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Good evening @maveric09 and an enthusiastic welcome to Connect. By introduction, i also have SFN and chronic myofascial pain syndrome. Mine was determined by a skin biopsy which indicated that it is severe at this point. Is that what determined your diagnosis.?

Let me see if I can answer your first two questions.....SFN is progressive as it takes way too long to regenerate replacement nerve cells. It is not fatal, however, many folks will encounter some form of it during their lifetime. And at this moment, there is no cure. There are some studies being done on possible regenerative medications.

Do you know how your SFN came about? Was it from chemotherapy or diabetes? Did your neurologist have a name for the type you have? Mine is from multiple traumas including accidental injuries and frequent surgeries. If the source is unidentifiable, it is labeled as idiopathic.

We can help you with the research information. I am going to introduce you to @johnbishop. He is our research expert and is quite familiar with the work done by the two professional organizations. John is also a neuropathy patient at Mayo Clinic in Rochester and knows what the relationship has been like. The only thing John doesn't have is pain......he only has numbness and what I call the tingle tangles.

Before I send you off to John, I would like to mention that there are options for treating SFN. For example, I started with Gabapentin for pain and numbness and Nortriptyline for depression and anxiety. I was quickly introduced to medical cannabis and now use only tinctures and topicals.....with CBD and THC, in appropriate dosages and formats. I have also found that mindfulness and meditation practice make a huge difference. Exercise is always very important including yoga and walking. At some point, you may want to try MFR, myofascial release therapy. I have two sessions a week and the goal is to keep my quality of life positive. As the pain and irritation progress, I will probably have to move to three sessions a week.

So....that's a start. John?????? please join us.

May you be safe, protected and free from inner and outer harm.
Chris

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Replies to "Good evening @maveric09 and an enthusiastic welcome to Connect. By introduction, i also have SFN and..."

three months ago I went to bed with normal feel. next morning I had cold toes. since that time they feeling has extended to the middle of my foot.

Interesting that you are using CBD tinctures and topicals. I have SFN and have been taking Gabapenten and Duloxetine. I had some CBD tincture on hand and decided to rub it on my ankles and legs before bed. It helps!

Thank you so much Chris. I was diagnosed via skin biopsy. I wasn't told what type i have but I can confirm I am not diabetic or prediabetic. I do have Hashimotos Thyroiditis, and my doctor said that it may be an underlying condition although she said it could also be idiopathic as my hypothyroidism is well managed with Synthroid. What I'm finding very discomforting is the best pain. It radiates from the center of my chest across my ribs. I've been to the hospital many times thinking I am having a heart attack, but multiple EKGs, a cardiac MRI and a CT Angiogram have all but ruled out any heart disease or dysfunction.