Education, Hashimotos, Hypothyroidism, Teaching

Hashimoto’s, Hypothyroidism and Autoimmune Deficiency = Me!  A High School Teacher.

I get to navigate through a whole new experience.  I tread lightly because I really don’t know where this is going to take me.  

 I’ve always cheered for the home team or underdog.  It’s just part of my nature.  I found my calling in the field of Education  just after my sophomore year in high school.  I delved and dug.  I asked Veteran Teachers.  I asked Academic Advisers.  Everything just seemed to fall into place and point me in the direction of teaching high school English.  

Folks already in the field told me that their profession was anything but easy.  They warned of late nights grading and weekends spent in the school building making copies and writing lesson plans.  God forbid the evenings of writing sub plans with Kleenex in one hand and a pen in the other.  It really is easier to suffer through work with the flu than writing Sub-Plans- no lie.  Public schools are full of sniffles, coughs and germs looking for new hosts.  

All mentors conceded to “…tenure status being the saving grace in the stress of high school teaching”.  That was in 1994. 

 I graduated college with a double major in Extended-English and Secondary Education.  Somehow my first “real” job was in 1998, teaching Kindergarten… talk about runny noses and sticky hands.  This lasted for five years.  Note, this assignment was not high school nor English specific.  However it was a nice introduction to the field and I am forever grateful.  Those kids taught me a lot!

By 2003, I was ready for the student loans to pay off -so to speak.  It’s now 2016, half way through the academic calendar and I am still fulfilling my calling.  Shakespeare, Poe, Prepositions, Diagraming Sentences, College Application Essays, Harper Lee… sigh, thump of my heart, breathe.  Yet,  I fear that it may be time to stop.  Gasp!  Nooooooooooo!

Things are changing.  I am changing.  I struggle with being “myself”.  Simple add on to teaching duties are becoming chores and more difficult this year.  Is it age?  Is it menopause?  

You see, three years ago I sought the advice of my local practitioner regarding the following symptoms:  fatigue, headaches, depression, anxiety, temperature hypersensitivity, lack of desire for anyone/thing.  I had a nasty run-in with hives on my upper torso and random food allergies.  She ordered the tests and my blood was drawn.

My blood work came back to say “Help Needed!”  I was forwarded to a Endocrinologist, Psychiatrist, and Gynecologist.  But I was busy teaching, broadcasting sports events, working with students on the school yearbook and trying to be a decent daughter, wife, community member and tutor.  Something would have to give.

On the day before Winter Break 2014, I had my first, full-scale, anxiety attack.  I was a mess.  My principal found me climbing into my desk and sobbing.  He needed to hand me a copy of my disciplinary letter.  You know.  The kind they put into a personnel folder because you screwed up.  

I’ve NEVER, EVER gotten a reprimand before!  This was nuts.  I was losing “it” and hating myself more than usual.  My husband knew it and my students were catching “wind” of it through the daily interactions.  I had to do something.  My world was falling apart.  Why?! 

Angry and cruel internal dialogue put me in a very dark place.  You know, the kind of place.  I made appointments and started my journey into understanding my body.

Hashimotos disease with hypothyroidism seemed to be the one diagnosis that everyone in the medical field could agree on.  Having Autoimmune Deficiency allowed Hashimotos to hold hands with Hypothyroidism and all sorts of vitamin deficiencies.  The psychiatrist did away with my current medications and started a whole new regimen.  The Gynecologist offered ablation to help with the hormonal fluctuations and pain in being a female.  Keep in mind, this started in January of 2015.  I had to manage it all while staying committed to my teaching duties.  I did!  I was.  At least I thought I was.  I’m not.  I wasn’t.

Instead, I am forgetful, exhausted, moody, overwhelmed, panicky, awful and lonely.  I’m afraid that I’m losing “it” and won’t be able to get “it” back.  My name is the same, but my demeanor is a whole different story.  Every blog, magazine article, medical journal, and website says the same thing… 

This is going to hurt and it is NOT going away.

Teaching, in and of itself, is difficult.  The stressors with the ever changing habits of teens, scoring/grading, mounting pressures from administrators, curricula, professional development, directives and testing are enough to have a perfectly healthy individual experience stress eating as well as sleep deprivation.  Imagine what it does to a person with Hashimotos Disease, Hypothyroidism plus Autoimmune Deficiency syndrome. 

It is painful -both emotionally and physically.  Frustration and humiliation are running amok.

I am at a loss.  I am too distraught to be sad.  I am too tired to fight.  I have lost touch with friends and hobbies.  My weight or physical size has grown in the wrong direction.  My patience is at an all time low.  

I look forward to sleep (the good, deep, relaxing kind) and quiet time.  I have changed my daily diet only to change it back.  My hair is falling out and my skin is dry like paper. I order a special vitamin for that.  I even forget words or ideas within moments of mentally drumming them up. 

I get seizures now. Those are surreal. I seldom remember them unless reminded by another person (i.e. my husband who held me through it). They scare us both.  I have a pill for those now.  My medications are tweaked every three weeks to three months.  Better living through chemistry, right?  

 Fun stuff! 


 (Yes, Sheldon, that was sarcasm.) 

Reality isn’t really fun right now…

I’m worried that my disease has become a  real disability.  It’s affecting my home, work and social life.  I have qualified for FMLA due to my increasing sick days.  The Amercian Disabilities Act has a section just for Thyroid issues.  There are work place accommodations listed that (before 2014) I would have never needed.   It’s a good start, but my system needs so much more attention, understanding and help.  A “scheduled potty break” in the afternoon just isn’t going to cut it for me.

Obviously Hashimotos doesn’t seem to bode well with High School -right now.  

Flare-ups, seizures, high anxiety levels, pressure, stress, fatigue, mystery body aches and mood swings are not conducive to the classroom environment.  I struggle with all of these things DAILY.   I feel like my body is at war within itself.  OH!  Wait!  IT IS !  

So, do I redial my calling or what?  Hashimotos and High School… (sigh).

3 thoughts on “Hashimoto’s, Hypothyroidism and Autoimmune Deficiency = Me!  A High School Teacher.”

  1. You need to get tested for Mast Cell Activation Syndrome. They need to check your Prostaglandins and your tryptase levels. If your Prostaglandins are high but your tryptase is normal, chances are you have MCAS. This is a relatively new illness that most doctors don’t know about. The Mayo diagnosed mine. The NIH can also diagnose- if you can get in. But Dr. Afrin at University of Minn is an expert. He will work with your doctor on diagnosing and treatment.

    You can get his book Never Bet Against Occam at Amazon. I tried the library but mine didn’t have it.

    These conditions and symptoms are typical MCAS reactions.

    Liked by 1 person

  2. Hello! A day in the life of someone who has hashi’s! I know exactly how you feel as I sit here with lack of focus and brain fog as I leave this comment. I say good job to you for fighting and pushing through your days! Thats how it is! Its all about balance. But even “balancing” everything can be exhausting! Keep being strong and I’m so proud that you continue fighting everyday!

    Liked by 1 person

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