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@johnbishop

Welcome @michc, While you wait to see if anyone else with EDS has experienced similar problems with fingers, I thought you might find this information from Mayo Clinic which mentions some additional noninvasive treatments helpful.
--- Trigger Finger - Diagnosis and treatment: https://www.mayoclinic.org/diseases-conditions/trigger-finger/diagnosis-treatment/drc-20365148.

Did your hand specialist suggest any therapy or stretching exercises to help the mobility of your finger?

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Replies to "Welcome @michc, While you wait to see if anyone else with EDS has experienced similar problems..."

Hi, Thank you for the link. I did ask for recommended non invasive specialized therapy for people with EDS. He just told me to take the anti-inflammatory and see him in 6-8 weeks if it doesn’t improve for a steroid shot. That’s why I switched to someone else. I gently massage the fascia. I try to keep it straight especially at night, because in the morning it’s locked in super tight. I can hear and feel it click as I maneuver it to open.