DEL2020Jul-11
junior member
- Joined
- May 23, 2020
- Messages
- 51
My right hip was replaced with a posterior approach. I had several years of OA pain before I decided to have surgery. My thanks to all of you, who have helped me through this difficult time. I also would like to wish the best for Josephine and to say that her wisdom is extremely appreciated!
Here is where I am now:
1) My worry that something will go wrong with my implant is less with time. These include worries about dislocation, infection, loosening of stem and cup, etc. From my personal experience, and from reading many of your stories, it seems I have a lot of company in the worry department.
1A) I believe that there is no guarantee of success with any surgery, no matter how well you prepare. For those who excitedly report that there is nothing to fear, I disagree. I only hope everyone recovers and I appreciate my improvement over time.
2) Posterior approach was the best option for me, as that is what my surgeon did. For me, again just my personal opinion, I would never choose a surgeon who does the anterior approach. There is a small chance of cutting the femoral nerve, which controls the motor function of one's leg.
3) While I am happy for those who have less pain after surgery, I had different pain, often worse pain for many months following surgery and poor sleep (I finally learned to position a pillow under my thighs, so I could adapt to sleeping on my back).
4) Physical therapy saved me. My tissues were extremely 'upset' by being cut and stretched and did not settle down. My close friend had her hip replaced 3 weeks before me, also posterior. I realized I was having trouble recovering when I asked her what she did about the stiffness on the side of the hip, which I had constantly, all the time, and she replied, "What stiffness?"
5) I have been in outpatient Physical Therapy for 4 months (wearing a mask, as does my PT). Now, my stiffness is resolving, my gluteal strength is almost back to normal, my gait is fluid, and my range of motion is good except for external rotation, but it is getting there. My PT has specialized training in manual approaches, and has also done PNF, which is a technique of proprioceptive input, stimulating the nervous system, which gave me back my trunk rotation and activated my gluteal muscles.
6) Without help from PT, no matter how much I tried to do heel to toe walking, I did not improve my gait because I felt no connection between my gluteal muscles and my heel strike. A total disconnect until several months of therapy.
7) Feed back to my PT was essential, as for the first two months I could not do the kind and number of exercises that he prescribed, due to pain, weakness, and fear. We worked it out, I did less than he wanted, while he did a great deal of hands on work (called soft tissue mobilization) on my tight, restricted, sore, painful tissues.
8) By 5 months plus, I can do all the exercises and feel my body being restored. It includes lots of bridges, but I tweak the position by providing support for my upper body with pillows (to take strain off my lower back).
9) My post-operative course has been difficult, at times truly awful. But, my pre-operative state was also awful. I am grateful for the chance to have my life back, which for me is to move. While warned by your wonderful forum not to overdo, once I could walk more than a mile, I was eager to go 2 or 3 miles. I gave myself a whole bunch of tendinitis, in multiple places, in both legs (when I am tired, my opposite leg starts to do more of the work). Again, thank goodness for my gifted PT, who rolled his eyes when I asked if he thought i had given myself tendinitis by walking too far, too often. My PT and I got my inflamed tendons under control. While I have to space out my longer walks, I can go 4 or 5 miles, on some reasonable trails a few times a week and for me, this is everything....
Here is where I am now:
1) My worry that something will go wrong with my implant is less with time. These include worries about dislocation, infection, loosening of stem and cup, etc. From my personal experience, and from reading many of your stories, it seems I have a lot of company in the worry department.
1A) I believe that there is no guarantee of success with any surgery, no matter how well you prepare. For those who excitedly report that there is nothing to fear, I disagree. I only hope everyone recovers and I appreciate my improvement over time.
2) Posterior approach was the best option for me, as that is what my surgeon did. For me, again just my personal opinion, I would never choose a surgeon who does the anterior approach. There is a small chance of cutting the femoral nerve, which controls the motor function of one's leg.
3) While I am happy for those who have less pain after surgery, I had different pain, often worse pain for many months following surgery and poor sleep (I finally learned to position a pillow under my thighs, so I could adapt to sleeping on my back).
4) Physical therapy saved me. My tissues were extremely 'upset' by being cut and stretched and did not settle down. My close friend had her hip replaced 3 weeks before me, also posterior. I realized I was having trouble recovering when I asked her what she did about the stiffness on the side of the hip, which I had constantly, all the time, and she replied, "What stiffness?"
5) I have been in outpatient Physical Therapy for 4 months (wearing a mask, as does my PT). Now, my stiffness is resolving, my gluteal strength is almost back to normal, my gait is fluid, and my range of motion is good except for external rotation, but it is getting there. My PT has specialized training in manual approaches, and has also done PNF, which is a technique of proprioceptive input, stimulating the nervous system, which gave me back my trunk rotation and activated my gluteal muscles.
6) Without help from PT, no matter how much I tried to do heel to toe walking, I did not improve my gait because I felt no connection between my gluteal muscles and my heel strike. A total disconnect until several months of therapy.
7) Feed back to my PT was essential, as for the first two months I could not do the kind and number of exercises that he prescribed, due to pain, weakness, and fear. We worked it out, I did less than he wanted, while he did a great deal of hands on work (called soft tissue mobilization) on my tight, restricted, sore, painful tissues.
8) By 5 months plus, I can do all the exercises and feel my body being restored. It includes lots of bridges, but I tweak the position by providing support for my upper body with pillows (to take strain off my lower back).
9) My post-operative course has been difficult, at times truly awful. But, my pre-operative state was also awful. I am grateful for the chance to have my life back, which for me is to move. While warned by your wonderful forum not to overdo, once I could walk more than a mile, I was eager to go 2 or 3 miles. I gave myself a whole bunch of tendinitis, in multiple places, in both legs (when I am tired, my opposite leg starts to do more of the work). Again, thank goodness for my gifted PT, who rolled his eyes when I asked if he thought i had given myself tendinitis by walking too far, too often. My PT and I got my inflamed tendons under control. While I have to space out my longer walks, I can go 4 or 5 miles, on some reasonable trails a few times a week and for me, this is everything....
Last edited by a moderator: