by James Chan

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PUT YOUR BEARD IN MY MOUTH

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if i look back, i am lost

izzy's playlists!
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Love Begins
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art blog(derogatory)
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"I'm Dorothy Gale from Kansas"

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@lymelogue-blog
by James Chan

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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Is Prozac...Prosaic?
Lyme amplifies my predisposition to anxiety/depression...Iām sure this is the case with most of you out there, sigh. Perhaps Iām speaking to the void, or to myself, but nevertheless, I'm hoping Iām not the only one who feels like their anxiety has felt entitled to my entire body through chronic illness. Bleh. (A daily Fuck You to Lyme Disease. Thanks.)
After 6 years (and a 2 year Lyme diagnosis) I decided to try my hand at antidepressants. First, Lexapro. Anxiety managed...yay. Depression magnified...boo. Zombie mode was in full effect, I went to work, I ate little, I slept, too much. Iām taking a week off of meds to see how my body feels, is this who I am? Am I just an emotionless zombie now or was the medication affecting me into abnormal detachment?
Next week Iām starting Prozac - does anyone out there in the void have any thoughts on this? I feel like Iāve heard horror stories, but canāt think of anything specifically and Iām too nervous to google literally anything. You know, one trip to WebMD and you have 7 different types of cancer, so Iām all set there. Maybe someone out there has a Prozac love story theyād be willing to share to a first timer?Ā
Itās Not Just a Phase, Mom
I think itās so interesting (perhaps interesting is the incorrect wordĀ āinterestingā with emphatic eyeroll at the end perhaps)...when individuals who have never experienced anxiety/depression/bpd/mental illness etc.Ā give you a hearty *pats* āyouāll get through this...itās not foreverā or something along the lines that this is temporary. To anyone out there who reads this who feels theyāre in stable mental state, donāt say this to me. Iām not speaking for the broader mental health community, but I donāt need to hear the equivalent to a snarkyĀ āthis is just a phase, mom.ā In my opinion, through my personal experience, mental health or mental stability isnāt something you overcome; youāre not going to wake up 10 years down the line and realizeĀ āhey...Iām all better!ā I mean; itās really not the equivalent of a broken bone.Ā I know thereās a lot of these graphics floating around the internet:
and I think theyāre great...to give substance and merit to mental struggles, being well, a struggle, but on the same accord I think we need to remember that the achievement of a stable mind may be through constant, consistent management throughout life. Perhaps, itās not something we can beĀ āhealedā from like appendicitis, food poisoning or a broken rib. Perhaps, it is simply a battle everyday to find will, purpose and fulfillment.Ā
Me: I donāt have the energy for this
Someone: For what?
Me: *gestures vaguely*

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everyday i drag my feet, but i get it done. where did my energy go?
by Davide Carovana
Depression (and/or chronic illness) is kind of weird in the sense that itās 2:30am and I just found the motivation/energy to do everything I needed to have done 12 hours ago.

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How is this not socialism?
What was that sound? And other mysterious creeks my body makes.
One semester of undergrad left! I completed my last final today. Iām excited, but also terrified, but also ready to go forward. I was trying to finish my final today, you know ā one of those essays where youāre supposed to compile literally everything that was crammed into your brain over the past 14 weeks into a few a eloquently synthesized pages. Well, I knew what I wanted to say, but I was really creeky today. Does anyone else out there in the void have those days? Where your body just makes noises and youāre not really sure where itās coming from? Iām pretty sure I have acute carpal tunnel after five pages of droning on about how media diversity/representation is really just a capitalistic ploy. (It is!)
(Here is a brief explanation as to not let anyone who stumbles upon this believe Iām some sort of postfeminist/post-racial culture enthusiast... diversity and minority representation is one of the best things thatās happening to mainstream media right now, but I think we have to think about it a bit smarter than that. Weāre representing minorities, but are we accurately representing minorities? Modern Family for example; does the gay community appreciate this representation? Does the antithesis of nuclear family? What about the Latina community? I canāt answer any of those questions, because Iām not an explicit community member. BUT, my point is weāre not going to know the repercussions of the romanticization of poverty (Shameless - although great entertainment), classism, racism in modern media until after post-production UNTIL we have equal representation in the production boardroom. We need minorities inside the creation process to fully represent diversity. My second point (and I donāt think this can ever truly be proven) is that diversity is expected in 2017, networks have entire sectors dedicated to the management of diversity (mainly liabilities, I presume), but diversity = profit. Diversity in the mainstream shows progressiveness. Progression = MONEY. Thereās more but, thatās for later).
I digress... my joints are creeking. The anthem of my gait. The stitch in my mouth is not hurting me though. Consequently, fighting Lyme doesnāt allow for me to really have the time to fight off peripheral infections; so I decided to get my tooth pulled after my dentist letās say āmismanagedā a dental procedure I had done. Resulting in A.) Root Canal, that may not 100% clear out the infection. B.) Extraction - 100% clears out the infection. I chose B. My body is tired. So here I am, tapping away, with my soft foods and stitched mouth; writing about creeks and media theory.
I hope your day was filled with friendly creeks.
(It's funny that I made this blog for an outlet for Lyme, but would rather talk Mass Comm. theory instead. Sigh. Nerd. Out.)
Where do we go...now?
Iāve been struggling a lot over the past couple months coming to terms with some of the newer symptoms Iāve been experiencing. Hip/knee pain, bruising, headaches have been a strong presence, but those are easy to deal with. Physical pain manifest a lot differently in my life than mental pain. The mental pain has always been at the back of my mind; for as long as Iāve been aware of my own āinternal monologueā Iāve noticed doubt and darkness. I am sure that is something we all experience at times.
The past couple months have shifted mental pain to the forefront of my mind. Mental pain I describe as an alteration of reality, a constant crippling sense of anxiety etc. When youāre dealing with an illness in your mind itās easy to have your presence in reality broken. Over the past few months Iāve seen myself analyze the interactions between me and others, constantly. Am I burdening them with my illness? (Yes! I convince myself). Am I guilty, should I feel guilty? (YES! I convince myself again). Iāve found itās getting more and more difficult to be able to accept and receive love when I have this consistent sense that Iām burdensome - Iām filled with guilt.
I didnāt ask for Lyme to enter my life, but am I doing all I can to get it out? Somedays (most days) it feels that getting dressed is a mental exercise. Making a grocery list is unthinkable. Iām a student; and Iāve always been a āgoodā student. Iām aware I put an inordinate amount of pressure on myself (as Iām sure you do too - reader of this rant!). Iām aware that I alter my reality into thinking that I am difficult to love. Well, I am difficult to love, but Iām not unlovable. There is this tenuous line, I think. You know that your mind is challenging you, warping you, you know itās happening! But, knowing itās happening and not allowing yourself to be consumed in doubt are two separate things.
My mind feels a lot like this post today. Jumbled. Where do I go from here? What do you do on days your mind is on fire?
This isnāt a blog about Lyme Disease.
Hi there - welcome to my firstā¦blog? I'm not sure what you've stumbled upon either, but nevertheless, greetings. I suppose I should introduce myself first.
I'm a young woman residing on the upper east coast. Currently, trying to balance out my life; finishing my education (B.S in Business Marketing, B.A in Media Studes/Mass Communications with a graphic design minor), captaining my university's track and field team, fulfilling internship duties and a part time job. I'm busy - I like to be busy. In January (2017) I was diagnosed with Lyme Disease, through the IgM and IgG blood test. Unequivocally. At the doctor's appointment I just remember smiling? Odd. I had no idea what Lyme Disease meant for me, or for anyone. I suppose I had a case of one those moments where you're entirely and utterly overwhelmed with confusion so you just revert to some sort of expression that you think won't offend anyone. My mom and my doctor sort of just stared at me tentaively, I think they were waiting for me to explode. I didn't, then. I think in that moment I felt relief, or it came over me within the next few days. The diagnosis explained a lot of things for me; my body's allocating resources to fight off not only the Lyme, but the coninfections as well, this gives my body less time to focus on processing the overwhelming anxiety that it builds. Most days my brain feels like it's on fire, but I understand why now and that gives me great relief. The diagnosis explained that I wasn't any crazier...than usual :). My body just doesn't have enough reserves to handle everything. To this, I shrug. I've chosen to battle Lyme through Naturopathic medicine and a very restricted diet. That means Iām currently taking low dosage antibiotics, managing coinfections and boosting my immune system, while strictly adhering to the Low FOD diet. My doctor's not crazy about the idea that I'm continuing to run. But, Iām stubborn, have to for mental sanity :). And sometimes mental sanity is more important. Somedays, I feel ānormalā. Somedays, I really, really donāt. I think Iām on a path that will tip the scale - I'm on the road to having more normal days. This isn't a blog about Lyme Disease. But, it is a part of my life. So it will be a part (and only a part) of this adventure. I've always been unable to define myself concisely, I hope that everyone finds those "describe yourself in 3 words" get to know you missions a very difficult joke. I'm a young girl who loves a lot of things; writing, running, photographing; I'm a sister, daughter, friend; I'm quiet, ambitious, headstrong (sometimes a bit too much). I'm a lot of things. We're all a lot of things. I'm battling Lyme, but my life is still happening. My joints hurt, my brain hurts - but I'm not putting life on hold. Neither should you. This is a space to synthesize thoughts, that I hope will help to serve me on my journey of healing. So welcome, I'd love it if you stayed too. Xo, K.