Nov 24, 2018

#Spoonies: Compression Socks - yay or nay?

WARNING: Not medical advise. Not paid review.

Quickie: If you're not familiar with compression socks they're used to help blood flow in your legs. People who stand all day, flights, or exercise frequently use these. They can help prevent varicose veins. They're an item that disabled/abled wear.

Background:

First pair of compression socks I decided to purchase were on a limb (heh). It was out of fear because I was having swelling in my legs and no one could explain why.

I feared that I was developing a blood clot or something and needed to do something. I mean, if your doctor isn't sure what's going on (or even cares)...ya gotta do what ya gotta do.

My first pair looked as if a hospital gave birth to them. They looked like medical gear and not in the good way. I was young and super vain. More vain than I had ever thought before.

They didn't match anything and they were hard to get on. I ended up throwing them away -- my health be damned.

The Present:

Just got paid the Friday before Thanksgiving break, and went onto Amazon. It's ran by an Antichrist more than likely but the availability and ease as a disabled person.. I use it a lot.

Anyway, I discovered that  compression socks don't all look as horrendous as what I had. I've found several companies who make cute compression socks. I purchased a three pack of plain black compression socks. They are knee high length and snug.

They look nice and fancy. I wear black socks to work to match with my shoes and my pants. So, I purchased these to blend in with my work wear.

The size I purchased are a S/M. They are snug with some stretch to them. They are more stretchy when they're not on your leg. This isn't the best showcasing how stretchy they are.

They are extremely easy for me to put them on by myself. I had difficulties with my original pair that I bought way back when. These do not act like my original pair at all.





What they look like outside of a shoe and not dangling around my fingers. I am 5ft 4in they reach the edge of my knee but do not go passed it.

They look like a regular pair of knee highs or leggings. Which I wear a lot of so they blend in well with what I already wear.

The big draw for me is that they look like regular socks and do the job that they're supposed to do.

Day Use:

I decided to wear them today while I was cleaning and doing my workout. My legs usually swell IMMENSELY during these things.

For me when my legs swell, they feel gross and don't want to move and they hurt. They hurt as if you're being punished for some sin you've committed that you have no idea. But boy do you wish you could repent it.


They have helped so far I do not have any noticeably sin-punishing pain in my legs and haven't swelled. Which is a relief to me because while wearing them I was working out to this: Keaira LaShae Dance Workout for Beginners.

I usually stick to step with a step, modified jumping jacks and some yoga here and there. Stuff that I can do without major swelling and pain. So, I am hoping this is a new normal for me to be able to do the "fun"exercises without too much pain.

They come in this packaging large print telling you what they are for.

The three pairs of socks come in their own packaging with the label "S/M" (whatever sizes you picked out). I have had them only for a week so I'll update how they last later on.

But overall my experience with these have been very positive. I plan on wearing them during my school day to see if there is any major benefits to them.

There are several brands on Amazon selling a variety of these. They don't look like medical gear -- they can look professional or colorful depending on what you want.

I plan on getting compression socks that are ankle length since I prefer my socks to be shorter. I am hoping to purchase some that have colors to them because they're ankle socks -- can't much see the color and they won't be too loud down there hiding in my shoe. Surely.

They can be purchased here. They are currently $15.98 at writing this. If you know Amazon well enough the prizes fluctuate  a lot.

One thing I've found in many brands is the giant ass logo printed at the top that can't be covered. I don't like advertising for brands -- if I like it I'll tell people about you ..y'know? So, these aren't branded so there's that, too.

Do you use compression socks? Do you like them? What brands do you prefer/recommend?









Aug 26, 2018

#SundayQuestions: Outdoor or Indoor Reading?


Alexas_Fotos

Prefer indoor curled up in bed or partially cuddling the boyfriend. He's usually playing video games or something not book-related as he doesn't read. I know it's hard to think of but I am with someone who doesn't like reading.

But he doesn't mind if I read parts of a book to him or talk about a book I'm reading .. so it's manageable.

I have allergies so I don't have the passion or interest to reading outdoors.

This is an updated version of this post




So, where do you prefer to read? Inside? Out?

Jul 21, 2018

#Spoonies: New House & Things

Anyway, tl;dr --- I'm now in a disabled-friendly house and haven't been able to leave on my own yet.

more below ...

We've been here a bit over two weeks. We need storage for a lot of what is left hanging out in the moving boxes.

Waldo, our calico cat, is getting adjusted to the new place. She still bolts when she hears anything peculiar or if someone walks into the yard.

I have YET TO LEAVE MY HOUSE FULLY. Not due to illness but because of our gas situation. The week we moved in scheduled to turn it on.

The gas company sends someone who then tells me that he cannot because there is a LEAK.

Inspector eventually shows up to tell us that there needs to be a thermostat on the heating unit in the living room.

So, our landlord Wednesday? comes to remove the heating unit.  Landlord on Friday says we should have received gas that day but..in reality who know? So, we are hoping that someone shows up Monday and sets up the gas.

Since my boyfriend works out in the elements he has to bathe everyday. He's not enjoying the cold showers. Me, I've been bathing every 3-4 days at someone's house.

I still need help with paying for surgery! Please share link

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Jul 7, 2018

#Spoonies: 5 Ways I Relieve Migraines




Five ways to possibly relieve migraines. I'm fairly certain these are pretty common ways to try to relieve yourself of the migraine pain. When I have migraines they last for days. Most of mine start at the base of head / neck and stretch outwards toward face. It's fun, don't recommend. I cannot afford to go get shots or another medication to add to the list of meds I already take. 


1. Drink Caffeine

Excedrin Migraine is Acetaminophen, Aspirin and Caffeine. I cannot take Acetaminophen or Aspirin. Before I was diagnosed with Rheumatoid Arthritis my other doctor just drowned me in NSAID's so I'm laying off those for awhile. And aspirin with my other medications can cause kidney problems which I don't want. 

So, I drink tea, coffee or soda to help with the migraine. 

2. Darken surroundings. 

If the migraine comes with sensitivity to light blackout what you can -- close curtains, turn off lights, dim cellphone/computer brightness. I turn down my cellphone and computer to as dark as possible and with the windows blackout and lights off it gives a softer presence and can use it. There is still the migraine and the pain but it's less, especially, if you're still needing to get work done.

3. Pressure. 

I place pressure on my head to help relieve the pain. I press a pillow or lay a blanket on top of my head and it helps dull the pain. I can't walk around with a blanket or pillow smooshed to my head. But when they're this bad I'm not mobile anyway. 

4.  Heat Pad/ Ice pack/ hot shower

I lost my heating pad years ago but I have a heating blanket. I wrap that around my shoulders and neck curled up on the sofa or bed. Ice packs on my neck or forehead .. or both.

 Ice for some migraine sufferers may make it worse....so I'd go slow with that before doing it.

I will also set the heat of my shower to the hottest temperature I can tolerate and let it pour over my neck and head.

5.  Medication

My migraines don't die or quit with over the counter medication. I don't take medication specifically for migraines. But I take muscle relaxers which does help with dulling the migraine. When I do this I also do slow neck stretches/whatever they are that they showed me when I was in physical therapy.


What are ways that you kill or make your migraines tolerable?



I am still in need of donations toward my gallbladder surgery. Sharing the link or donating is appreciated!

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Jul 1, 2018

#Spoonie: My Reasons to Stay Alive

Content Warning:  Suicide


Content Note: I wrote this over several days and haven't re-read it so I'm not 100% grammar, spelling or what the hell I wrote about. But I am scheduling it anyway. Good luck.


To other people, it sometimes seems like nothing at all. You are walking around with your head on fire and none can see the flames. And so -- as depression is largely unseen and mysterious -- it is easy for stigma to survive.” - Matt Haig, Reasons to Stay Alive


Inspired by this post. She started hers from Reasons to Stay Alive by Matt Haig.  One piece of the book was to list your reasons to stay alive. Example: one of hers is to watch Elf every Christmas. I read it a few days after she posted. Ever since I've been thinking about it. A few days ago I decided to go back to her blog to let her know.


Four in the morning, Tuesday June 19th I started this. It’s hot and humid, the humidity feels as if it’s trying to melt my bones. My joints disagree with this predicament striking loudly and painfully at this. While I’m laying in bed reading blogs and parts of Rough Justice in an uncomfortable state. When this happens there is no escape.

Some reason when heat gets trapped in the bedroom my medication and their usefulness dies.


Confession: I have suicidal thoughts and struggle with depression. I’ve been this way since I was a child. Before you panic with this information I want you to know I don’t need a pep talk, suicide hotline or reported for at-risk. This is one of those things where the stigma of depression and suicide stops conversations.


“Stigma is particularly cruel for depressives, because stigma affects thoughts and depression is a disease of thoughts.”


For me, suicidal thoughts are more like a gossip who comes along with an oldie thinking it is a goodie. I have no interest in gossip in my mind or with people so it doesn’t work well. Chronic illness has not helped with this, however, I am still here and will be.


At nine or ten, I knew I would not live until twenty-five. Either by my hand or something. It’s possible that my child mind simply thought twenty-five was fuck’old.  For me, I believe having conversations openly can help end the stigma and the isolation.


“... you internalize everything, and you are so scared that people will alienate you further you clam up and don’t speak about it, which is a shame, as speaking about it helps.”


Depression does things to us in different ways. Some of us can reach out for help and get the help without fear or insult. While others we struggle with acceptance, medication and getting the help. Either because of the people in your life, your financial situation or where you live. So, we keep everything within ourselves which does not help but y’know what? We know that and it is still going to happen.



The mentally ill know they are ill. They know they need help. They know. Sometimes the problem is the underestimation of the problem before they’re able to get help because they don’t have anyone to talk with.


“Words -- spoken or written-- are what connect us to the world, and so speaking about it to people, and writing about this stuff, helps connect us to each other, and to our true selves.”


Now, here are some of my reasons for staying alive:

  1. Cool mornings where the sun is clear and I wake up early. I get to sit in this weather on days where I’ve nothing to do.
  2. Writing parts of my stories at my mom’s house while I wait for them to wake up.
  3. Writing stories. I’ve completed many.
  4. Sharing memes and jokes with my boyfriend when we’re home together.
  5. Playing very active games and only slightly guilty for using up the spoons.
  6. Creating things. I crochet, sew and make wreaths beside writing.
  7. Reading. It is an adventure and a fun distraction..even before my chronic illness.
  8. Walks, hiking and anything naturewise I get to do with my family.
  9. My cats! Dogs! And the animals we spend time with to care and rehome when we find them alone/in a bad place.
  10. Having conversations on weird topics.
  11. Creating fictional worlds with my sisters or “what ifs”
  12. Sitting on the porch watching the animals roam around at my mom’s new house.
  13. Arguing. I like to argue. Not the red-face almost putting hands on someone. Just conversations disagreeing/agreeing. Lol. I’m not doing it to prove right what I’m saying (though I do participate in a lot with misinformed people lol).
  14. Teaching. I don’t have a full-time teaching position yet but I love subbing.
  15. My up-and-coming niece who will be released August something. We are slowly planning out my sister’s baby shower. She wants a preggo cake but the kind that would traumatize the kids who will be at the shower.
  16. Just doing everyday things with my family.
  17. Being alone and listening to music
  18. Dancing (I have no rhythm & never learned how to dance lol)
  19. Laughing
  20. Grocery shopping with my sisters


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Jun 29, 2018

#FF: Spoonie Blogs


Follow Friday: Blogs I like. June 22, 2018 edition Books and Fandom. Spoonsnbooks.com



Follow Friday: Blogs I like. June 22, 2018 edition Books and Fandom. Spoonsnbooks.com

  • No obligation to follow them or me for this.
  • Can ask me to remove promoting your blog - no worries!
  • No set # of blogs will be listed
  • Blogs will be from Wordpress, Blogger, Tumblr & Others
  • Comments about blogs are either things listed on their blog or what I like about them. 

Spoonie Blogs:

linktr.ee/katethealmostgreat  RA blogger - blogs about makeup and tips & trick, books, etc kinda place

notjusttired.com ME/CFS awareness and blogging about life with it. 

migrainemantras.com     focus on migraines and conversations around them.

Chronic Illness Advocacy & Awareness - not so much a blog but gathers info about Chronic Illness/Advocacy (it's in the name I know). 

thinkingoutloud-sassystyle.com Blogging about life with disabilities 

www.jumbledbrain.com   - brain injury blogger

A Chronic Voice  Chronic Illness and informational type of blog posts

Jun 8, 2018

#FF: Books & Spoonies



Follow Friday Blogs I like. June 8, 2018 edition Books and Spoonies. Spoonsnbooks.com


Follow Friday: Blogs I like. June 8, 2018 edition Books and Spoonies. Spoonsnbooks.com

  • No obligation to follow them or me for this.
  • Can ask me to remove promoting your blog - no worries!
  • No set # of blogs will be listed
  • Blogs will be from Wordpress, Blogger, Tumblr & Others
  • Comments about blogs are either things listed on their blog or what I like about them. 


Books & Spoonies:

fibroqueen.com  Chronic Illness, Advocacy & Positivity

themystiquereader.wordpress.com    Book blogger, participates in fun Tags, blog is COLORFUL 

irelandms.com  Blog about MS , positivity & thoughtful posts


Jun 7, 2018

#Spoonies: To Use Or Not To Use A Cane


Mentally check off if any of these questions apply to you:

Does it hurt to walk or put weight on the leg?

Have you tried everything to still have issues with walking?

Do you use furniture or walls to stay upright?

Did you recently injure your leg and everything just hurts?

Do you struggle up and down stairs or even struggle to step up on a sidewalk?


Congratulations! If you're able to check off any of these – you may need to use a cane.

I understand the concern of getting one because your doctor hasn't suggested it. If you've repeatedly told them that you struggle with walking due to pain or balance and they haven't advised it then what other things are they ignoring that you've told them?

When I started struggling with walking I thought it was a stupid idea to try to use a cane. My doctor didn't say I needed one, so why even think about it? At the time of this thought the whole my doctor doing a half-ass job didn't come into this thought process.

My journey toward using a cane started in my early twenties. Mobility issues IN MY HOUSE? You wouldn't believe it. Honestly, I didn't accept that I needed it no matter what symptoms blossomed in front of me

It didn't make sense for me, a young healthy woman to develop these issues. When trouble started to brew I had a common problem: shitty doctor after shitty doctor. Also, I still thought I was a healthy person with minor problems that would go away if I ignored it (Or over time).

It took almost falls, falls, and brain on fire causing falls for me to accept it. Whether my doctor told me I needed one or not.
 
Shitty doctors prevent better care that you deserve. Doubt that you're not sick enough to use assistance prevents better care that you deserve. Combined, you, me and others live a quarter of the quality of life we deserve or need.

If movement is blemished by balance issues, falls or pain a cane may help alleviate these issues.


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Disclaimer: Not a doctor. This is not meant to dictate what you and your doctor has agreed on for your condition. Always consult your doctor or other medical professions you talk with about your health concerns. 

Jun 5, 2018

#Spoonie: Update! She answered!

It took a lot longer than necessary to get through to the financial person to receive the cost of my surgery. But I've learned she does exist and the price of the surgery. I have to pay 2 places for the surgery, one for the facility and the other for the physician.

I updated my YouCaring with what it's going to cost in total. So, it's going to be close to 14K so I rounded. I'm at $80 in donations now and appreciate them all. Thank you! Please, if you can't donate share so I can get this done. I appreciate it so much!
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May 31, 2018

#Spoonie: Youcaring / Health Update


Image contains colorful pills and the words: You caring and health updates, #spoonsnbooks and spoonsnbooks.com on a dark pink background



YouCaring Update: I still need donations to help with paying for my surgery. I am at $50 so far. I am super grateful and appreciative of everything. I still haven't got hold of the lady in Financials. I don't know if I could just waltz up to the building to talk with her. But since the school year has ended I feel very tempted to do this.

General Health: I am having to modify my food once more. I've been eating as little as possible to prevent stomach issues. But the last few weeks have been lazy and just eating what's been cooked here. Which is generally spicy and meats I'm not supposed to have. 

Last night my pain levels were terrible that they'd incorporate themselves in my dreams. We had another night storm the room became hellish for me but couldn't do much about it. 

#May: Overview/Wrap Up


Post Count:

I created 67ish posts in May. Nine more than what I created in April. These posts are a combination of book reviews I've read this month, in the past, Spoonie up dates and various off-topic posts. Not everything about May will be in this because I've forgotten or added something since creating this post. I'm compiling it on the 28th.

Comments:

33 this month

Likes:

179

Books I've Finished in May:



Blood Will Out by Jo Treggiari 

The Electrifying story of Multiple Sclerosis by Vanita Oelschlager

Harriet Tubman by Isabel Sanchez Vegara

Georgia O'Keeffee by Isabel Sanchez Vegara 

Great Polar Bear by Carolyn Lesser

If All the World by Joseph Coelho 

Room 119 by T F Lince

Fish-Boy An Inuit Folk Tale by Vanita Oelschlager









The Stereotypical Freaks by Howard Shapiro

Books I've Abandoned in May:


I don't think I've abandoned a book this month. Woo!

Books I've been reading since April:

Or beyond April -

The Forest Beyond the Earth by Matthew S. Cox
A Nighttime of Forever by Matthew S. Cox


Book Reviews in May:

Not including books I read this month. These are just reviews posted.




Sunday Questions:


What are you top 5 reads for 2018 so far? 
How Many Books Are On Your TBR Pile?
Would you rather read digital or paper books?

Weeding Wednesday:







Writing Prompts:






May's Lists, Nat'l Days & Others:





All things Spoonie Updates:




Thanks for reading!


May 27, 2018

#Spoonie: Zoo Trip

Our three day weekend started with waking up and going to the Tulsa Zoo. Tweeted the zoo to find out how to access a wheelchair from them. It costs eight dollars. Fourteen something all together. You return it and get the five dollars back from the experience.

We haven't been here in years there were many updates. Wheelchair was fine. The trip through the was a bit rocky.

Some of the paths aren't even which I'm okay with. It happens nothing is perfect in this world. An aspect of my health problems is pain levels and dealing with that garbage so in parts the roughness was painful.

I worried things wouldn't be fun or manageable if it kept the way it was.

Exhibit buildings were fun. Our zoo is huge but smaller than others but it's still entertaining. Monkeys I hadn't seen the last time I was here. Got to see the giraffes -- usually physically I don't get to see a lot so I'm not 100% if EVERYTHING was new I experienced was simply new to me or new-new.

Some of the facilities the handicap buttons did not work and there wasn't any signs to indicate that they weren't operational. Thankfully, my boyfriend was pushing me around Saturday and was able to maneuver around these issues. We received assistance from other zoo visitors, too, which was a relief as some of the doors were not handicap accessible at all. If I was there alone my navigation would be longer to get to a main door... or asking strangers for help.


The loose animals around the park are very used to human contact. My boyfriend bought us ice cream and was surprised at how much they cost. But they came with in a way...free entertainment. A Peacock quietly watching him silently asking for a share of the ice cream. My boyfriend told him, "I have a feeling you shouldn't have ice cream." But pointed at the fallen pieces anyway. He wasn't going to outright hand over anything but figured if it wanted some he'd have to find it on his own.

He didn't take the hint that food was JUST right there. He eventually wandered away and we were met with two geese. Both calm and waiting for their share of the ice cream. Boyfriend did point, and lift the pieces to him which he did eat.

Thought I took more pictures through our journey inside the zoo but apparently did not.



 I got this little guy, too! Squishy toys and pillows are great little things that I can use to rest my limbs on without much pain. Plus, it's adorable so there's that. But seriously, it can cause bruising and pain if my legs sit on one another, or rest my hands on top of the other. It's really painful, annoying and extremely stupid. Stupid because why do basic normal people thing to do .. cause injury?

So, have another cutie pie arm rest. If cannot tell it's a green/yellow Budgie.







After the zoo we went to my parent's new house. They got the furniture included in the move and it looks and feels super fancy. So, good for them with that. They were having a BBQ to celebrate with the family, etc.

My youngest sister and her family didn't make it as they were on a 3 day camp trip on some lake. I don't remember which one.

My other sisters and nieces were there though. We watched Game Night and Black Panther. Already knew Black Panther was good but Game Night surprised me...hilarious and only smidgen of dirty humor at the beginning of the movie.

Today I caught up on Shadowhunters and I think ..almost done with season 1 of the Librarians.




=

May 22, 2018

#Spoonies: Surgery Progress...so far.. if it can be called that.

So...

Yesterday's surgery phone calls started optimistic and quickly crumbled within an hour.

Didn't get voicemail but actual people for financials and appointment setter. Except voice mail again for the person who is supposedly the one to tell me how much the surgery is going to cost when everything is said and done.

Found somewhere that I can email. Suggested for billing and other but finding out the cost of my surgery is technically...billing , right? I decided it was. Hopefully, someone somewhere answers my question.

I looked up the cost of the surgery and I've completely underestimated what it will be where I'm at. I don't understand why the estimate for our capitol seems lower than where I'm at. I've increased the donation amount on my youcaring account. I appreciate any and all shares of it.

Every school year I make between 2k-3k and I'm just frustrated at how the heck am I going to get this done and over. So, any shares of it would be amazing because this is at the moment the only thing that I can think of. Unless I can sell a body part.






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May 20, 2018

The Electrifying Story of Multiple Sclerosis by Vanita Oelschlager

Title: The Electrifying Story of Multiple Sclerosis
Author: Vanita Oelschalger
Publisher: Vanita books
Publish date: May 1, 2015 -- it's been out for years!
Rating: 4 out of 5

Summary:Because Multiple Sclerosis is a disease that someone will live with for years, or even decades, it is important for family and friends to understand what the person is going through and learn how to give support.

Multiple Sclerosis used to be feared because it was so unpredictable and doctors knew very little in how to treat it. Thanks to good research and great doctors, people can live with MS even though there is not a cure yet. The Electrifying Story of Multiple Sclerosis is written to help people understand what it feels like to have the disease and how to help.

My Review: 

The Netgalley page for this lists it as Nonfiction (Adult) so I was thinking it was going to be an intense read. But it's easy to follow along that a younger person could benefit from it. It has simple illustrations almost cutesy with some.

Easy to follow and learn from. Even goes into detail on how to try to see how someone with MS deals with everyday chronic issues.

Recommend? Yes, great for people who have someone in their life with this. Or, just for something to learn about in general. It doesn't go into great detail but it's good information.

Downloaded from Netgalley.

My other Vanita book reviews:


Signposts
A Tale of Two Mommies
Postcards From a War
A Tale of Two Daddies
Birds of a Feather

May 19, 2018

#eBooks and why I love them


I am aware I don't own the books when they're eBooks. Info: Here. Here. Here. Here. I still purchase them.

The feeling is probably because I don't purchase many books to begin with. I've only maybe ten books I've put down real money for digital reads? It's maybe knowing Amazon isn't going to die tomorrow may help, too.

But under my Where to Buy tab I list Indie book store finder first above all. You own a physical copy once you've purchased it. The bookstore owners aren't going to track you down and ask for it back at will.

1. Can carry a book in my pocket.

I can fit my phone pocket in my back pocket or on rare occasion my front pocket. I've lucked out in wearing women pants that have functional back pockets but decorative/fake front pockets. 

This allows me not to have to carry a purse (to the anger of purse makers everywhere) to bring books along. This frees up my hands or lessen the pain on my shoulders (they irritate my neck/shoulder) when walking around or at work. 

2. Ease of Access!

When I'm not able to go to the bookstore or the library I can just get it through my computer, tablet or my phone. I can checkout a book while laying in bed not having to go anywhere. Every bookstore that I've entered has miserable flooring. I can walk any other store and my feet are fine but at the bookstore? They usually aren't cushioned or whatever compared to other business floors, especially, the Barnes & Noble in my city. My god, I can't even sit down on their floor to gain access to the bottom shelf.

But my bed, blankets and pillows are always comfy softness so...they win.



3. Less Space.

I have 1 bookshelf that is dedicated to my children books for when I get a classroom. I cannot fit anymore books on it than what's already there. So, books I've purchased are eBooks they fit and easy to move around my room.

I still use physical books from my library. But more than not they all come through as eBooks. I'm currently reading three books that are the real thing as they say.. but they're from the library and won't live here that long.

4. Settings

I don't have to pay extra for a larger print size or carry a massive book because the font is larger. I wouldn't be able to hold the book very long. This would lessen my time with the book. Which would suck. 

I don't have to wait for the large print to get around to being published. Some books are never made into large print so they aren't accessible. 

I can change the font and the size in a book so it's easier for me to read. I don't have to pay extra for the visual boost that is given to me in an eBook.

I don't have to read on a white background. There are physical books that have SUPER WHITE paper which makes it hard for me to read on. Words will start dancing on bright white paper for me which is extremely annoying to deal with.

I can fix this by sitting in the shade to darken the page or wear sunglasses. But why would I want to wear sunglasses inside? 
Every digital book I'm reading is green or the beige background not white. 

I absolutely love reading physical books and enjoying the time with them. But since the use and ease of reading digitally I've been able to read and enjoy my time A LOT. I know there are disadvantages of both kinds and that they're not all perfect.

I'm not saying to stop reading physical books. I advocate purchasing them from indie stores and renting through your public library. I read and use them. But these are the reasons I love them.