Chronic Fatigue Syndrome and Small Fiber Neuropathy: What helps?
I read an article recently about the possibility that CFS is connected in some way with SFN. I find this interesting because my first dx was CFS and I recently had two punch biopsies done that both showed SFN. I am 95% certain my CFS was triggered by some horrible virus I had (3 rounds of antibiotics didn't touch it and I couldn't go back to work full time for a good 6 months even after I was "better"). Would this indicate that neuropathy could be triggered or "woken up" by a viral infection? Anyone know any good research articles on this topic? Inquiring minds. 🙂
Interested in more discussions like this? Go to the Neuropathy Support Group.
Good evening @sharka, Well, you got me. I would not have guessed Australia. I am not concerned about pesticides and heavy metals. My cannabis choices come from the same company I have been with for about 9 years. They have progressed significantly and are very responsive to patients. They have two websites: the first is http://www.papaandbarkley.com and covers a wide range of medical cannabis options. The second website is http://www.papaandbarkeycbd.com and covers only CBD products. The sites explain the products and resources well.
The reason I trust them is that I have been with them for so long and watched them grow. I also know that in CA, the producers must follow certain regulatory protocols. That, in and of itself is one of the benefits of legalizing cannabis..........regulations.
So....have a look at those sites. Perhaps you will find some helpful information.
May you have happiness and the causes of happiness.
Chris
Thank you so much Chris!
Even though this website don't ship to Australia, it's helping me to read some very useful information 👍 👌
Good for you. Knowledge is power! I think you will become a good student of your own condition. Way to go!
Chris
If it's any help to find others with your condition, here I am.
After finishing up 15 months of heavy chemo for Lymphoma, the good news was it is currently non detected. The problem after finishing chemo was terrible fatigue, and an increase in chronic pain. The only thing that allowed me to get up for work in the morning is Adderall.
I'm a 68 year old male who has played sports my entire life and woke up everyday at 6:00 to go to the gym. These days (with Adderall), I'm lucky if I can start out for work at 9. During the past 2 years, I've had 2 complicated Cervical surgeries and a visit from Covid in January, my symptoms have gotten worse. When I bring it up to my Oncologist, he looks at me like "sorry, I did my job" and never has any suggestion that the fatigue could be caused from the chemo. I've seen so many specialists who have the same answer; Everything looks fine, you should be happy. My quality of life is non existent right now, without any answers
Thank you for the dosing website you recommended Chris, it is exactly what I was looking for!
My heart goes out to you. I am fortunate enough not to have had anything as serious as the Lymphoma and therefore no Chemo. I do however understand the debilitating heavy fatigue and the inability for my doctor to tell me what is causing it and how to make it better. I have lost an straight week of my life to fatigue this month. Everything is a struggle, What use to be automatic becomes a forced thought process as in walking up the stairs. It feeds depression and depression can feed fatigue. I am currently looking for answers also. I want a productive life that I can enjoy and help others. Have you tried Functional Medicine?
And yes it is helpful to share for all of us!
Hi, @sharka.
I have had sfn for about 30 years. Started meds in 2011, gabapentin, and it was slightly helpful pain-wise, but made me high and I gained about 25 lbs. Then to nortriptyline, which was ok, but my neurologist recommended medical marijuana. That was about 5 years ago. It took about a year to figure myself out. Some of it was that they didn't say, or I didn't hear, that you need a consistent dose so that you have a consistent blood level. and it takes a month for it to build up. So I played around with it and didn't get much relief. But, then I got it and now it is helping well.
I do not smoke. I know many do, but my disease is pretty advanced and I need to have that consistent dose, and smoking doesn't provide that. I take pills. I am sensitive to thc, so I can't have it in the day. So, for the day I take medical cbd only, 60 mg. Then, at night, I take cbd and thc to help me get to sleep and stay asleep. dose depends on if it worked the night before and, if not, I take more.
I hope this helps you even though this is almost a year after you originally wrote.
Dear @ kmom5942
Thank you so much for the info, didn't know about the consistent dose every night and or day! My doctor didn't explain the importance of this and so again thank you for this valuable information ! At the beginning I took less then I should have and not every night! Now I'll try your advice.
And can you please let me know what ratio of CBD/THC is helping at night?
I've been prescribed 10mg/10mg in one ml. It's definitely helps me with sleep!
And I will ask for CBD only for the day, seems like a good idea.
You mentioned 60mg CBD only , is that in one ml?
Thank you very much 😊!
Dear @julbpat, please know that you are not alone in this fight. I also experience similar symptom. I find it a challenge now to do any tasks I used to be able to do easily. I can still do them now, but afterward pain comes at a vengeance. I still force myself to do them because it's the only kind of exercise I can get these days. I'm not sure how much longer I can keep doing this. I have been on intermittent fast to try to keep my weight down from little activity, so far it has helped me not gaining weight. I hope you feel better and wishing you well.
I’m 50 and have been diagnosed with autonomic dysfunction and small fiber neuropathy and am non diabetic. I feel my condition getting worse but the fatigue is ruining what little bit of enjoyment I have left. What can I do to help this?