Just diagnosed with osteoporosis. What are my options?

Have you had side affects from the Reclast infusions? I appreciate your information. It was one of the very few non-scary Reclast posts. My first infusion is at end of August and I can't stop reading posts about nightmarish side affects. While I understand that people who have good outcomes don't post about it very much it seems the bad outcomes are overwhelming. I saw endo in June and I wish the infusion was right away bcz waiting 2 months is pure agony. I am scared to death reading these posts and it was refreshing to hear someone's positive story so I thank you. Does anyone know if having mild TMJ is a concern when getting Reclast infusions or am I just making myself crazy because I feel crazy and confused and lost.