← Return to Symptoms Concentrated in Legs?

Discussion

Symptoms Concentrated in Legs?

Polymyalgia Rheumatica (PMR) | Last Active: Mar 23, 2024 | Replies (8)

Comment receiving replies
@nyxygirl

I agree with John - recently my sister had a bout of pain, because I have PMR ( and our cousin 10 yrs ago) she already knew what that was .
But she had positive Rh factor AND she has pain in her feet -basically PMR has been ruled out. And her rheumatologist used this term: ENTHESITIS (which i had heard of on THIS site - can't remember who said it )
https://creakyjoints.org/living-with-arthritis/symptoms/what-is-enthesitis/
She will be having an ultrasound soon .

Jump to this post


Replies to "I agree with John - recently my sister had a bout of pain, because I have..."

Oh no! Glad your sister is getting it checked out. It may have been me—I have an inflammatory arthritis that causes enthesitis (inflammation where the tendons insert into the bones). It’s very painful, but much more localized than I would imagine PMR to be (my dad is the one with PMR).

I read the updates on this forum when I wake up in the morning before I get out of bed. Today this enthesitis topic hit me right in the face so to speak. I have literally been hobbling around the last three days with heel pain. I had this once before awhile back, went to the foot Dr in my orthopedic group and got diagnosed with Haglund's deformity. I did some PT which helped somewhat. What really helped was wearing open backed clog type shoes. About a month ago I went to this Dr because I could hardly walk, the top of my foot was swollen. I assumed it was from previous OA surgery at the base of my big toe. I opted for a cortisone injection and it got better. This week it's the heel pain. He already told me heel injections are a no-no. So this will be day 4 of limping and my bag of frozen peas on my heel throughout the day. My heel is swollen, has a lump and is red. Walking is very difficult. Enthesitis or Haglund's deformity??
I have been on 3mg pred for weeks now, just started my 6th year of pmr. The last 3 months my crp has been elevated, sed rate is normal. I have tolerable morning pain, stiffness but I am fighting increasing the pred dose. Rheum will tell me to try the mtx again, am not taking mtx. I don't see rheum until May.
I see my pcp on Monday and will be making a list of questions.
I did ger up a little while ago, made chamomile tea and took tylenol.