I am having major symptoms still, major burning/tingling in both hands, joint popping (sometimes pain), stiffness and tightness in my ribs(this one is 24/7 for the past month). I am pursing lyme, my Igenex tests arent in as yet but for the past week I have put myself on 400mg of Doxy a day and haven't seen any major differences. I will see a Stanford ID doctor this Tuesday. How are ya doing on the abx Ginak? How did your MRI's come out Stef?
Stef,
Sounds like you and Chris are in the clear. Padro, it sounds as if we have not made any more progress. Are you all still having symptoms? This is such a lonely feeling.
Doc advised he did not think it was Post Viral due to the time that has gone by--he advised he could see 15 weeks NOT 15 Months
Well Chris, you will have to let us know how your lyme test results are. I know someone who has lyme with neurological symptoms and it took a long time for her to get diagnosed. The doctors initially mistreated her when she was diagnosed and didn't give her antibiotics for a long enough period of time. She had many of the symptoms that we do and is now better. It took her a year of antibiotics that she took 4 times a day to get better. Ginak, hang in there, maybe you just need more time on the antibiotics. And Padro, I am curios too, why do they think it's not post viral anymore? You've had intestinal issues, did they test you for Celiac?
I go for my MRI tomorrow (Friday) of my brain and cervical spine with and without contrast. How is the procedure? Is it easy? I am so nervous. I requested an open MRI because I don't like enlcosed spaces. I have good days and bad days. One day my finger stiffness is better, but I may be twitching more. Then I have less tingling, but my back is tight and stiff. It is so bizarre to feel this way. I hate the tremors though. My hands and arms shake and it makes me feel so fragile sometimes. My neuro said that I am not weak and that the sensation of weakness that I am feeling is fatigue. She also mentioned chronic fatigue syndrome as a possibility. Who knows? I'm just thankful for this website. When I feel really down I read our posts and realize that other people have the same symptoms as me and I have hope that we are all going to be ok. I am trying to take the advice of one of the doctors that I work with and to try not to think about what my body is doing as much. He suggested that if I can just try to forget about it (much easier said than done since there are always symptoms) one day it just might be gone. He was giving me alot of examples of patients that he has had who let their mind kind of take over and how it made everything worse. I am not minimizing what we are all experiencing, because I know firsthand that my symptoms are not in my mind. I am just trying to focus a little less on them so I don't get so freaked out. I hope that after my MRI tomorrow I will feel better.
Glueclose Tolerence Test---The doc advised he would search for some things, he is also taking blood checking some Hormone levels as well--He is a Internal Med doc and said that Post Viral should not last as long as I have had it 16 Months--so it must be other issues. Post Viral is a cacth all when they dont know according to him
I am on abx-Doxy and a ton of other supplements. I am still having a lot of neurological symptoms. I really don't know what I have. I have been on Doxy for 3 weeks, still lots of ringing in the ear, tremors at night, muscle twitching at night, new symptom of tingling around mouth area. I just don't know anymore. Sometimes I feel like everyone else is getting better but me.
Padro, what is a GTT? Also, if the dr doesn't think Post Viral, what does he think this could be?