maine, USA - our motto is "The Way Life Should Be" for a reason!
* R is my son, and my first child - although his arrival prompted my PS rupture, he's honestly perfect. I'm a total goner for this kid.
* E is my husband - the love of my life, and a tremendous support throughout the last 2 months.
* The title of my blog is a line from the lullaby that we sing to R before bed each night. My dad used to sing it to my sisters and I, and his dad sang it to him. Somehow it seems like the right fit for this space.
* Stay Thankful is my life's motto. I have it inked on my right wrist.
All for now -
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