Skip to main content

Argh Matey, Me Eyes...

Thankful for Halloween:

One picture can say a lot. For example:  This picture (besides saying I just woke up) Also, say a few other things:  I have lung problems (Cystic Fibrosis) since I'm doing a vest treatment & nebulizer, It's Halloween or I have eye problems.


Well, actually it's all three! I'm thankful it's Halloween, because it makes my eye patch blend in more.
Why am I wearing an eye patch? I don't wear glasses or contacts, right....

Did you know that I did have glasses for many years. I had such bad eye sight that as a baby that I got my first set of (thick) glasses by 6 months old.  I had bifocals by the age of three. However, the eye problems were corrected (sort of) by age 11 and I could ditch the glasses.  Only in the last year have I noticed them coming back. Lately, they have been pretty bad. I've hit more curbs while driving and stopped driving at night all together.I keep running into things and tripping, I'm usually accident prone to begin with...But not to this extent. Clearly, it is time to take action.

It's mostly depth perception problems that stem from my right eye. The problem has always been with my right eye, it's muscles are too weak to focus. So if I close my left eye I can't read. I can recognize words, but can't follow a sentence across, because I can't focus. This may explain why I have had more headaches recently and why I'm not a big fan of reading latetly (sadness). Eye focusing problems run in my family. I have two cousins who have to look certain ways in order to see. One is not as bad and not noticeable at all. The other younger cousin has to always turn her head completely to the side to see, she can only see out of the corner of her eyes. 

So I probably have some genetic disposition for eye problems, but I also have mild Cerebral Palsy. To read more about my years doing physical therapy & wearing a leg brace, which pretty much lead to me loving dance and performing click HERE!  My CP only affects the right side of me. My right foot is 1.5 size smaller than my left and the leg is slightly shorter too. I have always struggled to use my right hand with certain fine tuned skills. I can't tie a shoe to this day. I have trouble doing anything that takes skill from both hands. Forget playing instruments, chopping vegetables, most sports etc. My right hand just doesn't listen to me sometimes, same thing is happening with my right eye again.

I wear the patch over my left eye, to force my right to work harder (like physical therapy for the eye). I also scheduled an appointment at the eye doctors. But until my appointment, I get to wear this patch and see if it helps. 

But like I said Luckily it's Halloween and I can pretend I'm just rocking the pirate look! 

ARGH, Matey, Andrew & I are getting our pumpkins tonight!!!!!! YAY! 

Here are the last two years' pumpkins we did...

                       2013: Mine is the Spider & Andrew's the face     
   


        2014: Mine is Jack Skellington & Andrew's the Minion



Please Note: I don't carve pumpkins with my depth perception problems, I draw & he carves...

 I will be sure to share pictures after we carve them! Keep updated on my CF Blog Facebook Page!

Comments

Popular posts from this blog

Today's BIG Appointment

 I discussed last week about my recent struggles & goals. I have been dealing with a lot all at once! Family planning (update on that in 2 weeks), my Grandma's funeral, lower lung function. Through it all I have remained very compliant with my meds! My health is VERY important to me. So this last weekend I took my vest machine, wabi sterilizer system , and packs of ensure to my parent's for the weekend. I wanted to make sure I did everything. While it was a sad occasion, it was still pleasant seeing almost all of the family together again. Actually 27 out of 29 of the cousins made it to the funeral. Grandpa is in the middle of the picture (can you find me?) LOL   On top of my medications I have been doing some dancing & walking, but no jogging or anything. I'm still counting calories on my fitbit (hitting over 3000) a day (& 40 grams of protein, 50 grams of fat at least). I knew I was feeling a bit better than before, but wasn't sure what to expec

Post- Surgery Appointment

Post Surgery Appt: As you prolly know, I had Laparoscopic Triple Hernia Surgery last Tuesday. Here was a picture of me devouring a piece of bread so I could go home afterward the surgery (4 hours post surgery and 20 mins post waking up from recovery). I was ready to go home! Today I had my post surgery check up. He said everything in the surgery went well and besides the finding the 3rd hernia there were no surprises. He pointed out where the staples/stitches (they are holding the mesh in place) are in me. I have two on each side at the end of the mesh (so 4 on top) and two down farther in my groin. Apparently, I just have one huge piece of mesh that runs the width and length of my whole abdomen/groin area. Bahaha. I am Inspector Gadget after all. He said a few more weeks before I can lift stuff or exercise. Also, he said the area where the staples are will hurt when bending or twisting. However, I only notice really when I twist or turn too fast. Overall, it was a nice appointment

Theatre and Life...how to fit in CF?

Fitting CF into my life: Cystic Fibrosis won't be hard to fit into my schedule right now. As I just finished my job watching my babysitting kids for the year. I'm currently job hunting and taking classes on Mondays at the local community college (as a pre-req for Grad programs/and for fun). Mulan Jr, just ended today. We had two shows. Back-to-back performances are harder, since I had a busy day before the shows, I didn't get a chance to do my meds before the shows. Therefore, I end up bringing my therapy machine along.  Yep, sitting in the light booth and doing my meds, while watching people take their seats. [Note: I turned my therapy machine off when the house lights had to go out.] Its not that hard to fit them in. You just have to be willing to do them sometimes in unexpected places and be willing to have others find out about it. I had two people in the light booth with me, neither knew I had Cystic Fibrosis, but neither were bothered by the nebs. So bottom line