Just Diagnosed with Small Fiber Neuropathy
Hi . I am a bit scared here. Had positive skin biopsy for small fiber. What tests will the Neuro ask for to find causation? Was diagnosed prediabetic in Fall. My Dad had similar issues and eventually lost a toe. Always felt he was walking " on fire ". My feet have similar issues. This is just one big Ick. Boo
Interested in more discussions like this? Go to the Neuropathy Support Group.
@jesfactsmon
Chemo-Induced Peripheral Neuropathy: Quality of Life and Treatment Planning
The Foundation for Peripheral Neuropathy is bringing together a panel of experts for this webinar to discuss CIPN and its impact on patients and their physical and mental health.
https://www.foundationforpn.org/events/?blm_aid=116106
Date: November 10, 2020
Time: 12:00 PM – 1:00 PM ET (Please note that this lecture starts at 11 a.m. Central, 10 a.m. Mountain and 9 a.m. Pacific)
REGISTER NOW - https://register.gotowebinar.com/register/5174813403335669772
Panelists for the webinar are:
Thomas Smith, MD FACP FASCO FAAHPM
Professor of Oncology,
Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University
Stefanie Geisler, MD
Assistant Professor, Neurology,
Washington University, St Louis, MO
Krista Nelson, LCSW, OSW-C, Oncology Social Worker
Providence Health Systems
CIPN (Chemo-Induced Peripheral Neuropathy) can be an unexpected side-effect of certain breast and other cancer treatments. While the treatments save lives, the resulting CIPN can be life-changing and devastating.
CIPN, depending on its severity, may impact future treatment decision-making requiring effective doctor-patient communication about future options and goals of therapy. Patients often find it difficult to find information about CIPN and are at a loss as to how to discuss treatment options with their medical care providers. Patients are equally unaware of the impact on their ongoing mental health that CIPN can cause.
The panelists will provide the latest information about the causes and treatments of CIPN, offer insight into the patient-doctor relationship, and explore the emotional challenges and medical options in coping with CIPN. The webinar will conclude with a Q&A session.
This webinar is generously sponsored by:
The Foundation for Peripheral Neuropathy
485 Half Day Road, Suite 350
Buffalo Grove, IL 60089
847-883-9942
http://www.foundationforpn.org
Jake, I agree, the dizziness, memory problems, brain fog, balance issues went away after a few weeks or so, and I also had decreased my initial dosage from 3xday to 1x night. Luckily, the gabapentin works for me and I have only increased my dosage 2 x in 3 years now taking 300 mg. Helen
@steeldove
Hi Marilyn, at first I was not sure what this was, but upon further inspection I see this is about a CIPN webinar being held next month. Thanks very kindly for passing this along. Best, Hank
Here is a link to the webinar that @steeldove shared. It looks like it is free and hosted by The Foundation for Peripheral Neuropathy
- Chemo-Induced Peripheral Neuropathy: Quality of Life and Treatment Planning https://www.foundationforpn.org/events/
@steeldove - I hope you don't mind that I edited your post to remove the extra text from the cut & paste of the events page on the Foundation for Peripheral Neuropathy website. I also added the link to the events page for the webinar and the link to register for the event. John
@strikeanerve
Gabapentin/neurontin didn't help me, and my wife says that it affected my thinking. I have 5 siblings, and Gabapentin worked for all of them.
By this point in my pn journey, I am willing to try any medication my doctors prescribe. I've had idiopathic sfpn and autonomic polyneuropathy since 2012, and I've tried a lot of medications. Some just did nothing, some didn't have any effect on my neuropathy, and had unacceptable side effects. Some reduced my pain for up to six months, then stopped working, and had no side effects. I have a team of great doctors whom I trust to give me any appropriate treatment, whether it's medication, or stimulator or surgery. After working with them for up to 15 years, I know that they have my best interest in mind.
I wish that one of the medications I've tried would treat the non-stop pain. Neuropathy is one of the diseases that has no cure, but there are many things that treat symptoms. I wish you the best in finding a treatment that works for you, and that you're comfortable with.
Jim
Hi Jim, I just read about Belbuca, supposedly a new 12 hr. opioid? It is a thin square strip which you place in your cheek to dissolve. I don’t have any idea about it’s effectiveness. Helen
This group is very helpful. May I ask how long did it take to get your skin biopsy back? I’ve been waiting 7 weeks, it was sent to Mayo
@kyc117
I had an appointment with the neurologist 4 weeks after the biopsy, to discuss the results, so I'm pretty sure your doctor has your report by now. Have you called or texted them? Sometimes it takes some nudging (sometimes it takes a lot of nudging).
Jim
That time frame seems excessive, I would call and make sure it's been processed. I had mine done at an outside clinic, it was read by two different specialist but I had results in less than 2 weeks.