-Stay Beautiful ♥
-Stay Beautiful ♥
-Stay Beautiful! ♥
Here are some FREE printables I have made to help keep organized with important medical info!
♥ Cover page for a medical binder! ♥
♥ Vital information to keep handy! ♥
♥ Medical information ♥
♥ Your medical history ♥
If you all would like different designs feel free to message me! I hope this can help you like it helped me! Watch out for more chronic illness / medical organization post! Very helpful for my EDS binder!
-Stay Beautiul ♥
Hello everyone! I apologize for it being a little while since I last posted! I finally graduated so i can spend more time blogging/vlogging! Here are some of my EDS/Chronic illness summer essentials! ♥
Sunglasses are a must for everyone! My eyes are super sensitive to light because of my keratoconus, but it’s also important to protect your eyes from the sun!
Even if the sun isn’t out and shining bright, the UV rays can harm your skin more if left unprotected.
Even if i don’t get sun burn i apply this, because my skin gets really sensitive during the winter months and it helps the pain from the sensitivity.
A lot of times I get heat flashes and it makes me feel sick and dizzy so it’s always nice to have this handy for nice quick cool down!
It’s always important to stay hydrated and keep up with your medications, but sometimes it can be hard to remember to take your pills throughout the day! This makes things easier to do both – stay hydrated and on schedule with your medications.
I hope these can help give some ideas on what may help you! Thank you all for the support and visiting my blog! Feel free to contact me and talk! I love you all so much!
Stay Beautiful ♥
I was checking through my blog and I’m absolutely amazed by where everyone is from! I can’t believe my blog has reached so far! I hope you all are doing well and hopefully my blog can/has help even the slightest bit! No matter what Country you’re from I’d love to hear your stories! If you would like to share your stories enter the tag edspaoutreach !
The following country’s have visited my blog!
♥ United States
♥ United Kingdom
♥ Burkina Fasco
♥ Puerto Rico
♥ South Africa
Thank you all so much!
Again, if you would like to share your stories do the tag edspaoutreach !
Everyday we all go through this constant pain that keeps us limited and unable to a lot of things like those who don’t share our struggle. A lot of people say the physical pain can’t be too bad, but they cant see the excruciating pain that goes not only through our bodies, but heart and soul.
Every Single Day…
What are you doing after school?
Are you going to college?
Whats you dream job?
What does your future look like?
Those questions eat at me more than the physical pain.. All my dreams since is was a young child are gone..
Dance, College, work, family, etc… Taken away right in front of my eyes from an illness that left me sick throughout my teen years. No answers to what it was or why i was feeling this way, but it didn’t stop there.
After 7 years I was finally diagnosed with Ehlers-Danlos Syndrome. The questions kept coming..
You know you can’t manage that, right?
You will never accomplish that, why even try?
Why don’t you just give up?
Those are questions people ask that makes me want to break down and cry.
It pains me knowing I won’t ever be the same person living the dreams i planned on for so long.
But I won’t give up…I can’t give up.
The love and support from my family and friends keep me going! Wanting to make a difference keeps me going. Together we can do this..
Thank you for visiting my blog!
♥ Stay Beautiful
♥ The Mighty ♥
Hello everyone!! I apologize for the long wait! I wasn’t feeling the best and was busy, but I’m back!!!
I’m going to be talking about a website that was very informative and helpful to my family and I! A lot may already know about it but for those who don’t I hope it can help in some way!!
♥ The Mighty website (Link Below) has many different categories that could hopefully help just about anyone!
The Mighty has helped my family and I so much! It informed us about my chronic illness more than any doctor around here could.
When I first got diagnosed, I felt like I was all alone and couldn’t relate to other people my age, Most of them just thought it was some type of joke. My mom then found the Mighty and showed me, I felt connected because a lot of them were feeling and going through what I was..I finally realized..I’m not alone in this fight. I have my families support through everything as well as the amazing people I have starting to talk to throughout my blog and the Mighty!
From reading and watching the Mighty i have learned to not be ashamed or embarrassed about having a chronic illness (EDS). Everyone is unique in their own way but that doesn’t make us any less beautiful!
Seeing so many stories i related to helped with the diagnosis, before i was confused and scared. It’s helped me open up more so I hope to share more often on here for you all!
Thinking of doing a QA any questions?!
Thank you all!
-Stay Beautiful ♥