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He had me wait one week after the shot to start PT. The cortisone helped somewhat. It basically took the edge off and I no longer feel like I want to cut my arm off, but I am still very uncomfortable and can't sleep at night. I started PT yesterday.
I am not scheduled to go back to see him for another 2 1/2 weeks, but I am desperate for some type of pain relief. I simply cannot bear the pain and I am making a lot of mistakes at work because I am so distracted by the pain. I know I have a high pain tolerance because other physicians have told me so. I have recovered from knee surgery and gall bladder surgery without pain medication of any kind. This doctor is very reluctant to prescribe any pain meds, but I think I have a right to some kind of pain relief. I don't know whether to go back to him before the 2 1/2 weeks is up and try to talk with him, or seek another doctor who understands the pain of this condition. This particular doctor specializes in treating professional athletes, and I feel like to him, I am just a middle-aged woman complaining of some superficial condition that I should be able to tolerate until it decides to remedy itself.
Thoughts/opinions appreciated. Thank you!View Thread

I was never able to get any help from the medical community except for the cortisone injection that I got early on. I waited it out, and at about the 9 month mark, it started to become less painful. I am now at about the 13 -14 month mark and while my range of motion is better, it is still not back to normal, and I am unsure that it ever will be. I still cannot sleep on my left side because of pain, but the pain is nowhere like it was when I was first diagnosed. The last pain mgmt dr. I saw said that he had no problem with putting me on disability, but suggested to me to be careful with that decision because of the economy. I decided to still keep working full time, which was very difficult at times.
I must say that it's true that in time, the condition improves on its own, but it's a long time to wait considering the severity of the pain. I will admit that the cortisone injection did take the edge off the pain, and made it hurt just a little less. My suggestion would be to try the cortisone injection, but make sure you get a dr. who has done them before for frozen shoulder. If they don't get it in the right place, it will do no good, and can even cause damage. Only after another member in my family was diagnosed with frozen shoulder did they then understand the severity of the pain that I had gone through. Unfortunately, many people (including drs), do not understand how painful this condition is unless they have experienced it for themselves. Good luck to you and I hope you can find some relief.View Thread

He said he agrees with the first doctor's Dx, ( and I agree too, I am not questioning that), and that I should get the MRI and decide what to do from there. Well, I am positive that that MRI will show FS, and if it does, my first doctor already has said that he cannot do anything more for me, and was only going to refer me to a pain dr, who I have now already seen.
I can't understand the reluctance of these dr's to help me by giving me some pain medication. I have been compliant in everything that they have asked me to do. I don't have a history of substance abuse or addiction, am on no current meds for any conditions, and sometimes wait out a headache instead of taking Tylenol. I am not drug seeking, but I am looking for help with pain.
At this point, I have given up any hope that anyone will help me. I told my husband that if he finds me trying to cut off my arm, he knows why. And it is not inexpensive for me to see each doctor. I have insurance where I must meet a $3,200 deductible before insurance kicks in. Today I paid $137 for no help. I have paid my other doctor $340 so far. And each time I go to physical therapy, it costs me $78 and I have gone six times already.
I guess I will just wait for my FS to go away on its own. I don't see any other choice at this point. I had so much hope that I would get some type of help today, but now I just feel defeated and depressed. I am so angry at the medical community right now.View Thread


I neglected to mention in my first post that I cannot take NSAID's because I have a tendency to develop ulcers while taking those types of meds. So, those are out. He still won't give me any pain meds because he is afraid of dependency, and I understand that, but I need help with the pain. Don't they make pain medication for a reason? I'm at my wits end still, cannot function in daily life, and quite frankly, suicidal at times because of the chronic pain. I sleep maybe 2-3 hours a night, and do so with my arm packed in ice and propped on pillows because that it the only thing that gives me some relief.View Thread
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