#behcetsdisease

[emily-strange]

So I have 3 chronic conditions in total (cos 1 isn't enough) and my joints are heavily effected....but....with a lot of breaks 😂 I managed to crochet this for my friend who's expecting.

Gotta say, I'm a little bit proud 🤷🏼‍♀️🥰 (it's meant to be a giraffe but also kinda looks like a jaundice cow 😂).

[kenziecamillexo]

I didn't know back then that life would change forever. I didn't know that I would have to give up the things that brought me the most joy because I just couldn't do them any more. I didn't know how my limits would change from one day to the next. I didn't know I'd have to fight so hard for what I need. I didn't know I could be okay with wearing socks that don't match. I didn't know how good fuzzy socks feel. I didn't know doctors could be wrong. I didn't know that there were others going through this. I didn't know there was support from people like me. I'd say I wish someone had told me all of these things back then, but I know I would't have believed them. 💙

[chronicallypos-blog]

#Repost @youngpeople_chronicillnesses with @repostapp ・・・ March is autoimmune disease awareness month! We've decided as a part of our #SpoonieSpotlight project to post a lot of #Autoimmunespotlight stories throughout the month! If you are interested in sharing your story please direct message us for the details on how. Entries close on March 10th. All entries after that will still be posted but as a general #spooniespotlight within the future. Our goal is to help people understand that our bodies can attack themselves. We deserve a voice and a outlet! This is your chance. Tag your friends with autoimmune diseases or # some diseases that are autoimmune or even give this a repost! . . . Thanks for your help everybody. Much love -YPCI Family. . . . . #behcetsdisease #neuromyelitisoptica #lupus #rheumatoidarthritis #addisonsdisease #autoimmunedisease #transversemyelitis #opticneuritis #crohnsdisease #Bulluspemphigoid #celiacdisease #chronicinflammatorydemyelinatingpolyneuropathy #Encephalomyelitis #gullianbarresyndrome #GravesDisease #graftversushostdisease #* Inflammatoryboweldisease #irritablebowelsyndrome #chronicillness #spoonie #invisibleillness

[emily-strange]

Someone knows mummy isn't feeling well 🤒😻 Time to play RDR2 before checking my favourite blogs in bed.

(@callmehopeless , @babbushka , @porkchop-ao3 , @strwxberrymilk , @shethenightwolf expect many likes and comments haha I apologise! 🥰)

[emily-strange]

Just something I put together on my insta a while back. Just incase anyone wants a little bit more insight into me or my main condition 🤷🏼‍♀️ you never know lol 💊😷

[emily-strange]

Made it to the 5th January without a hospital visit 🤦🏼‍♀️😭

[emily-strange]

Just a little personal message to my Tumblr friends!

So this is to anyone really who follows or interacts with me via my blog or messages! If you've messaged me/commented on something and I haven't responded please don't take it personally and be assured that I will reply 😊😉

I don't really have to explain anything but you're all so lovely and understanding that I feel safe to....I have 3 chronic health conditions (cos 1 isn't enough right!?) and with that comes a lot of anxiety and depression. A lot to deal with at 29. As well as feeling that my 20's have been lost to illness 🤦🏼‍♀️

If I fall off the radar, which is kinda happening atm, please know that you not forgetting about me means the world. I've lost a lot of real life people because I couldn't always 'keep up' and it's truly heartbreaking.

Knowing that I can disappear due to my health and still have your support is something that means more than you can know.

So, to the few people who have sent me anons, I am alive haha and I really do appreciate you checking up on me ☺️ I will always be back 😉 nothings killed me yet!

And to those anons who have questioned why I haven't replied yet, please be patient ♥️ xxx

[theadventureoflauren]

Being in hospital now for almost a month sucks but when this one visits life is so much better ❤️❤️