#treatment of adhd
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Lack of impulse Control In ADHD ADD Children | Autism Homeopathy Treatment Cure #adhd #adhdkids
About Video: Uncover the challenges of impulse control in children with ADHD/ADD in this insightful YouTube Short. Learn how impulsivity affects their behavior and decision-making, leading to quick actions and reactions without forethought. Understand the impact on their daily lives and relationships, and explore effective strategies and techniques to manage and improve impulse control. Tune in for practical tips and a better grasp of this common ADHD/ADD trait!
#impulse control#children with adhd#impluse control#impulsive child#symptoms of adhd in children#out of control teenagers#self control#adhd children#adhd in children#impulse#teaching self control#tre ating children#teaching self control to kids#how to raise children#young children#raising children#impulsive teen#self control for kids#childrens charity#adhd in young children#impulsive teenager#treatment of adhd#impulsive#control issues
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I really wish there was more interest in how to handle ADHD other than just addressing the symptoms that affect the people around us.
Like, the best pharmaceutical treatment we have right now is stimulants, and I agree that being on stimulants 24 hours a day, 365 days a year is probably not good for your body. Hell, I’m on a less-than-ideal dose of my medication from a concentration perspective because the ideal dose had my resting heart rate sitting at a cool 115BPM. I know taking med holidays is important. I know all of this.
But because ADHD isn’t just an attention problem (or may not actually be an attention problem at all at its core), it sucks that the only time period medical professionals seem to be concerned about treating are the “important” times: the length of a school or workday. Forget the fact that ADHD affects executive function, forget the fact that people with ADHD often experience chronic and unending anxiety and/or depression as a result of the ADHD, forget that there are important times that have nothing to do with an 8-hour school or work day, forget the rejection sensitivity dysphoria, the sensory issues that make things like clothing, food, and group situations a nightmare to try to navigate, the household stuff that has to be taken care of outside of the 8-hour school or work day. It feels like none of that matters because it doesn’t affect a group of fifteen or more people.
On top of ADHD, I have been plagued with anxiety-related issues for the majority of my life. I likely have a form of OCD and I have a history with a restrictive eating disorder; both of those conditions are very closely associated with high levels of anxiety. I’ve been on anxiety medications before. I was first given an as-needed medication that took the edge off but also made everything feel a little fuzzy, like there was a pane of glass between me and the rest of the world; I was put on an SSRI that somehow made my OCD-related intrusive thoughts about 50x worse than usual and had me wondering at one point if I should be hospitalized; and I’m currently on buspirone, which is doing what it’s supposed to do without the side effects of the others thankfully. But nothing, and I mean nothing, has reduced my anxiety as much as my ADHD medication.
Two hours after my first stimulant dosage, I just suddenly didn’t feel on-edge any more. I estimate that being on ADHD medication has reduced my anxiety by about 70% (buspirone’s for the other 30%). I started taking it in the summer of 2020 and I remember, in 2021, when I saw my boss in person for the first time since lockdown, he remarked on how much more confident I seemed, how I was more likely to speak up in meetings, etc. And I was like…yeah, man, it’s a wonder what not feeling anxious every second of every day will do for someone.
ADHD affects so much more of my life than just attention and anxiety, too. I have sensory issues with mine, which is pretty common, and they make eating — an already sometimes-complicated task due to the ED history — difficult at times because, while I can eat foods that I don’t particularly like, if something is what I call “the bad texture”, I will gag no matter how hard I work to overcome it (believe me, I’ve tried). And my brain sometimes decides that foods that were previously fine are now “the bad texture” and they may or may not shift back to being okay eventually; I don’t know.
The sensory issues affect me socially. My therapist and I have recently come to the conclusion that I’m probably not actually an introvert, but if I’m around larger groups, that means noise and movement and probably being touched, and too much of that causes my brain to either freak out or shut down. I used to always say, “I love people, but when I’m done, I’m done.” And that was likely because the overstimulation was building and building in the background, and at a certain point, my brain would just be like, “We gotta get outta here.” I was Queen of Irish Goodbyes for a very long time because of this.
And the executive dysfunction affects…well..everything? Not just work, not just school (but also those because if my environment is chaotic, my brain feels chaotic, and it is difficult to maintain a non-chaotic environment if you keep getting stuck on order of operations when picking up a room).
I’m not saying that I want to be on longer-lasting stimulants or that I want to be on the higher dose that I know helps my concentration more, cardiovascular system by damned. What I’m saying is, I wish treatment research had been more holistic rather than just figuring out what would give teachers and managers an easier time despite what the person with ADHD might be dealing with as soon as their meds wear off.
Maybe current research is working on it; I don’t know. I just know that, the older I get, the more frustrated I am with my brain and the more apparent the deficiencies I used to be able to counteract with pre-chronic-illness energy and crushing perfectionism become, and I wish there was an answer to this that actually helped me most of the time rather than forcing me to pick which parts of my day/week is “important” and making sure I’m medicated for those parts.
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Just read the Barriere Du Maine chapter
#poor grantaire I bet the only treatment for adult adhd at the time was like laudanum#enjolras#grantaire#enjoltaire#exr#les mis#les miserables
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I cried over the dishes today
Happy tears, mind you
It's been about a month on this new ADHD medication. The stimulants weren't working out for me. One gave me heart palpitations, the other I couldn't remember to take reliably.
But I've been on a new medication for a little over a month now, one that I take every day like my antidepressant. It's supposed to increase the precursor to dopamine, which ADHD people struggle to regulate. Like an antidepressant is supposed to give me the ability to make my own serotonin, this is supposed to just give me the ability to make my own dopamine.
It's a rainy day, I've been productive and pushing myself all week, I was going to take a rest day. But I still did the dishes, because the dishes needed doing.
And as I almost finished, I realized I felt satisfied. I felt good about it. I did the dishes.
For so long I thought the "good" feeling you got when finishing something was relief. Relief that it wasn't hanging over your head, the loss of shame that you felt for Not Doing the Thing. It was a passive sort of thing, the removal of an ongoing internal punishment rather than a reward.
It wasn't a high, it wasn't like I felt elated doing the dishes. I was just... satisfied. I was glad I had gotten that out of the way. It felt nice.
And I went to my mom, and I asked her, "is this how it feels for everyone?"
She held me, and we cried together, cried that I had missed out for so long, cried that I was buried in shame for so long thinking I was lazy and broken, cried for joy that things are looking up.
To think I spent my life without this basic neurotransmitter doing its job properly. It's like putting on glasses for the first time.
I wasn't faking. I wasn't lazy.
I'm. Not. Broken.
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When you finally have access to things like healthcare, therapy, and medication that helps you function and have made a to-do list that includes doing taxes and calling your insurance company and somehow none of it makes you anxious at all. What the HEEEEELLLLLLLL, HOW IS THIS NORMAL????
Where are the very slow tigers that are chasing me??
I'm. I'm not excited about anything on that list but I'm not not excited???? It's just things to do, that I gotta do, and I'm gonna do them because I can? I can!!
I'm making this a good luck post. May you get one big step closer to healing/recovering/getting the proper treatment and diagnoses for whatever is ailing you. Whether that's mental illness, chronic illness, disability, or simply a hardship you have to endure, may good things be on their way to you swiftly ❤️💕
#mental health#chronic illness#disability#positivity#happiness#wellness#good luck#good luck post#but really it hasn't even been a full 2 weeks and i feel like i can just DO the thing#and i haven't even TOUCHED on getting a diagnosis for adhd and barely brought up autism#i know this won't stay exactly the same forever but this feels good and i can't wait to see how well i do with real treatment
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Fighting off cold and flu has always been difficult for me and it's only getting harder as I get older. I find the transitioning from being "sick in bed" back to "functioning person" can often be the hardest part, especially when it comes to congestion which can take days if not weeks to clear up, so even if I'm able to walk around, do basic tasks, etc. I'm uncomfortable the whole way through. At least when it comes to my back pain, that's something that I'm used to and can predict and accommodate; getting sick is none of those things.
What's making it even more difficult this time around, compared to every other time, is the fact that I went from being healthy and medicated to sick and unmedicated. So that transition back into "functioning" is being slowed further by my returning inability to focus, to push myself through the uncomfortable feeling of doing literally anything, to be at peace with boredom.
Every single time I want to do anything that isn't laying in bed, it's met with both "I don't know if I'm physically capable of doing that because I'm sick" and "I don't know if I'm mentally capable of doing that because I'm off my meds."
And it's incredibly exhausting.
#self post#update#off topic#idk sorry for whining on main#my brain just. feels awful rn#part of me thought “huh i don't think being unmedicated is actually causing me issues”#but now that i'm on my third day (???) without meds i'm not feeling so sure LMAO#and for anyone wondering why i'm not taking them#it's because i have to play triage with my meds and treatment#i don't want to be stacking decongestants - some of which are designed to make me drowsy - on top of concerta which is a stimulant#this would kill the liver LMAO and also my brain would become an even bigger mess than it already is#so considering i'm on bedrest i've just decided to forgo taking my concerta meds until i don't need to be hopped up on sinus pills#then once the worst of the sick has passed and i can get by without needing pain and congestion relief i can go back on concerta#thankfully i was only on 18mg anyways so the crash isn't as bad as it would have been if i was taking stronger doses#but it still sucks and it means i'm at war both with the flu and my ADHD u.u
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Okay, I need advice. I’m getting diagnosed with autism and I just went through the first screening for speech therapy. My dad found out about it and he’s really upset bc he feels like my mom is trying to “label” me and “she goes to church and socializes and loud concerts and she’s fine so obviously she’s not autistic”
For perspective, I’m 100% okay with being autistic and have known it for years. I know there’s nothing wrong with me or wrong with being autistic. My mom spent her twenties working with adults with disabilities, like the deaf and blind, autism, ADHD, Tourette’s and other disabilities. She thinks anything but less of me for my disability and I know she’s not trying to label me.
Any thoughts or ideas on how I can help my dad see things from my perspective, or at least stand my ground against the idea of “labeling” and that being able to function doesn’t mean I’m not autistic?
#autism#autism things#autism tag#autism test#autism thoughts#autism treatment#labeling#advice#adhd#disability#disabilties#disabled#neurodivergent#neurodiversity#neurodiverse stuff#actually autistic#actually neurodivergent#actually neurodiverse#neurodivergencies#neurodiverse things#neurodiversesquad#neurotypes
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hi…i recently discovered that there is a very high chance i have ADHD. after doing lots of research, i brought this up to my therapist, who also has ADHD. she had me do a screening, told me she’d noticed the signs awhile back & believes i have it; however, she is not authorized to give an actual diagnosis. later, i talked to my doctor about it to see if it would be worth seeking one & what my options were. she told me that to get a diagnosis i’d have to see a psychiatrist, which would take at least a year because of wait times. but she asked if, for the time being, i’d like to be prescribed a 7-day supply of 15 mg adderall to see if it helped. ive done an okay job managing symptoms throughout my life, but some of them have really taken a toll on me, especially emotional dysregulation, so i thought it was worth a shot.
but im on day 3 of the pills and i don’t feel any different. ive looked all over reddit & see people saying that it kicks in instantly, but i haven’t felt that at all.
is this normal? should i be concerned that’s something’s not working right? could this be a sign that i dont have ADHD? and in that case am i harming myself by taking this medication?
sorry to dump this here. im just extremely new to this & i dont know what i should be expecting.
Sent August 5, 2024
Okay, first of all, a medication trial is not a reliable diagnostic strategy. Different meds work for different people, and it can take time to find the right dose. So don't worry about that.
Not feeling any different isn't a sign that the medication isn't working. It's possible that things are different but you aren't noticing because the changes are subtle. It's also possible that the dose is wrong and you need a higher one or even a lower one. Or you need a different medication. In particular, if your biggest issue is emotional dysregulation, guanfacine (brand name Intuniv) can be very helpful for that.
I think it's worth getting on the wait list for the full assessment, but also talk to your doctor about trying something else in the meantime.
Followers, what are your experiences with medication just after diagnosis? Can you offer any advice here?
-J
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Sure didn't have "methylphenidate is going to partly solve my anosmia" on my 2024 bingo card YET HERE WE ARE
#there have been a couple of double blind studies that seem to indicate a lack of olfactory sense could be a bio marker for adhd#AND#that treatment with methylphenidate can increase olfactory sensitivity#fucking whack
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Call : +917997101303 | Whatsapp : https://wa.me/917997101505 | Website : https://fidicus.com
Why Golden Period Is Important For ADHD ADD Hyperactivity Kids? | Treatment Cure Medicine | Autism | Homeopathy | Autism ADHD Treatment Cure #adhd #adhdkids
About Video: Understanding the golden period is crucial in treating ADHD or ADD in hyperactive kids. This period, often during early childhood, is when intervention is most effective. Addressing ADHD or ADD symptoms early can lead to better outcomes, improved focus, and fewer behavioral issues as the child grows. Early homeopathy treatment can help manage symptoms naturally, promoting long-term well-being. Don't miss this critical window for your child's future success.
Dr. Bharadwaz | Autism ADHD | Health & Fitness | Homeopathy, Medicine & Surgery | Clinical Research
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had to stop taking the new adhd medication but the good news is i can drink coffee and iced tea again
#it's the bright side to every time a medication has failed lol#gotta set up an appointment for alt treatments#pretty sure my insurance doesn't cover counseling and i can't afford it... which is why i've been going for meds#it's one of those things where if i have enough going on in my life i can manage my adhd relatively ok but i'm severely under-stimulated rn#i have too much time on my hands so there's nothing for me to force me to do the things that aren't as interesting as say. fucking around#so the variety of stuff i do keeps narrowing and it just gets worse#so all i really need is a kickstart#which!!!!! if stimulants weren't so hard on my body! would be great!!!#i need structure in my life but setting up structure myself is boring#like yoga is something i LOVE doing but it's still hard to get on the mat even though i used to be able to do it every day#i think that more yoga would definitely help but i don't know how to get myself there#rum.txt
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Also, I'm getting medicated for my adhd IN TWO HOURS. No more constant suffering and feeling like a failure, IN ONLY TWO HOURS, after years of waiting to even get diagnosed.
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Fml 🙃
Trying to study without meds feels like trying to build a house without mortar. It can work on a day when the weather's really good but even then it can all fall apart so easily, let alone if there's wind and rain!
I've studied med free before and I'm sure I can do it again but whether I'll achieve all that im capable of is another thing entirely!
Time to stock up on good diet and exercise and other compensatory strategies, take cover and hope for the best! 😩
#adhd#adhd memes#adhd meme#student memes#uni memes#adhd student#adhd struggles#adhd medication#adhd meds#adhd awareness#adhd women#adhd treatment#adhd problems#adhd life#adhd brain#actually adhd#audhd#uni life#memes#student life#adhd hacks#adhd tips#ineedfairypee#fairypeememes#i need fairy pee
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🍒
#mine#ts4#sims 4#the sims 4#simblr#sims#ofmd#ed#ofmd sims#i had an appointment w my psychiatrist 2day and it went rly well and im feelin rly good about it and myself rn 😂#she said she thinks i do have adhd and since i already take adhd meds (off label for treatment resistant depression) she said that it would#be a good idea to talk to my therapist abt this too#and we can adjust some therapy stuff to be more suitable#got a zoloft prescription for during ovulation because i guess that is supposed to help w/ pms#and she's gonna try and get my insurance to cover dyanavel so i can try that too#good things good things!#like. idk i feel like im on the cusp of something good and i NEVER feel this way lol#but this could maybe be part of the puzzle and one step closer to figuring myself out
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I am tired of being in the DSM-V, please put me in another book. am i irritable, hyperactive and and forgetful because i have adhd or because i am a werewolf on my lunar week. is it the depression or my ancestral curse coming to bear. Is it anxiety or am I haunted by the ghosts of the city around me. let's keep some whimsy in the world plz and not make literally everything about how we're incorrect in some way.
#take mental health seriously and all that. Destigmatize it &c#But i am exhausted with this culture of pathologizing EVERYTHING.#I had a student writer make a series of character profiles and a must-have category was “disorders”#Like christ. Our personalities are not our diagnoses.#Let's chill with this trend of grouping all normal human behavior into diagnostic criteria.#I am glad you see yourself in the experiences of the mentally ill! Relating to your fellow humans is good!#But maybe take it as an opportunity to empathize FIRST rather than instantly taking the opportunity to slap another label on yourself#You don't have to be autistic/psychotic/etc to relate to and love autistic/psychotic/etc ppl#Because they're PEOPLE of COURSE you're going to relate to and understand their experiences to some extent!#You don't need to “have” a disorder to benefit from their treatment/coping strategies/etc#It's not effing chemotherapy.#What's good for the goose is good for the gander#Earplugs help people with autistic/adhd/etc sensory overload and also you??#You don't have to give yourself a diagnosis to use earplugs.#Promise.#Mental health#mental illness
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how it's going
yah my second experiment with adhd meds is like. well, this time it's making it so i can't sleep and my appetite gets shitty, which is what they normally say but i didn't really have that problem last time. i do now!!!
cut for discussions of eating/weight gain/loss shit, and the Horrible Yearnings
lil PSA, because a friend said something about this-- yah SSRIs make you fat (i gained 25 permanent irrevocable pounds on Celexa in 2012 and that's that, it's never gone away no matter what I did and it never will short of some other medical crisis I think), and it's reasonable to in a kind of not-healthy but understandable way wish that the amphetamine ADHD meds would thus make you thin. Seems like it, yeah? If you have no appetite and your metabolism is higher? I'm not finding that, though, so here to nip that in the bud is my observation that if you have trouble with comfort eating, losing your appetite does not take that impulse away, it just makes it disgusting. I actually am not a big comfort eater, but I do, like many humans, tend to derive comfort from eating food I enjoy? This takes that away without removing the need to do it. I still need to eat; if I don't, I get heartburny, emotionally distraught, and more, just like always. But now instead of enjoying the food at least, I find it unappetizing, have to force myself to prepare it, and then eat it so slowly it's always cold/mushy/melted by the time I'm done, and it's not satisfying. And instead of an occasional Fun Lil Treat as a pick-me-up, I wind up roaming the house with Formless Yearning, because I know food won't make me feel better, but nothing else is making me feel better, and I'm not getting any pleasure chemicals from anything I do, any more than I ever did. Friends have reported the dreaded afternoon/evening time when their ADHD meds wear off as being always a notable time for the Yearnings, but I'm finding that I get that just Whenever, so.
It ain't fun and it ain't cute.
But I'm determined to stick this test out to the end of the week because every day has been somewhat different at least, and I'm really trying to write down what happens. Because I was given two weeks' worth of this shit, and I tried it for a week and hated it so much I stopped, but then I didn't write down what happened so I have no fucking idea what to tell the doctor. (I also collapsed into despair and stopped calling that doctor back, but like, that didn't solve anything, and being bitter that finally getting a chance to attempt to fix my ADHD didn't work on the first several tries and in fact seems to still be beyond my capabilities because it requires me to have pattern recognition skills plus medical knowledge I simply don't have... well, it isn't helping anything.)
So we shall see. I have no attention span whatsoever and a MUCH worse working memory than usual, I routinely get up and leave the room to go do something and by the time I get to the next room I have NO memory of what it was, and unlike my normal life, I don't ever get the memory back. Usually I can retrace my steps but now that entire train of thought is JUST GONE, which is way more severe than the problems I normally have. And my usual coping mechanism, where I get up the oomph to do something by daisy-chaining several tasks together, is WILDLY ineffective now because the moment I add a second task the first one falls off and vanishes and I again, cannot recollect what it was.
I normally am no great fist at to-do lists, but I was told it's the Only Way To Make Vyvanse Work, but what I'm finding is that i am also even less capable than normal of making a to-do list have any relationship to reality. Plus I forget I made them, so. They are in fact not helping me.
I have had reasonable (like... 5 hours or more) sleep two nights this week so far, all other nights have been significantly less than that, two or three hours in most cases, which is not all that unpleasant-- at least my bed is comfy-- but does mean I have even less that I am capable of doing when I am awake, since I am so fuzzy-headed from lack of sleep. Also I can't nap, which is usually what fixes me; I am a world champion napper, but this is actually an issue from about the last six months, I cannot actually fall asleep during attempted naps, so it's futile to try. Discouraging!
Last night was a reasonable night though, so I'm carefully observing my capabilities and let me tell you I am not impressed.
So, what I'm finding is that stimulant medications make me MORE ADHD than I was before, which is. I don't know what that means and neither does my doctor so far.
I was going to write about my writing process but now this seems too whiny so I will not, I'll do that separately lol.
#about the author#adhd treatment#or whatever this is#who knows#still holding out a theory that i am just uniquely broken#more likely than you think!
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