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Nodules
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?
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?
Happy5
in
NRAS
2 months ago
Finally a spring day šš¼
Going into foot doctor tomorrow to have injection in my good ankle to help with
bone
spur
. Always something going on.
Going into foot doctor tomorrow to have injection in my good ankle to help with
bone
spur
. Always something going on.
Kenu
in
My MSAA Community
6 months ago
To Bone marrow biopsy or not to bone marrow biopsy that is the question.
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.
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.
Tellingbones
in
CLL Support
3 months ago
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I donāt know what to do!!!
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.
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.
Dolphfan47
in
Anxiety and Depression Support
10 months ago
(Full break) spiral humorous fracture; surgery or let bone heal?
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
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
MotherofDragonsUSA
in
CLL Support
7 months ago
AT LAST
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 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
Fingerandus
in
Restless Legs Syndrome
9 months ago
Need advice on getting diagnosis
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.
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.
Twin4Life
in
Pelvic Pain Support Network
6 months ago
Update on Dental Implant Surgery
A quick note to say that it all went well. I am currently on 3mg pred. The dental surgeon advised 10 mg the morning of the surgery. I was also given paracetamol and antibiotics. Tooth extracted, implant inserted with some bone graft. Not pleasant but it didnāt hurt at all. Followed the hygiene instructions
A quick note to say that it all went well. I am currently on 3mg pred. The dental surgeon advised 10 mg the morning of the surgery. I was also given paracetamol and antibiotics. Tooth extracted, implant inserted with some bone graft. Not pleasant but it didnāt hurt at all. Followed the hygiene instructions
Janet57
in
PMRGCAuk
11 months ago
Stem cell transplant
I just wanted to let everyone know that I made my decision and Iām going through with a SCT. I have been seeing a transplant doctor at Dana Farber in Boston for about a year and he feels Iām strong enough now to have one. Now we have to find a donor and I have to start making preparations. We are shooting
I just wanted to let everyone know that I made my decision and Iām going through with a SCT. I have been seeing a transplant doctor at Dana Farber in Boston for about a year and he feels Iām strong enough now to have one. Now we have to find a donor and I have to start making preparations. We are shooting
Cja1956
in
MPN Voice
4 days ago
Diagnosed with Richters follow up - great news
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
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
Louie_CC
in
CLL Support
8 days ago
Finally, weaning off prednisone after 15 years.
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
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
phebamom
in
PMRGCAuk
8 days ago
Iām still here :)
itās been a while and my last post was not very positive . This is a quick update . Iām 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
itās been a while and my last post was not very positive . This is a quick update . Iām 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
Hilo13
in
CLL Support
19 days ago
Venetoclax
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
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
jroon08
in
CLL Support
20 days ago
Continued Journey
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
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
FiArt12X
in
CLL Support
25 days ago
Still Hangin in There
Hi everyone. 9+ years on (take a peek at my bio.) Stage IV pca. I'm still hormone sensitive with undetectable PSA. Living life and enjoying my time with friends and family. In November I will enter year 2 of multiple myeloma DX. Have been through induction but not needing a stem cell transplant
Hi everyone. 9+ years on (take a peek at my bio.) Stage IV pca. I'm still hormone sensitive with undetectable PSA. Living life and enjoying my time with friends and family. In November I will enter year 2 of multiple myeloma DX. Have been through induction but not needing a stem cell transplant
swwags
in
Advanced Prostate Cancer
25 days ago
Richter's and Novel Treatments/Combinations
We've had a few members post about Richter's recently so I thought it might be time for a bit of an update on new treatments. In these reports there is not a lot of information about clonality and which mutations the patients have. Extensive pretesting for these variables as well as the clinical ones
We've had a few members post about Richter's recently so I thought it might be time for a bit of an update on new treatments. In these reports there is not a lot of information about clonality and which mutations the patients have. Extensive pretesting for these variables as well as the clinical ones
Jm954
Administrator
in
CLL Support
1 month ago
Diagnosed with Richters
My history is a CLL diagnosis around Sept of 2016. I started the Ibrutinib/Venetoclax trial at MDA in Jan 2017 achieving MRD U in April 2019. Clear sailing until April ā22 when my blood test showed .07 CLL cells that doubled every 6 months. Showing no symptoms, my Doc did not recommend treatment.
My history is a CLL diagnosis around Sept of 2016. I started the Ibrutinib/Venetoclax trial at MDA in Jan 2017 achieving MRD U in April 2019. Clear sailing until April ā22 when my blood test showed .07 CLL cells that doubled every 6 months. Showing no symptoms, my Doc did not recommend treatment.
Louie_CC
in
CLL Support
1 month ago
11 months Post SCT
Iāve been wanting to update my Stem Cell Transplant journey with good news and today I was going to post that, instead Iāve been told that a lot of my lymph nodes are enlarged again. Itās so disappointing to say the least, not what I was expecting as I feel quite well and most of the GVHD issues have
Iāve been wanting to update my Stem Cell Transplant journey with good news and today I was going to post that, instead Iāve been told that a lot of my lymph nodes are enlarged again. Itās so disappointing to say the least, not what I was expecting as I feel quite well and most of the GVHD issues have
Billarina
in
CLL Support
2 months ago
SCT journey update No.4
Hi all, just to give you an update on my journey towards my *Allogenic Stem cell Transplant. Last tests @ Addenbrookes yesterday, was a very early start as Lung function testing was @ 8.30am and itās about 2 hour journey. Wife and I were up about 3-4am ( to be fair, couldnāt sleep anyway ) The drive
Hi all, just to give you an update on my journey towards my *Allogenic Stem cell Transplant. Last tests @ Addenbrookes yesterday, was a very early start as Lung function testing was @ 8.30am and itās about 2 hour journey. Wife and I were up about 3-4am ( to be fair, couldnāt sleep anyway ) The drive
LFCLove
in
MPN Voice
3 months ago
ASXL1 mutation 39% Worried about MF turning into leukemia
Hello Everyone, I have almost taken Rux for more than 7 years. and added interferon during the time. Actually my platelets are already very low now because of prolonged suppression of signaling pathways and the use of interferon. China site only available Rux in the markets. and I also have the ASXL1
Hello Everyone, I have almost taken Rux for more than 7 years. and added interferon during the time. Actually my platelets are already very low now because of prolonged suppression of signaling pathways and the use of interferon. China site only available Rux in the markets. and I also have the ASXL1
merlisa
in
Fight MPN
3 months ago
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