Depending on the severity of your condition, you may be able to qualify for Social Security Disability Insurance or Supplemental Security Income. You will need to meet certain medical criteria in order to be eligible, so it is best to consult with an experienced attorney to see if you qualify.
What is Sjogren’s Syndrome?
Sjogren’s syndrome is an autoimmune disorder that affects the body’s moisture-producing glands, such as tear and saliva glands. It is often referred to as a connective tissue disorder or collagen vascular disease, since this type of connective tissue helps support many areas of the body, including organs. The main symptoms of Sjogren’s syndrome are dryness in the mouth and eyes due to decreased production of saliva and tears. It can also cause fatigue, joint pain, dry skin, difficulty breathing, dry cough, and difficulty swallowing.
The underlying cause of Sjogren’s syndrome is not yet known; however, there are certain genetic and environmental factors that increase risk for developing this condition. There have been some studies that suggest genetic components may play a role in Sjogren’s syndrome development. Additionally, it is believed that environmental factors may increase susceptibility by triggering the body’s immune system to attack its own moisture producing glands.
Debate around the causes of Sjogren’s Syndrome has centered on whether genetic or environmental factors should be considered more important in terms of risk. Some argue that genetics are largely responsible as evidenced by research findings demonstrating familial patterns of occurrence. On the other hand, others contend that environment has a greater impact on developing the condition since various studies point to common triggers such as viral and bacterial infections or sun exposure. Ultimately, while the causes are still unknown it appears likely that both genetic and environmental elements contribute to its development.
Now that we understand what Sjogren’s Syndrome is, let’s explore what symptoms and signs individuals should look out for to better detect onset of the condition.
- According to a 2017 study, the most common symptoms of Sjogren’s syndrome were dry eyes (86.6%), fatigue (75.2%), and oral dryness (71.4%).
- The same study found that “musculoskeletal involvement” was reported in 46.7% of individuals with Sjogren’s syndrome, with arthralgia being the most commonly reported symptom.
- A 2016 meta-analysis found that Sjogren’s syndrome is associated with an increased risk of developing certain types of autoimmune diseases, including systemic lupus erythematosus, rheumatoid arthritis and antiphospholipid syndrome.
Symptoms and Signs of Sjogren’s Syndrome
Sjogren’s syndrome is a chronic autoimmune disorder characterized by the destruction of the body’s moisture-producing glands. Common symptoms include widespread dryness in the mouth, eyes, and other mucous membranes. Other signs and symptoms may include severe fatigue, joint pain, dry skin, musculoskeletal pain, dry cough or hoarseness, antigenic keratoconjunctivitis sicca (dry eyes), recurrent infection of the upper respiratory tract or bladder infections and decreased tear production leading to increased incidences of eye inflammation.
It has been noted that many with Sjogren’s Syndrome experience changes in their central nervous systems which can lead to an increased risk for developing depression or neurological problems such as numbness, tingling and weakness in the limbs. For some with Sjogren’s Syndrome these conditions can be temporary while others experience persistent issues. It is currently debated if this condition is co-occurring with depression or if it is caused by Sjogren Syndrome itself.
It has also been speculated that Sjogren’s Syndrome may increase a person’s risk for developing certain auto-immune diseases such as rheumatoid arthritis, lupus and thyroid disease though-out their life span. While experts are still researching this connection more data must be collected before drawing definitive conclusions regarding this association between these diseases.
Though there are various treatments available to help those living with Sjogrens Syndrome manage their symptoms, some have opted for alternative treatment methods based off anecdotal evidence and experiences from those living with the condition. Supporters of these alternative methods point out that not everyone responds positively nor equally to traditional treatments, even when prescribed in combination with lifestyle changes such as proper diet, exercise and adequate sleep. Detractors on the other hand caution against attempting to self-diagnoses or treat oneself due to possible serious complications that could arise from ignoring medical intervention from a trained professional.
To understand how best to get benefits for living with Sjogren’s Syndrome it is essential to understand the potential complications associated with the condition in future sections. Therefore, coming up next we will discuss “Complications of Sjogren’s Syndrome” and how they might relate into receiving social security benefits.
Complications of Sjogren’s Syndrome
Sjogren’s Syndrome is an autoimmune disorder that can be debilitating for those suffering from it. It affects the tear and saliva glands, leading to dry eyes and mouth, along with other painful symptoms. Unfortunately, this condition can lead to several other serious complications.
One of the most common complications associated with Sjogren’s Syndrome is the risk of infection. The decrease in saliva production caused by Sjogren’s Syndrome often leads to dental problems such as cavities and gum disease. In addition, the dry eyes can make a person more likely to develop eye infections. Both of these issues can cause further health complications if left untreated.
Fatigue is another common complication for those with Sjogren’s Syndrome. This fatigue can be severe and cause problems with daily activities. People with this condition are often forced to expend extra energy on everyday activities due to their symptoms. This can also lead to difficulty sleeping, which then worsens fatigue and causes additional problems.
While fatigue and infection are two of the most common complications associated with Sjogren’s Syndrome, there are also more serious issues that may be experienced. Joint pain and swelling, nerve damage, kidney function problems, and even cancer are all potential outcomes that must be monitored closely by a physician.
Given the potential simultaneous presence of multiple complications that may arise due to Sjogren’s Syndrome, it is clear that this condition should not be taken lightly. Regular visits to your healthcare provider are essential in order to catch any signs of a potential complication early on so that it can be quickly treated. With proper management and treatment, it is possible for someone with Sjogren’s Syndrome to lead an active lifestyle with fewer health concerns.
The effects of Sjogren’s Syndrome on one’s physical and mental health must not be underestimated or overlooked in light of its possible disabling implications. Knowing how this condition may affect an individual allows us to understand the need for disability benefits from the Social Security System as we transition into the next section discussing how to get them.
Disability and Social Security System
Disability and the Social Security System
Those suffering from Sjogren’s Syndrome may be able to file for disability benefits through the Social Security Administration (SSA) under two programs: Social Security Disability Insurance (SSDI) and Supplemental Security Income (SSI). Filing for either of these can be difficult and time consuming, so it is important to understand which one to apply for in order to get the most helpful benefits.
SSDI provides a monthly benefit based upon an individual’s prior work earnings as covered by Social Security taxes, while SSI is a needs-based program available to those who meet specific income limits. To qualify for either program, applicants must have a disability that has prevented them from working for at least 12 months or is expected to last longer than 12 months.
The application process for those seeking disability benefits through the SSA involves both medical and legal aspects. The medical aspect requires applicants to accurately describe their debilitating medical condition and provide evidence such as detailed medical records which support their limitations and inability to work. For the legal aspect, applicants must prove that they have enough credits from their previous employment to qualify for SSDI or demonstrate that their income and assets fit within the limit of SSI eligibility requirements.
Applicants will also be required to attend a consultative examination with a doctor of the SSA’s choice. This examination is used to help determine if the applicant meets the SSA’s definition of disability, which includes having a severe physical or mental impairment lasting over 12 months or longer that prevents gainful employment. It is important for individuals with Sjogren’s Syndrome Disability to understand how this examination works and what types of activities are evaluated during it.
As filing for disability benefits requires a great deal of information gathering and paperwork, many people find it beneficial to use an attorney or qualified representative throughout the application process. Having someone experienced in navigating the SSA’s rules and regulations can ensure that all forms are filled out correctly so as not to delay an application being approved.
Understanding how these programs work as well as any eligibility requirements can help make applying for disability assistance easier. As such, this section has provided an overview of the basics concerning disability benefits through the SSA. The next section will discuss how best to apply for Social Security Disability Insurance (SSDI) or Supplemental Security Income (SSI) benefits in more detail.
How to Apply for Disability Benefits
Applying for disability benefits due to Sjogren’s Syndrome (SS) can be a long and tiresome process. The Social Security Administration (SSA) is responsible for the nearly 9 million SS beneficiaries all over the country, so their application process is fairly stringent and detailed.
The first step is to obtain a medical diagnosis from your physician or other qualified healthcare practitioner, who must determine that you’re unable to work because of your SS-related disability. Your doctor must also document the diagnosis and list any acute or chronic symptoms and limitations due to SS that prevent you from working. This information will then be used by the SSA to decide if you meet their criteria for benefits.
Applicants are encouraged to apply online, as this format allows them to upload corroborating medical evidence directly and enables them to receive faster decisions from the SSA. Paper applications are also available and provide detailed instructions regarding the documents on how to submit supporting evidence such as medical records, laboratory tests, and other related materials.
It’s important to keep in mind that applying for SS disability benefits can be complex: applicants may not understand some of the technical terms and/or feel overwhelmed by the sheer volume of paperwork required. Additionally, though disability hearings provide an appealing option, they have a long processing time, often having wait times of over a year before they even start an evaluation process. Fortunately, having legal assistance in your corner can help streamline this process, providing peace of mind in an otherwise uncertain situation.
Unfortunately, there’s no guarantee that those suffering with SS-related disabilities will qualify for benefits through SS. Those rejected initially may reapply at a later date when their condition worsens or if they have additional supportive medical documentation confirming their disability has progressed beyond what was previously submitted.
Now that we know how to apply for disability benefits related to Sjogren’s Syndrome (SS), let’s move onto the next section which discusses the limitations on activities that qualify for these types of benefits.
Limitations on Activities that Qualify for Disability Benefits
Determining whether or not an individual with Sjogren’s Syndrome qualifies for disability benefits can be complex, as it depends upon how much the disorder affects a person’s daily activities. Generally, disability benefits are reserved for individuals whose Sjogren’s impacts their ability to perform basic job functions—including physical tasks, communication, socialization, and activities of daily living (ADL).
When applying for disability benefits, individuals must provide detailed information about their condition and its effects on specific activities. To qualify, a person must prove that their symptoms prevent them from being able to work a full-time job, or that they require significant assistance from another individual during ADLs. Furthermore, applicants must demonstrate that these limitations are consistent over time and have been caused by Sjogren’s.
It is important to keep in mind that there may be gray areas when considering an individual for disability benefits. For example, an applicant may have difficulty engaging in some activities due to limited energy or other physical symptoms linked to Sjogren’s, but may still be able to perform certain types of jobs part-time. On the other hand, other activities may be harder to quantify and assess with respect to degree of limitation. Therein lies the challenge of evaluating individuals with Sjogren’s Syndrome on an individual basis within the context of obtaining disability benefits.
The jury’s still out on this controversial matter; however, the impact of Sjogren’s Syndrome on a person’s ability to work must be taken into account when deciding if someone is eligible for disability benefits or not. Ultimately, it is important for individuals with Sjogren’s Syndrome to communicate openly and honestly about the limitations from their disorder when filing for disability benefits.
Now that we’ve examined what activities may qualify for disability benefits for those with Sjogren’s Syndrome, let’s move on to exploring treatments available for managing this disorder.
Treatments for Sjogren’s Syndrome
Treatment for Sjogren’s Syndrome is largely found in relief of symptoms, as the underlying cause is unknown and there is no cure. While there are some medications that may reduce the severity of symptoms or target some of the underlying tissue damage caused by Sjogren’s Syndrome, focus for most with Sjogren’s Syndrome should be on symptom management therapies.
Immunosuppressives such as methotrexate and cyclophosphamide can be effective to bring slight relief from some of the pain associated with Sjogren’s Syndrome but they also come with potentially harmful side effects that may make them less than ideal treatment options. Additionally, corticosteroids (like prednisone) can help reduce tissue inflammation, however these can lead to other health complications which makes their use dependent on individual circumstances.
On the other end of the spectrum, proponents argue for a more holistic approach to treating Sjogren’s Syndrome that incorporates lifestyle adjustments rather than prescription drugs, such as adopting healthy sleep patterns, mild exercise regimens and proper nutrition. Some believe that such lifestyle changes don’t just help manage pain levels, but may also provide long-term benefits in slowing down the severity and progression of the condition over time. As treatments go, this approach is usually seen as preferable due to its lack of any serious side effects.
Ultimately each treatment option for Sjogren’s Syndrome will need to be tailored to each individual’s assessment by their doctor. Medical professionals must be consulted before implementing any course of action or ‘treatment’ to ensure potential damaging effects are taken into account.
Whether it be under medical supervision or personal initiative, understanding what treatments could work and their potential benefits is an important part of claiming Disability Benefits due to Sjogren’s Syndrome. Now that we have explored potential treatments for navigating symptoms associated with Sjogren’s Syndrome, let us turn our attention to understanding Support Services available for those who are living with Sjogren’s Syndrome disabilities.
Support Services for People with Sjogren’s Syndrome
People with Sjogren’s Syndrome (SS) often experience a range of specialized needs due to the complexity of their condition. To help ensure that these needs are met, access to a variety of support services are available for people with SS. These services can include medical care, financial assistance, educational resources, and counselling services.
Medical care is an important resource for those with SS. It is recommended that those impacted by SS receive both primary and specialty care from doctors who have specific expertise in treating the condition. These doctors may be part of a multidisciplinary treatment team that includes dentists, ophthalmologists, rheumatologists, and other specialists depending on the individual’s symptoms and needs. Furthermore, occupational therapists or physical therapists may be necessary for those struggling with compromised mobility or other physical limitations caused by the condition.
Financial assistance may also be available for people living with SS. Health insurance can cover medical costs associated with treating the condition, as well as prescription medications or assistive devices needed to manage symptoms or side effects from treatment. In addition, there are some government assistance programs that can provide additional assistance to people affected by SS in meeting their medical expenses. Furthermore, financial counselors can provide advice about debt management, budgeting strategies and other money matters for those facing financial difficulties due to the condition.
Educational resources may also help individuals cope with the demands of SS. Information related to understanding SS and its impacts is available online through various educational sources such as patient advocacy groups and websites like sjogrens-foundation.org/living-with-sjogrens/. In-person support groups are also available in most areas offering an opportunity for individuals to connect with those managing similar issues and learn coping strategies from one another.
Finally, counselling services such as cognitive behavioural therapy (CBT) and psychotherapy can be useful in helping manage the emotions associated with living with a chronic illness like SS while helping individuals establish healthy coping mechanisms that empower them to take active steps in improving their quality of life. Counselling is not only beneficial for individuals affected by SS but family members and caregivers as well who may be dealing with related stressors or changes to their daily routine caused by the condition.
In conclusion, people diagnosed with SS have a variety of support services available to them including medical care; financial assistance; educational resources; and counselling services. Accessing these services can allow individuals to better manage the demands of living with this complex disorder while affording them opportunities to improve their overall health outcomes and quality of life.
 Miller F., & Zembower T., (2005). “Psychologic impact of systemic lupus erythematosus: Differential effects of depression and anxiety.” Arthritis & Rheumatism 52(6): 1903–1910
Responses to Frequently Asked Questions with Detailed Explanations
How is the severity of Sjogren’s Syndrome evaluated for disability?
The severity of Sjogren’s Syndrome can be evaluated for disability through a critical assessment of the symptoms and signs of the condition. A doctor may evaluate symptoms such as fatigue, joint pain or stiffness, dry eyes, persistent dry mouth, a very high sedimentation rate or ESR (indicating chronic inflammation in the body), recurrent oral yeast infections (candidiasis) or recurrent sinus infections, difficulty concentrating or difficulty with simple mental tasks, and frequent hoarseness. All of these factors contribute to the assessment of the individual’s disability level due to Sjogren’s Syndrome. Diagnostic tests such as blood tests, biopsies of the salivary glands, and imaging studies such as MRI scans may also be used in determining the severity level. Additionally, the Social Security Administration (SSA) uses guidelines that take into account the debilitating effects of Sjogren’s Syndrome when evaluating someone for disability benefits.
Are there any benefits available beyond disability for Sjogren’s Syndrome?
Yes, there are additional benefits available beyond disability for those with Sjogren’s Syndrome. The U.S. Department of Veterans Affairs provides a wide range of specialized services and programs to Veteran patients that help address the specific needs associated with Sjogren’s Syndrome such as immunially mediated diseases and autoantibody production which can be difficult to manage. Many states also provide state-specific benefits for those living with a Sjogren’s Syndrome diagnosis. These might include housing assistance, medical care, low-cost drug therapy, and even training and job placement programs. Additionally, many local volunteer organizations offer various types of support to those affected by Sjogren’s syndrome including educational resources, support groups, advocacy events, public awareness campaigns, and even fundraising initiatives. Finally, employers may provide certain accommodations for employees with a Sjogren’s Syndrome diagnosis in order to reduce the physical demands associated with their job duties or allow them more control over their work schedule. Overall, there are multiple forms of benefit beyond disability that those living with Sjogren’s Syndrome can access if they look hard enough to find them.
Are there certain conditions that need to be met in order to qualify for Sjogren’s Syndrome disability?
Yes, there are certain conditions that need to be met in order to qualify for Sjogren’s Syndrome disability. In general, applicants must demonstrate long-term and/or significant limitations resulting from the syndrome that impacts their ability to perform activities of daily living and/or isolated functioning problems.
In addition, applicants must provide medical documentation, such as physical examinations, X-ray imaging, or lab tests confirming the diagnosis, a history of chronic dry eyes or other symptoms associated with the syndrome, and any other evidence needed to prove their eligibility. The Social Security Administration may also contact healthcare providers or a specialist to review the case before a decision is made. By carefully documenting the claimant’s impairments and how they affect everyday activities, an individual may significantly increase their chances of receiving benefits for Sjogren’s Syndrome disability.