What to expect and chances of getting in?
Hi! So I just had my first initial call yesterday and they went over paper work and my symptoms. Is it going to be a phone call or will it be on the portal? What are the chances of me not getting in? I'm going in for heart issues and a lot of other problems. What should I expect these coming weeks?
Interested in more discussions like this? Go to the Visiting Mayo Clinic Support Group.
@sbtheplumber1, I'm confident that @jenniferhunter will have suggestions for you. She is so helpful, especially in back issues.
With respect to your finding a suitable hotel with a recliner in Rochester or other Mayo Clinic location, I recommend contacting Mayo Clinic's Concierge Services.
@cheyennepeterson and her colleagues can recommend options for you:
Concierge services
https://www.mayoclinic.org/patient-visitor-guide/minnesota/concierge-services
By phone 7 a.m. to 6 p.m., Monday-Friday: 507-538-8438
Email: concierge@mayo.edu
@sbtheplumber1 I am doing well. Even though I was turned down by 5 spine surgeons prior to coming to Mayo, it was the right thing because those surgeons missed the diagnosis. They didn't have confidence in knowing what was causing the symptoms, so they should not operate if they don't completely understand the issues.
From what I understand, your spine surgery was a year ago. You are having L3 nerve issues, but the operated levels were L4 to S1, correct? It is possible that further surgery could make you worse off than you are now, and only a specialist can make that call. Prior to my spine surgery, my physical therapist was buying me time by doing myofascial release and using a Dolphin Neurostimulator on the nerve roots in my neck to disrupt pain signals. That prevented pain for about a week. All surgery creates scar tissue, and myofascial release may be something to try to see if it helps loosen the tight tissue. I have done a lot of work on my scar tissue both from my cervical spine surgery and surgery for a fractured ankle. It has helped a lot. Time helps too, and perhaps a year isn't long enough. Another surgery will add more scar tissue. I am 4 years out from the ankle fracture and have just recently improved a lot, and I'm now walking without pain.
If you do get an appointment at Mayo, I would recommend looking at Candlewood Suites for accommodations. They do have kitchens and recliners in the room and you can add pillows as needed to make it comfortable. I would recommend requesting a handicap accessible room that has a roll-in shower. Those are usually on the first floor, and I stayed in rooms like that with my ankle fracture when I could not weight bear at all. You would need someone to accompany you to drive. In Rochester, there is a hotel shuttle to Mayo (and most Rochester hotels have them). My drive between my home and Mayo was 5 and a half hours, and I did fine right after my surgeries coming home in the car. I was uncomfortable because of the surgery, and the drive didn't make it any worse. If you do get to go to Mayo, you'll find a way to figure out the travel part of it.
Here is our discussion where you can learn about Myofascial Release which is a type of physical therapy.
Neuropathy - "Myofascial Release Therapy (MFR) for treating compression and pain"
https://connect.mayoclinic.org/discussion/myofascial-release-therapy-mfr-for-treating-compression-and-pain/
They won’t take me in :((
I'm sorry to hear that. That is hard news to get. Please know that you can continue to connect with other members in the Heart Rhythm Conditions support group here: https://connect.mayoclinic.org/group/heart-rhythm-conditions/
I actually did get in! It was internal medicine that denied me but I’m getting into cardiology.
That's great news. I'm not surprised. General internal medicine is a very very busy department. Given that you're primary concern is heart-related, you've landed where you need to be based on the review of your medical records by Mayo Clinic experts.
Once you have your initial appointment, testing and assessment, additional appointments in other departments (including internal medicine if necessary) will be arranged. Your cardiologist will be your main provider and will quarterback any additional needs.
Here are a few discussions that may help as you prepare for your appointment:
- Your Tips on How to Get Off to the Best Start with a New Specialist
https://connect.mayoclinic.org/discussion/your-tips-on-how-to-get-off-to-the-best-start-with-a-new-specialist/
- First Visit to Mayo Clinic: How do appointments work? What to expect?
https://connect.mayoclinic.org/discussion/new-internal-med-patient/
- Mayo Clinic Patient Portal: How do I find it? Do you use it?
https://connect.mayoclinic.org/discussion/mayo-portal/
Have you downloaded the Mayo Clinic patient portal?
I self referred to MD ANDERSON IN Houston. I was offered an appointment within a week and met with a GU Oncologist within 4 weeks. I was seeking a second opinion for advanced prostate cancer. The entire process was straight forward and seamless.
Wishing you a successful outcome! The cardiology department at Mayo is the best in the world for many conditions and shares top rating with the Cleveland Clinic for a few others. You are in the best hands.
This was not my experience. Last week I self-referred for my essential tremors.
I was seen by 3 movement specialists (2 in GA my previous state, and now in FL).
I received a call ~2 days after I sent in my referral. No appointments - even into 2025 - schedule isn’t open that far up. Could not put me on waiting list either.
I’ve failed every med I’ve been put on. Am in process of getting the TAPS device by Cala.
Saw the Neuro yesterday. He is such a waste of space. As a nurse practitioner, I read the current journals and google current thoughts on meds when refractory to the established ones.
He never knows what I’m talking about, and has never touched me - to do strength measurements etc.
I brought a ‘cm’ ruler as he didn’t have one. Thank God I read where and how to measure my wrist, as he had no idea.
Ironically one of the docs in his office has her name come up when on the Cala site, looking for docs. Told him this. He couldn’t care less.
We just went up on my useless Propranolol. He referred me to a neurosurgeon ~3 mo ago at my last visit. He had a ‘tude yesterday, ‘why didn’t I see the neurosurgeon’. A first, I would NEVER go to a doc he referred me to for brain surgery - not down here in east coast FL, B. When I looked him up - quite a few lawsuits with verdicts! That’s a hard no in my book!
He knows I’m a traveling nurse practitioner, so I was out of town. “Oh, ok, call him again”. Yeah, no.
I guess at this point, Mayo is not the only hospital on earth. I’ve been to Emory, and am looking at UFL.
I also was unable to get an appointment at Mayo Jacksonville for dx of CIDP. I now am seeing Dr Michael Pulley, neuromuscular neurologist with Univ of Florida in Jacksonville. I now have a new and correct diagnosis and am very happy with the care I receive from him. I would not change physicians now even if I was given an appointment at Mayo.