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

CF isn't all tears and saddness. Get a Full Picture.

  CF and Laughing Cystic Fibrosis can bring sad times and times of tears (like losing a close friend with CF, etc) BUT, it can bring so much joy and love. I've noticed most people love to talk about the people they meet while traveling. This is usually, because they have learned something from the person. Or the person is considered unique to them. I can do the same thanks to my Cystic Fibrosis. I may not have traveled much in my life thus far, but I have learned mountains of lessons from my CF. [Picture right:  Me ready for surgery in 2nd grade!] Forgive my shoutouts (but I must recognize a few amazing people) I have met some of the most amazing doctors: Chatrath, Dr. B Nurses: Sara & Marie (from Clinic), Lizzard, Melody (best IV stick ever), Deb, and Kris (you know a nurse is amazing if you love her after putting tubes down your nose!) Respitory Therapists: Jeannette, Lanell, and Don (you da Man) And Cookie Marrow (Musical Therapist- She would sing to me a...

Video Blog: Life in the hospital (as a child)

The daily life in the hospital! Most people cringe at the idea of a hospital. However, when I was little I never minded going into the hospital. I usually would have at least one other friend with Cystic Fibrosis to hang out with there (before we knew about the "CF Bugs"). I didn't love being sick, but I loved my CF friends that I would hang out with. Also the hospital, nurses, and my parent's tried to make it a "normal" environment. I got up and put on cute clothes, "walked to school", flirted with a couple CF boys, did homework, came "home" (back to my room), my friends would ask my parent if I could go play with them. We'd hang out in the play room or go on a walk with one of my parents! My dad loved taking me on walks and I LOVED going on our walks! Here is a video blog of the route we took and bit of information on what is was like growing up (for a chunks at a time) in the hospital! (it is posted via youtube, let is dow...

How Fostering and CF impact my work

I haven't been on my blog much.... I think that is because most of my blogging is currently been done on Health Union's Cystic-Fibrosis.com (here is link to all my posts on their site: https://cystic-fibrosis.com/members/cherizkunkel/ ). I decided last fall to step away from real estate after 3 years in the business. It was tough to say good-bye, especially since I had tripled my volume and business in the last year. However, I didn't have time to add any new clients; I kept saying, maybe next week, next month I can fit more work into my schedule. The truth is fostering takes a lot of time. We have between 5-8 monthly visits at the agency, 1 court ate a month, 2 home visits from the caseworker a month, plus e have 2-3 doctors/specialist appointments for our current kiddo. We have lots of paperwork we fill out, gas mile logs, receipts to add, and more! Our kiddo also participates in gymnastics and dance two nights a week. We go to a fosterparent support group with our kid ...