Small Fiber Neuropathy and genetic testing?

Posted by hypotemusea @hypotemusea, Oct 9, 2020

Hi everyone, it was great to find this forum and all of you wonderful members on it. This is my first post.

I was diagnosed with idiopathic small fiber neuropathy earlier this year. I was wondering if anyone has undergone genetic testing for this condition (specifically the SCN9A and SCN10A genes)? I have an appointment with a geneticist next month. I think I'd find it helpful to look for answers as to the cause of my condition, and if they found any linked genetic mutations it would affect my reproductive choices as well.

Backstory if it's helpful to anyone: I'm a 27 year-old woman, previously active and relatively healthy but then I started having constant pain in my hands and feet last year. At first my doctor thought it could be RA but then they did nerve conduction studies and QSART test to diagnose SFN. I've seen multiple rheumatologists, neurologists, gastroenterologists, etc. I also have some joint hypermobility (I think a 5/9 on the Beighton), especially in my limbs and upper body... I might consider genetic testing for EDS as well. I was diagnosed with PTSD years ago, so I have definitely put my nervous system through a lot. I couldn't find any research linking it to SFN specifically though.

It's been really challenging to go from being healthy and active to having chronic pain, and to know that I am only 27 with 50 years ahead of me with this condition and no treatment available. The pain is worst in my hands and wrists so it makes work and everyday tasks painful -- I recently quit my job partly because of this. I used to teach yoga part-time and enjoy activities like rock climbing, cycling, even the occasional run for fitness but I've had to give up on those things. I've also lost almost 10% of my body weight in the past year from this and related stress (I was already borderline underweight to begin with).

Things that I've tried: I've been receiving acupuncture for about 6 months, most of the time it helps keep the pain to a manageable level although when I get pain attacks (like last month when I decided to go for a run it triggered two weeks of severe pain) even acupuncture is ineffective. For some reason I've found that the TCM herbs the doctor prescribes have been more helpful than the acupuncture itself. Lyrica helps me to sleep but doesn't actually reduce the pain -- I can't tolerate anything more than 50mg due to side effects. Tramadol gave effective pain relief but made me too drowsy and gave me flu-like symptoms even after just once dose. And when I can manage it, very gentle yoga and meditation is helpful.

My doctor prescribed a low dose of amitriptyline but I have yet to try it. It's more of a "last resort" for me because I'm very sensitive to medications and speaking from experience I have a very hard time with drug withdrawals, even on supposedly low and unproblematic doses. I will likely start taking it next year if my acupuncture shows no further progress.

I would love to hear from anyone who's had similar experiences! Sending thoughts and good vibes to everyone here 🙂

Interested in more discussions like this? Go to the Neuropathy Support Group.

@jesfactsmon

@hypotemusea
Welcome to Mayo Connect. I am so sorry to hear that you are experiencing such bad health issues at such a young age. That is simply not right! One question about medications. Did the doctor run you through a course of neurontin (gabapentin) before moving to Lyrica? That is the standard way it's done. It sounds like that was not the case for you. Gabapentin, Lyrica, Cymbalta, then duloxetine and amitriptyline, Tramadol, and others are usually tried first, and if none of them seem to work they might step you up to opioids and benzos, at least eventually. I would keep that attitude of yours to be reticent to take all medication such as these, and if/when you do, stay on them only if they truly benefit you, don't stay with them one minute longer (i.e. taper back off under doctor supervision). Know that medical marijuana and kratom are good for pain also.

I have heard of a few people here who underwent genetic testing for neuropathy. Wish I could remember who, it's been a few months. Have you exhausted the internet searching for info? You might want to use the search feature here on Connect (magnifying glass at top of this page) and see what you can come up with. Do you think you may have inherited neuropathy? Do other family members have it? Hope your geneticist appt. provides you useful info.

If I can figure out who it was I heard had gone for that type of testing I will let you know. Want you to know that this forum is FILLED with compassionate and smart people (as well as people like me - just kidding). I am pretty sure @johnbishop will touch base with you with something helpful, he always does. Some other good contacts and resources for good feedback here are @jenniferhunter @artscaping @lorirenee1 @jeffrapp @avmcbellar @rwinney (currently doing a 3 wk Mayo Pain clinic) and a ton of others. The site is well supervised as well by some great moderators.

Keep in touch. Good luck. More later. Best, Hank

Jump to this post

dr levine honor health group phoenix az will do that test

REPLY

he is well known by mayo clinic here in phoenix

REPLY

In case you missed the FPN Webinar: Hereditary Neuropathy and Genetic Testing

REPLY

How do you get on the list for these types of webinars and more info on neuropathy.

REPLY
@pitepalten

How do you get on the list for these types of webinars and more info on neuropathy.

Jump to this post

You just have sign up for their newsletters and you will receive news updates when they occur.

https://www.foundationforpn.org/
REPLY

I'm 33 and feel like I too don't know how I'm going to live with this for the rest of my life. My neuropathy has spread to my hands, feet, arms, legs and back. I'm trying to keep it together too.

REPLY
@kat600

I'm 33 and feel like I too don't know how I'm going to live with this for the rest of my life. My neuropathy has spread to my hands, feet, arms, legs and back. I'm trying to keep it together too.

Jump to this post

Kat600 - I’m almost twice your age and I also wonder. Will it get worse? Etc. I feel your pain. Hang in there. Medicine is moving fast these days. There is always hope. Lars.

REPLY
@pitepalten

Kat600 - I’m almost twice your age and I also wonder. Will it get worse? Etc. I feel your pain. Hang in there. Medicine is moving fast these days. There is always hope. Lars.

Jump to this post

Hello @pitepalten and @kat600, I would like to welcome you both to Connect. I'm 78 and first noticed my neuropathy in my late 40s with some numbness in my toes. Other members and myself have posted their neuropathy story and what has helped them in another discussion you might find helpful here -- Member Neuropathy Journey Stories: What's Yours?: https://connect.mayoclinic.org/discussion/member-neuoropathy-journey-stories-whats-yours/

There are a couple of really good sites for learning more about neuropathy and different treatment options that you might find helpful.

-- Neuropathy Commons: https://neuropathycommons.org/neuropathy/neuropathy-overview
-- Foundation for Peripheral Neuropathy: https://www.foundationforpn.org/

Do you mind sharing what treatments or therapies you have tried or found helpful?

REPLY
@pitepalten

How do you get on the list for these types of webinars and more info on neuropathy.

Jump to this post

@pitepalten, The Foundation for Peripheral Neuropathy has a YouTube channel with all of their webinar videos if you want to view any of their previous webinars

https://www.youtube.com/channel/UCLtOWy1tDeZLdUsMXz_bnfQ/videos
REPLY
Please sign in or register to post a reply.