Brian’s Story

Site created on June 24, 2023

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.


As most of you know,  Brian was diagnosed with ALS in September 2022.  In hind sight, Brian noticed that he had lost a little strength in his right side when working out as early as 2021, but chalked it up to age, lack of testosterone, etc.   Finally, when I (Robyn) noticed several changes, I insisted that he to go to the doctor to find out what was going on.  There is no specific test for ALS, so basically they have to rule everything else out (immune disorder, lyme disease, tumor, Parkinson's, etc) before they can diagnose for sure.  At the time of diagnosis, he had an almost imperceptible limp, slight loss of strength on his right side and major loss of energy.


In October of 2022 he went to St. Petersburg, FL for a stem cell transplant that is experimental (insurance does not pay), but thankfully because of many of YOU we were able to afford this treatment.  The stem cell protocol consisted of several intrathecal injections (injected directly into the spine/CSF) as well as several IV treatments.  The spinal treatment caused severe headaches and body aches for the first couple of days, but then subsided.   As a direct result of this treatment, Brian gained a significant amount of energy and felt much better.  We are unsure how much effect it had on the progression of the disease.


Throughout the Fall of 2022 and the early Winter of 2023, Brian continued to lose strength in his right side and relied on a walking cane to steady him and aid in walking, but was able to walk.  He is right handed, but has had to switch to doing everything with his left hand.  In the last four months, we have seen a significant change in his strength on both sides.  He is now almost exclusively in a wheelchair.  He is able to transfer himself from the chair to the couch or the bed.  He is able to stand for a small amount of time as long as he can hold onto something to support himself.  


In late June of 2023 we went to St. Petersburg, FL again for a more advanced stem cell transplant.  These stem cells are specifically designed to target motor neurons. The hope is that these stem cells will stop the progression of the disease and possibly restore some function.  This procedure is experimental, therefore it is not covered by insurance.  We are currently playing the waiting game to see if there is any change.


Brian's attitude is amazing.  He has such a strong faith in God, that he faces these extremely difficult circumstances with the attitude of knowing that God is in control and He will work all things to His glory.   Brian doesn't complain or whine about his situation.  I, on the other hand, throw daily fits and sometimes Brian has to talk me down.  I will be totally real with you, this disease is horrible and I cannot think of anything worse.   This disease does not discriminate; it doesn't care if you are healthy or not.  Brian has always been super active and fit.  He was an ultra runner, running as much as 100 miles in a race.  He is now in a wheelchair.   Throughout this journey, Brian has been the epitome of grace and strength.  His mental discipline and emotional strength absolutely  amaze me.  He remains a wonderful husband and father.


So many of you have stepped up with donations, meals, calls and texts, and I cannot begin to tell you how much this means to us.  Thank you from the bottom of our hearts.  Thank you for your continued prayers.  We know that this journey will not be an easy one, but are thankful to have such a loving community beside us as we travel it.   


I will try to keep you update on our journey.  Love to you all. 
Robyn

Feel free to drop comments or good thoughts below.

Newest Update

Journal entry by Brian Boatman

I am so very sorry that it has been five months since my last CaringBridge update.  I thought about it a millions times but I haven't taken the time because when I do, it seems to take forever for me to get it all out in a logical manner.

I am not really sure where to start since it is been so long, so I will give you a quick highlight of the last four months and then tell you where we are NOW.  When I last updated you in November, I was super transparent about my feelings of the lack of contact and support that some of Brian's friends and family had had with him..... Although I felt badly about being so harsh, I do think that it was divinely inspired because many good things came from it.  Some of his friends said that is what they needed to hear to make themselves do what they knew they needed to do.

In November and December Brian had several special visits.  Brian had wonderful visit with his friend Phil, who now lives in Norway.  Phil made a special and intentional trip to come across the ocean to spend a few short, but very meaningful days with Brian. I think Phil needed it as much as Brian did.  In December, Tommy James, an old helicopter Army buddy that we met while living in Germany came to visit Brian.  It was like no time had passed as we reminisced about the good old days in Hanau, GE.  It is so beautiful the way old friendships can fall right back in step.

We also started seeing more support from our small group at Hunter Street.  They started coming to us once a month for small group since Brian can no longer come to them.  His friend and fellow "crazy" ultra runner, Bob Watters, has been a constant in companionship with Brian. Coming over for visits every week or two and sitting with Brian for hours.
Brian's friend, Rich Glaves, has showed up many times to visit or stay with Brian when I needed to leave.  Rich is always good for a little comedic relief, and we need all the laughs we can get :).  

The man that has showed up time and time again, and continues to show up every week to shave Brian, is Mike Davis.  When Mike shows up to groom B, it is a totally beyond salon experience.  He give B a hot towel shave,  massages his neck, shoulders and arms, trims his nose hair, cleans out his ears... just a few things that he does.  I even bought him an barber's apron that says "Magic Mike" (picture below :).  The man gives Brian two hours of his full attention.  Y'all, I  cannot express enough the gratitude I have for Mike Davis.  I love you, Mike Davis.

The community has been absolutely amazing providing meals via "Meal Train"   We have been fed so well, and loved so well. This has been a blessing to me because I rarely have the time or energy to devote to cooking.  I am so grateful to everyone who has taken the time to bring out meals, send gift cards, etc.  Some of you have cooked multiple time!  You are a blessing.   


February- Roby married Joey Mollica, our new son, Feb. 3rd.  This wedding could not have been more perfect!! The day was perfect, the venue was amazing, the bridal party was beautiful!  Everything went so smoothly that I felt like a guest rather than the "hostess" of this event.  All of this ease was due to my dear friend, Corinne Ver Meer, who took on the role of wedding planner the minute Roby got engaged.  I will never be able to fully express the gratitude and love I have for this woman!!!!  Her sweet and amazing husband, Anthony, served as bartender/everything else Corinne needed him to do.  Love you, Antoine.  And my sweet friend Sasha and her husband Lance selflessly volunteered to be servers at the wedding.  Sasha and Lance, you are the best servers ever!!!  My group exercise staff paid for the flowers, the cake, and breakfast and lunch for the bridal party.  My heart overflows with joy and love for all of the above people who made this day perfect.  I felt unbelievably bless during this time.

A huge thank you goes to Brian's mom, Elaine, and Brian's brother, Todd, who cared for, dressed, transported, ect, Brian during the weekend of the wedding so that I could focus on Roby.  I am eternally grateful for their help.

Ok, now onto what you are really here for....how is Brian?  First let me say, that Brian is the bravest person I know.  He has handled this journey with courage and grace.  HE IS A ROCK.  I am a disintegrating piece of sand compared to him. 

Over the two months he has slowly lost complete function in his left hand (this was the only limb that was hanging on to function).  He is now unable to move his legs, arms, or hands.  If he has an itch, we scratch it, if his nose needs cleaning out, we clean it, if he gets a "hot spot" then we move him; we feed him, we do everything as he is unable to do nothing.  He is still eating a little bit through his mouth but we have to put it in the food processor to get it completely smooth so he does not have to chew at all.  We give his meds through his feeding tube.  We feed him a liquid meal a couple of times a day through his feeding tube.  He is still able to move his head a little bit, and is able to talk (with great effort) as long as he has his bi-pap/triolgy machine on.  This is the machine that blows air in so his diaphragm can expand (this is not O2).  If he doesn't have it on then he is unable to take a deep enough breath to be able to talk.  Brian thinks that his ability to talk will be gone within the next month, but of course, you never know. 

We spoke candidly with our Hospice doctor last week, and Brian asked him what his estimate on timeline would be.  He said he would guess two to four months.  But, of course, with ALS, you just never know.  Brian has started planning his funeral with more detail than I planned my wedding.  If you know Brian, he doesn't do anything half-assed.  Brian actually feels "lucky" to be able to have the time to actually put thought into what he wants his funeral to look like. The funeral that Brian is planning is actually not about himself at all, it is about HIM.   It is about the bigger picture in life and life ever after.  I would urge all of you to come to this service if at all possible because I do think it has potential to be life changing. 

The past year and a half has been long and arduous, and sometimes I don't think I can bear another minute of it.  Luckily, in February,  Brian's mom, was able to move in with us several weeks out of the month.  I could not do it without her help.  There is always something to be done for Brian and sometimes it takes two, three, or even four people to do it.  Roby and Mitt have continued to be such a help to both of us.  Often being asked to do things that a child should never have to do for a parent.  However, they never complain (at least to us ;) and always run to help when needed.  I know that this experience with make them more compassionate, empathetic, and beautiful humans.  They are truly special "kids" and I have never been more proud.

As we continue this journey, we know that it will only get harder.  We ask for your genuine prayers for strength to go on and also peace with what this life has brought us.  We greatly appreciate the help that you have given us already, and will continue to accept more, because I have discovered that I cannot do it on my own.  You just have to know, if you are here, you may get drafted into doing something you hadn't planned on doing ;).  If you want to hear Brian's voice, then I would reach out sooner than later. Thank you for loving us well and helping us, hopefully finishing this race strong.

With love, Robyn, Brian, Roby and Mitt




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