feeling ignored

hello everyone, I just want to say thank you in advance for any support or advice you can provide me. I have been feeling so alone through this diagnosis and finding myself with more and more unanswered questions. I am trying to do my own research and advocate for myself but it has been very hard. 

my story (TW: sexual assault) - 

a full year ago I was forced into unwanted, nonconsensual sex with someone that did not involve a condom. I believe this was how I contracted the Mgen and have been plagued with this bacteria and yeast infections since. over the last year I have struggled with recurring yeast infections. I have made many visits to various doctors trying to figure out the underlying issue of why i am getting wrecked with yeast infections when I have previously never had one in my life. the very first visit I made to urgent care regarding yeast I tested positive for yeast cells and also positive for abnormal clue cells. now, I know the abnormal clue cells could have been an indicator of BV, along with the yeast, but I was not having any odor or BV symptoms at the time of the yeast infection. they are similar, so I guess it is hard to tell.

anyway, my most recent sexual partner tested positive for Mgen after he told his doctor that I struggled with yeast infections. I find it very frustrating that none of the medical professionals that I have seen in the last year (2 urgent care doctors, 2 family practice/primary doctors) thought to also test me for Mgen. each time I visited for yeast issues, I had SPECIFICALLY asked for a FULL STI panel. is it possible that I have been dealing with Mgen infection for a year and the symptoms of it are chronic yeast infections? I feel so defeated and ignored that my male sexual partner received tests for this after telling the dr that his partner (me) was struggling with yeast. yet none of my doctors listened to me or thought to test me for other STIs not included in the normal tests.

after receiving my positive results for Mgen, my doctor prescribed me one week of doxycycline (100mg, 2x a day) + one week of moxifloxacin (400mg, 1x a day). day 2 of taking the doxy, 4 pills, I broke out in a horrible itchy/stinging rash on my neck, chest, shoulders, and legs. I have no history of medical allergies other than seasonal allergies but I do have occasional eczema breakouts. I contacted my doctor twice yesterday feeling desperate and annoyed. a nurse finally called me this morning and said to stop the doxy and move on to the moxi. will only one 2 days of doxy and 1 week of the moxi be effective enough treatment? they told me to finish the 7 moxy pills and then test again in 2-3 months. I am extremely worried that this won't be effective enough to treat the Mgen and don't want to wait 2-3 months to find out if it even worked. obviously I will be finding a new doctor as I have yet to have one positive interaction at this place. I have asked them many questions regarding yeast infection prevention while on antibiotics, the allergic reaction, and the efficacy of shortening my antibiotic treatments. I always end the phone conversations feeling more confused and ignored than when I started. 

thank you if you made it this far, I just really needed to tell my story and wish I had someone to hold my hand and tell me it will all be okay. I wish I had more answers about the timeline in hopes that treating the Mgen will treat the chronic yeast.

TLDR; questions I am still left with:

  1. is it possible that the test for abnormal clue cells was an indication of Mgen?

  2. are the chronic yeast infections an indication of Mgen or is this a separate issue? is this something I can ever find out? (i guess yes, if the yeast stops if/when the Mgen clears)

  3. is there more I can do for yeast infection prevention? I am taking a daily probiotic (on an empty stomach ~30min before a meal) and plan to use boric acid suppositories at night

  4. most importantly - will taking only 1 week of moxifloxacin be effective enough to clear the Mgen or will I need to advocate more for myself?