Experiences with

Bone spur

My elbows are looking deformed these days nodules on nodules and a small bone spur. Know lots of you get this in various joints , but wondered how you "treat" them if you bother to?

Going into foot doctor tomorrow to have injection in my good ankle to help with bone spur. Always something going on.

I am wondering if anyone has had this surgery,I need to have it carried out with an iliac crest bone graft and tendon transfer. I have exhausted all other avenues. If anyone has experience with this I would be interested to hear.

In the meantime I had 2-3 years wait for a hip replacement (no cartliage) and it turned out a bone spur had grown off the ball.

After a morning of being at the hospital helping my mom who has several medical Issues I was rushing to my own pulmonary rehab for persistent respiratory damage following my first Sept. covid infection then BOOM! Slipped on ICE in a parking lot, fully broke arm bone between elbow & shoulder. Surgeon

I have a tear in my labrum, osteoarthritis and bone spur. I started PT because in 2001 I had both knees replaced and my one knee was bothering me so they figured a little PT would help it.

She was told she has swelling around her coccyx, the coccyx bone is bruised, she has a small bone spur on one of her sacrococcygeal discs displacing the ganglion impar (which the doctor was weirdly unconcerned about), and she has muscle spasms in her lower back.

i have finally got a kind of an answer. i went to docs and asked for an X ray on my spine she sent me instead for a CT scan. there are several things going on with my spine. firstly arthritis, secondly i have a bone growth [ spur ] which is touching a nerve, so i am going for a steroid injection

I've got a long and varied CLL history. Long story made short for those not familiar, I was diagnosed in 2013 in my own lab when I was working as a NHS healthcare scientist in Haematology. I am. 11q del and rapidly enlarging nodes meant I started treatment with Ibrutinib in October 2015. Six years

this is the email i Got, what do you think Hello, Thank you for your interest in Biostar’s stem cell therapy for Parkinson’s disease. The treatment is recommended for patients with early to mild stages. The cell dose for treatment will be determined on the patient’s stage of the disease. This will

will be needed a stem cell transplant after my third round for Flagida Chemotherapy. Has anyone had similar?

Hey all. I don't know if I'm asking a question or just venting so bare with me.Brief history- 31yr old female. Diagnosed Jak2+ ET start of this year but going by bloodwork, I have had it since 2019. Had a BMB in the summer which showed "mild fibrosis" and "hypercellular marrow" but diagnosis remained

It’s been awhile for an update, here is the latest. I’m at Day plus 127 from my Bone Marrow Transplant. I saw my doctor (main specialist) on day+119. This was after a BMBiopsy +105 and colonoscopy +109! Those results revealed the great and not so good! There’s no sign of cancer in my BoneMarrow, and

Hello! This is my first post. Since my teen years, I know I've had some repetitive movements of my fingers, ticks/twitches of my eyebrows and face, and counting even and odd numbers, often imagining doing so on my front teeth (sounds a bit odd, but that's what it is!) It was manageable and possibly annoying

I just wanted to let everyone know that I made my decision and I’m going through with a SCT. I have been seeing a transplant doctor at Dana Farber in Boston for about a year and he feels I’m strong enough now to have one. Now we have to find a donor and I have to start making preparations. We are shooting

Late April prior to treatment September after 4 cycles This is an update to my Diagnosed with Richters post a month or so back. I now go to MDA every 28 days and every third visit is a PET/CT scan and bone marrow along with

I have not posted in a while. About 5 years ago my blood pressure went up (180/110). I was put on over 10 different blood pressure meds. Nothing took it down. Last November I was diagnosed, via kidney biopsy, with something called MGRS (monoclonal gammopathy of renal significance). The illness

it’s been a while and my last post was not very positive . This is a quick update . I’m still unclear as to how I got here with my illness but I received palliative chemotherapy six cylcles one every three weeks. I think it was a variation of chop plus an immunotherapy drug beginning with B . The treatment

Hi everyone , I am so glad with this site. My name is Anja, 67 years old , and I live in the Netherlands. I was diagnosed with CLL in september 2010. In 2012 I got FCR for six rounds. After that I was stuffy and it occurred that I had heart failure because of the chemo therapy. It took me years

This is day +67 for me since by Bone Marrow Transplant. Happy Labor Day here in the USA. I had been cruising along with a few seemingly minor issues. GI tract at times has been an issue especially with bowel movements. As I was weened off the steroid Prednisone I have recently been put on the steroid