It seems obvious my 19 year old child has autonomic neuropathy. It’s so sad. She is suffering a lot and doctors (ER, and a neurologist) aren’t diagnosing and helping her so she continues to suffer while waiting weeks for an emg which alone won’t confirm a diagnosis anyway. Her primary care doctor put her on gabapebtin (painkiller for neuropathy) but it only covers 20 to 50% of the pain at best and only for part of the day. Her health is declining. How can I get her real help ASAP? What can I do to best support her? I’m trying my best to help her.