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The patient is able to switch from one medication to the other and the clinican guides them on which one to pick.
-create a decision tree or prioritization matrix mapping symptoms with highest impact and more effective treatment WHILE optimizing add this or treat this sequentially. Give a clinical review step at the end to ensure patient is self-medicating appropriately. Make sure the explore treatment options are presented up front; it look me a while to find it. User journey is currently a little more open ended than may be effective?
Need to give the option to delete a form to start over (can't edit info)
Love what you’re doing. Can you figure out a way of offering your service in the U.K.? It’s not clear from the site whether you can post to us. I think there would be big take up due to nhs (which whilst free which is great, consequentially means access to doctors, testing and medications is very limited and/or slow).
It is extremely hard (likely impossible unless you live in New York City or urban California) to find physicians aware of, and experienced in treating, Long Covid and other infection activated chronic conditions. The ME Action physician finder doesn't go far enough. In the absence of appropriately experienced physicians, the availability of short primer for physicians describing the features (breadth of symptoms) of IACCs and first line treatments along with key references would be tremendously helpful for patients who are having to educate their providers - presupposing that the providers are willing to be educated by their patients. The ME/CFS Clinician Coalition letter is a start, but doesn't go far enough.
Unlimited assessments for a monthly fee.
Hello, I just wanted to give you some feedback on this treatment. I tried Oxaloacetate at the dosage that you had prescribed. It made me quite agitated and muddleheaded. I almost gave up but decided to split the capsules. 1st in half and then in quarters. At 125mg(2x), it started to work! I'm much less tired and while my cognitive abilities are challenging, I don't get as tired with mental activity. I thought I would pass this along for those who are trying it and may have given up.
Please expand your care to Connecticut as I know of a lot of people here struggling with LC symptoms :)
Option to have epi pen prescribed for MCAS patients that have trouble getting access to allergists.
Instead of wandering around the research articles in the Rthm community or the very limited conditions summary, present summary documents similar to NIH Clinical Digests: - current (updated within 6 mos.) - summary of current research by treatment approach) - clinical guidelines - additional information