Alan Beaulieu

My name is Alan Beaulieu.  I am 29 years old and was just recently, within the past few months, diagnosed with Ankylosing Spondylitis (AS).   My story begins like so many others that suffer from this disease.  It involves pain, stiffness, fatigue, frustration and feeling hopeless.  AS is a complicated disease, there are not a lot of “specialists” that have a lot of answers; without answers there are not a lot of options for relief.  However, we must not just give up.  Even though we have our daily struggles and pain, we must not give in to it.  We must do whatever is in our power to face this disease and defeat it.  I hope in writing my story I can get a lot of my own questions answered, as well as, maybe help those that are unsure of what AS is and what it does to the bodies of those of us that suffer from it.

Background:  I joined the United States Air Force in March 2001 and became a part of the Security Forces career field.  For the first six years I was a regular “Air Force Cop” The last four years, I was fortunate enough to be able to be a Military Working Dog Handler.  I have worked both drug and bomb detector dogs.  It was the best job that I have ever had.  During my time, I have been stationed at Ellsworth AFB, South Dakota, Ramstein AB, Germany and currently at Joint Base Mcguire-Dix-Lakehurst, New Jersey.  During the last ten years I have been deployed 4 times, twice to Iraq.  I have enjoyed my time in the military.  Unfortunately, it is coming to an end.  I am being medically retired due to having AS, 6 bulging/herniated discs, moderate Traumatic Brain Injury and PTSD.  I look forward to “hanging up the boots” and re-starting my life back at home in Michigan.

The Pain and The Journey:  My story of AS starts in spring of 2006.  I had just returned from a 7 month deployment to Kirkuk, Iraq.  During my deployment I noticed some back stiffness but really didn’t think anything of it.  I figured it was just from all the gear and ammunition, little did I know, I was in for one rude awakening.  One morning, while on R&R, I woke up out of bed.  When I went to take a step I feel to the floor.  I had no idea what was going on.  I felt terrible pain in the lower part of my back,  along the spine and debilitating pain on the lower left side and down the left leg.  My entire lower back and left leg felt “seized up”  It felt like it was fused together.  Each step was painful, each movement that involved the left leg or back was excruciating painful.  I limped slowly for the next few months.  No one really had a clue as to what was going on.  When I went to the medical clinic on base the doctors thought my hips were uneven.  They layed me down on the table and my left leg was yanked on twice in an attempt to even out the hips.  Obviously, this made my pain worse.  After several failed chiropractic visits,  I was sent for an MRI.  The results showed a bulging disc in the L4-L5 area of the spine.  After receiving the results of the MRI, I was sent to physical therapy.
Physical therapy was a waste of time. I rolled around the floor on a ball and did a bunch of stretches.  The point was to keep my back straight and my core muscles strong.  They said it would help with the pain.  Notice, I previously said, it was a waste of time.  It didn’t do anything for the pain.  It took months, upon months to start running again.  After a few months, it got easier to walk.  The easier it got to walk the easier it got to job ever so slightly.  When I finally tried running it was horrible.  As soon as I got a few steps my entire lower back and left side would tighten up and eventually seize.  My left leg would go numb and feel like “jello” The more I tried to run through it the worse it seized up before eventually I would hobble around.  I was baffled.  I had no idea what was wrong.  All the medical doctors would do is feed me motrin or naproxen.  They couldn’t understand why I was in so much pain.
I wasn’t able to run until the summer time of 2007. Even then it wasn’t like what I was used to.  I was still slow.  I was still barely passing my physical training tests.  Sit ups and running were painful.    As much as I wanted to say something, the mentality in the military is to “press on.” You don’t show weakness.  If you’re hurt then you better suck it up and keep going.  For the next year, all I did was take naproxen for the pain and do my best on my PT tests.  It got so bad; I had to take 6-8 naproxen just to keep the inflammation down so I could pass my tests.
In August 2008, I was deployed to Baghdad, Iraq.  My bomb sniffing dog, “Cici” went with me.  I was really worried that my back would give out on me during the deployment. I had to do whatever I could to keep my dog and I, in the mission.  I went to the medical tent several times for the back pain.  I spent many nights laying on heating pads and taking NSAIDs and motrin like crazy.  At this point, I have been dealing with this pain along the lower back and left leg for 2 years now.  With no understanding of what the problem is.  No one knew what was going on.
My problem took a turn for the worst in the fall 2010.  The pain was getting more frequent and worse.  The exacerbating episodes lasted longer and longer.  Before, I would hurt for a few months then it would return to normal.  This time it never went away.   This time was like all the others, except it never left.   I was never ever to stabilize my back again.  For 4 years I felt pain.  It would be extremely painful when getting out of bed, off the couch or even off the floor.  It felt as if my back and leg area was fused shut and every movement was forcing it “open again” There were times I would be in tears from the pain.  There were times I had to use a cane just to help me walk.  It was horrible.   In November, 2010 I underwent another round of MRIs.  This time they found bulging/herniated discs in my C-spine (3) and L-Spine (3)   the doctors were still at a loss as to the pain in the lower left part of my back and down my left leg. In Jan 2011, I was sent to physical therapy (yet again) for the fourth time.  Again, it was a waste of time.  I couldn’t run, nor could I walk more than a hundred yards without pain in my back and down the left leg.  In Feb 2011, the physical therapist told me there was nothing more that could be done for me.  She said, “Since your still having the pain and the numbness when you walk or try to run” this is more than just something that I can fix.
I spent the next few months going to two neurologists and pain management.  Both neurologists confirmed I had Degenerative Disc Disease.  Pain management really didn’t do anything for me.  Upon the initial examination the doctor noticed when I sat down; I didn’t have the strength to lift my left leg off of the ground.  It was crazy, It felt like I was paralyzed and had lost all strength and functioning in my left leg.  I was prescribed a whole slew of narcotics and pain medications during these months.  None of them provided relief.  I underwent an EMG test and the results were “normal.”  I was growing more and more frustrated.  I was in so much pain and no one had a clue as to what was going on.
My frustration reached its peak in the spring of 2011.  I was in the office of my former Primary Care Manager.  After all the visits to the specialist he was growing more and more suspicious that I was faking it.  He sent me for a round of blood tests.  About a week later, I was called back in. He looked at my tests and said, “You know I was real skeptical about your pain when you first started coming in.  However, according to your blood tests you have some real issues going on.”   I wanted to scream at him. I wanted to smack him for basically telling me I was lying. However, I could not.  After all, he is a Captain and I was just a Staff Sergeant.  I asked to go to a Rheumatologist.   I pleaded by saying, “there is something wrong and we haven’t tried everything.  What about a rheumatologist?” My request was shut down.  I was instead sent to mental health for a psychological evaluation.  He seriously thought all my pain was just “in my head”  I was at a loss.  I started to feel like I was going crazy.  I began to think, “am I just making this up?”  I knew I wasn’t, but after 5 years, no one had a clue as to what was going on.”  To make matter worse I was also told, “you can no longer work with military working dogs”  The physicality of the job is too much for your health.  I was devastated.  I had been working with bomb/drug dogs for 4 years.  I deployed with a bomb dog who saved mine and others lives.  I was in tears.  It hurt badly.  I was moved to an office job, where I am currently working as I await the results of my medical retirement board.
(on a side note: It is a good thing I was sent for the mental evaluation. I was having problems from my time downrange for a while.  It was then I was finally able to be diagnosed with PTSD and mTBI, so all was not lost in getting sent to mental health.   There is a stigma in the military about PTSD.  Those of us that suffer it are seen as weak.  When I was taken off of the road and away from dogs, it allowed me to quietly get help without fear of being judged and tormented.  It’s not my fault I saw what I saw and experienced what I experienced.  To be judged and viewed as weak by my own brethren was painful.)

When I went to mental health, the LCSW that was working with me noticed my pain.  She noticed i walked with a limp daily.  She noticed I couldn’t sit in a chair for more than 10 minutes without grimacing and having to stand up due to the pain. She asked me what was wrong.  I told her the whole story.  She looked at my blood tests and made a few phone calls.  I was then able to switch to a different Primary Care Manager.  Finally, after 5 years, I had a doctor who gave a damn.  She immediately sent me to a rheumatologist.  The rheumatologist sent me for more blood work and a bone scan.  The blood work showed high levels of C-reactive proteins and I tested positive for HLA-B27.  The bone scan showed high levels of inflammation a long my lower back and in my SI Joints (sacroillitis)  The bone scan was unable to show inflammation in the neck.  I wasn’t able to sit in the machine that long.  I freaked out in MRI and bone scan machines due to my PTSD.  If I feel trapped with nowhere to go, I immediately fear for my life and undergo a panic attack. After listening to my symptoms the rheumatologist finally diagnosed me.  It was ANKYLOSING SPONDYLITIS.  Now, normally people would be devastated upon hearing they have a lifelong debilitating disease.  I was actually relieved.  I was so relieved because I knew I wasn’t crazy.  I knew I wasn’t faking it.  It’s pretty hard to fake 5 years of back pain.
Currently, I am on Humira.  I inject myself every two weeks.  I think I need to go to weekly injections.  For the first couple of days I feel okay.  I don’t have the inflammation in the SI joints and the pain in the left leg. However, my neck is still stiff and my lower back (along the spine) still hurts.  If I try to do any type of physical activity the pain in the neck, back and even the sciatica gets worse.  The only time I feel okay is when I don’t do anything at all.  After a few days, the pain starts coming back on its own.  It’s frustrating.  I fear getting bamboo spine.   Over the last few weeks I have been getting a pain in my chest and I have had shortness of breath for a while now.   I see the rheumy on the 17th.  I am worried the spondylitis has attached to the joints in my rib cage.  If this is indeed true that means my chest is seizing up and my lungs can’t expand like a normal person.  I am 29 years old.  I can’t lift more than 29 lbs, I can’t sit for too long without being in pain.  I can’t bend over very much, nor can I bend to the side.  I can’t turn my neck too much without being in pain. I am on an immune suppressant which leaves me tired all the time.  When I tell people what I have I get the same response, “what is that?”  It’s frustrating.  It’s frustrating to have a disease that impacts my life so severely, yet no one has a clue what it is.
Even though I get frustrated, I am focused.  I won’t let this disease beat me.  I am confident they will find a cure.  I have read numerous articles and even read about how this disease could be caused by bacteria.  Who knows?   All I know is this disease is real. It has the potential to be extremely debilitating.  However, I can’t focus on that. Each day I try to stretch as much as I can. I try to stay active.  It is difficult because I am limited but I do what I can.  I am looking at the disease like a blessing in disguise. Instead of doing 20 years in the military I am able to get medically retired.  I will be able to move back to Michigan and achieve my life long dream of graduating from the University of Michigan.  I also have the assistance of a great service dog named Bella.  She’s a service dog trained to the specification of the American with Disabilities Act.  She is trained to assist me not only with PTSD symptoms but also to “fetch” things off of the ground so I don’t have to bend over at pick it up.  She is a lifesaver.  Once, I get medically retired, I will be able to re-start my life.  I understand what I have. Now I just have to find what I call, a new “normal” I have to learn to live within it and also figure a way to defeat it.

I am Alan Beaulieu and I have Ankylosing Spondylitis!

Joint Base McGuire-Dix-Lakehurst, New Jersey United States of America


6 Responses to “Alan Beaulieu”

  1. Dear Alan,
    Thank you for sharing your story with us. I am a person who is always looking for a “sign” to know that I am moving in the right direction. I had just posted that I needed a “face” because I had not received any for the day. I am finding that I “pout” if I think I am not going to get a “face” for the day. I have received one every single day since I started this journey. A few have asked me why I would take on a project that would consume so much of my time and energy. I wonder sometimes myself. After posting, I received your email. I was so excited to see that I would indeed have a “face” for the day!
    I was shocked that you were a veteran and so tickled, then I was totally in shock when I realized you would end up being A.S. Face 0111.
    My 1st story on the 11Th Verterans Day was a veteran who would be :face” 0111.
    1 /11/111/ Equals my sign!
    Sincerely Cookie
    Thank you for the sacrifice you and your family has made in order that I may have the freedom to do this site safely in my home.
    Bless you always.

  2. Hi, I am Taku (AL) & I suffer from SA too (SpondyloArthritits-the general name of a group of inflamatory imunoreactive diseases, part of which is AS).
    Little is known 4sure about this kind of diseases, and most of it came from people talking about their own sufferings from SA.. and yes: I’ve been into all the troubles you talk about in this confession, + more..
    While there are many types of SA and they all have their own caracterisstics, they also have many simmilarities and they all involve some kind of genetic malfunction of the Central Nervous System (CNS) and/or some sort of outer-factors-triggered weakness of the body’s Immune System (IS) and CNS. Now this is the effect of (?) .. and I wonder if the cause (?) is the same for all them.. One thing is for sure : doctors wonder too!
    In my case, my blood’s white cells doesn’t seem to like my connective tissue, hence they attak each and everyone of them.. continuously, especially the ending parts of ligaments and tendons right at the place where they attach to the bones.. …. now I know I must live with my pain and I’m getting used to it.. after 10 years.
    Knowing what you are dealing with is deliberating and contributes especially to your mind’s health. Lately I have found some information about food & diet involving SA.. not yet confirmed as useful information though.. but I think you may want to make researches about this.. I am!
    You mention you are on some sort of Modern Medicaments.. In my experience NSAIDs (Non-steroidal anti-inflammatory drugs) will only make your IS weaker, possibly damage your Digestive System, consume your time and money as well as play strange games to your nerves, general will and the dose of optomism/pesimism they inject to your brain.. if you know what I mean !!
    I started to feel better when I quitted my relationship with NSAIDs – 2 years ago I was litterally Druged and self-suggested from using them. When I finally stopped taking them for real, I suddenly came to realise that they did nothing at all to stop my pain.. It was only my mind..
    Now I’m getting better or worse, depending on my LIFESTYLE – I can’t stay seated for too long or too frequently, I have to walk (sold my car – bought a bicycle). I spin everyday, swim everyday, do a little stretching every other day (sadly can’t stretch as much as I want to.. it will make my muscles sore for days).. I’m starting some light resistance training and see how it gets.
    Pain comes and goes.. and comes again.. I am oriented to see the god part of it.. pain can make you a very modest person and limit your personal needs.. because Evey Person Have Dreams.. But a Sik Person Only Dreams Of Better Health !!

    I wish you a better health my friend, feel free to comment on this or if you wish, contact me stargo@live.com

  3. Hello Alan

    My name is Brian and I to have AS. Diagnosed in 2010. I am a veteran medically retired in 1989. I have recently been having trouble with my AS. I went to the VA to process a claim and was shot down. They told me that it is a autoimmune disorder. I don’t believe that I did not have any problems with my spine, SI joints, for neck until I joined the military I have been taking INSAIDS like candy throughout my military career. I was wondering if I should appeal there decision. I have read several cases that have been over turned. I think it’s because the military is really trying to understand this disease. Do you have any suggestions for me to help my case be granted a percentage award. Would take any advice you an offer. Thank you.

    Brian Farrar, USA MEDICALLY RETIRED

  4. It’s definitely a relief to have answers. I have been dealing with the symptoms of AS since I was 12, I am now 35 amd have been recently diagnosed… appropriately. Now I am dealing with the depression of having to completely change everything about my life. I can no longer lift weights, or do deadlifts. I can no longer do the biking and cardio I’m used to that brought me peace of mind, and I am depressed over it.

  5. Thanks for sharing your story. I’m 27 and have AS. How and where did you get your service dog? I think I really could benefit from one.

  6. Dear Alan,
    First, thank you for your service. Having provided freedom to all Americans it seems only fair that the Lord should provide you with freedom from your pain. I to have AS and I believe you. I hope you living retirement now you deserve it and it is possible to have peace and happiness even with this disgusting and missunderstood disease.
    Peace to your heart and soul.

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