Teaching my phone to swear

Those of you that have ever talked to me on the phone, in person, gotten a text message from me etc, know that I have a “potty mouth”..  Not only do I frequently talk about “potty” and my bag of pee, but I just can’t seem to utter more than a few sentences without a cuss word or two popping out.  Popping, not pooping, although I do talk about pooping or not being able to alot also.

Last month, or the month before, I had to do a warranty trade on my smartphone, which in my opinion is Not very smart, although some would claim operator error. 😦

I have always struggled with the talk and type technology, because I speak quickly and do not enunciate.  This was proven when I asked my kids to “fix the damn phone” and they politely explained that I don’t enunciate when I speak.  To prove them wrong, I turned on the talk and type and said “ENUNCIATE”, the phone responded by typing E9C8!

SMDH AGAIN!

So now I have this ‘New’ smartphone AND I am cutting down on the number of cigarettes I smoke each day, in effort to quit on August 15, 2018, so needless to say I have been swearing a bit more lately.

After talking out a message that contained some “cuss words”, I forgot to turn off the talk and type feature on my phone before I said,

“It’s not duck, the word is fuck.  I really don’t understand your objection to ass, and on that note what the hell is wrong with shit or even hell?  It’s not like I used all the words in one sentence”

My phone typed….

” It’s not duck, the word is duck.  I really don’t understand your objection to ASK, and on that note what the he’ll is wrong with fit or even ****?

Immediately after reading that I said, “Bastard”, which for the record translated into “Last Turd”.

So I have decided to teach my phone to swear.  I have been correcting THEN saving each of the words that it misspells or ***** out.  So far I have added

piece of shit

fuck

shit

damn

hell

I cant say the C word, but it would probably come out as CANT anyway.

This morning I said, “I am coffeeing” which I know is technically not a word (its a way of life).  The phone typed doddering…which I left because I probably was.

Can you think of anything that I am missing?  When the day comes that I am finally ready to tell that ONE person that got on my last nerve off, I want to be prepared.

 

NOT THE TUBE!!!!

By the time this post appears, I am probably already stuffed in the tube for my annual MRI.  Nothing new really, I’ve only had 40 or more, I should be a professional by now.  But Today is a First for me.  I am going to attempt to go in without being drugged.  Lately, I have been pushing myself to do things outside my comfort zone, you know like dealing with FEELINGS and shit….. :(,  So I figured why the hell not….?

Tonight (well now last night) Thing two looked at the dry erase board with all of our schedules on it.  She saw that I was scheduled for an MRI at 10 AM Friday, and asked who was taking me.  Like a proud 4 year old that learned to tie their shoes, I replied, “I’m going by myself.”….. The NEIGHBORS could hear her laughing……smh heh Thanks for the support kid!

I guess I should start at the beginning and maybe share some of my MRI tragedies with you.  The very first time I went in for an MRI was 20 years ago, when I was diagnosed with Multiple Sclerosis.  I had never even heard of such a thing.  The doctor explained,  “it’s just a glorified xray machine, but it will take much better pictures”.  If she was still in practice I would find her and let her know exactly how I feel about her bullshit explanation by placing my foot in her ass.   SMH….

So about 20 years ago, My sister in law and I show up at the hospital for my first MRI of my brain. I thought they were looking for a pinched nerve or something simple to explain the numbness in the left side of my body.

c spine coilI was 25 and had no idea that I was claustrophobic.  I laid down on the table and they put something that is called a coil around my head.

Coil my ass!  This thing felt like a vice and I couldn’t breathe!

While they were trying to calm me down, the doctor called down to say that she wanted a cervical spine and thoracic MRI as well with GAD otherwise known as Gadolinium for contrast.  This meant another coil and two more hours to the one I was already committed for.  The second coil looks like this.

head neck

Oh fuck no!  Although the coil is very lightweight, it felt like 100 lbs on my chest.  I started panicking  and hyperventilating before they even put me in the tube!!!!

Hey guess what…. I’m claustrophobic as fuck!!!!!!

They called the doctor back and told her I was being ‘uncooperative’, could they give me something to relax me?  After all these years, I still can’t believe I was the first person to ever freak out about being put in a tube, in fact I am positive that I wasn’t.  Seriously though, no warning!!!!

I don’t know what they gave me to sedate me, but I kind of remember climbing back onto the table, being “strapped down”, given a little “panic bulb” and being  pushed inside the machine.  I must have fallen asleep.  When I woke up, still inside the machine, I tried to squeeze the little panic bulb, but I had dropped in in my sleep.

I started yelling, and kicking the machine from the inside.  No one was coming!!!!!  My sister in law could here me yelling in the waiting room and came busting through the door yelling, “can’t you hear her in there, get her out!!!!”…. That is the LAST time I ever let anyone put me in an MRI machine without being drugged to some degree.

In fact this is the perfect time to share another MRI mishap.  It was 5 years and several MRI’s after that first bad experience.  This time I was going to be smart though…or so I thought…. I had scheduled the MRI for 6 am on Black Friday.  My thoughts were, that I would stay up the entire night before shopping and I would be so exhausted that I wouldn’t need as many drugs to go in the tube.  Sounds like a good plan right?

We went to Thanksgiving at my parents, did black Friday shopping, but I couldn’t stay awake.  The last time I looked at the clock it was 2 am Friday morning.  The next time I looked at the clock it was 11:30 am.  I started yelling at my husband, why didn’t you wake me?  I had to be at the hospital by 6 am!!!!  When I stopped yelling, he said, “Grace, you were at the hospital and you had your MRI, Honey it’s 11:30 on Saturday!”

NO fricking way!!!!!

My stomach was growling so loudly, so I went in the fridge to find something to eat.

veggie tray I found something like this with a section filled with turkey, another with sweet potatoes, and so on and so on.

When I finished stuffing my face, I told Ken that he his idea of filling the veggie tray with leftovers was brilliant.

He responded, “I didn’t do it, you did.”  “after we went for your mri, we stopped by your parents, you ate almost a full plate of deviled eggs, and filled this up with leftovers”

I have absolutely no recollection of anything after 2 am Friday morning.  Apparently, everything he said was true though.  Looking back, I Think I self medicated TOO much.  That’s the only explanation for it.

I really scared the shit out of myself with that one!

Since that time, I have learned better and SAFER coping mechanisms for being placed in the tube, but it has taken me years to work up to this.

  1.  I know how to disconnect the coil myself.
  2.  I only schedule one mri at a time.
  3. I do keep my eyes closed the entire time.
  4. I keep the music on very loudly in the headphones
  5. I “tie” the panic bulb around my hand
  6. I make the technician talk to me between each picture and tell me how long the next image will take.  (so I can break it down into 5 minute segments)
  7. and perhaps most importantly, I go to the same place with the same technicians each time, so I have developed a bit of trust for them.
  8. I know that if I can’t make it, I always have the option of LIMITED drugs

I hope to write tomorrow (later today) that it was a piece of cake.  I have to try!  MS is not going away, nor are the yearly MRI requirements to stay on Tysabri, so I might as well give it a shot.  If you are interested in learning more about my experiences, with Tysabri, please type tysabri in the search box, I think I have made several posts.

How do you deal with repeated MRI’s?  Any tips?

 

7 day B&W Photo Challenge Day 0 (my rules)

I was tagged a few days ago to participate in the black and white photo challenge by Kim author of I Tripped Over a Stone.  If you haven’t “met” Kim or visited her website, please do.  Kim’s blog is primarily geared toward living with Fibromyalgia, but it’s not only informative about her disease, she offers great advice and support for so many people no matter what they have on their plate.  I definitely consider myself blessed to be able to call her my friend.

When Kim tagged me a few days ago, I only saw the words “post a black and white picture for the next 7 days”….. OK, I can do that.  I took black and white photography in college, I will just upload some old images…..never did it occur to me that I could just use my phone and edit on the computer.  (technologically challenged much?)

So the rules…..

You know there are always rules to everything in life! The rules for this are straightforward. Seven days. Seven black and white photos of your life. No people. No explanation. Challenge someone new each day.

Tomorrow, I will follow the rules, but first I would like to share some of the pictures I took 20 years ago….just because I dug them out 😛  I don’t remember what the assignment was…. I think something about shadows?

If I tag you this week, please don’t feel like you have to join the challenge.  After rereading the rules… I really do like the part about  Seven black and white photos of YOUR LIFE. 

I’m curious to see the world through your lens!!!!!

Will you hold the flashlight?

So Yeah, I’m in a really dark place right now…. I chuckle as I say that because I think it almost goes without saying if you have talked with me recently, or read anything that I have written in the last month or so.

So now what?  What’s next?  What’s the plan?  How do I fix this?

I’m gonna stay right here for a little while and just be.  I am going to let myself FEEL each emotion GOOD, BAD, or UGLY and NOT judge them.  I am also not going to give myself a time limit on this.

I have mentioned before that I don’t “do feelings” well.  When I ‘mention’ it though, I say it offhandedly or in a joking matter, as I immediately begin looking for the next task or chore I am supposed to complete. (anything that I can do to “get out of my head”)

Over the last couple months, I have tried eating, drinking too much, smoking more, taking xanax and sleeping as much as possible.  If you have tried these things you know that they don’t really help, and are a temporary fix at best.  In fact, usually as in my case, they cause more problems.

So for now, I’m done running.  I need to sit in the dark a bit and just be, without a time limit.  I am, however, asking for someone to ‘hold the flashlight’ as I let my eyes adjust to the darkness that I have let consume me.

As I get ready to hit enter, I am acknowledging that I feel Fear.  I also feel vulnerable, and kind of weak at the moment.  I know these feelings will pass, but they are there.

ME and my bag of PEE

I wrote last week that I was going on another “adventure”.  Maybe I shouldn’t have SAID anything?… Somehow MS found out that I am going away and decided that there was no way in hell I would be traveling without it.  GRRRRR

I realize that MS has a place in my life.  I make room and accommodate it’s demands all the time, but just ONCE I would like it to stay in the background a little more.

I should probably get to the actual point of this rant huh?

As I finished packing this morning, I had to pee again FOR THE 4th TIME IN LESS THAN AN HOUR!!!! Seriously?!?!  I just had PTNS last week, and Botox surgery in February for this.  I shouldn’t be having problems again this soon!

Thinking that it is  better to be safe than sorry, I called the doctor’s office.  They agreed that maybe I had a UTI and should come in to rule that out.  (yah for getting me in so quickly)…. Urine test complete, no UTI, but they still want to put me on antibiotics anyway, and suggested I use the Foley catheter for my whole trip. 😦

I am actually ok with having to use the catheter, lord knows I’ve been dealing with incontinence long enough, and who would want to have to pull off the interstate 4 times an hour for a 16 hour road trip?  The thing that stresses me out is having to deal with people’s reactions to seeing someone with a bag of pee strapped to their leg in public.

Well you could cover it up Grace?

Why?  So other people are more comfortable?  Not a chance!  The weather in Texas and Las Vegas is supposed to be in the 100’s, no chance in hell I am going to wear pants.  I have already given up half of my suitcase for incontinence supplies, medications, and such.  The only way I have half a chance in hell of surviving the heat is wearing shorts and tshirts or tank tops.  I had hoped to stay in/or by the pool while in Vegas, and I realize if I can’t get these symptoms to calm down I MIGHT have to give that idea up though :(… we shall see….

I’ve got this!…The only thing left is to come up with a name for my “companion”….Any suggestions?