When I accomplish two things in one day
[Gif of Jace from Shadowhunters holding a sword while saying,Ā āSheās out of control.ā]
Mike Driver
Keni
Three Goblin Art
NASA
noise dept.
hello vonnie
Jules of Nature

@theartofmadeline
Aqua Utopiaļ½ęµ·ć®åŗć§čØę¶ćē“”ć

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⣠Chile in a Photography ā£

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YOU ARE THE REASON
š
Lint Roller? I Barely Know Her

izzy's playlists!
PUT YOUR BEARD IN MY MOUTH
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@mschronicles-blog
When I accomplish two things in one day
[Gif of Jace from Shadowhunters holding a sword while saying,Ā āSheās out of control.ā]

Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
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I feel like somebody steamrolled me with Tired ⢠and then buried me in cement
@woozis-vodka-aunt (via chronicillnessmemes)
It is okay to let your illness define you. Itās part of who you are and if youāve been suffering a long time it can shape your life and personality. It can change who you are for better or worse. Stop listening to these ādonāt let your illness define you!!ā Or āyour illness is not your identity!!ā posts. If your illness defines you and is a huge part of your identity thatās okay. If your illness doesnāt define you and you donāt see it as part of your identity, thatās okay. Just stop telling other people what should and shouldnāt define them.
My social calender is just so full
*Has 2 things planned in one week*
My autoimmune disease

Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
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Does the reality of having a chronic illness ever just slap you in the face? Its like wow Iāll never be able to do that thing that Iāve always wanted to do.
Post 3 day steroid infusions
I haven'tĀ posted in a long time! My MRI came back with an active lesion so I had to do a 3-day steroid infusion!! Fun times!
After the 3,000mg of steroids with no taper I have been feeling horrible! My blood pressure dropped and I am just constantly sleeping and feeling dizzy. Where is the burst of energy everyone was saying I would feel?! I guess it took away my leg pain but I wonder if it was really worth it. Plus I got sick with a cold to top it all off...
Anyway, Iām glad itās over.Ā ĀÆ\_(ć)_/ĀÆ
Hey kids! Letās play The Worldās Least Fun Guessing Gameā¢!
[Image Description:Ā Fry from Futurama meme- not sure if flare, or just the flu, or just the tacos, or just the allergy, or just the injury, or just too much coffee, or just not enough coffee, or just angry and bloated,Ā or just the side effects of meds,Ā or just <insert symptom here>]
MRI
Moments before your first one
and before your fiftth one
Step back, bitches, I donāt need your stupid instructions. Iām a professional!
You canāt prepare for a sudden impact. You canāt brace yourself. It just hits you, out of no where, and suddenly, the life you knew before, is over.
Meredith Grey, Greyās Anatomy (via blossoms-things)

Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
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Why Do You Hide?
āWhy do you hide your illness?ā
Maybe itās because people donāt even believe me when I tell them Iām sick.
Maybe itās because I can feel people become uncomfortable when I talk about it.
Maybe itās because Iām tired of having to disclose extremely personal medical information to random people.Ā
Maybe itās because Iāve had doctors doubt me.Ā
Maybe itās because Iāve had people I love doubt me.Ā
Maybe itās because Iām looked down upon when I need help.
Maybe itās because of all of the times itās been implied that Iām just not trying hard enough to get better.
Maybe itās because itās easier to pretend Iām okay than it is to explain that I am in fact in pain this very minute even though Iām out of the house because if I didnāt do anything every time I was in pain I would literally never do anything because I am in pain every minute of every day.
Maybe itās because Iāve had my sanity questioned when I try to open up.
Maybe itās because Iām terrified of the harassment I would face if I identified myself as disabled.
Maybe itās because I know youāll never understand unless you experience it (and I would never want you to).
Maybe itās because Iām so f*cking sick of hearing the judgment in healthy peopleās voices.Ā
Maybe itās because society has made me feel that disabled people are lesser than able-bodied people.
Maybe itās because I donāt feel important enough for anyone to care.
Maybe itās because I feel like nobody would want to be around me if they knew how bad things really are.
this user has multiple sclerosis
Get up. Survive. Sleep. Repeat.
Donāt tell me I talk about my illness too much. Every movement. Every breath. Is a reminder that Iām not ok. That I may never succeed.That I canāt do things that normal people do. That everyday is a struggle. Never ever tell me I talk about it too much.
Quick PSA
Thereās a huge difference between being tired / fatigued and being chronically ill and exhausted / fatigued due to illness.
I know because I wasnāt always sick.
Please, donāt tell disabled / chronically ill people to ājust push throughā or say something that invalidates their exhaustion (especially if itās literal energy producing dysfunction) like ā you donāt know tired till you have kidsā.
Yes, both of these have been said to me, no, I was too exhausted to say anything.

Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
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Does the reality of having a chronic illness ever just slap you in the face? Its like wow Iāll never be able to do that thing that Iāve always wanted to do.
My body is tired and Iām tired of my body.
Unknown (via hayla86)