jeanoz
I’m going in for my third tennis elbow surgery and I believe it’s caused from PsA is there any information anyone has that I could give my orthopedic surgeon? When he did the surgery last time he said he didn’t see any signs of arthritis but I don’t think he understands PSA
Jill.Brodie Community Admin
Hi
Jill, Team Member
tiffany86 Member
Yes, tennis elbow can be caused by psoriatic arthritis. It causes inflammation where tendons and ligaments connect to bones. My rheumatologist told me this, and has had to give me steroid injections in my left elbow a couple of times the past few months.
robert Member
I got diagnosed with psa a few years back. At that time I wasn't experiencing the many varied symptoms I've dealt with since.
I did have a bout with tennis elbow. My daughter suggested I try some CBD oil for it, and to my surprise, it relieved the acute symptom within a day, or two.
I seem to have issues now with the lower part of my arms from elbow to wrists, weakness, stiff, heavy feeling, but no acute pain,
It seems from your posts we have similar symptoms.
My skin issues have been calm for the past year and I have no obvious changes in the appearance of my joints that I can see.
What does give me an annoying degree of discomfort are tendons in the neck, shoulders, and groin and hips. I had issues in my GI tract which have improved greatly in the past six months.
I'm not on any meds, yet.. They might be in my future.
I have pain, stiffness daily. I keep moving, but I'm constantly reminded things are different these days.
This mysterious disease is changing my life dramatically.
It plays with my mind, mood and physical abilities but,
Stay strong, good luck on your journey!
Lori.Foster Community Admin
Hi
robert Member
Thank you so much, Lori!
I did read the article and I'll re-read again.. I'm one of those who have been leary of the medicines available, or maybe, I'm in some sort of denial that I can get by without them.
I had started on methotrexate but my body didn't seem to like it and I told the rheumatologist I didn't want to go that route. There were financial challenges, too.
I said "thanks, but no thanks".. I'm sure he didn't intend to come off as arrogant but all he said was "you'll be back."
It's been robbing me more and more of what I used to be able to do, the things that I love to do. No one gets it. It affects my relationships. I don't like talking about it. That's why I come here. I have much in common with the people here.
I'll heed your words regarding (permanent damage) and consider talking with the reumotolgist again.
Thanks, again..
Jill.Brodie Community Admin
Hi @robert, I can totally understand your concern with medication. I wish this illness was not taking away the the things that you love to do. I am so glad you have found our community. You are welcome at any time to share or just to vent. We are here for you. Jill, Team Member