Has anyone who is on treatment noticed their grip getting weaker? I haven't had any joint issues except for my left si joint this whole time but since I started treatment this week I swear I am noticing I can't grip a pen like I use to which scares me. My LLMD said to stop taking the meds if I felt something wrong in my gut (meaning more harm than good not my actual gut functions) but I know I have to get worse before I get better. Oh the troubles. :(
29, F prior to Feb '13 healthy, outgoing, dating, active, worked out 4 times a week, taking no medications only multivitamin/calcium.
Current: Dizziness, numb tongue, si joint pain, fatigue, numbness in left leg/arm, anxiety, out of body feeling that comes and goes, floaters, light/heat sensitivity, pain in rib cage, stay home except for work.
Lyme Diagnosis:2/2014, MTHFRC667T gene mutation (1
Post Edited (gingeranne8) : 4/11/2014 11:08:29 AM (GMT-6)