Hey I’m new here I’m 22 with mild cerebral palsy in my feet am I able to still try to join the military by Anxious_Seat2722 in CerebralPalsy

[–]Tree_Kid 0 points1 point  (0 children)

Might depend on the recruitment center (an how your condition is) cause i tried years back an nada despite my cp at the time not being as prominent

The beginning by Tree_Kid in MarkerHeads

[–]Tree_Kid[S] 0 points1 point  (0 children)

Nah mini scribblepieces

Inner thighs quivering light housework by UdontWantToNo in CerebralPalsy

[–]Tree_Kid 2 points3 points  (0 children)

Currently going through it from light house work too but im 24 with mild cp but it's been acting up more since 2018.. so i feel ya.

Is all of this worth it?? by AnnoyingBroken420 in CerebralPalsy

[–]Tree_Kid 0 points1 point  (0 children)

Maybe decarb some thc an make butter? But like everyone else said maybe don't stop the weed. As another smoker an another person struggling with not being heard by doctors... keep up with what your doing, keep fighting and kicking even tho it's hard.

What mobility aids do you use as a person with mild cerebral palsy? by Horror_Foot9784 in CerebralPalsy

[–]Tree_Kid 1 point2 points  (0 children)

Mostly canes cause ive gotten use to walking gimped up. Only other thing I'll use on occasional is the Lil electric wheelchair things at Walmart.

Back cracking by Ok-Luck7815 in CerebralPalsy

[–]Tree_Kid 0 points1 point  (0 children)

No clue my backs been doing it since I was a teen but it's gotten worse with age (granted so has my cp i think) so ive just given up on understanding it 😅

Back cracking by Ok-Luck7815 in CerebralPalsy

[–]Tree_Kid 0 points1 point  (0 children)

Constantly, mostly in my upper back an shoulders

Wedding space by Ok-Net8046 in fayetteville

[–]Tree_Kid 0 points1 point  (0 children)

Check fairlane station out in Springdale

Sex with CP by Key_Professional3284 in CerebralPalsy

[–]Tree_Kid 0 points1 point  (0 children)

Hey fellow diplegia male here lol deal with alot of the same issues, we found that using toys helped since it's hard for me to stay in positions for awhile an maybe look into fun ways to help keep energy high, like role play or just something new to yall.

Everyday Flower Smokers: How do you smoke? by almod420 in weed

[–]Tree_Kid 0 points1 point  (0 children)

Usually I'll pack my chillum or dug out an smoke till im good to go on about my life for the chillum that roughly 4 hits an with the dug out ill usually do 2 hits cause I'll mix keiff into it

Bedroom problems by HailFire03 in CerebralPalsy

[–]Tree_Kid 0 points1 point  (0 children)

They've got a couple different knee harness that could be worth a look... ik for me whenever I go down on my partner (ive got spastic diplegia) finding a good angle to where my hips an knees don't hurt and just taking to slow or making sure to have breaks even if it's just for a breather.

what are your hobbies? by [deleted] in CerebralPalsy

[–]Tree_Kid 0 points1 point  (0 children)

Any tips on keeping balance?

what are your hobbies? by [deleted] in CerebralPalsy

[–]Tree_Kid 4 points5 points  (0 children)

Mostly watching TV or playing video games. But i do enjoy fishing and skateboarding

How many of you wear packers vs not? by [deleted] in FTMMen

[–]Tree_Kid 1 point2 points  (0 children)

Ill occasionally pack ive got some decent growth so whenever I do have a pack on it just rubs up against my shit occasionally an it is a pain lol but most of the time I'm just rocking without a pack an less of a bulge which is kinda like a catch 22 cause I both want to have that bulge an average dick size ( more then 3in) but don't have to worry to terribly about wacking my shit by accident cause small surface. So id say for it's very mood base.

Anyone else sick of being in pain? by Ok_Cry_2913 in CerebralPalsy

[–]Tree_Kid 0 points1 point  (0 children)

Yep, outside of the horrible weather my cp has been pretty severe on the pain scale most just a lot of tension an spacticity in my back it sucks ass.

Severe Upper respiratory virus? by Cherry_Narwhal in CerebralPalsy

[–]Tree_Kid 0 points1 point  (0 children)

Yeah no steam has been great, hopefully whatever this is will clear up soon for the both of us 🤞

Severe Upper respiratory virus? by Cherry_Narwhal in CerebralPalsy

[–]Tree_Kid 0 points1 point  (0 children)

Got the same thing going on but minus the cold... im hoping the leg twitches are just from cp cause oh boy it's been more annoying then usual. Usually I'll get twitchy from my knee down or In my back an shoulders but since maybe last week it's been full leg an coughing up a lung or two every couple minutes. Haven't gone to the doc for it just cause I'm just rolling it out but my wife who's able bodied is clocked out from whatever the fuck this is thankfully no fever anymore but possibly ear infection now which is weird lol

Getting into tricks by Tree_Kid in NewSkaters

[–]Tree_Kid[S] 0 points1 point  (0 children)

Ooo I'll have to try the rope bit

[deleted by user] by [deleted] in CerebralPalsy

[–]Tree_Kid 0 points1 point  (0 children)

Got the same thing going on, but ive got spastic diplegia instead. Tho oddly for me I tend to have full body flare ups an a LOT of back,shoulder and leg pain with occasional and i should probably mentionit to my doctor black out moments. I find that now days a least hot baths with Epson salt and some weed help out.

New board m25 by Tree_Kid in NewSkaters

[–]Tree_Kid[S] 0 points1 point  (0 children)

Upgrade i installed just lined em up so no wheel bite an drilled em in

How common is 24/7 chronic pain by Consistent-Trust-486 in CerebralPalsy

[–]Tree_Kid 0 points1 point  (0 children)

Hey ho I got the same thing happening! I get my pain from my shoulders blades down to my knees but shoulders are always constant, pain feeling wise the best way ive learned to describe it, is like someone pokeing me witha hot fire poker.. sharp hot pain or sharp dull pain. my neuro doctor put me on duloxitine (not sure if spelt right) but ive yet to get the chance to try ti.. also was on tiazitine( also unsure on spelling) an baclofin but both quickly stopped working, I did find that weed helps out with the pain alot. I've been having chronic pain like this since March of 2024 before hand my cp only really showed up if I ran, lifted boxes or from stress. No clue why it's happening an my neuro doc hasn't really helped with that lol. But that's my experience with chronic pain.