Question: Hi. I recently turned 40 in Dec 2018. I suffered a cva: 2 MRI confirmed : right parietal juxta cortical region parafalx on 12 XXXXXXX 2019, but have made a full recovery (after experiencing left arm loss proprioception and sensation as well as weakness and loss of range of motion for 3 days, with inital loss of coordination and abnormal sensation in lower limb as well- although briefly). CT angio was clear as was echo. TOE found a PFO and after bubble injection and valsalva confirmed paradoxical flow. I am taking warfarin. Along with this, i had a Erythema nodosum rash two weeks prior to the cva and ANA titre 1:160 suggesting autoimmune reaction. Along with this, i have clinical features of ehlers-danlos syndrome (stretchy translucent skin of hands and feet, stretchy eyelids, soft doughy skin, high arch in palate, fallen arches in feet, clawing of toes, right shoulder dislocations x25, lax ligaments, big eyes, short stature, long arms). The Opthalmologist has examined and content with vascular and pressure in eyes. There are 3 possible causes of the cva, but taking warfarin may be contraindicated in ehlers-danlos type4. Am having follow up with neurologist in 2weeks time and redoing ANA in April. Should i have the genetic testing done for ehlers-danlos, as this is very expensive and only offered overseas -R33000.00? Am i being managed fairly or should i be seeking additional opinions/investigations?