Living with Neuropathy - Welcome to the group

@artscaping - I wouldn't say I found it 'definitive' - but it did sort of confirm something I have believed about my own situation. I just don't know what to do about it....

@iceblue - I have frequent pain in my SI joint. My daughter, a physical therapist. keeps encouraging me to follow an exercise regime. (I hate execise!) She also points out that I probably have PN stenosis scoliosis and sacral arthritis all at the same time, which makes diferential diagnosis and a treatment plan challenging! You might have a similar complex of conditions? And my chiropractor friend keeps reminding me that pain in say the foot is just as likely to reflect a back problem as it is a foot problem. In plain language we are statistically unlikely to get a comlete diagnosis or a complete treatment plan unless we are very lucky in our choice of Dr. or Specialist. I have tried injections, medical marijuana, chiropractic and accupuncture to no efect. Ibuprofen helps but The long term side effects are risky so I limit myself to 400 mg perhaps twice in a month. Mindfull meditation, weight control, cycling and a healthy diet have helped me to a) to reduce pain from say 8 to 4 on average...and b) to "accept" my condition with a consequent reduction in stress, anxiety, depression. ( previously depression and anxiety relating to my condition caused more problems than the physical conditions!)

Have a happy new year!

I completely agree. I have been chasing a diagnosis (cure actually) for years, and suspect it is highly unlikely that I will ever find out the underlying cause of my pain. I am not a fan of 'exercise' either. It seems so much like work. I used to walk a LOT because I really enjoyed it - but the pain in my feet has eliminated that joy from my life...

Hi. I'm Robyn. 6 months ago I was hospitalized because of low magnesium and potassium. My hands were numb and hypersensitive. 2 years before I was hospitalized for low potassium and water weight gain.

I lost nearly 100 pounds of water weight during the 7 day stay. Only discharged me when my K was normal.

They said that I had neropathy this last time due to my drinking. 6 months later, the neropathy has gotten worse even after I stopped drinking. My magnesium and potassium are normal. BP normal. BS normal. B counts normal. Heartrate still high.

I have lupus in my family (Systemic and Discoid), my tests came back as borderline as did my mothers.

Is there any hope for me?

Btw, I am only 44.

@roxye Have you spoken with a neurologist? We can share our experience with regard to the things you wrote, but it would be inappropriate for anyone in this discussion to give you medical advice or diagnosis, and you probably wouldn't want us to. The subject of the relationship between alcohol and neuropathy is being discussed in one of the Living with Neuropathy discussions, and @johnbishop is active in it.

I'm sorry you have been through a difficult time with health issues, as many of us have. It's a very real challenge to sort through multiple signs and symptoms, medications and diagnoses, seeing multiple doctors. I can attest to the fact that the process can be overwhelming and frustrating.

I hope that you will find responses to your note helpful.

And, yes, there is surely hope for you.

Jim

@roxye

I was around 50 when I started noticing signs of neuropathy, beginning in my feet. I'm still ambulatory at 69, so neuropathy isn't a death sentence.

Jim

Hello @roxye, I would like to add my welcome along with @jimhd and other members. I definitely agree with Jim that there is always hope. Staying positive is a big help. Here is the other discussion Jim mentioned that you might want to read through and post any questions.

> Groups > Neuropathy > Small fiber peripheral neuropathy and alcohol
— https://connect.mayoclinic.org/discussion/small-fiber-peripheral-neuropathy-and-alcohol/

As Jim mentioned, have you seen a neurologist yet or had any tests done to diagnose neuropathy?

Hello. This is my initial post and my main question is: Are there patients on this platform who have idiopathic progressive peripheral neuropathy? I have had testing and do not know where to go next! Thanks in advance for any helpful information
Larry

Hello Larry @oldshep, Welcome to Mayo Clinic Connect. I also have idiopathic small fiber peripheral neuropathy. I posted my story and what helps me earlier on Connect here: https://connect.mayoclinic.org/discussion/anyone-here-dealing-with-peripheral-neuropathy/?pg=42#comment-65985.

I know it can be frustrating trying to find something that helps with the symptoms of your PN. Can you share a little more about your symptoms and any treatments you have tried?