ohhhhh yes. yes i needed a migraine today on the day where a local music festival is being held near my house. yes please.
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ohhhhh yes. yes i needed a migraine today on the day where a local music festival is being held near my house. yes please.

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There is A Game I Play. Try to make Myself feel Okay 🤣
#TheCloserIGetTheworseItBecomes
There Is no Place I Can Go
There is no place I can Hide🔥
It feels like it Keeps
Coming from The Inside🤯
whenever ur vaguely allergic to something it’s like oh well my symptoms are probably flaring up. symptoms of what? they’re just my symptoms
idk it just feels like I’ll never be pretty and I’ll always be 2 steps short of living what could be a really kickass life
im gonna get a burger
i go outside to stop Experiencing Symptoms. and then i Experience Symptoms outside

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Check out @risingabovera’s latest linkup for raising awareness about RA! For more details: . #Repost @risingabovera with @get_repost ・・・ This past week many of us arthritis warriors raised awareness for World Arthritis Day. I recently shared a poem on The Mighty giving a glimpse into #MySymptoms I experience while living with rheumatoid arthritis. ___ So I created a LinkUp thanks @achronicvoice for the inspo. All you need to do is publish the poem on your blog, then add the URL to the post on my blog by clicking the ‘Add Your Link’ button. To view more information and my poem go to, www.risingabovera.com. ___ *Note: This is an ongoing LinkUp. If you don’t have a blog but would still like to participate, you can email me your poem at, [email protected] and I will share it on my Instagram stories where it will then be featured in the ‘Community’ highlight section. I can also add it to the blog if you like, just let me know! . . . . . #chronicillness #chroniclife #chronicpain #RA #rheumatoidarthritis #arthritis #spoonie #spoonies #spoonielife #spoonieproblems #painwarrior #spooniewarrior #arthritissucks #arthritisawareness #poem #poetry #chronicblogs #awareness #chronicpainwarrior #chronicillnesswarrior https://www.instagram.com/p/Bo9Ye4DHpxj/?utm_source=ig_tumblr_share&igshid=1dc1m9jt9ioi2
My symptoms made simple
This particular blog is the closest I’ve got to explaining how my particular brain damage works. It’s not been an easy journey, but with the relevant help from Neurologists and new understanding over the 8 years I have been writing, I am getting there.
The frontal lobe section, known as the ‘emotional centre’ is the part of my brain that is extensively damaged. Generally, it is the place where our emotions are controlled and where our personalities are formed. This area also plays a role in controlling movement, judgments and behaviour, as well as social and sexual behaviour.
If this part of the brain becomes injured from birth or through an accident, it can affect many functions in the body, as I am just beginning to understand. The type and severity of our symptoms depend on which section of the front lobe is impaired. As my brain is extensively damaged in the frontal lobe area, I struggle with emotions. I have always known that I have, I just never understood why.
As a result of impaired emotions, I also deal with anxiety. That explains why I used to hold on to bad thoughts and have difficulty releasing those. As a child, it would takes weeks, months, even years to let go of them. I used to have to keep myself busy so that my attention was diverted, even if it was for a short while.
Because the cells that control movement to that area of my brain is damaged, I also deal with weakness in my arm, hand, fingers, leg and foot on my Cerebral Palsy side. And as a child, although my difficulties on my left side were down to a paralysis that I didn’t know I had, although I still have a certain amount of paralysis, with continued exercise my leg is slightly stronger. I have little muscle tone and weakened muscles on my Cerebral Palsy side and can’t point my toes.
I also struggle with fine motor skills such as writing and forming outlines on those. Frontal lobe damage has an impact on non-creative thinking, and problem-solving ability and I struggle with both of those. I struggle with spontaneity, memory, language initiation, judgments and impulse control. I have mostly learned to adapt and find ways through most of what I deal with, although I often get caught out on one or most of those.
I know that if this injury were to have happened to me as an adult, my personality and social behaviour would have changed drastically. As a child, I found social situations difficult and as a result didn’t mix in very well, particularly in school. I failed to interact and think that was part of why I became so insular. I have learned a different method for me to cope.
Through my intuition, I am able to read people and understand their body language enough to know how I need to behave and what to say. But more importantly I am able to piece and link together the missing pieces to the jigsaw on my symptoms and how those play out in daily life.
For more inspirational, lifestyle blogs, please check out my site https://www.thecpdiary.com
My Symptoms
These are the symptoms I feel:
-Hot or cold flashes (at one point I was so on fire whatever I touched was left burning too, almost like I had a fever) -Nausea, vomiting, dizziness, very upset stomach -Shortness of breath (sometimes feels like I am breathing through a straw) -Feeling like I am going crazy (this is by far the worst symptom)
Feeling like I am going crazy/being out of touch with reality is by far the worst symptom I have ever experienced and continue to experience struggle with. Not sure how many of you out there who struggle with anxiety feel this too. This feeling is almost to the point of disconnection. You look in the mirror and you do not see the same person, you don’t recognize your reflection. Feel out of depth with your environment, like you are watching your life go by. It’s not necessarily you feeling fear, but you feel so disconnected. The feeling of going crazy brought on a panic attack - it goes back and forth, panic attack and feeling crazy, panicking about going crazy, and freaking out because of my panic attack. It is the most dreadful thing that I would never wish upon anyone.
This feeling of going crazy doesn’t happen everyday though. Rest assured with proper care it only happens once in a while or sometimes disappears all together. During these times I surround myself with people who I trust and love. Even though they may not understand or I feel like their presence isn’t working, it eventually does help, and I do feel better.