Patient Reviews ? Write a Review
I have had epilepsy for many years and have seen many doctors who would put me on meds that seemed to make the seizures less but never go away. Finally i met dr. Beall for the most part my seizures have stopped due to treatment instead of every week or at times every day I am having them every few months and for me that's a huge accomplishment. Thank you so much Dr. Beall for knowing what you are doing and for helping :-)
I have been dx'd with ms for almost 13 yrs . I have seen 6 neurologists. I am very impressed with Dr Beall. He is the first Dr to do a complete exam. He talks to me like I am a person not just a number. He found numb areas that I didn't even realize I had. I highly recommend him.
This doctor diagnosed me with ms and put me on daily shots of copaxone. He told my husband if I didn't treat it I would be in a wheelchair. Turns out I have Lyme disease which I am now treating and am recovering. Thank goodness I stopped the copaxone an d am treating for lyme. My symptoms are disappearing with treatment. I tried to tell this doctor that my symptoms of fatigue and brain fog were constant, but he kept telling me with ms the symptoms go away when the flare is gone. But mine did not. This man didn't listen to me! It was so frustrating! So now three years later I am much, much better. I don't have ms and my lyme is getting better. Also had a CCSVI procedure which helped tremendously.
he is a doctor who cares! you will never find another doctor like him!
Dr. Beall first off would like to say thank you. You believed me when i came to you for help. I have been having symptoms for years. it seems every time some Dr. would tell me i have MS but then no you don't nothing shows in your MRI. How aggravating right away they want you to see a psychiatrist. I'm not imagining how i feel. I came to see you in 2010 you gave me an extensive workup, you used the kurtskye method. 2011 i had another flareup. you sent me to the hospital immediately. I was in for about 3 weeks. I was so surprised that you never followed up with me in the hospital, but knowing your staff you probably didn't even know i was still there. We tried to get me on the oral Gilenya but you know insurance companies,you have to try other things first. Unfortunately because of my cognitive thinking and memory problems we both talked about my decision to take a leave of absence for my job. I had no insurance and i could not get any state aid because i lived with my daughter.After 2 yrs i finally got insurance in April. In the later part of June i Started feeling fatigue, my right foot started dragging, but there was one thing i never had before facial pain. I called the office to make an appointment they said you left the practice, i asked for information but they could give nothing to me. Well my daughter searched on line and found that you went to Deckerville Mich. which is 2 hrs away from us. I asked if she could take a day off work to take me to your new office we had to wait till sometime n July. So we found another neurologist. I took all the tests again MRI, evokes, kept asking if i had a spinal tap kept saying yes, which was the final test that gave you my Diagnosis of MS, you were so compassionate i hope that is one memory i don't forget. The Neuro i went to said i didn't have MS nothing showed up on the MRI. Showed him the records of my spinal tap, didn't matter, told him about the methods you used Kurtzke,. Mcdonalds he did't want to hear it. He said i could get a second opinion. I was very aggravated , then he mentioned to see a psychiatrist. Before a could get an appointment with another Neuro my symptons got worse i noticed a pain in my right eye and a twitching with my lips. Iwaited a couple days. one morning i woke up didn't feel right the right side of my face was drooped. It looked like i had a stroke. My daughter took me Mclaren Macomb was no bleed showing on the CT was relieved. they admitted me so i could see the Neuro on staff there. Turns out he was from your other office gave MRI said nothing showed doesn't think i have MS told him about the spinal tap i had twice which came back positive in 2007 and 2010 oh you may have it in your spinal cord you can come back our practice and see another doctor. i am home now and going to make an appointment with you i am on prednisone for 10 days. I hope you will see me as a patient again. You were the only one that believed me i have been going through this for years. I no its not proven but my brother was diagnoised with MS in his early 20's. I hope you read this and to all the non believers of Dr Steven Beall i'm certainly not one of you. The Man is very educated and has dedicated his life to this complicated disease. my rating for you is from the other office!!! Hope to see you at your new office, Paulette Snarski
No other doctor in my 23yrs has ever been more helpful or caring! Hooorah!!
In response to the latest letter written praising Dr.beall iw as not only misdiagnosed was told to take interfon which is traumatic and hospitals MRI records show no lesions ever existed must, must get another neuro U,of M fabulous beware seriously
This is Dr. Steven Beall. I am now the Director and C.E.O. of the Multiple Sclerosis Centre of Michigan, P.L.C. I have had a chance to look at all of your comments and would now like to respond to them. First of all, I wish to thank all who have responded positively. Thank you soo much TCM for finally setting the record straight. On the 16th of May, 2011, I resigned from my former group Michigan Neurology Associates because I wanted to focus on stopping the disease I was trained to fight starting with seven years of fellowships (National Institutes of Health and the California Institute of Technology, continuing as a faculty member at the University of British Columbia (UBC), home of the largest MS Centre in the world, and most recently building a practice of 1500 CIS and MS patients. Up until this point in time (16 May 2011), although I was intensely involved in caring for patients with strokes and other neurological diseases I realized it was taking time away from my devotion to the diagnosis and cure of MS, so I decided to start my own company: the Multiple Sclerosis Centre of Michigan. My previous contract prohibited me from treating or contacting the patients of my former practice for three years (this is known as a non-compete clause and is typical in the field. For the 1500 patients I have taken care of in the past, I am still very concerned about you. I think of you all of the time and my heart aches for you. I also wish to thank all of the patients who have made the trek to my Northern and Eastern Michigan clinics hoping to see me again but only to be turned away because of the non-competes which will soon expire. I hope the above can at least help the patients who wrote negative comments about me because I was no longer available. I know you are hurt, scared, and thus angry. The earlier comment from TCM expresses it beautifully in her last sentence of why I left. The non-compete expires on 17 May 2014. Next, I would like to address the comments about alleged misdiagnosis. Clearly, you are confused. Since 1983, I have had the fortune to be trained and associate with the best in the world at diagnosis and treatment of MS, first at the NIH, then at Cal Tech, and then the University of British Columbia. (UBC) We performed the first drug trials for MS at the NIH and UBC. For 20 years, I was surrounded by experts in the field as detailed in my bio on my website: www.mscentremi.com. I basically "grew up" with the criteria for diagnosis of MS. As a consequence, I learned after doing around 50,000 exams and Kurtzke scores precisely the same way every time to pick up the first signs on the neuro exam and MRI of MS and thus stop it in its tracks. For all of my patients who have had a seed of doubt planted in their minds about misdiagnosis and for those who wish to learn more about their correct diagnosis, I urge you to go the library and have the librarian copy this article for you. It was written my my Canadian friends (I spent 10 years in Canada) who are especially adept at the neuro exam since they are not as enamoured by the technology as the US neurologists. They are rightly so more hands on and spend more time with the patients and thus discover the disease earlier and hence can actually make a difference at that point. The article is entitled MS, MRI, and the 2010 McDonald Criteria: A Canadian Expert Commentary. The reference for the librarian is Neurology, Volume 29, Number 23, Supplement 2, December 4, 2012. www.neurology.org. It reviews all of the criteria I have used to make your diagnosis. Please remember that for many of you patients who have CIS (clinically isolated syndrome) I have treated you with the interferons and Copaxone because we have known since 2000 that this "vaccinates" you from getting MS. I often found it does stop the disease in its tracks and lesions DO go away. It doesn't mean you have MS. CIS is also discussed in the article. The CHAMPS, BENEFIT, and PRECISE trials discuss the "vaccination of CIS" Please copy this article and give it to your present neurologist, ask for a copy of all of my office notes and ask him to compare my office notes to this article and tell you why you don't have the diagnosis based on this article and my notes. To the comments re: MRI showing no lesions: As the article explains on page S3, only two lesions measuring at least 3 mm are needed to now satisfy space if in the appropriate areas. Unless one uses a specific 3 mm gapless axial/sagital colocalization protocol one will miss these lesions. Also it requires conscience searching for the first lesions which often hide under the anterior tips of the frontal horns (which is needed to prescribe treatment for CIS according to the CHAMPS, BENEFIT, and PRECISE trials. These lesions are often overlooked. The juxtacortical areas are also overlooked because they are inappropriately ascribed to chronic white matter changes if the patient is middle aged or older. Finally, MS is a clinical diagnosis as Don Paty used to emphasize. As the article illustrates, the first attack has to be documented on the neuro exam. My experience of doing around 50,000 exams has taught me that the first part of the nervous system to show the first signs of MS is weakness of about 18 different muscles starting at the fingers and toes. ALL of my patients can attest to the fact that every examination I performed on them tested weakness in these 18 muscles. Patients who have contacted me wishing to be treated by me again have the same complaint: Dr. Beall, my other neuro never touches me. I would urge all of the patients who have doubt about their diagnosis please ask their neurologist to give them their Kurtzke score. I hope the foregoing addresses all of the past comments :) thank you very much Steven Beall, M.D. Director and C.E.O. Multiple Sclerosis Centre of Michigan, P.L.C. www.mscentremi.com
I'm still a current patient at MNA & I agree the majority of the staff are rude, seemingly uncaring, confused & overworked. Dr. Beall was the only neuro who has ever actually examined me there. Any other neuro has only looked at my MRI results or asked me how I'm feeling. I feel like I'm doing their job & telling what I need for my health. 2 PAs have done actual neuro exams on me since Beall left. For those who claim misdiagnosis, I'm curious what lead you to a neurons office in the first place? Clearly, it was bad enough to go there. We all know are own bodies & should trust our gut. Personally, knowing the nuances of MS, I believe in my diagnosis & Dr. Beall. There are a few PAs, MAs & nurses who are caring enough to help while I figure out what to do next. Dr. Beall is too far for me now, so he isn't an option. At the moment, leaving MNA isn't one either. I don't know where to turn or who to trust. I don't have an answer for my next neuro cuz no MS specialist exists within St. John. What I do believe in is my diagnosis & in Dr. Beall. Don't lash out in fear & doubt. Know Dr. Beall would never want to abandon his patients. In the long run, to be the kind of neuro he wants to be to his patients; a small hiatus & vow of silence was necessary. Patience is a virtue & a dr who will risk so much to be better than the practice he left wanted him to be is priceless.
I had a great experince as his patient in Clinton Twsp. He disappeared unannounced and could not be located. I think that he is questionable because he is very elusive. An MS Dr should not leave his patients since the disease is so mysteriose. I definetly would not recommend him to any MS patients. I have run a support group for 27 yrs.
For those of you looking for Dr. Beall, he has recently opened a cllinic in West Branch. At the present time, he sees patients every other Thursday and it isn't too hard to get in to see him. The staff, although a little confused at first is very caring and attentive. You are more than just a number at this office.
I read all the prior comments and most issues were of waiting time and staff. I was referred to Dr Beall in 2004 by a well known Neurosurgeon. When all other doctors were scratching there heads, he allowed me to have a name to what I had and meds to help. He stood by me and my family answering questions,listening to problems,while ALWAYS allowing whatever time it took. For that patients would wait longer at the office but having a doctor like him was well worth it. If you want a doctor that will help you and not make you feel like your symptoms are all in your head...see him. A very kind,caring doctor who I miss terribly since he re-located. Thank you Kindly for helping me for all those years Dr. Beall.
Terrible MD should lose his license misdiagnosed for 6 months received and received unneccessary treatment ..horrible staff.
Please see my response to the comment posted 8 Apr 2013 and ask your current neuro to provide a Kurtzke score. Thank you
Dr. Beall is a horrible neurologist. Very uncaring. Office Staff is ridiculous. GO FIND A BETTER DOCTOR! He misdiagnosed me with MS when it's now been proved I never had MS.
Please see my response to the comment posted 8 Apr 2013 and ask your current neuro to provide a Kurtzke score. Thank you
Dr. Beall diagnosed me with MS and was treating me for MS. After getting second opinions from two other neurologists, it is 100% certain that I do not and never had MS. Dr. Beall talked me into believing I met the standards of MS, despite clear CSF. I would recommend to anyone who has been treated for MS by Dr. Beall to get a second opinion.Michigan Neurology, where Dr. Beall used to practice, has the worst staff I have ever encountered anywhere. Rude, disrespectful, uncaring, etc. etc. etc.The entire staff should be fired. No patient ever deserves to be treated the way I was.I have found a new Neurologist, at a different location, who is amazing. Good luck to all of Dr. Beall's patients. Be very wary of any MS diagnosis he tries to give you.STAY AWAY from a new site opening soon in Deckerville, MI. It's called the MS Centre of MI, with Dr. Beall the Medical Director. Good grief :/
Sorry that your neurologists never read the McDonald's 2010 criteria for the diagnosis of Multiple Sclerosis. These criteria as well as McDonald's 2001, 2005 don't require CSF positivity. Hope you are doing well. If you start dragging a leg or go blind, I would be happy to see you. You need to review: McDonald's Criteria for MS 2010. If you go blind, please don't say I didn't warn you. (please see my response to the comment posted 8 Apr 2013. Thank you
I found Dr.Beall at: www.mscentre.miDirector of the M.S. centre of Michigan, Dr. Beall is serving a very underserved patient population with the Michigan Rural Health Preservation Network.Check Dr.Beall's diagnostic and treatment credentials compared with other money mill operators or self styled "specialists".People--do your research on diagnosticians.
For those of you disapointed: Dr. Beall specializes in M.S. He was the only one @ MNA that did. I will miss him. After my MRI and L.P. He advised me to start treatment, even before I met my clinical diagnosis(2 1/2 years later). For that I am thankful to him. Some drs. would have waited. That would have been 2 1/2 years of my disease getting worse. I even got a second opinion, which confirmed that Dr. Beall was on the ball! Thank You Dr. Beall
Those of you interested in Dr. Beall he has opened a new clinic in Deckerville Mi. He cannot except patients that he seen through the Michigan Neurology Associates, it was in the contract he signed
According to an article in a July issue of Macomb Daily this doctor is being sued along with three other doctors from the practice.
Dr. Beall left Michigan Neurology some months ago. To be honest, it has been the best thing in my neurological journey. Beall treated me for MS only. Dr. Voci doubts very much that I have MS. It's possible I dont have any Auto Immune disease at all. Dr. Voci and his PA's are looking at other reasons I have brain lesions. The Office Staff at Michigan Neuro are the worst staff I have EVER encountered. They treat me like crap any time I call. Act all put out that I have bothered their day. I wonder if Dr. Voci truly knows how horrible his staff is.If not for Dr. Voci, certainly, I would seek another Neuro Office.
Please see my response to the comment posted 8 Apr 2013. Thank you.
4705 Towne Centre RoadSuite 201Saginaw, MI (989)799-2770
I share the opinion that he is the best MS Dr. I've ever seen. Worth the wait if he's running late. I also HATE the staff. MNA is a MONEY MILL. They have ZERO regard for patients and are infuriating. No one but Dr. Beall has/had a clue what the F they are doing over there. SOoooo sorry he's MIA. If I have to see a PA who thinks she's hot stuff and knows more than Dr. Beall again, I'm going to lose it. Only problem is, no one else in town seems to have a clue either, from what I'm hearing. Thank God I'm stable right now. If I have a bad exacerbation, I'm in trouble. God help us all. If he resurfaces, I'll drive to Timbuk2 to see him again.
I really don't know how I'm supposed to start over with another neurologist. I have been with Dr. Beall for 8yrs. now. He is absolutely the best. He is so thorough and doesn't skip a step at each and every visit. I really just feel sick after reading that he is gone from the practice. I was told by the staff and the Dr. that replaced him at my last scheduled appt., that they weren't sure when he would be back. If they are going to out and out lie just about that then how can I trust them. If anyone does find out where he is, PLEASE let me know. Good luck to everyone, it's bad enough having MS but to loose a great Dr. is like having a major flare up.
I HAVE BEEN A PT AT THAT OFFICE FOR MANY YEARS...I HAVE HAD AN MRI ALMOST YEARLY...NOTHING HAS EVER SHOWN UP UNTIL I SAW DR. BEALL... HE SENT ME TO SOME MRI PLACE UP NORTH AND ALL OF A SUDDEN LESIONS STARTED TO SHOW UP IN THE WHITE AND GRAY MATTER OF MY BRAIN...I WAS DEVESTATED WHEN HE SAID I HAD MS..WE STARTED TREATMENTS THAT SEEMED TO MAKE ME FEEL WORSE, HE ASSURED ME IT WAS THE MS AND NOT A SIDE AFFECT... RECENTLY I HAD TO SEE DR. VOCI AND HIS BIG BLONDE HAIRED ASSISTANT...ITS A MIRACLE MY LESIONS ARE GONE....SINCE THERE IS NO CURE FOR MS WHAT HAPPENED.....VOCI WAS KIND ENOUGH TO GO OVER ALL MY PAST MRI'S THAT WERE DONE AND EVERYTHING WAS FINE..THERE WAS ONLY BAD NEWS FROM THE MRI PLACE BEALL REFERRED ME TO...DR BEALL IS A JOKE! NOW I AM IN BILLS UP TO MY ROOF WITH NO MONEY BECAUSE I WAS TO SICK TO WORK.. DO YOUR RESEARCH PEOPLE...
I found your lesions at the place up north that was missed at MNA. Your lesions were gone perhaps because of the treatment perhaps "miraculously" the lesions disappeared. Hopefully, you will not be afflicted with paralysis, tremors, bladder incontinence, blindness in the future. Please see my comment to the post 8 Apr 2013. Thank you
Dr. Beall has been my neurologist for a long time. It's disturbing that no one will tell me what happened to him. I thought he was a good doctor, but would a good doctor just up and leave his established patients? His staff have always been rude and unprofessional, but because I thought Dr. Beall knew his stuff, I put up with their crap. I am at such a loss not knowing what to do next. Appointments with Dr. Voci are always handled by PA's, and trust me, they are NOT neurologists! Where can I go to find another neurologist? I certainly refuse to remain at MI Neurology. Meanwhile, my MS remains untreated by a neurologist, but thankfully, my MS is in remittance.
Please see my response to the comment posted 8 Apr 2013. Thank you.
Well, Dr. Beall is gone...his choice...and yes, possibly opening his own special place...I just feel he should have contacted his patients. Dr. Voci was great trying to explain what he could about the situation. I am going to stay w/Dr. Voci, and not follow Dr Beall. If his clinic opens, it would not be here on the East Side anyway. I have always found the staff at both offices I go to, very helpful. Understand, it is not there place to explain why Beall is not there...Good luck everyone! MSucks!
I agree that his office staff is rude and does not care about their patients' problems. Dr Beall went "MIA" very soon after my appt with him in mid-May and of course no one in that office will let us know whether or not he is coming back. I have treated with him for a very long time and he is one of the few doctors who know what they are talking about and treats his patients with respect. He knows all there is to know about MS; I went through several neurologists before finding him and even then, he did not diagnose my MS despite lesions on my brain until after months of additional testing.His staff refused to give me an appt after a hospital stay for treatment of a MS flare-up even though he told me they were to add me on even if his schedule was full. I had to wait for my next already-scheduled appt over two months later to see him!!!I called the office in June (and many times afterward) to tell them I have major medical issues which are affecting my MS treatment and medications; they were rude and told me I had to see another doctor, one I had seen as a consult in the hospital and had no intention of ever seeing again!!!I have LOTS of horror stories about what his schedulers and testing departments have put me through, inflicting stress and pain needlessly!!! The long delays in my office visits were because the staff overbooked him and his assistants would make deragotory remarks about him just because he tried to give his patients the time they needed!!The only departments I never had problems with were the MRI and physical therapy ones!!I had always told my husband that if Dr Beall left I would be gone also as he was the only reason I put up with all the misery his staff and other doctors put me through!!!Please let me and everyone else know if and when Dr Beall opens his clinig!!
This is infuriating. Dr. Beall is no longer with this practice yet no one in the office gives a rip about his patients who are left in the dark.PA's are now taking the place of Dr. Beall. The remaining neurologists wont even face us. Dr. Voci needs to step up and stop giving Dr. Beall's patients the run-a-round.The ENTIRE staff is useless, rude and crass.The Office Manager, if there even is one, should be fired as he or she has no control over the actions of the staff.
Please see my comment responding to the post on 8 Apr 2013. Thank you.
I showed up at my last appointment only to be met (not by Dr. Beall) but by a P.A. who was obviously doing major damage control. I was told that I had abnormal results on two MRI's from over a year ago - and this is the first I am hearing of if! I feel like I'm getting the run-around and the staff, in general, is being less than helpful/not accomodating. No compassion - just c.y.a.
Please see my response to the comment posted 8 Apr 2013. Thank you.
We were trying to find where his next adventure would take him. We drove around the location where we heard he would reside & didn't see his name. Hopefully all of the legalities go thru quick for starting his own practice. WE WANT TO FIND YOU DR BEALL! WE WILL MENTION IT IN OUR SUPPORT GROUP, IF AND WHEN WE FIND AN ADDRESS & DATE. Dr Beall is worth the wait in GOLD! He cares about his patients.
I have learned that Dr. Beall will be opening his own private practice very soon, called The Multiple Sclerosis Centre of Michigan. Can't wait for this doctor to re-emerge independently!
Love my neuro Dr. Beall. Went yesterday for appt., waited over an hour, went to ask why it was taking so long & was told I was seeing a different Dr. Was told that he is on leave...sounds permanent...Hope all is fine w/him...but what about us patients? What is going on?
IVE BEEN TOLD DR. BEALLE IS ON AN INDEFINITE LEAVE OF ABSENCE. WHAT HAPPENED? WHERE DID HE GO? HIS OFFICE OFFERS NOTHING! THE STAFF ALL NEED "NICENESS" LESSONS! WHEREVER; WHATEVER HAPPNED TO DR. BEALL, I HOPE HE IS OK. HE WILL BE MISSED.
I was referred to a neurologist after my primary doctor was concerned with some symptoms that could be early signs of MS. For my first and second appointment Dr. Beall was wonderful. Knowledgable, thorough, and kind. I've had to wait over a month to get the results for all my tests and diagnosis. I was called today to say Dr. Beall is not available for my appointment tomorrow but I can see a doctor who has never seen me. If I want to see Dr. Beall I'll have to wait another 3 weeks! The staff show absolutely no compassion for the anxiety patients must go through waiting for results and appointments. The desent thing to do would have been to fit me in at the latest for another appointment this week. As another patient mentioned the tremendous amount of patients they see only make you a number, not a human being. We'll see how it goes tomorrow.
Dr. Beall is a decent doctor. Pros: he seems to care about his patients and spends a decent amount of time per visit. Cons: He doesn't remember patients. I've spent 7 months with Dr. Beall coming in every 2 to 4 weeks and he still doesn't have a clue as to who I am. Asks same questions every visits. He also spends too much time discussing solutions for symptoms I told him I do not have. My main issue is fatigue and Cognitive issues is second. He told me cognitive issues were not an MS Symptom yet it's listed as a symptom on all the MS sites. He is also a bit arrogant and doesn't listen to me. Every appointment he brings up how he is the only neuro who does thourough exams.I'm used to my doctors knowing who I am and respecting my input. I like to play an active role in my treatment plans. If you are the type of patient who thinks doctors are Gods, then he may be for you.
DR. BEALL GAVE ME A DIAGNOSIS OF MULTIPLE SCLEROSIS RECENTLY WHICH WAS TO ME,A LIFE-CHANGING DISEASE. I WAS CERTAINLY AFRAID OF MY FUTURE. DR. BEALL EXPLAINED EVERYTHING IN TERMS I COULD RELATE TO AND GAVE ME ALL THE TIME I NEEDED DURING APPOINTMENTS.HIS BEDSIDE MANNER IS VERY CALM, KIND AND GENTLE.HIS KNOWLEDGE IS SECOND TO NONE AND HAS WRITTEN AND PUBLISHED ARTICLES ON VARIOUS SUBJECTS.I FEEL BLESSED THAT I WAS DIRECTED TO DR. BEALL.
he has the education...the experience...the bed side manner...***but we had way to many repeat conversations!!...missing files!! wanted to repeat tests that had been done that we had talked about repeatedly*****he seemed to forgot who I was btw visits and apparently to refresh himself by reading the chart before coming into the room! dismissed symptoms that were very troublesome to me without explaination to me...maybe not a big deal or nothing that could be done about them but...shouldn't have been dissmissed without comment** seemed to me he had to many patients and not enough time?? just my opinion
I think Dr.Beall is wonderful doctor. I have recommended him to other people in my family with MS. He immediatley found my left side weakness and then set up lots of other testing. My family doctor said nothing was wrong with me but I knew there was. Dr. Beall reassured me that I was not imagining my symtoms. My father's neurologist that he is treating him for his MS never told him about streching, massaging, or strength testing. I think that is important. I have not been diagnosed with MS, but I am been treated for it. I am thankful that it was caught so early.
Dr. Beall is very knowledgeable about MS. He is one of the best Dr.'s I have been treated by. I strongly recommend him to anyone who may have MS.