Skip to main content

Ultrasound Guided Cortisone Injection

Today was the big day. I woke up at 5AM, I firmly believe no one on the planet should ever have to be awake at this hour. It was still dark out when I embarked for HSS. The only good thing about getting up this early was how pretty the view was from the waiting room window. I have discovered both the x-ray waiting room and the ultrasound waiting room over look the east river, which is gorgeous in the morning.

View from the ultrasound waiting area at 7AM
Soon I was called back to an ultrasound room. First they just did an ultrasound of my hip, the radiologist pointed out that I have Cam impingement. I asked if I also have pincer but he said it was nearly impossible to see on an ultrasound but most people have both.He also said that my labrum was not detached, even though he could not tell if it was torn, but at least the fact it is not detached is a good sign. I was really surprised he told me so much when I have gone for MRIs and x-rays the radiologist usually say they can't tell me anything.

Next it was time for the injection. First they sterilized the area then they put a sterile field around it, and then sterilized again. first they insect some numbing stuff, although it didn't feel numb but hopefully helped, it burned a little while they injected it. Instead of injecting the cortisone in the same manner, first the needle by itself went it. The doctor was using an ultrasound to see where it was going. The needle hurt when it first went in and there was a painful pop when it enter the actual joint. Next the cortisone shot was injected, there was a sharp pain as it went in but after a few seconds all that was left was a residual soreness. 

The first few hours afterwards my hip was stiff from all the extra fluid and a little sore but not too bad. At hour three or four however I was in a lot more pain. The radiologist told me to relax for the day, but me being me I went to school anyway. I would not suggested that to others. Right now it hurts to move my leg or put any weight on it but hopefully it will get better soon.
Labels:

Comments

Post a Comment

Popular posts from this blog

The Swollen Wrist

This morning I woke up to a red painful swollen wrist. My right wrist was not happy or useable for the better part of the morning. Of course my mom wanted to make a rheumatologist appointment for this week but I really did not think it is worth it. Since I am now in the 2 week period before my hip surgery I can not take anything but Tylenol anyway (no voltaren or fancy cream), so there is not a whole lot that can be done. We finally settled on me going to my GP (for the 2nd time in one week as I had a pre-op appointment with him on Monday), and I took a picture so I can show my rheumy at my next appointment. I managed to get an appointment at 11AM because my GP was in the office this Saturday. By the time of the appointment my wrist looked pretty normal, although I had the picture so he could see something was up. He had it x-rayed just to rule out any issues non rheumatology related, and as we both guessed the x-rays came out normal. My Lovely Wrist this Morning I was left wit
Post a Comment
Read more

The Perfect Body?

Today I am going to write about a taboo subject- body image, and how living with chronic illness/pain has affected it. I get told how great my body is a lot, I am tall and fairly skinny. Not to be egotistic but I look pretty good in a bikini. I should love how I look. I should be confident of my body, after all I just bought a pair of size 2 jeans. Yet I still struggle with loving my body. My New Jeans! In middle school I thought my legs were fat, that was when I had muscles from horseback riding, today I miss my muscular legs. My thighs tend to be two different sizes, the left one is almost always smaller. The reason for this is simple, my left quad has atrophied from months of limping and being on crutches when I was 15/16, at one point it was so bad my doctor measured it and the difference was a good 2 cm in circumference. Today they are almost the same size, and probably look the same to anyone else, but to me they still look different. If you haven't guessed it yet,
4 comments
Read more

30 Things You May Not Know About My Invisible Illness

I am doing this post for invisible illness week which is this week.  1. The illness I live with is: Enthesitis, Amplified Musculoskeletal Pain(AMP), and Uveitis 2. I was diagnosed with it in the year: Uveitis-2012, Enthesitis and AMP-2013 3. But I had symptoms since: 2006 4. The biggest adjustment I’ve had to make is: I have had to learn I can't do everything I want or everything that other people my age are doing. 5. Most people assume: I am perfectly fine or I just have osteoarthritis and not an autoimmune disease. 6. The hardest part about mornings are: Getting out of bed, doing my hair, and figuring out what outfit will be the most comfortable for the day (and accommodate any swelling I may have) 7. My favorite medical TV show is: Grey's Anatomy (and Scrubs even if it is no longer on) 8. A gadget I couldn’t live without is: My Freezer 9. The hardest part about nights are: Not being able to fall asleep in a comfortable position and waking up in the middle of the night in p
5 comments
Read more