How do I help my new doctor understand what I need in terms of adult adhd?
I was diagnosed at 44, (within the last year) though I’ve pretty much guessed that I have had it for a long time. My kids have both been diagnosed and were struggling in school, they are pretty successful now with appropriate supports.
I had to change doctors due to an employment and insurance change, and just had my “new patient visit”. Took a while to get an appointment so now I have about 9 adderall left. (Only take 5 mg because my previous doc was worried about medication tolerance). I’m not married to the idea of meds, but I was a bit disappointed in the doc’s attitude towards my diagnosis.
She basically wants me to go get re-diagnosed. I mean, fine I will jump through the hoops, and probably go through the merry go round of being diagnosed with depression and anxiety, and treating the symptoms rather than the problem. And/or sleep apnea. I don’t think I had that when I was in middle school struggling to turn in homework, probably not in college when I pulled all-nighters to cover up for not being able to break down a project into manageable chunks.
The doctor said that, because I managed to “cope” and get good grades, hold a decent job, etc that I must not really have adhd that needs to be treated.
Apparently, that means it is perfectly healthy to need to have control over every detail of your job and have no surprises so that I reduce the changes of falling flat on my face. It’s also healthy to avoid seeing friends socially in case I might be expected to reciprocate by having people over to my constantly messy, always-under-construction home. It’s healthy to not make any volunteer commitments at my kids’ school because I am afraid I won’t be able to get my part done on time, or afraid I won’t be aware of the unspoken expectations of field trip chaperones or what have you.
I would love to see a counselor or adhd coach “instead” of medication, but guess what? They are like 100% unavailable right now. She also mentioned that adult adhd diagnoses increased significantly in the last couple of years, and her interpretation of that is essentially that perfectly healthy people are just stressed out and think it is adhd; and of course a stimulant medication is going to give anyone a “boost” but that doesn’t mean they “need” it to function. I see the logic, but I would counter that the pandemic finally “broke” a bunch of people that had been hanging on to “normal” by their fingernails, there was finally not enough coping or symptom masking in the world to make up for that extra dollop of stress and expectation and demands on us, and we finally had to recognize the truth.
As with many psychological and neurological conditions, being named a “disorder” or a treatable problem often hinges on an assessment of how much one is able to meet societal norms for behavior and function. This is a very subjective measure; adhd diagnosis may very well be more prevelant in societies like ours simply because we only accept a narrow standard of “being” and functioning in society. But that doesn’t make it any less real; it is still biologically and neurologically based. Furthermore, I may be able to manage to meet society’s expectations, but the other part of that measure is, at what cost? Is denying caring for myself, having normal relationships, or working myself to death to maintain the fallacy that I exist like everyone else, a reasonable cost?
Or, is it reasonable to receive support (medication or otherwise) that helps me to not need all of those coping mechanisms just to maintain normal functioning?
How have any of you been successful in having this conversation with your doctor?