Anyone here dealing with peripheral neuropathy?
Anyone here dealing with peripheral neuropathy?
Interested in more discussions like this? Go to the Neuropathy Support Group.
Anyone here dealing with peripheral neuropathy?
Interested in more discussions like this? Go to the Neuropathy Support Group.
Hi @16jody, I think it's a good idea to discuss it with your doctor to make sure there are no interactions if you are taking other medications. The doctor can order blood tests to see if you have any B vitamin deficiencies.
John
Thank you,
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1 ReactionHI @johnbishop, I think there is a problem again with the post the last one I got was from @16jody yesterday. And then I got the Digest this morning. Could you please look into this for me?
Thanks
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1 ReactionHi @mikween, I'm pretty sure they are still making some tweaks to the website after they made some major updates. Please hang in there as it should return back to normal soon. I've seen a few glitches myself.
John
Yes, dealing with it - trying lots of different suggestions - prescriptions, etc. Nothing seems to quite do the job and some (prescriptions) make me worse. Just wondering if anyone has heard of DMSO. My granny had rheumatoid arthritis and used DMSO which seemed to help her. She was on pain meds too - percoset (or something like that and became addicted to it). Now, I'm over 80 years old so you kind of know how long ago the DMSO story was and granny was 92 when she passed away. What I remember was that it was a clear liquid that she rubbed on her knees and ankles and it made her breath smell - not really bad but kind of like garlic... anyway, wondering if any research has been done on the use of DMSO to treat PN?
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2 ReactionsFor anyone living in the Minneapolis area, the Minnesota Neuropathy Association is having a meeting this month. I attached a meeting flyer. Great place to meet with and discuss peripheral neuropathy issues.
Next Meeting: Thursday, May 25, 2017 – 1:00 PM
MINNESOTA NEUROPATHY ASSOCIATION - 3rd Program of our 21st Anniversary Series
We welcome Nick Rich, PharmD (doctor of pharmacy), a compounding pharmacist, owner of Lake Elmo Pharmacy, who will be speaking about: alternative treatments to conventional medicine for the treatment of neuropathic pain. He will also tell us what a compounding pharmacist does, and how it may be different from what your pharmacist does. He has over 13 years of experience as a compounding pharmacist, and is one of two accredited compounding pharmacies in Minnesota. This is a program you won’t want to miss!!!
Meeting location:
St. Michael’s Lutheran Church
9201 Normandale Boulevard,
Bloomington, MN 55437
Directions/Map are on the website: http://www.neuropathy-mn.org/ (redirects to minnesotaneuropathyassociation.org)
MNA flyer 5-17 (MNA-flyer-5-17.pdf)
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1 ReactionHi @mfobrien36 - I haven't heard of DMSO (Dimethyl sulfoxide) but there is some information available on it from Mayo Clinic - http://mayocl.in/2ptIQ3m.
There is a discussion started here by @dongee and @alysebrunnella - http://mayocl.in/2r2pOB1
John
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1 Reaction@colleenyoung
I have taken Multi vitamins, vitamins b complex, c, and d. I stopped taking vitamin e some time ago. These in addition to the long list of meds: for peripheral neuropathy (Duloxetine and MScontin and Lidocaine cream), depression (Bupropion), anxiety (Clonazepam), allergies (Claritin and Benadryl), breakthrough pain (Percocet), reflux (Omeprazole), arthritis (NSAIDs and Voltaren cream), and occasional lower back muscle pain (Orphenadrine).
I was scheduled to have a spinal cord stimulator implant, but blood tests showed anemia. Over the past couple of weeks, with a series of blood draws, the hemoglobin has been going back up, so I'm getting back in line for the implant, sometime in June. The trial gave me a wonderful week of pain relief, so I'm looking forward to the permanent implant. Can't wait! I'm hoping that lessening the pain level will mean reducing or even eliminating some meds.
Jim
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1 Reaction@johnbishop, Hi John I wanted you to read over the questions that I came up with for the doctor since you were the only one that replied
last time. Let me know if you can think of anything else. Thanks for all of your help. I will let everybody know how my appt. goes on May 16th.
Have you ever heard of Alpha-Lipoic Acid?
Have you ever heard of Lidocaine injections? And could that work on me or the patches?
Can you even fix my neuropathy through surgery with my Foot Drop?
The Specifics about the surgery?
Could it make it worse?
What is the success rate for the surgery?
How long will I be off of my foot?
In a cast and for how long?
Therapy afterwards and for how long?
How long before I see improvements?
Do you have any referrals?
How many procedures like this have you performed?
Are they all the same kind of surgery?
Even though people may have different reasons that might have caused the neuropathy
Does it matter how long someone might have had the neuropathy as to how the outcome might be to the surgery?
Have you ever heard of Alpha-Lipoic Acid?
Have you ever heard of Lidocaine injections? And could that work on me or the patches?
Can you even fix my neuropathy through surgery with my Foot Drop?
The Specifics about the surgery?
Could it make it worse?
What is the success rate for the surgery?
How long will I be off of my foot?
In a cast and for how long?
Therapy afterwards and for how long?
How long before I see improvements?
Do you have any referrals?
How many procedures like this have you performed?
Are they all the same kind of surgery?
Even though people may have different reasons that might have caused the neuropathy
Does it matter how long someone might have had the neuropathy as to how the outcome might be to the surgery?
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1 Reaction@mcween
Some excellent questions. I've learned that if I don't write out my questions, I forget to ask them until I walk out the door.
Jim
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