The person I know who was diagnosed with EDS did not have pain.
He was diagnosed based on his flexible joints as the main symptom. I think he also had the 'soft' skin...sorry I can't remember. But, definitely no pain.
When I was looking into whether my son had EDS - he also never had pain.. but that wasn't even a factor at the time.
There are many types of EDS and various symptoms.
If your pain came on since Lyme disease - then it's likely from LD.
What Im trying to say - is maybe you've had EDS all along but the pain is from Lyme. Muscle and joint pain is very very common with LD patients.
If I were you - I would focus on Lyme treatment and try not to worry at this point whether the joint pain is from EDS or Lyme. If it is from EDS - there isn't any treatment anyway, right?
Moderator, Lyme Forum
Symp started April/2013; Buhner's Lyme May 15-July24/14; Igenex pos. July 3/14
Doxy: July 4-Aug.24/14;Zithro July26-Aug24/14; Amox + Proben. Aug. 29/14;
added biaxin Sept. 26/14
Disc. amox,added Ceftin Nov. 20th.;
Disc. biaxin added Buhner bart herbs Dec/14;Jan/15 pulsing Tinda (w/ Ceftin);
Abx/herb break Apr-July/15; July-mino; Aug. added Rif;
Nov./15 mino - to biaxi
Post Edited (Girlie) : 11/27/2017 3:44:52 PM (GMT-7)