Life with MS
Anna Gramlich: Senior Capstone

Incurable: Multiple Sclerosis

Supporting the people living with life-changing, chronic illnesses. To their strength, bravery, and patience: a page dedicated to expand the knowledge of MS.

Anna Gramlich

Capstone & Website Creator

My name is Anna Gramlich and I am a senior attending Oxford High School in Oxford, Connecticut. I have always found an interest in the medical field. Throughout high school, I have gotten the opportunity to learn from and volunteer at the Oxford Ambulance Association to help provide medical services to people in town. I always knew I wanted be a medical professional, and getting experience through the Oxford Ambulance Association has helped my passion grow exponentially. 

My capstone project is a research-based medical website to help me personally gain knowledge about Multiple Sclerosis (MS), and then teach it to others. I chose MS because my uncle had been diagnosed with it and battles it each day; I have seen how the effects take a toll. I feel that it is very important to spread awareness about chronic illnesses and the mental affects it can cause on both the patients and their support systems, like family and friends. It is very important to learn how to cope, and to be aware of anything that may bring comfort to these patients. 

Part 1

My Inspiration

Why I Chose This Project and What It Means to Me

Family means everything to me, as it does to many people. If you think about it, someone you know is probably battling a physical or mental disability, whether it is obvious or not. The man pictured on the left is my uncle Thomas. He was diagnosed with Multiple Sclerosis in 2005. As I've gotten older, and his condition has grown worse, I am able to see the impact this disease has on him and on the rest of my family.

One of my favorite subjects to learn is medicine and human anatomy/physiology. As I am entering college next year in 2022, I am planning on majoring in biology, with the end goal to be involved in medicine and possibly neuroscience. I thought, what better idea than to research and write about the condition that affects my family first-hand. In the production of this website, I have gained knowledge about my uncle's worsening health condition, and also got exposure to the process of medical research, as it will be a prominent skill for my education in years to come. 

Part 2

Multiple Sclerosis

Studies and Research

Multiple Sclerosis is the condition in which one’s own immune system attacks the myelin sheath of the central nervous system and deteriorates it. The myelin sheath is the protective covering of nerve fibers. It is important to have healthy myelin sheath that remains intact because without it, the nerves in your spinal cord cannot properly send messages from your central nervous system to your brain. It is like if you had a wire transporting electrical signals, but at some point along the way, that wire was stripped or cut. The message no longer gets sent, and that signal is lost. Your own body is attacking itself and there is no way to stop it.

Some cases are worse than others depending on how damaged the myelin sheath is. Once it gets destroyed, it cannot be repaired. Unfortunately, this means that the condition can only worsen over time, and there is nothing a body can do to fix itself. The severity of the deterioration that has occurred and the types of nerves affected will determine how prominent a person’s symptoms will be. Symptoms are experienced to all different degrees, but incorporate issues from head to toe within the body. 

  • Lhermette’s Sign/Phenomenon is when shock-like sensations shoot down the neck and spine in a relatively painful manner. This is usually one of the first symptoms people report as this disabling shock can branch out into your arms, legs, and back. It is most commonly felt when your neck is bent forward in the position where your chin can touch your chest. 

  • Tingling and complete loss of feeling in your limbs results in body numbness, causing much worse side effects. Numbness will inevitably lead to immense difficulty in walking, moving, and holding objects in your hands. It will also cause tremors and unsteady limbs.

  • Weakened muscles and muscle stiffness occurs, making muscular movements very hard to accomplish. Mobility becomes extremely limited. With this, canes or wheelchairs can be of use. Many struggle to stand up, walk up and down stairs, or even something as small as holding a pencil in your hand and writing on a piece of paper with it.

  • Movement of the eyes can cause pain and in worse cases, lack of vision, double vision, and blurriness. This effect may start in one eye and eventually affect the other. Due to sensory interaction, poor vision can lead to poor balance, since being able to see what is in front and around you helps aid in coordination. 

  • Because of the extent of such nerve damage, one may also experience losing control of their bladder. It is not rare to find MS patients urinating on themselves without knowing. Sexual arousal and bowl movements may be affected as well. 

All symptoms do not necessarily occur at the same time. With multiple sclerosis, people can experience recurring symptoms for a short period of time, as in weeks, or an extended amount of time, as in years. But for all, it is everlasting. They may experience times of relapse, when their physical state gets noticeable worse, or remission, where they are in a window of small, temporary recovery.

There are different kinds of multiple sclerosis. Primary-progressive MS is the trend of the progressively worsening conditions, with no early-on signs of relapsing or remission. There are different stages with PPMS, as one can be in an active state, where they may relapse, or an inactive state, where they are stable. In this case, the deterioration is not linear. However, the other kind is secondary-progressive MS, where your condition will only worsen. There is little to no chance that you will find yourself experiencing windows where your symptoms fluctuate. Your health will rapidly decline and it is unlikely for remission at any point. There is also relapsing-remitting MS (RRMS), where it is characterized by continuous relapsing and larger, more serious attacks of MS symptoms. The average lifespan for those with PPMS is 41.4 years old, whereas for those with RRMS, it is 77.8 years old.

Every person experience multiple sclerosis differently. Age, gender, heredity, race, and other varying factors, like being a smoker, determine the severity of one’s condition. Interestingly enough, women are 2-3 times more likely to be diagnosed with RRMS than men. Multiple sclerosis is also the type of autoimmune disease where if another family member has it, you are at risk, and more likely to genetically develop it. 

The National Multiple Sclerosis society has concluded that over 2.3 million people worldwide have this condition. Although it is easy to look at this like a statistic, it is crucial that we realize 2.3 million people is not just a number - they are 2.3 million families, 2.3 million lives, 2.3 million stories, and 2.3 million people suffering each day. The ones with the illness are not the only ones being devastatingly affected. These people are parents, brothers and sisters, children, friends, and coworkers. In my family’s case, my uncle has two young children who are not even teenagers yet. Taking care of kids is a job itself, especially young ones who need proper guidance and attention. It is any parent’s best wish to do anything for their children, but what happens when that ability is compromised by something that cannot be controlled? Multiple sclerosis is not just a change to one’s body, but a lifestyle adaptation too. Those with jobs may have to quit due to the inability to work, or, are at high risk for being fired for the same reason. Employment discrimination due to disabilities is unfortunately very common. The Bureau of Labor Statistics report that in 2019, 66.3% of non-disabled people were employed, and only decreasing to 61.8% in 2020. However, in 2019, only 19.3% of disabled people were employed, and decreased down to 17.9% in 2020. You can see where unemployment will become a problem for those who are chronically ill. With an increased number of doctor or hospital visits, their medical bills are likely to be skyrocketing. Other life luxuries such as driving a vehicle are restricted. The activities and daily occurrences we do not think twice about are heavily compromised for those struggling with multiple sclerosis. 


Part 3

The Interview

A Series of Questions and Answers about MS

My uncle was kind enough to do an interview with me about his personal experience with MS. I had previously prepared the questions listed below and the answers are his honest, word-for-word responses.

  • Question #1: When were you diagnosed with MS and how long before that did you start to experience symptoms? 

"I was diagnosed with MS in 2005.”

  • Question #2: What are some of the hardest challenges you face in having MS?

“None until about 2015 when I started having ‘drop foot’ where my left foot doesn't pick up all the way while walking. Sometimes when I do a lot of walking, like on a site visit for work, it is difficult for me to walk.”

  • Question #3: What are everyday activities you can no longer do due to your illness?

“Because of the drop foot, walking, jumping, and running. Writing as well.”

  • Question #4: How do you feel your sickness has impacted your loved ones and those around you?

“Nobody has said anything, so I guess they are okay, and I am not much of a burden.”

  • Question #5: Have you learned anything about yourself while fighting this illness? 

“Don’t take easy things like walking or writing for granted.”

  • Question #6: What is something you wish you had to make your experience with MS easier, or more bearable? 

“Nothing comes to mind.”

Part 4

Coping with a Chronic Illness

Treatments and Remedies to Ease the Severity of Multiple Sclerosis

Multiple sclerosis is not an illness that can be cured. However, there are various remedies that can help treat the pain and symptoms of this condition. The first option is medication. There is not a single medication that can soothe all aspects and symptoms of MS in one take. However, being on multiple medications that are designed for each kind of symptom are available. 

 Injections:

  • To modify the disease as a whole, by delaying progression activity, one may be prescribed: Avonex, Betaseron, Copaxone, Extavia, and more. 

 Oral Medications:

  • Aubagio: A pill taken once daily used to enhance the ability of compromised immune cells. 

  • Bafiertam: A medication used to treat relapsing MS, such as relapsing-remitting disease (RRMS), and secondary progressive disease (SPMS).

  • Dimethyl Fumarate: Also used to treat relapsing forms of MS.

For more specific symptoms, these medications are commonly used.

  • For bladder issues: OnabotulinumtoxinA, or Botox is given. 

  • For bowel dysfunction: Coclace or Dulcolax is given which softens stool to treat constipation or stomach discomfort. 

  • For depression: Prozac or Zoloft can be given, which are two common medications to treat depression. 

  • For walking difficulties: Ampyra may be given, which is a muscle strengthener to improve walking and muscular abilities. 

Therapies may also be of use to MS patients. As their mental health may rapidly decline due to drastic life changes, speaking with a therapist may ease them mentally. Physical therapy is also of great use. Especially with a condition that will decline their ability to walk and move due to muscular weakness and instability, PT can help them get back on their feet and be able to move again. 

It is important to be as understanding as possible for those with multiple sclerosis, or anyone with a chronic illness. It is scary, threatening, and uncertain. Be the additional help someone needs, and you may change a life in ways you never knew you could. 


Thank You

-Life with MS-

For more information or to donate to the cause, please visit The Multiple Sclerosis Foundation at: https://msfocus.org/