Skip to main content

Macbook features

There's so much I don't understand about technology, especially my computer. I know, that's slightly problematic.

Well, we can't all be a computer genius.

As my graduation present, my grandparents bought me a computer. It's the traditional graduation gift that they give all of their grandchildren (Thanks again!!) Anyway, I got a Macbook Pro. I probably should have spent extensive time learning all the features about my computer and trying to understand how it works, but I didn't. If you know me well, you may be saying to yourself, "Yep, sounds like Emily." You see, I'm not the most patient person in the world. I want to understand things right away. I am not a fan of reading long, boring instruction booklets (I usually leave that task to my dad and then ask him to explain in actual English). So, naturally, I did not spend a lot of time reading the instruction booklet that came with my Mac. I jumped in and started using it right away, as if I knew what I was doing. Because of this, there are A LOT of features that are on my computer that I either 1) don't know about 2) don't understand how to make it work or 3) I know how to do it but can't figure out the practical application of it. For instance, this weekend, I learned that you can change the highlighter color when you click on something. I also learned you can change the various settings of the trackpad, like swiping to scroll, tapping to click, etc. WHAT?! There are about a million different choices for different aspects of the computer that I didn't even know I had.


So the lesson I learned? Always read the instruction booklet. Unless you can get someone to explain it to you. Then, that's definitely the better option. I will be exploring the different functions of my Macbook this summer, for sure!


Comments

Popular posts from this blog

CF Letter 2020

Dear friends and family, It's May 2020, which means it is another CF Awareness month and another time to talk about all the amazing things happening in the CF world! This has been a very good year in the CF community. In October of 2019, Trikafta was approved by the FDA for all people with CF with at least one copy of the dF508 mutation. 90% of people with CF have at least one copy of this specific mutation. This is a HUGE deal in the CF community because it is one of a handful of drugs that addresses the underlying cause of CF and the only drug that such a huge percentage of people with CF can take. Trikafta is a total game-changer for so many, including me. I have gained stability, I require fewer IV antibiotics, I gained lung function I thought was long gone, and I feel like I can plan things in my life again. The hard work of the CF Foundation, willing researchers who continue to search for a cure and medicines that will increase quality of life, and the generous donations fr

CF Letter 2019

Dear friends and family, I hope you all are having a happy and healthy 2019! The Great Strides CF Walk is just around the corner, and we are gearing up for a great walk day! Since my last CF Walk letter, my health has had its ups and downs. Just before the CF walk last year, I got the sickest I have been in awhile and had to fight off pneumonia with the help of 4 weeks of IVs. I also had to do IV antibiotics in August and November. However, I have stayed relatively healthy in 2019, and for that, I am extremely grateful! Although I’ve had to fight off 2 colds, my body has been able to get through it without needing IV antibiotics. While I know I will need another round of IVs eventually, I am thoroughly enjoying being IV free. I credit this to the amazing CF therapies available to me, my compliance to my treatments, and all of your prayers for my health. I continue to take 30+ pills a day including enzymes to digest my food, vitamins and supplements that my body cannot absorb

The spirit of giving

It’s the end of 2017. That means it’s time to send in those end of year donations. Want to give to some amazing charities actually doing good in the world? I’ve compiled a list for you!  The Cystic Fibrosis Foundation- Obviously, I’m biased toward CFF. They fund amazing research that is saving people’s lives! Don’t you want to be part of that? Not only that, but 90 cents of every dollar goes directly to advocacy and CF research. If you donate to the Cystic Fibrosis Foundation, you know your money is going to be spent wisely and is going to make a difference. Since cystic fibrosis is an orphan disease (that means it’s really, really rare), people with CF rely on your donations to fund research. As well, Congress just cut the orphan drug tax credit, meaning companies are not going to get as much incentive for studying orphan diseases and creating drugs to treat them. The CF Foundation needs people like you to donate to CF research so we can find a cure for CF SOON. —www.cff.org