Unknown Cause or Idiopathic SFN
Hello. I was wondering if there were any folks out there who were at one point labeled “idiopathic” or “unknown cause” SFN, BUT later found the cause?
I’m asking because my son (15 years old) has a positive biopsy for SFN. We have done every blood test imaginable and thorough genetic testing to try and pinpoint what is causing his SFN so we can guide treatment. So far, nothing shows up out of the ordinary on any test. His B12 is high, which is weird since he is homozygous for MTHFR, but other than that everything comes back normal on blood tests and his genetic testing shows no known mutations.
His doctors have tried many medications and he doesn’t respond to those in either a negative or positive way. The doctors are pretty stumped, so I was wondering if anyone else has had a similar situation and finally did find something (maybe outside the box of normal testing) that they think is causing the SFN and were better able to treat it? Ideally we’d like it to be autoimmune, so we could start IVIG or another type of immunotherapy (even though he didn’t respond to a 30 day high dose of prednisone) but nothing in his bloodwork is pointing in that direction.
Thanks so much!
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Hi, @grahamb - how long have you had diabetic neuropathy? Have you taken any medications to date for it?
I'd like you to meet @manassen1 @johnbishop. @blocker @jeffrapp @harper7745 also may have some thoughts for you on medications for this condition.
Has your doctor indicated that the fevers you are experiencing have a tie-in to the neuropathy?
Hello @grahamb, I would like to add my welcome to Connect along with @lisalucier and other members. Mayo Clinic has some good information on the different treatments/medications for pain relief for diabetic neuropathy as well as some lifestyle and home remedies information here: https://www.mayoclinic.org/diseases-conditions/diabetic-neuropathy/diagnosis-treatment/drc-20371587
About 5 yrs I've had neuropathy. No I have not taken any meds for it trying to do research to find something that will help. No doctor can figure out the fevers low grade 99.2-99.9 and some nights I can have a fever as much as 101 ???? I have psoriatic arthritis but my rheumatologist says it's not causing the fevers.. This has been going on since Feb 2015
@artscaping thank you so much for your detailed schedule and info on medical marijuana. I’m sorry I haven’t responded earlier but just saw the replies. I did start a new thread on cbd and need to go there also to see if anyone has posted. I went to the neuro that specializes in SFN and pn. He wants me on lyrica but I’m holding off as long as possible. I upped my imipramine to 200 mg 2 days ago. I was at this and also 30 mg cymbalta earlier in the year but had to cut back as I was getting tremors. Going back to 200mg imipramine has helped me sleep at least 5-6 hours the last 2 days. I’m feeling slightly better but know it’s short lived. I still don’t know why tinnitus has started this year and increased steadily. I was told also that my back has 3 really bad herniations - 1 cervical and 2 thoracic and should see a neurosurgeon . Said don’t think I need surgery right now but should see him now so you know who to go to as it will one day become a problem. Have to get signed up medical marijuana to try
@albiet, Good evening. Thanks for your response. I wanted to show how you can totally "manage" the SFN pain during the day with a natural medicine without side effects, that simply relieves symptom pain.
We know that at this point there is no cure for SFN, so we are not trying to treat anything.... just mask the pain so that we have the best quality of life possible.
When I read your current list of medications, it is overwhelming. And even with medical cannabis, you may still need to address the anxiety and depression that most of us try to conquer. I take Cymbalta in the morning to help my anxiety enhanced recent memory issues. It has made a huge difference in how I approach my day......sort of "Que sera, sera." Sleep peacefully, Chris
Hello...I'm feeling good about my recent choice to stop lidocaine infusions. I have been approved for Medical marijuana and will be visiting a dispensery tomorrow. Hoping it provides the masking of pain and discomfort I need and will allow for discontinuation of hydrocodone...2 years coming. Thank you Chris for your positive encouragement since I've joined connect. You and many others have been a big help in my discoveries of how to live better with SFN. Fingers are crossed for a better tomorrow.
Rachel
@rwinney, @artscaping, Great news. I am excited to learn about your visit to the dispensary. I am here for you. Be safe and protected. Chris
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Found this on the dispensaries website and I find both very helpful in general as an overview and comparison. A little tough to read, sorry.
@rwinney, those are helpful. I would be very hesitant about extra strength dosages. I don’t think the pain from SFN requires those levels. The times seem pretty accurate. Oral mucosal is my preferred distribution method. Find joy today. Chris