I am going for the back consultation. Then, the second appointment is the nerve block. Hoping I can get the nerve block first, and delay the nerve block. I will hopefully be seeing the doctor. You never know. I am constantly surprised by how I am told something on the phone that turns out to be incorrect (insurance especially).

I am going for the back consultation. Then, the second appointment is the nerve block. Hoping I can get the nerve block first, and delay the nerve block. I will hopefully be seeing the doctor. You never know. I am constantly surprised by how I am told something on the phone that turns out to be incorrect (insurance especially). Also , what works for you?

What treatment worked for you??
I am a nurse also. I am scheduled for a punch biopsy in Nov. Hoping that it leads to some sort of diagnosis or helps to clarify things at least.
I am 75 now. I have led a very active and healthy life. I have no heart disease, diabetes, cancer, hypertension, or osteoporosis. What I do have is lots of degenerative arthritis and have had many orthopedic surgeries related to that: Bilateral knee replacements 2009/2019, Spinal Fusion at L3,4,5 in 2018, Torn hamstring surgically repaired 2021, Kyphoplasty L1 2022. I also have long term familial tremors of both hands that slowly increased over the years.
The history of my current situation actually runs from about 2017 to 2022. During those years I experienced occasional and increasing unexplained falls. My family and I observed that something was different about my gait. That being that I was catching my toe and tripping or misplacing my step. I sought medical help at that time with PCP and referral to neurologist. Had appropriate testing at that time including brain MRI. Testing was negative but toe catching was able to be observed once with observation by that neurologist. To watch and wait was the plan. Along the way, I did perceive increasing muscle fatigue in lower extremities when doing a typical walk of 2.5 miles between 2021-22. Also, I could not walk as fast as I was used to being able to. As listed above I did have ortho surgeries in and around that time frame. Related??
In the spring of 2023, there was a change in my symptoms with increased back pain and weakness in legs and significant decrease in ability to climb stairs due to strength not pain. To begin with my increased back pain and symptoms were thought to be related to the condition of my spine. There were plans for a major back surgery. However, before surgery could be scheduled, there was an acute increase in symptoms of bilateral numbness in toes and feet, inability to lift forefoot or to move my toes and severe loss of balance and ataxic gait requiring 100% use of a walker. I seem to be losing function hour to hour. Sensory Motor Nerve Conduction study showed major change over a matter of days from previous study and indicated nerve demyelination. I was hospitalized at that time and treated for GBS for 5 days with IVIG. I stabilized but the symptoms did not go away.
What followed were months of extensive testing and image studies to rule out whatever could be ruled out. What turned up besides the abnormal S/M conduction studies was a recessive gene (POL G) I inherited and that has potential for pathologic expression, mild elevation of spinal fluid Protein and GAD levels. I also had a Sural nerve biopsy that showed essentially normal nerve i.e. no demyelination. At Multiple consults/2nd opinions at specialty centers followed. You know the drill.
I HAVE seen improvement slowly over time. I can walk now with just the use of a cane and I can cruise counters and walls at home fairly well, but balance is still a major issue as well as a residual L footdrop. I must be very careful and always be conscious of my footfall and balance issues. It is exhausting. I fall about 1 x per month despite my best efforts to stay upright.
I am on monthly IVIG. I cannot correlate anything with IVIG treatments. I could not tolerate steroid blasts.
Your experience has buoyed my hopes that the Skin Biopsy may lead to some additional clarity. Thank you.

Have you found treatment that works?

I had my nerve biopsy yesterday; 3 places on left leg, which is somewhat worse than the right. I had messaged my rheumatologist who made the referral about the experience I had on my first appointment, and he actually contacted the doctor that does the biopsy. I was told it would take at least a month, possibly 2 months to come back from the lab. He is leaving this practice, so I will have an appointment with a different doctor when the report from lab comes in. I am canceling the injection until I know more.