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DiscussionAnyone here dealing with peripheral neuropathy?
Neuropathy | Last Active: Oct 28 4:54pm | Replies (3050)Comment receiving replies
Replies to "Sept 17th meeting for the 20 Year Celebration for the MN Neuropathy Association (www.neuropathy-mn.org). If others..."
Hello @johnhans, welcome to Mayo Connect and thank you for your question. I also have small fiber peripheral neuropathy which was diagnosed as idiopathic and possibly hereditary.
The Minnesota Neuropathy Association normally puts the monthly meeting schedule on their website - http://www.neuropathy-mn.org/ but it still shows the July 28 meeting and has not been updated since then. They normally hold 10 monthly meetings a year and are currently looking for people who are interested in serving on their board of directors. The September 17th 20 year celebration meeting with the speakers above was to try and bring in new members. We had around 100 guests at the celebration. I am a member of The Minnesota Neuropathy Association and will post the next meeting here on Connect as soon as I find out when/where it will be held.
Hope to see you at the next meeting!
Here are my notes from the meeting:
Program for Minnesota Neuropathy Association’s 20th Anniversary Event
Sept 17th, 2016
Dr. David Walk: “The Basics of Neuropathy”
http://www.neurology.umn.edu/profile_walk.html
Dr. Walk gave us the high level view of what neuropathy is along with the basic anatomy of the nerves and how the small and large fiber nerves work with the brain to tell us what we feel, etc. He told us his work is primarily research but that he does see some patients. Some, but not all of the topics he discussed:
- Effect of VM202 injection for patients with diabetes induced PN https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3677315/
- PCORI – Patient Centered Outcome Research Institute Trial
http://www.pcori.org/news-release/pcori-board-approves-21-million-fund-research-managing-and-reducing-opioid-use-chronic
https://trialbulletin.com/lib/entry/ct-02260388
- CMT – Charcot-Marie-Tooth
Dr. Walk discussed the genetic component and that the hands and feet are affected.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392824/
- PXT-3003 Study for CMT1A
https://clinicaltrials.gov/ct2/show/study/NCT02579759?show_locs=Y#locn
- CIDP – The Gripper Study: IVIG Treatment Related Fluctuations in CIDP
https://trialbulletin.com/lib/entry/ct-02414490
Pam Shlemon – Director of Foundation for Peripheral Neuropathy
"What’s new & living well with PN"
Pam shared how The Foundation for Peripheral Neuropathy got started and presented a slide show of the foundations current projects. Some of the topics she discussed:
- Clinical Trials - https://clinicaltrials.gov/
- Peripheral Neuropathy Research Registry - https://www.foundationforpn.org/research/research-registry/
- Exercises & Physical Therapy for PN
https://www.foundationforpn.org/living-well/lifestyle/exercise-and-physical-therapy/
Dr. William Kennedy
“Simple inventions that quantify touch on finger, vibration on toes and sweating in neuropathy”
My favorite speaker of the day. All of the speakers had a Q & A after their talk and one of the burning questions of the day was how many people are affected by neuropathy in the U.S. and around the world. Pam and Dr. Walk had both said they thought the numbers were around 20 million in the U.S. and up to 128 million in China. Dr. Kennedy said he would take exception with his younger counterparts and said it’s more like 100% if you live long enough. Since there was some discussion of idiopathic PN, Dr. Kennedy asked if we knew how the diagnosis is made for idiopathic. Got my best laugh of the day when he told us it got the name from the idiot neurologist who diagnosed it.
Dr. Kennedy went on to talk about his research work on developing a tool he would like to make available in every GPs office to easily test for neuropathy.
More information can be found on his website:
http://kennedylab.med.umn.edu/
John
Thank you for the update on what happened at the meeting. This is some very interesting and informational material here in the links.
When is the next meeting of this group? I have ideopathic peripheral neuropathy and live in the St. Paul area. My friend had Dr. Walk as his doctor for many years for his neuropathy. I hope you had a good meeting in September.