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)What do you do? do you take meds? do physical therapy? do hot baths.???
cece

i cant even leave the room when i have students in class- also i have teens!! for 90 min per period... just wondering if there was anyone else dumb enough to try to teach and deal w/ this monster! 
I am not a teacher, but I know alot of people who are...and I do work that requires me to be "on", keep a smile on my face at all times, allows little time for rest, and is quiet laborious...I'm a massage therapist at a 5 star resort hotel. And it's not so much what I do during my time there, but what I do when I'm at home...
At home is when I stretch and breathe, take hot baths and recharge, reach out to my loved ones who are kind and supportive...I know you probably have to bring alot of your work home with you, but taking as much time as you can to do things that rejuvenate your body and your soul are extremely important...
However, there are things I do at work...In the 15 minutes I have between appointments, after changing the linens on the table and setting my supplies up, I do a little light stretching or I sit down and I breathe, even if it's just for a few minutes...I stare out the window at a pretty tree or any birds that might be flying around...or I drink some water and scarf down an energy bar...whatever I can get in in the few moments I have...
I hope some of this helps...I can't even begin to imagine what it's like to teach teenagers, especially in today's world...I commend you for your hard work and your perseverance! Good luck and keep coming back for more knowledge and support!
Soft hugs,
~Susan~
I am a teacher with fibromyalgia, so yes, I do know the unique difficulties in getting through the days as a role model to teens.
I must admit, however, that I do not teach in a classroom setting anymore. Thank goodness. (More on that later.) I am now an Independent Study teacher, so I meet with the students more on a one-to-one basis.
When I did teach in the classroom, I often befriended my students. I explained my condition and difficulties. Surprisingly, they were actually quite understanding and helpful. We would joke about my "brain farts" in the middle of an Algebra lesson. So, that became an opportune time for one of the students to come to the rescue, to review what we had covered and where it was going next. Sometimes, we all groaned when I told them, "Sorry, I need a break right now, so it's worksheet time." Then, I would just ease up on everything until I could muster myself back up.
Obviously, I made changes though. I saw that I was not going to be able to keep the neck-breaking, bell-ringing schedule. I don't know how anyone can really keep that pace for an approximate 30-year career. Luckily, I have the flexibility that I need in the alternative ed setting now.
I might also mention that I get an ADA accomodation as well. Fibromyalgia is a qualifying condition. I currently have a schedule that gives me Wednesdays off, so that I can rest from the daily grind that can be so difficult to maintain. In your situation, it might be having 1st period prep so that you can have more time in the morning to get going. (Just a suggestion.)
I don't know your climate and environment, but I had to fight for my rights. I got information from JAN Network on the Internet, got the backing of my union, and jumped through all the dr. and paperwork hoops. It took 1/2 the school year to do that. But in the end, for my situation, my request was reasonable and the district had to accomodate.
I hope that gives you ideas for help and encouragement that things can be changed for the better.
But i know the truth of having to change to a less stressful situaion- i feel hopeful to see that you have done so!
Sad to say, when i have tried to bring the class in on how i am feeling- many of the boys used it against me- one even told me to 'get out of his face and go take my meds"- this was an honors 12 english class... am considering just not saying anything at all this year, and just dealing with situations as they arise. i am much better adjusted on meds, re dry mouth, etc... but i do still have A LOT of brain farts... it hurts to not be ' on my game' like i used to be....
Anyway- sorry to be so long- just curoious about the ADA stuff, like do i have to register myself with some gov agency? if you can tell me more
and thanks!!
I know that there are rules here about how other sites are posted, so I hope I am doing this right. If not, those of you who know better of how I should be posting reference, just go ahead and let me have it -- the correct info, that is.

http://askjan.org/
This site is called JAN for Job Accomodation Network. It has excellent references to ADA laws and information. I had to call them, and I actually got an expert on fibromyalgia. He was quite knowledgeable and answered all my questions. He explained what I needed to do, and what to do if I had any problems.
Secondly, I would suggest you get a union rep to support you. Not only is there comfort in the comraderie, but they can go to meetings with/for you. Finally, the union rep needs to know what is going on, so if you do need an attorney, the union will be on board and supply one for you. Just a word of warning, most school districts do not give accomodation(s) without a fight. Or at least a little bluster.
Finally, don't give up your career too easily. There are a lot of benefits that go along with that pay, like medical, retirement, and even tenure. My accomodation has made it to where I can function and not give up the life I worked so hard to do.
BUT I won't give up!!!!

When I drove a school bus I just stuck with the autistic ones and when I made a wrong turn I just said we were taking the scenic tour.
I had always meant to go back to school and teach but after fibro fog came along I am not sure if I could have ever kept the pace you teachers must so my hat is off to those who can teach with fibro. I gave up the teaching/driving instructions part of my job 7 yrs into fibro and was just a bus driver.
laurab

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