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So disheartened
It’s been a while since I past posted as things had improved with LDN and also becoming a patient of Dr. Brent Goodman at Mayo Phoenix. Of course it was too good to last. Dr. Goodman decided to leave Mayo and move states, Mayo Neurology declined to keep me as a patient, and now I am worsening or the LDN is becoming less effective. My pain is back in force and so far I have struck out finding a new doctor.
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Go to pharmacy & ask them to recommend a doctor. You could also join the LDN Facebook group & they may have some suggestions. Don’t give up - LDN works for pain
I am still taking LDN @4.5mg… still better than nothing (I tried to disastrous results ). Just like I don’t believe in paying a $2,200 membership fee to see my previous neurologist at his new practice, I also don’t believe in shopping around for a doctor to get an LDN prescription or any other prescription for what it is worth. My PCP said I would have to find another doctor to get a medical marijuana prescription as Mayo won’t do them and that effectively ended the ask.
Have you tried Rochester mn. They will take me but Phoenix’s not accepting neurology patients.
No I haven't. I was trying to keep it relatively local as travel is difficult at best - right side affected by cerebral palsy, left side (formerly known as my good side) affected by this SFN, and deathly allergic to black pepper (and other things) so have to cook all of my food - haven't eaten in a restaurant in 9 years.