Neuromuscular   

Are there any protocols in place? Aside from telling patients to use ice packs or bags or immerse hands/feet in ice water baths from 15" before to 15"...

Have you tried Vitamin K2? In light of a recent publication: Tan et al., PMID 39466236

B5 deficiency can be seen in patients with burning feet syndrome, do you typically screen for this when assessing for neuropathy?

When it seems fairly certain that this is a drug effect is it something that can just be monitored or requires a change in approach?

How do you counsel young adults with antibody-negative necrotizing myopathy on prognosis, risk of recurrence, and long-term monitoring/treatment?

What referrals do you recommend/imaging orders?