Chronic Pain members - Welcome, please introduce yourself
Welcome to the new Chronic Pain group.
I’m Kelsey and I’m the moderator of the group. I look forwarding to welcoming you and introducing you to other members. Feel free to browse the topics or start a new one.
Why not take a minute and introduce yourself.
Interested in more discussions like this? Go to the Chronic Pain Support Group.
@johnbishop John, you are so fortunate to live so close to such an amazing facility. Although I do not live close enough to Boston to have my PCP there I am happy that I am close enough to be able to go there for anything more specific. I regret so much not going there sooner so that the mystery of what I had could have been solved, it was difficult to go for so long not knowing what was wrong, waking up every morning afraid that I might have an HE episode that day. Thankfully though, at this point it is all history and I am doing fabulously, only glitch being side drug side-effects.
"House" was great, one of the shows I miss.
JK
Hi John
Thanks so much for your response. I truly appreciate your insight and suggestions. I will look at the links and I am pursuing getting an appointment for my daughter at the Mayo. There are a lot of physicians at Mayo - I am wondering if anyone of the site has any suggestions of a good physician to start with or someone that they have had good luck. Thanks again and have a wonderful holiday weekend!
Michele
Hello Michele (@micheledeville),
I think when you make your appointment they will setup a series of appointments based on the symptoms you tell them so that they can help you. I am tagging a few folks that may have a better insight and can give you some information on what to expect with your visit/appointment - @cynaburst @dawn_giacabazi @IndianaScott @katemn @kariulrich @kdubois @rosmarya @colleenyoung @jamienolson.
Please let us know when you get your appointment set up and you have more questions.
John
Hi Michelle,
Here are a few links that may help you with any questions you might have about an upcoming appointment at Mayo Clinic.
A typical visit:
http://mayocl.in/2r3YzUw
Frequently asked questions about visits to the Rochester Mayo Clinic:
http://mayocl.in/2iqtsjl
Sharing Mayo Clinic - Stories from patients, family, friends and Mayo Clinic staff
http://mayocl.in/2rolpJp
John
for @micheledeville When I went to to Mayo-AZ, things were very different. I went there having spent many days and nights trying to learn as much as I could about amyloidosis, having had a MD give me what he called an "informal" Dx. I at least had a place to start. Anyway, I was at May four (4) months, and it was only in the last few days that amy... was given any credence. The docs spent the rest of the time looking for any other excuse they could find for me having the symptoms and signs. They even sent some blood and biopsies to Rochester. The found a few things, but nothing that would excuse the situation. In the last few days the docs showed me a list of cancers, but nothing which would impact the amy. Only on the last two or three days did I get to see a hematologist, who knew next to nothing about amy. Only after I had been back home for a few months did I get a report from Rochester that said "We cannot rule out AL (light chain) amyloidosis, Gelsolin, Cystatin-C, Apolipoprotein, or other systemic, primary, familiar" amyloidosis diseases. In other words, the waffling-around by Mayo for 90% of the visit cost me several thousand dollars, with very little in return. So I say, be careful. You have to protect yourself at all times.
Thanks for the tag, John.
@micheledeville, John has given you some great things to read about getting an appointment at Mayo. Should you wish to inquire about an appointment, please fill in the online form here: http://mayocl.in/1mtmR63
There are several great discussions in the Visiting Mayo Clinic group about getting your first appointment and preparing for your visit. Check them out. Ask questions of people who have been there:
- Visiting Mayo Clinic http://mayocl.in/2bGLTKj
I am nelsonpowell,constant pain all day iwant to know if anyone has had a wire inserted in ther back forpain
Doctor wants to insert a wire in side my spine and transmitter out side for 7 day trail
Welcome to Connect, @nelsonpowell.
I'm wondering if you are talking about an implantable neurostimulator, sometimes called a spinal cord stimulator? We have several members who have experience with this chronic pain treatment, including @ladyjane85, @jimhd, @medic7054 and others. You may wish to read their comments as well as many others on this discussion:
- Has anybody had an implantable neurostimulator for chronic pain? http://mayocl.in/2aOZaR0
Nelson, when will you start the trial?
Yes, I had the trial SCS stimulator done and it did not work for me but the trial is relatively simple and painless. I wish you the best of luck and any specifics I can answer.
Kristine