Hip MRI Results and Surgery Date

I saw the hip specialist here in Cincinnati about a week ago in order to get the results of my MRI. It shows that I have a complete acetabular labral tear with detachment in my left hip. The acetabular labrum is the ring of cartilage that is between the head of the femur (thigh bone) and the pelvis. This is what we thought was the issue with my left hip and the MRI confirmed this.

I will have to have surgery to fix the labral tear and detachment. He will go into the hip arthroscopically, meaning through multiple small incisions, and fix the tear. The surgeon will remove any of the tissue that is dead or beyond repair and repair any of the tears that are able to be stitched back together. This is a relatively minor surgery and is the same type of procedure I have had done on my wrist and knee. I have done very well with both of those procedures, so I am not too concerned about this one!

The one other concern that he did note on my MRI is that I have a moderate degree of anteversion. Anteversion is another way to say that my hip is turning inward toward my other leg. This is perfectly normal in young children, but disappears in 99% of children by adolescence. While I am not that old (22) I am past adolescence, so it is not considered normal for me at my age! This is a condition that is not uncommon in people with EDS and I only seem to have it on the left leg. Since the degree of anteversion is moderate and the surgery to correct the anteversion is very involved (it involves shaving down bone in the femur and pelvis) we have decided to not treat the anteversion at this point. If after the labral tear repair I am still having hip pain then we will discuss if we need to address the anteversion at that point, but the surgeon is fairly confident that once we fix the labral tear I will have relief!

I have already been to see my primary care doctor and have been declared “medically optimized” for surgery. This just means that he does not see any reason why my health should cause complications during or following the surgery. I have had a number of surgeries in the past (six under general anesthesia and multiple under twilight sedation) and have always done really well. I need medication to prevent vomiting after surgery because that is one negative reaction I have to anesthesia, but we know this ahead of time so we can medicate for it before the vomiting starts (about 4 hours after surgery)! There are a few other minor things that we need to watch out for like making sure I stay well hydrated, ensuring the anesthesiologist des not dislocate my jaw when they put the breathing tube in, and making sure that my neck does not get bent too far backwards because of my cranial cervical fusion, but in general I do really well with surgeries!

This surgery will be in about 3 weeks on Tuesday May 17 at 11:45 a.m. Of course this date and time may change, but as of right now that is the big day. I will let you guys know if anything changes, but prayers that everything goes smoothly would be greatly appreciated!

Primary Care Appointment

I had an appointment last week with my primary care physician (PCP). I had a wonderful PCP when we lived in the most recent town we were in in Illinois, so I was extremely sad to leave him! Thankfully my geneticist used to live in Cincinnati (where we recently moved to) and still has connections here! He was able to give me a recommendation for a PCP who is knowledgeable about Ehler's-Danlos Syndrome (my connective tissue disorder). This doctor was not taking new patients, but since my geneticist referred me to him he was willing to take me on!

I had a few questions for him, so the appointment was timed perfectly. Firstly, I have been taking a muscle relaxer for about 8 months now for the extreme tightness in my neck down into my shoulders.  The muscles that run down from my neck into the top of my shoulders get as hard as rocks (literally, not an exaggeration). This can be caused by many of my conditions (chiari, EDS, and instability) and is extremely uncomfortable for me. When I saw my genetesict last fall he recommended that I start a muscle relaxer called Flexiril to attempt to alleviate some of this tension. This helped a little bit, but every time I saw a new doctor or therapist they still were amazed at the amount of muscle tension that I held in my neck and shoulders. I asked my PCP if I could increase the dosage of the Flexeril, but he said he was not comfortable increasing my dosage. Flexeril can cause electrical changes in your heart and that risk increases as the dosage increases. Instead he recommended that I change to a different muscle relaxer called Baclofen. He started me out on 10 mg once a day and I will increase that dosage to twice a day and then finally three times a day over the course of three weeks. I am currently on 10 mg twice a day and it has helped so much!!! My muscles are not constantly tight and do not feel like rocks! It is so nice to have some of that tension reduced! One note of caution is that my doctor did say that if I had not had my cranial cervical fusion (screws from my skull down to my second cervical vertebrae) that he would absolutely not recommend a muscle relaxer since I am an EDSer. This is because the tightened muscles are actually helping to hold your cranial cervical joint stable and when you relax those muscles the instability that many of us with EDS have gets worse.

I also asked him to check my thyroid and my electrolytes. My thyroid is considered to be borderline hypothyroid, so I like to monitor my levels and make sure they do not tip into the range where I would need to be medicated. My levels were still borderline, so for right now we are good to go! I get my electrolytes checked because a medication I take (florinef) depletes my potassium and thus I need to take prescription potassium. Low or high potassium can cause serious issues with your heart, so it is essential to monitor my levels to make sure we are not over or under supplementing my potassium. Thankfully my electrolyte levels all look good! I was able to take my orders for the blood work down to the cancer center and have the labs drawn through my port. It is incredibly convenient that the cancer center is located in the same office as my PCP because then I do not have to drive to a separate office just to get my labs down.

As I mentioned in my last post that I also was able to get a recommendation for for a doctor who will do the botox injection into a muscle in my stomach (see this blog post for more info on that), so I was incredibly thankful for that! I will see that doctor next week, but I am excited to try the botox inject and see if I get a symptom relief from my gastroparesis. I also got a prescription from the PCP for a brace that my physical therapist recommended that will hopefully help support my spine and improve my neck pain and discomfort. I will write a blog post more on that when I receive the brace and have a chance to try it out!

I believe that those are all of the major this that we discussed at my primary care appointment. I will go back and see my PCP in 3 months. In the mean time I have a few appointments coming up in the next week or so, so I will update on those as they happen. I also had an appointment for my hip so I will write an update on that ASAP. Thanks as always for following along on my journey!

Cleveland Clinic Gastroparesis Appointment

Last week we went back to the Cleveland Clinic to meet with their gastroparesis specialists for the second time. We had been waiting on insurance to cover a test that they had ordered (a smart pill which measures time, pH, and pressure of your entire GI tract), but insurance would not cover this test and deemed it experimental. Since they wouldn't cover this test we had to go back up to Cleveland to come up with a new care plan without those results.

It is a four hour drive each way to Cleveland, which makes it quite a long day!!! My service dog Reilly DESPISES the car, so he was left at home with my sister-in-law. We live next door to my brother-in-law and sister-in-law right now, so to Reilly they are family and he is very comfortable with them. It is still hard on the both of us to be separated since we are together at ALL other times. I feel like I am without my shadow when I don't have Reilly because I do not go anywhere without him  (even the bathroom normally!!!).

We were able to meet with both the gastroenterologist and a general surgeon who works with the GI doctor. The gastroenterologist raised the dosage of a medication (Remeron) that is supposed to help my stomach empty. It is not a "traditional" medication used to treat gastroparesis, but he uses it with many of his patients who have gastroparesis in conjunction with autonomic nervous system dysfunction. The idea is that this medication will help the nervous system to effectively tell the stomach to empty. We doubled the dose and so far I have not noticed much of a difference in my symptoms since increasing the dose, but it has only been a few days so I will give it some more time!

After having a conversation with the GI doctor we decided that the gastric neurostimulator is not the route for me right now. This device is what we had discussed as the next step previously, but we decided at this appointment that this is actually not a good next step right now. One main issue with the gastric neurostimulator is that it is not MRI comparable. This means that I would never be able to have an MRI. Having EDS and needing MRI on joints and my brain and spine on a fairly regular basis this is not ideal. The alternative to an MRI is a CAT scan. Now CAT scans themselves are not a bad thing, but they do expose patients to radiation. Having a few CAT scans is no big deal, but if I had to have multiple CAT scans a year the radiation would definitely add up over the years and this is a huge concern.

Another issue we have with the gastric neurostimulator is that the success rate is only 50-60%. That is not very good odds in my book! The surgeon also said that since I have chronic constipation he thinks my intestines may be slowed down as well as my stomach so the success rate drops even further. It is a major abdominal operation to place the device and then an even more complicated operation to remove the device if it does not work. The surgery to take it out includes the surgeon removing a piece of your stomach because the nodes on the stimulator become embedded in your stomach. Obviously this is not an ideal situation!

Now all this aside, this does not mean that someday this device will be a good next step for me. Right now I am actually gaining weight and eating much more than I have in the past. I still have symptoms and discomfort, but in general my GI status has greatly improved. For all of those reasons the benefits  do not outweigh the risks at this time.

Since we decided we are not pursuing the gastric neurostimulator at the moment we discussed alternative options with the surgeon. After discussing a few different things we decided that the next thing we will try is injecting botox into the pyloric sphincter. The pyloric sphincter is the valve that allows food to pass from your stomach into your intestines. By injecting botox into the muscle that forms this sphincter the muscle relaxes. Once the muscle relaxes the hope is that food will pass easier from the stomach into the intestines since it does not have to work to get past the sphincter. If the botox does work I may notice results immediately or it might take a few days before I notice any results. Even if the botox does work, however, the results are only temporary. The general surgeon says that most of his patients only see results for about 6-8 weeks at the maximum. For this reason the botox injection is not considered a long term solution, rather it is used as a diagnostic tool. If I respond well to the botox injection then that tells the surgeon that I would be a good candidate for a surgery called a pyloroplasty (more on that in a moment). The botox injection is done via a scope, so there are no incision in the abdomen. There are very few risks of the botox injection itself, besides the risks of the anesthesia of course! For this reason we decided that there is no harm in trying the injection and seeing if it helps.

Since Cleveland Clinic is so far away for us to drive to the doctors and I decided that I would try to find a doctor to do the botox injection in Cincinnati. I had an appointment with my primary care doctor at the beginning of this week, so I asked him if he knew of anyone. He sent me the name of a doctor that will do it, so I set up an appointment with this GI doctor for Monday the 25. We will schedule the procedure to do the botox at this appointment.

If the botox injection provides relief from symptoms then we will most likely preceded with a surgery called a pyloroplasty. A pyloroplasty essentially does the same thing as the botox injection, but it is permanent. During the pyloroplasty the pyloric sphincter is cut so that the valve is widened. This provides a permanently opened pyloric sphincter. The Cleveland Clinic is one of the only places in the world that can do this surgery endoscopically. This means the surgery can be done through a scope down the throat rather than through incision made on the abdomen. The recovery is faster, the risks are lower, and there is no scarring if the surgery is done this way. For this reason we will travel up to Cleveland if we decide that this surgery is the best next step for me. The risks are very low and there are no long term complications with this surgery. We will not know whether or not I am a good candidate for this surgery until after we do the botox injection.

That was a very long update I know, but it was an extremely informative appointment! I will update as to when the date for the botox injection will be after the appointment I have schedule on the 25th.

Hip Appointment and Arthrogram

Since working with a new physical therapist in Cincinnati her and I both realized that there is something wrong with my left hip. We are not sure when or how I injured it, but with EDS that is quite common. My joints all pop out of place regularly and sometimes they do not go back into place correctly and can catch and tear.  Activity really seems to aggravate the hip (walking, stairs, etc.) and the pain is deep in the hip joint. We started trying to treat the pain conservatively and tried doing different exercises to see if it would improve, but it has not improved. After a few weeks of this treatment the PT recommended that I see an orthopedic surgeon in order to get my hip assessed.

I was able to get an appointment with an orthopedic surgeon at Cincinnati Children's hospital (they accept patients into their thirties, which is fantastic for me!). At that appointment he took some x-rays and did a full assessment of both hips. The x-rays looked great, which we expected them too, but based off of the amount of time I have had pain in the hip, the fact that the pain has not gotten any better, and the specific positions I have pain in the hip he recommended that we do further testing to see what is going on.

The test that he wanted done is called an arthrogram. An arthrogram is done when contrast is injected directly into the joint and then an MRI is done. I have never had one of these, so it was new experience! I was taken into an operating room (a sterile environment), my hip was numbed, and a needle was injected directly into the hip using x-ray guidance. This allowed them to put IV contrast directly into my joint so the soft tissue structures of the hip would show up much clearer on the MRI than they would if IV contrast was used.. While he had the needle in my hip they also injected steroids into the hip. The steroids can be used as a treatment for joint pain because they reduce the inflammation in the joint and can decrease pain. Sadly the steroid injection did not seem to help much at all.

The arthrogram itself was not painful necessarily because of all the local anesthesia that they used, but it was definitely uncomfortable! I could feel pressure and tugging as the needle was in the joint and when the procedure was completed my hip was VERY stiff. The doctor inserted so much fluid into the hip that it was extremely stiff and sore. I was on low activity for 48 hours, so we just used my wheelchair since we had family in town and were going out to a museum. Part of my connective tissue disorder means that I bruise severely and easily, so the point that the needle was inserted into the hip is definitely bruised and still sore a week later.

I will go back to the orthopedic surgeon next Wednesday (4/13) to get the results from the arthrogram. If it is a tear in the cartilage like we think it is we will then schedule surgery to repair the tear, but we will not know that until after I get the results from the arthrogram.