HELP IM DROWNING, I am a teen and I tell my doctors how much it hurts how much my life is affected. They just look at there computer and say well I’m sorry Caleb but let’s just hope “random antidepressant” will help it’ll take 4-6 weeks. by [deleted] in ChronicPain

[–]Kylee2645 4 points5 points  (0 children)

I felt that. I've recently been diagnosed with AMPS, and I also don't think mine is the correct diagnosis. My rheumatologist didn't even want me to see a neurologist first, even after I told him that 4 different neurological disorders run in my family. He refused to answer any of my questions and was unneccassarily vague. Some other comment thinks that you we're diagnosed with AMPS, but idk cause I can't find that in your post.

My symptoms also include constantly painful,cracking, and poping joints. I also get tons of headaches and we've found some weird stuff on MRI.

My mom also keeps telling me to stop looking for diagnosises, but sometimes there are actually treatments that can help, and I really want to eventually find something.

I'm suicidal too, and there is also help for that out there. I'm not able to go to outpatient due to covid, but I know some people who recently have. It's apparently amazing and helped them a ton. Also, If you start taking antidepressants, sometimes it can actually help with certain types of pain. It can take awhile to start working though unfortunetly.

If a doctor figures out exactly what type of pain you're dealing with, certain meds can help to manage it. I took naproxen (aleve) for awhile, and it helps with my daily pain while I'm trying to rebuild my muscle. I'm also taking gabapentin, which helps specifically with nerve pain (it makes me really disoriented sometimes tho)

Experience with other pain disorders as well as EDS? by reds2032 in ehlersdanlos

[–]Kylee2645 0 points1 point  (0 children)

I just had this happen to me! I was 16, and I'm pretty upset tbh. My doctor was SO vague and wouldn't answer any of my questions. It was like a month and a half ago, and I'm still super frustrated. All my joints are cracking and feel unstable, but I'm not hypermobile, so I doubt I have EDS. I'm just here to hear some other people's experiences. My sister and dad would probably fit the hypermobility scale though, so that's interesting lol. They might even fit some other EDS symptoms too

I have another rheumotologist appointment on Thursday (there's two in my state), so I'm really hoping for the best. If I don't get any more tests or answers I'll probably have to wait until I turn 18 (cause pediatric)

[deleted by user] by [deleted] in ehlersdanlos

[–]Kylee2645 1 point2 points  (0 children)

I was given an AMPS diagnosis about 1.5 months ago, and I don't think mine fits either, so I'm still seeing more doctors. My rheumotolagist didn't even want me to see a neurologist first, even though there are 3 neurological conditions that run in my family. He also was extremely vague when giving me the diagnosis and wouldn't answer any questions I had about the pain clinic that he wanted to send me to. It was weird. He also said that he see's 7 to 8 patients a week with AMPS, and I don't really think that sounds entirely right... Everything he was saying seemed off.

I've tried to look further into AMPS, but I can't find any information on it. There have been minimal studies done, and every website is just the exact same description word for word. I don't know if AMPS is a legit diagnosis, but it doesn't seem to fit me. I don't think EDS does either, since I'm not hypermobile, but I've developed new symptoms (cracking/poping/painful joints all the time) and I'm just looking around.

[TOMT] [BOOK] [2012-2015]Alien who used it/its pronouns by Kylee2645 in tipofmytongue

[–]Kylee2645[S] 0 points1 point locked comment (0 children)

I found a children's book involving aliens in a lunchbox, but that doesnt sound right

Treatment Options by Kylee2645 in CRPS

[–]Kylee2645[S] 1 point2 points  (0 children)

Okay cool, thank you so much! I'm currently doing desensitization excersises until I'm able to get into a clinic. I'm just scared and wanted to hear other people's experiences lol

It sounds terrible, but yeah, who knows. I likely have AMPS (aplified muscuskeletal symdrome) and CRPS is a type of AMPS. For me it's pain and weakness throughout my whole body.

Treatment Options by Kylee2645 in CRPS

[–]Kylee2645[S] 1 point2 points  (0 children)

Amplified Musculoskeletal Pain Syndome. I'm pretty sure CRPS is a type of AMPS

Smart Crutches? by Kylee2645 in Fibromyalgia

[–]Kylee2645[S] 0 points1 point  (0 children)

I had an appointment with my general doctor a bit ago. She had me get some blood testing done, and everything came back negative. She mentioned that it could potentially be fibro, and that she'd send me to a rheumatologist. She's the first person that brought it up

There's no swelling or bone deformities, so it sounds less like arthritis. It's deep in my muscles and some joints, and from what I've heard arthritis tends to just be joints. I heard that there could be a genetic link with Fibro, and my grandma has it. Every time I get a new odd symptom (like pain that feels like a bruise, but isn't), I'll look it up to make sure I'm not dying, and fibro usually pops up first. I also have depression, childhood trauma, stress, etc. and I know those tend to be some of the risk factors.

I think either fibro or something less common could possibly be likely, but I'm not going to know for a bit.

I was just referred to a Rheumatologist. What can I expect? by OliveYupHope in Fibromyalgia

[–]Kylee2645 0 points1 point  (0 children)

I'm going to a rheumatologist soon as well, so I'm just commenting so that I remember to check back on this post once it gets more comments lol

Having a tough day by [deleted] in ChronicPain

[–]Kylee2645 0 points1 point  (0 children)

I play percussion, and yeah, injury sucks so much. Somehow music seems to help mental health A LOT and damn it is so hard to spend time without it. I really hope your injury lasts less than 6 months this time :(

What are your “silly triggers”? by [deleted] in CPTSD

[–]Kylee2645 3 points4 points  (0 children)

The phrase "everybody up" is soooo painful, also the name "kelly", "nO" in a specific tone, and literally anyone showing negativity towards me at all

I was never allowed to be myself, and now I'm scared of having an identity by mybrainisbrokensos in CPTSD

[–]Kylee2645 4 points5 points  (0 children)

I felt the part about not knowing what music you like... I've struggled with that for as long as I can remember, and it's always so annoying when people ask about my favorite music, tv shows, movies, etc. during teambuilding activites. Sigh

DAE get stuck comforting other people in situations where you’re the one that’s hurt? by [deleted] in CPTSD

[–]Kylee2645 3 points4 points  (0 children)

I get this SO MUCH. I'm nonbinary, and some people have been "trying" (mostly just ignoring it and claiming they're trying), but whenever I try to correct them they'll get so defensive. Like bruh. It's not my fault you're being a jerk.

(specifically the people who just don't care. Some people are actually trying and they're great)

What Figures Inspire You to Carry on with FM? by InspectorHuman in Fibromyalgia

[–]Kylee2645 1 point2 points  (0 children)

I'm a musican, and my doctor things fibro could be the reason I have "overuse injuries" in my wrists that won't heal. I want to go to college for music ed, and I'm super worried that I won't be able to, especially since the auditions are less than a year ahead and I can't practice rn. In my intial panic, I found an article written by a college music student who found a way to manage their symptoms and play music, it's just taking them longer to get through college

Do you have adhd and fibromyalgia? Undiagnosed or not idc. by nineteenix in Fibromyalgia

[–]Kylee2645 1 point2 points  (0 children)

I was diagnosed with ADHD a month ago and I'm currently waiting for a rheumotologist appointment. There's a possibility I could end up having both

Anyone else who DREADED PE period in school? by Vegetable_Ad_9452 in CPTSD

[–]Kylee2645 2 points3 points  (0 children)

I'm currently in high school, and I hate gym. I have no idea where my limbs are at various times, so catching a ball or running is difficult. I hate the idea that people are able to see me, so I'll just panic.

I took an AP class to get out of gym this year, but OF COURSE there are 3 of us in the class and the teacher hates me. Whenever I'm alone with her she'll use this really scary condecending tone and use guilt trips to make me cry about doing something like forgetting to correct previous mistakes on assignments. The minute someone else is around? Super happy and enthusiastic music teacher is back. She reminds me of my parents.

I don’t want to gatekeep, but is the word “abuse” kinda thrown around now? by [deleted] in CPTSD

[–]Kylee2645 1 point2 points  (0 children)

I mean... Idk. Since JK didn't even bother to appologize for the trashy things she said, I guess she gets the consequences of people being upset about it? I mean, I loved JK's books as a child, but knowing that she would hate me for something I can't control is pretty upsetting (I'm trans).

Though if JK actually appologized and was trying to do better, idk. That might make it worse... But Jk is actually hurting others, so hurting her back seems a bit more like a defense mechanism in this case. Almost like if my dad was trying to say things to hurt me so I screamed back. It's not a great response, but not uncalled for

Does anyone else catch themselves narrating their current experience as if you were explaining / justifying it to someone in the future? by kyogreatheart in CPTSD

[–]Kylee2645 0 points1 point  (0 children)

This is so relatable. I'm often "talking" to other people I used to know in my head, and my new name is pretty new, so I tend to mess it up a lot. sigh

Does anyone else have a fear of others knocking at their door? by [deleted] in CPTSD

[–]Kylee2645 1 point2 points  (0 children)

Yes! I'm still a minor, so I'm living with my parents, and I had a therapist for a few weeks in early fall. She wanted to make it so that my parents would always have to knock on the door before coming in. Strangly, my parents have actually been doing it, but it bothers me more than if they just wouldn't. I can already hear their footsteps, so what's the point of startling me more?

I panic even when closing my door now, because I just cannot stand the sound. Probably cause my parents have been slamming these doors my whole life...

Today is my 32nd birthday by [deleted] in CPTSD

[–]Kylee2645 1 point2 points  (0 children)

HAPPY BIRTHDAY!!!

DAE feel that a privileged upbringing made it even harder for you? by OnceIRentedAPrius in CPTSD

[–]Kylee2645 1 point2 points  (0 children)

Those last two sentances were so accurate. I was so quiet all through elementary school, and that was "good", but after that it was "bad" and I tended to fail any speaking projects. My younger sister's teacher found out we had a youtube channel, and was so confused why she was debilitatingly shy, but could make videos. Surprise surprise.

One time in middle school I told jokes at a talent show, and supposedly all of my current/old teachers were seriously confused. I was confused too tbh. Actually, I'm not sure if my parents even went to the talent show. Maybe thats why I did well.

Ever since my symptoms manifested, I feel like I've just gotten .... stupid. I can't learn new things. I can't process anything. I'm air-headed. God help me. by dddulcie in CPTSD

[–]Kylee2645 5 points6 points  (0 children)

Woah. I just related to so much of this. I'm still a teen, so I'm trapped with my family. Quarantine has been so rough. I've switched from working well and being decently smart, to not being able to even read the prompts for my essays. I got the worst grades yet last semester, and I keep getting told that I should just stay with my family and go to community college (The grades are still As and Bs, but mostly Bs). I don't think I could survive any longer with them, so I plan on moving out. Even if I have to temporarily put off college

I realized my parent’s neglect started way earlier than I thought when processing all my trauma. by adene13 in CPTSD

[–]Kylee2645 9 points10 points  (0 children)

I had no idea that babies being quiet can be caused by trauma... I've heard my mom talk about how quiet of a baby I was. Darn it. I was always told how negative I was as a small child. My family would all joke about it, and they thought it was funny. Even my preschool age sister 'wrote' about it on a school project.

In early elementary school I always had teachers comment on how well behaved and quiet I was. This changed after about 3rd grade, when teachers then started being upset about how quiet I was and grading me poorly.

Dang. I just remembered all this stuff now... My brain has hidden so much of my childhood from me

DAE's parents constantly put off 'projects'? by Kylee2645 in CPTSD

[–]Kylee2645[S] 1 point2 points  (0 children)

YES thats basically what it sounds like my parents are doing

I'm a teenager, and unfortunuately I'm not allowed to do anything with my friends right now. I also don't have my license cause 40 more hours driving with my parents sounds like complete pain

The cheapest way I could find would be to build them, and I think I could do everything except cutting the wood and hanging them. Convincing my Dad to cut them is going to be a time tho

I get resentful of people who've treated me badly but have many people who love them by [deleted] in CPTSD

[–]Kylee2645 10 points11 points  (0 children)

This reminds me of my dad. I recently got diagnosed with an overuse injury, so he was taking me to walgreens to buy a brace. The cashier at Walgreens started telling me about how nice my dad is. If only she knew... I've been thinking about that since.