Author: msgracefulnot
Pushing my buttons…. battle of the sexes
Memories……
OMG, I don’t even know where to start!!!!!! Have you ever had a “battle, argument, disagreement or whatever” with someone that started as a somewhat serious issue, but just turned into the most laughable, ignorant thing ever. I am having so much trouble finding the words…… but Einstein has done it again…...DAMN BUTTON PUSHER!!!!
Ok So here’s the thing…. I am very very organized and have OCD about the cleanliness of my house….. most importantly things NOT being left on the floor. I can, and frequently do, trip on air, and have broken many bones from falling etc. ( to be honest though, I have probably always been OCD) Either way, I hate things on the floor!!!!!
Einstein has an issue with ….you guessed itleaving things on the floor….most notably his laundry. I have two hampers set up in our bedroom, the black one for his…
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Feel the Fear and DO IT ANYWAY!!!!
Remember THIS I love lucy type moment? I turned the camera on myself with no topic and lasted about 10 mintues. If you don’t remember, or haven’t seen the video, please check it out. I will try to make another one next week and see if I have improved at all
Two months ago, I decided to start a blog…this entire post is about my experiences in the last two months as I have challenged myself to step out of my comfort zone. (kind of like a roller coaster ride)
Today’s personal challenge was to make an unedited video and post it. TBH, I have been thinking about it for about a month now, and talking myself out of it for one reason or another……. but I finally jumped and did it.
Before you watch the video, if you choose to, let me again state that there is no real point to the video, except that I needed to challenge myself to do something I was afraid of and I did it and it didn’t kill me…..YET.… my stomach is still in knots….
I began my blog/ website (whatever the technical term is about 2 months ago.) I originally…
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It’s almost been a year
Sometimes it’s important to look at where you have been to remind yourself that you are going places, or to reassure yourself that you are moving in the “right direction”. This month is the one year anniversary of my blog, so I decided to spend some time reminiscing, not just about the contents of MY blog, but my entire blogging experience including the road blocks or problems that I created for myself. Who knew the experience would prove to be so rewarding?
I officially created my blog on September 30, 2017. In my first post, called “First Blog Post”, (I know how original right?) I attempted to explain what I was doing here. The goals for my blog etc.
Over the next week or so, I read any and everything that I could find about how to set up a blog (yes I now realize that MAYBE I should have done that first?!?!?) I read about copyright laws for photos, SEO, tried to understand backlinks etc. It really was NOT fun, and I ended each day with a migraine and a few of those days in tears. I started comparing my itty bitty baby blog to others thinking there was no way in hell I would ever measure up. But then I asked myself who was I competing with…. The answer was NO ONE but myself. I was at a turning point in my life and I didn’t know which direction I wanted to go next. The context of the next page I made is here under Disclaimer. (Now it looks nothing like the original, but the words are the same.)
During the month of October
I wrote about how and when I was diagnosed with MS, and how I decided to take the disease modifying drug that I am on. I have never been much of a writer, now talker on the other hand…., so I had NO IDEA how therapeutic writing could be. I couldn’t believe how much lighter my shoulders felt after “dumping it all out there.” I joined every facebook group I could find for Multiple Sclerosis and Tysabri. I wanted to help everyone, and be friends with everyone.
During the month of November
Looking back, I can tell you that is the single biggest MISTAKE, that I have made on my journey. I now realize I don’t want to spend my time with negative people!!!! As if dealing with MS isn’t enough, mean people suck! They literally suck the energy right out of you! I felt like I had run head first into a brick wall. I had spent so much time “friending” everyone that I neglected to be selective in the process. Even though, I had “met” and was still friends with some good people, I had let myself get sucked into a world of bitchy, whiny, sniveling people in Facebook groups. UGH!!!!! (Like I want to be sick ugh) People would complain that they were lonely and needed friends, yet didn’t want to do the work. Others would ask for help with an MS symptom, and when I would try to offer advice I literally got “yelled at” because I offended someone by being unsympathetic or condescending. SERIOUSLY?!?! I spent the rest of the month doing more soul searching. I spent less time in the FB groups, and more time seeking out positive people to spend my time with. I created an Instagram and a Twitter account, adding actually learning how to use them to my “to do list”.
The Month of December
I still had a “bad taste in my mouth” from all the cynical people from the Facebook Groups, so I spent less time there, and more time on WordPress. I began sharing what I thought were “funny events” in my life with my posts about Renaming my children and Not winning the mother of the Year Award. I pushed myself to see the positive in every negative situation that came up. In the process, I made some great friends. The kind that inspire you to be the best you. The kind that make you laugh, and are honest enough with you to tell you when you are being a dumbass. This is where I wanted to be!
In January 2018
It seemed like Everyone posted about new year’s resolutions. I didn’t have anything to say about that. I don’t make NY resolutions, for me it’s an everyday all the time “self check”. “Was I being the best ME that I could be?” “Would I be able to look at myself in the mirror in the morning if I had let the toxic thoughts that sometimes invaded my mind come out of my mouth?” NO I WOULDN’T. I felt that I was doing ok there, so I skipped the New Year’s resolutions lists.
When I originally started writing this, I was going to go month by month and talk about my experiences, but I am at 818 words already and since I usually lose interest around this time when I am reading a blog, I feel I should stop. I feel that I have been in survival mode for most of 2018, and I think it will be healthy for me to spend more time looking at where I have been this year, before deciding what my next steps are. Surprisingly for me I have made 148 post to date, and if I am going to reread them all, I had better get started.
Hope you all have a fantastic weekend!
ADL and Toe Mice
So Thursday’s post op visit with the surgeon didn’t quite go as expected. That isn’t to say I am disappointed with the results, it’s just that he said something I NEVER expected to hear….. EVER….
My friend Jeri picked me up and we, well she, drove to the doctor. My appointment was at 2:45, we where shown to a room at 3:45. (not bad as far as orthopedic visits go) I climb onto the table and the nurse begins asking me what my pain levels are. This is a trick question I am sure, because if I don’t walk on it and keep it elevated, my pain is pretty low on the scale. After I have been walking around a bit, or letting my foot hang down too long it climbs quickly. I told the truth…. kind of… I left out the part that I had been standing alot.
Do you want more pain pills?
I quickly answered, “NO!!!!!”, and pulled out the bottle of remaining pills that I had asking if she wanted them back. I can not stress enough, that I really don’t like the way the make me feel ( mood swings, maniac, nauseated etc.) and I NEED to be able to feel the pain to prevent me from overdoing things. I agreed to take Tylenol over the counter as needed. (in my opinion, advil is better at pain relief, but since I am a bleeder and it’s a blood thinner, I will stay away for now)
I took off the boot, the nurse removed the dressing, I took a quick picture, and then looked away. The doctor, and a student came in shortly after. As he pulled up a chair beside me to examine the stitches, he asked, “Did your father tell you what we found?”… I replied “um no, not really, he didn’t tell me that you FOUND anything, but what he did tell me was…… “So the doctor took off your big toe, reamed holes in your foot and then your toe, they put in a stud and then screwed your big toe back on”.” The doctor looked at the medical student and then back at me. He said, well “Yeah, that’s basically what we did”.
After seeing the horrified look on my face, he said, “No seriously though, let me tell you what we found.” “When I made the incision, two toe mice immediately popped out.”
ANOTHER Horrified look
“Toe Mites?”, I asked.
“No Toe Mice” he responded. and then continued, “It’s a medical term that we use to describe what we found.”
I really wish I had a picture of my face, because I can’t find the words to describe all of the things I was feeling at this point.
“Cmon doc, PLEASE tell me the truth, I am gullible as hell and completely disgusted that I have mice?!?!?!? My next step is to cry and I promise you don’t want that”.
He put his hand on my shoulder and said, “let me explain.” “First of all young lady, I can not believe that you were able to walk at all with the amount of damage in your foot. You had absolutely zero cartilage in your first metatarsal joint.” He pounded his fists together to demonstrate the bones hitting each other as I walked. He went on to explain that because I continued walking the bones starting splitting and breaking off into fragments (or mice). This had been happening for so long that the bones had turned into smooth marbles and kept chipping away more bone. The combination of those conditions, my unsteady gait, and whatever I was doing to compensate in my walking caused another break.
WOW that’s a lot of information. Crazy as hell too, but a lot to absorb.

As I tried to process what he was saying, he re-wrapped my foot in gauze and an ace wrap before sticking it back in the boot. While he says the incision is healing nicely, I am stuck with the stitches for another week still, but I am released to begin ADL in moderation.
ADL- Activities of Daily Living
Should be simple enough right? But for me it wasn’t….please take a minute to watch this video to understand why, especially if you don’t know me very well.
So this is what Jeri and I were doing BEFORE we saw the doctor. I get that I can’t use my right foot, so I thought we could just throw the ball and knock the beehive down. I didn’t realize that to get any “air” with the ball I would have to push off with……you guessed it, My foot….holy mother of……………………………
I was ready to give up, but Jeri was having fun, so I played video ographer…..
Anyway, I’m not sure that this is considered an activity of daily living, but since I do dumb shit like this all the time, I asked for further clarification. More specifically….
I am allowed to….
1. stand/or walk for no more than 5 minutes at a time. to be followed by a minimum of 1/2 hour break AND ONLY WITH THE BOOT ON
2. Take the boot off except for when walking or sleeping
3. I can resume sexual activities, so long as my toes don’t curl during orgasm (yes this was discussed)
I am not allowed to
- Curl my toes
- get the stitches wet
- put any weight on my foot without the boot
- specifically throw a ball at a bee hive
- mow my lawn
- go grocery shopping without a scooter
- drive 😦
I will call that progress……though not as much as I hoped



