Experiences with

Hand pain

Recently experiencing moderately severe hand pain (trigger finger). MO says it’s from the ADT injection. I’m currently taking Eligard and on Erleada. Prescribed a prednisone pack and suggested tart cherry juice and glucosamine could help. Any other warriors dealing with this?

I posted this earlier as a part of a reply to another post [i]I saw the doc today as I have been getting extra pain across my right hand, palm and fingers which doesn't respond to pain killers, which really knocks out it being my OA, but may be a sign that it's PMR starting to reappear or even RA or

Hi warriors - my husband and 3.5 months post taxotere chemo. Now on lupron and Nubeqa. He is having pretty severe pain in his hands and feet. We have discussed this with oncologist and he wants us to work with GP until we can see other specialists (rheumatologist and Neurologist). We went down the rabbit

hi everyone, it’s been a while since I have been on here as I have not been well. Serval things have happened to me especially in the last 12 months. I had to have a full hysterectomy due to pain/lupus. I had a fall and dislocated my knee cap and damaged my ligaments on the inside of my left knee joint

I wonder if anyone has any experience of wearing arthritis gloves? I have a lot of pain and stiffness in my hands especially in the morning

I had my third face to face consultation with Rheumatologist this week and 2 things were decided which might be of interest to others with the same problem. 1) We discussed the continueous pain in my right hand, after a thorough exmination of joint movement in fingers, thumb and wrist, he ruled out

Hi everyone I thought it would be useful to update you on the hand pain I have recently experienced. On the sound advice of everyone on here, I increased my dose by 5 and a bit mg to 10mg daily.

all over joint, muscle pain, hand pain severe right now, 8 yes on prednisone, tapering to 3 1/2 mgs now, cant take anti inflammatorys wile taking pred

joints, hand pain especially unbearable, in process of tapering. From 4 mgs to 3 1/2, tild was arthritis, since on very low dose now wondering if could take aleve, or naproxen temporarily see if get some relief of pain, ?

I’ve had PMR for over seven years… I’ve managed it quite well with a few flares along the way.,I did get down to three and half m.g for a while but now I am back up to 5. Over the last few days i am having pain in my wrists and the back of my hands. I seem to be losing my grip.. is this another flare

I have a letter telling me to stop taking pain medication for four weeks Before my hand and foot scan.

(my hips stayed the same and my wrists much worse, but have had terrible hand pain from carpal tunnel so no wonder can rebuild bone with muscle work after surgery! )

Good morning, I'm suffering from severe hand and feet pain.

The nerve pain in my arms/hand and legs comes and goes but the mechanical pain is more frequent and ranges from mild to very painful. 80% of the time is manageable but the other 20% can unbearable.

Not saying the hand pain is related but does seem a bit of a coincidence.

the awful pain i had in my hands is just worse by the day, i thought it would go cos maybe gluten related but after setting doc she said she can see joints inflammation. nothing can be done except painkillers. now i’ve realised and admitted to myself that it is arthritis 😢 after all these years of

I have been taking shot of Prolia and shot of methotrexate every Tuesday.i have no pain but have tender spots on my head and if does not hurt to touch. I only seem to have it in my temple are and top and back of head.. I had a mri of my head a few years ago. I have had a couple of bad concussions 2

I actually think the leflunomide is working better for me than methotrexate, less hand pain and stiffness-yeah!!! However, the past month my hair has begun thinning terribly which is a known side effect of leflunomide.

Has anyone in our group tried the antispasmodic Spasfon? Generic name is Phloroglucinol. It is approved and is an over the counter medication in France, Spain and I believe in a few other countries but not in the U.S. The research studies that I reviewed shows promise for IBS-D related pain and

Source: https://www.youtube.com/watch?v=L6CtKeOAzGE BUT the likelihood of patients to respond to these treatments is lower if treated for 5+ years with dopaminergics. The reason being the upregulation of D1 receptor responsible for sensitivity to pain and abnormal sensations.