Rob Kinney

First post: Jun 25, 2019 Latest post: Aug 6, 2019
Welcome to our CaringBridge website. We are using it to keep family and friends updated in one place. We appreciate your support and words of hope and encouragement. Thank you for visiting.

Here’s the back story:
In July 2018 Rob had what we now know as an “episode” or “exacerbation”. At the end of a CrossFit class Rob’s right foot went numb and he had trouble walking.  At the time we dismissed it as a pinched nerve or just the result of a really hard work out. The numbness went away after cooling down.  We assumed all was well until it happened again :(   During a walk around our neighborhood, nothing strenuous, a numb foot again.  I actually had to help him walk home as he was unsteady as he appeared to be dragging his right foot.  It was pretty scary and we decided that it was time to make an appointment to see the doctor.
August 3rd, 2018: Meeting with the Primary Dr.
We met with the doctor to discuss dizziness, blurry vision, eye pain, vertigo, headaches and the recent numbness in his right foot after activity, and curious about a bump on the side of his jaw that we assumed was an ingrown hair which hadn’t gone away after several weeks.  The doc asked lots of questions, seemed pretty calm, then suggested an MRI to “get an explanation for the headaches, dizziness, and vertigo”, and a follow up with dermatology to investigate that small bump on his jaw.
August 9th, 2018: Mayo Clinic Charlton for MRI on the brain.
Doctor called at lunchtime and informed us that it could be many things and the lesions found on his brain could be MS ( punch to the gut).... and he wanted Rob to return the next morning for another MRI of the spine and back.  Rob was working from home that day.  The kids and I were out of the house at the time he got the call from his doctor, he was home alone.  When I returned home I could see in Rob’s face that something was wrong.  He told me about the MRI results and the fact that it could be MS and that he would need another MRI the next morning. We both stood in the kitchen and cried.  What did this mean for us?  Our future?  Our family? We were scared.
August 10, 2019: Mayo Clinic Charlton for 2nd MRI on back and spine.
Another early morning at Mayo Clinic for another MRI (the lady actually remembered him from the day before).  After this MRI the doctor called again to inform us that there are multiple lesions on the neck and spine (likely causing numbness in the foot).  He then referred us to Neurology.
August 24th, 2018: Mayo Clinic NW Dermatology.
I went in to the dermatologist for them to look at my bump on my neck.  They removed the bump and they thought it was just a cyst and they would send it to pathology.  Dermatology called and explained that the bump on his jaw was the result of carcinoma that was growing in his neck.  Cancer was removed a few weeks later and no evidence that it spread beyond his jaw and neck.
August 27th, 2018: Met with Neurologist for the first time.
We headed downtown to the Mayo Clinic for this appointment.  The neurologist informed us that many people get misdiagnosed with MS because there are a few other things that look like MS.  We went through the MRI’s.  He confirmed it.... it was officially diagnosed as Multiple Sclerosis. There were tears at this appointment.  We discussed medication, future outlook, future mobility, and a lot of other things that are a blur because they are things that no one wants to discuss, or know the answers to.  A lumbar puncture further confirmed the MS diagnosis.  Multiple Sclerosis is a disease of the brain and spinal cord.  Rob’s immune system attacks the protective nerve sheath which will make it difficult for his brain to communicate with the rest of his body.  He will gradually develop more symptoms for the rest of his life. 
There is no cure for this disease..... BUT!!! There is a way to halt the disease!! It’s called HCST! HCST (Hematopoietic Stem Cell Transplant) is a procedure where Rob’s own stem cells are harvested and treated with the goal of restarting the immune system after the faulty immune system has been destroyed with chemotherapy.  Following treatment, Rob will age normally and not be a prisoner of this disease. The treatment is safe and performed regularly around the world.  

Rob met with Dr. Burt at Northwestern is Chicago to see if he was a candidate for the trial study.  Dr. Burt accepted Rob for treatment under the condition that he have his spine fixed with surgery.  X-rays showed spinal stenosis and deterioration between C5 - C-7.

April 2018- Rob underwent spinal surgery at Rush university medical center in Chicago.  A lot of the issues he had were solved with this surgery!  Dizziness, numbness, headaches all went away!  After surgery he will recover for 3 months, stop his MS medication to flush his system and then he will be ready for HSCT!