“Sometimes the night was beautiful…”

What a week!! Quick recap of big events:

I bought myself my first pair of sunglasses!!! I think they are pretty cool. 8-D (Yes, they go over my glasses–but they work great!)

I finished a painting. I tried Snapple’s new tea: Bret’s Blend Tea–Trop A Rocka. It has mango, pear, peach and cinnamon flavoring. Delicious! I got to talk to some friends from CO. My little sister comes home from college tonight! 😀 So exciting!!! 😀 We got to see some family friends who are in town and had dinner with them. And the biggest event of the week: yesterday’s hospital trip.

I had my annual 3-month MRI and doctor visits. It was a LONG day! I checked into radiology at 6:30 a.m. for my MRI. I got out around 9:30. Got a nice bruise on my right arm from the IV they used for the contrast. Went up to my regular doctor visits that lasted until 12:45 pm. Ate my sandwich on the run to my 1pm appointment for an ultrasound on my left leg to see how the blood clot is doing. I got out of there at 2:30. Back up for one more appointment and finally got to leave the hospital around 4 pm something. I was so tired by that time that as soon as I got in the car, I fell asleep. Thanks to my dad and mom for being there, because while I was sleeping, they were stuck in rush hour.

The day, although long, went well. It is my own battles of striving to be independent that cause me to build a defense wall when I attend appointments, especially when they are Occupation Therapy concerned. I like to do it on my own, even though my body is changing. And for me, it is harder to except the fact that my body is changing and getting more slow, than it is for me to adapt to changes. For example, when doctors ask me if I have noticed any changes…I say the obvious ones that I might be concerned with or notice getting harder to do. Then they ask my parents and they say things that I really have not noticed, because most often either I am used to it by the appointment so I forget the changes or I just don’t take note…like I can’t see myself walk, so I don’t notice how my right leg and ankle are working or seeming different. I am not mad at my parents for speaking these things, but my first initial reaction is to clarify with justification and try to prove that I am doing just fine. It is a hard day to sit and discuss about all the big to tiny changes noticed. It is not that any big steps are taken towards these changes–it is just discussing them. I think what frustrates me most is having to talk about all the options out there–possibilities–for when the time comes that I do need more assistance in maintaining my independence.

Independence. The word in itself is what I fear most I think. The thought of losing my independence causes me to strive to work harder to maintain what I can do right now in life. Like driving. The weeks following my blood clot, I could not drive and I struggled! When I was ready, driving and taking management of my schedule helped me get back towards feeling independent, even though I had just let go of my apartment. God only knows the future. He knows when I will need help and has surrounded me with an amazing family who helps me in more ways than I probably recognize and a team of doctors who have resources to help me as well. I just hope when it comes to that time, that I will have let go of my pride and recognize that I will need help. And not all help is bad. Not all help classifies me as helpless. Not all help labels me as disabled. The assistance at that point in time will enable me to continue to live independent for as long as I can. I must learn to embrace help, not build a defense against it.

I have not received the results for my brain and neck scans yet, but scans of the spine were stable. And the left leg shows stable as well. This is a praise!!! 🙂 Thank you for your prayers!

Last night before I went to bed, I went out to feed Muffy. The moon was bright, stars were shining, and it was a lovely warm evening!!! I sat on the patio and started humming Rich Mullin’s, “Sometimes by Step”. Of all the day’s worth of emotion, chaos of schedule, and long discussion…it was so nice to sit in silence. Just for a few minutes. No thoughts of the day spent or thoughts of tomorrow. Just a deep breath of wonder realizing how tiny I am in the universe, yet God knows me by name. He loves me and takes care of me. I am so blessed.

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Filed under Adjusting to NF2, Books and Movies, Hospital Trips

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