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The Ethicality of Sustained ADHD Medication

6 minutes ago
3 min read

40 mg of Vyvanse every morning —often before breakfast—, 20 mg of Adderall before  homework, and, don’t forget, a hearty dose of melatonin before bed to wear off the stimulants.  It’s the daily standard for millions of students with ADHD. Every. Single. Day. Initially a  characterization of neurodivergent individuals, the label of “ADHD” has quickly become the  basis of desensitization for the greater public. Tolerance, addiction, and withdrawal are among  the most addressed implications of substance abuse. Yet, when it comes to ADHD, we turn a  blind eye to the devastations of heavy stimulant intake, waving it off as “just a routine”. But the  truth is, children with ADHD are just as prone to dependance to these powerful chemicals, and  thus, it is imperitive that we don’t use their functionality as an excuse to ignore the long-term  effects of sustained use. 

Before we discuss potential solutions to dependance in children with ADHD and  establish a stance on the ethicality of the strenuous medication regimes, it is important to first  consider the neurological processes they influence. As a testament of their strength, let’s figure  out exactly how they work: 


A Deep Dive into ADHD Stimulants 

Stimulant medications essentially work by expediting the activity of dopamine and  norepinephrine, which are neurotransmitters involved in regulating focus, attention, and arousal  among other facets of mood, through a multitude of ways. In particular, the specific circuits they  alter are from the prefrontal cortex, the primary center of decision making, impulse control, and  memory in the brain. In regular neurons, when dopamine or norepinephrine is released by a  neuron into its corresponding synaptic cleft, they bind on to the receptors waiting for them on the  subsequent neuron. This binding process occurs for only a split second, though, before transport  proteins (dopamine transporter DAT and norepinephrine transporter NET) engage in a process  known as reuptake, where excess neurotransmitters are rapidly evacuated from the site. This  prevents an influx of activity in the synaptic cleft, ensuring the neurons aren’t overstimulated. This reuptake process is completely inhibited by methylphenidate medications like Ritalin and  Concerta, which block DAT and NET enzymes from carrying out their protocols. Adderall,  Vyvanse, and other amphetamine medications, on the other hand, amplify the effects of these  neurotransmitters by interfering with how much of them are stored inside neuron vesicles. This  interference yields significantly higher concentrations of them within the neuron itself, which in  turn results in their influx in the synaptic cleft, where they take effect. The increased stimulation  of the D1 dopamine receptors and the alpha-2A adregenic receptors that both types of medication  cause stronger, longer-lasting signals to the brain to lengthen attention span, filter distractions  from the environment, and maintain a goal. It’s important to note that a curated dose amount for each prescribed user is of utmost importance, since too little stimulation will hardly see any  effect, while too much will cause an overload that may lead to anxiety, agitation, and actually  worse concentration and cognitive performance. 


The consequences of long-term stimulant use and the potential to establish tolerance are heightened in children, whose pre-frontal cortexes and the neural pathways that are housed in  them are still developing. It becomes increasingly important to monitor side effects like physical  growth, weight-loss, sleep disruption, elevated heart rates, and changes in blood pressure in  children, whose neural circuits are not yet mature and thus prone to developmental  modifications. 


Drugs like Adderall, especially in unregulated use, are notoriously addictive. So naturally, a  measure we should adopt is a more tapered dose system in which doctors systematically lower  prescribed intake amounts as conditions improve. This ensures a smooth transition into  productivity without medication rather than a dependance on it.  


No one is denying the functionality of this medicine. These drugs allow for a more  regulated and ideal learning environment for children around the world. That being said, by  keeping a sustained or even increasing dose, we are perpetuating dangerously high levels of tolerance to these strong chemicals. Children wishing for the mitigation of the disorder and better  executive control in all conditions are instead sucked into a vicious cycle —a feedback loop of  medication— in which their intake only goes up. The more they take, the more they build up  tolerance and require more to feel the same degree of regulation. The substances that were  prescribed to help with productivity end up snatching any chance they have to function without  them. 









Shaurya Singh: IN HOSA State Representative (2026-2027)

 
 
 

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