AMR1879
member
Nonsense! a) there is always fluid in the joint, even in an artificial joint! It can't be avoided. b) that fluid always looks blood tinged because that is the normal colour of tissue fluid. Even saliva has a faintly yellowy-pink tinge. Perfectly normal.
I am very curious to see what, if anything the fluid shows. I hope you're right @Josephine and it is normal fluid! Then again, if there is a sign of an early infection, that may be the answer!
Haha! They totally didn't care, the Dr joked and said I can curse if it was okay if he did too! I said, as long as he curses for a good discovery, not b/c of something bad! And to my surprise, as I'm cursing away at the pain, he blurted out a surprised reaction with a curse included too....he was genuinely surprised at what he got out of the second aspiration deep between the ball and socket (the time it hurt the most).I can promise you that all surgeons have a fairly rich vocabulary of "medieval epithets" which they use freely in the operating theatre! I went in an innocent and naive young girl and pretty soon learned a LOT of words I'd never heard of before!
I still feel it is a loose stem (or a stem that never even got anchored)--but I am not the Dr, I am just the one living with the pain! The more I read about people's symptoms they experienced before their Dr's concurred w/a loose stem, the more I feel I fit the bill--but many situations are years after the THR.
There was an older post on another forum that I was reading, it was so similar to my situation, I actually had to check to see if it was written by me at another time, lol, it sounded almost exactly like what I am going through. The person, unfortunately, did not follow up so I don't know how they made out.
I can't seem to find many people who have experienced the same type of situation as me (being within a year of the THR), which is hard, because I want to feel like I am not crazy and that I am not being over dramatic or expecting too much at 4+ months out.
I revisit my previous posts in this thread when you (Josephine) said,
This is very characteristic of a loose stem. No doubt about it. It certainly IS the reason you are having increased pain! That's a definite no-brainer! Got nothing to do with haematoma or doing to much. You have a loose stem. It needs to be dealt with.
You have been the only one to talk definitively and confidently, not brushing me off or thinking I am being over dramatic....and it is appreciated. Thank you for taking the time to help everyone who finds this site looking for guidance or just empathy for their situation!
My pain has been worse since the aspiration on Friday. I am feeling more pain when I rest in both my hip and lower back/high butt area. I even tried icing last night because it was so irritating. I still have the lumpy side of my scar (it was referred to as a hematoma post-op) but it is still there and is has never been and still is not discolored, just ugly, and I tried massaging it yesterday with my massage tool, but it was actually painful, so I stopped. I didn't feel like adding to my pain!
@Josephine is there any chance the lumpy side of my scar, and my hip pain could be related?? Maybe I am just grasping for straws. The lumpy scar has kind of gotten pushed to the side (no pun intended!) and forgotten by my Drs, while dealing with my hip joint pain--I even forget to mention it. But I see it every day when I look in the mirror, dressed or undressed -- right side of hip goes straight down (pretty much) and the left side has a bulge/small saddle bag look.
I am so eager to go see the new OS tomorrow and hopefully figure out something! I hate to get my hopes up for some answers, because I have been disappointed many times. I honestly feel like I will have left hip pain for the rest of my life. For heavens sake, at the in-practice 2nd opinion, the OS was CERTAIN my hip was not the problem at all and wanted to do nerve blocks as a "way to diagnose" where the pain is coming from. That was devastating to me, not only did I not get any answers, but I was told by a hip replacement specialist that it wasn't my hip!
So I took the next step down the nerve block path and made an appointment with the pain management Dr within the same practice last week, I have met with him before for x-ray guided cortisone injections and I felt he was a knowledgeable Dr who would take the time to explain things to me. He very strongly recommended to hold off on nerve blocking, he feels (and I agree) I am too young to start messing with nerves and going down that road. He suggested I wait to do anything until I hit the 6-month mark, unless they find there is an infection, of course.
Anyhow, this has become more of a rant than an update, reply or even question! I'm sorry, sometimes just venting helps, especially if it is to an audience that has been through something similar.
Thank you @MyAussieGirl for the support! It is much appreciated!! And thank you @Josephine for your in-put, I can only imagine how full your inbox must be!Just sending you supportive hugs I have no wisdom being new to this myself but my heart goes out to you
United States

