STRUGGLE: Regaining Control From An Often Misunderstood And Misdiagnosed Skin Condition

The post STRUGGLE: Regaining Control From An Often Misunderstood And Misdiagnosed Skin Condition appeared first on Good News!.

Listen to “Hispanic Heritage Month (September 15th – October 15th) THE IMPORTANCE OF ACTING EARLY WHEN LIVING WITH LUPUS” on Spreaker.

Hispanic Heritage Month (September 15th – October 15th)

THE IMPORTANCE OF ACTING EARLY WHEN LIVING WITH LUPUS
Recognizing the Disproportionate Impacts of Lupus on Hispanic and Latinx Communities

Women of color are disproportionately affected by systemic lupus erythematosus (SLE), the most common form of lupus. SLE is a chronic, inflammatory disease that can result in permanent damage to major organs.[1] Notably, it is estimated that 21 percent of those living with lupus in the U.S. are Hispanic.[2] Patients of color, including Hispanic people living with SLE, also have significantly higher rates of lupus nephritis (LN), a potentially life-threatening complication of lupus, compared to White patients.2

Hispanic and Latinx individuals may also face distinct challenges that can impact access to healthcare that may make managing the disease even more difficult, such as language barriers.[3],[4]

Fortunately, early intervention with the use of FDA-approved medications can help reduce the risk of organ damage progression.[5]

In honor of Hispanic Heritage Month, on Tuesday, September 24, Guillermo Valenzuela, M.D. is available to discuss the effect of lupus on the Hispanic and Latinx communities. Dr. Valenzuela, who is the Medical Director of the Internal Rheumatology and Immunology Specialists medical center, can also discuss the unique challenges these communities face and the importance of early disease intervention.

Interview is courtesy: GSK

#hispanicheritagemonth #actingearly #livingwithlupus #lupus

The post Hispanic Heritage Month (September 15th – October 15th) THE IMPORTANCE OF ACTING EARLY WHEN LIVING WITH LUPUS appeared first on Good News!.

For the millions of people living with psoriasis, like Gloria, the impact on their daily lives extends far beyond the physical symptoms. Among some of the many grievances Gloria can share about her last 10 years living with the condition are:

Strangers commenting on her skin when she’s out in public

Leaving bits of skin on furniture — and even needing to vacuum her bedsheets

Wearing her hair down during the unbearably hot Texas summer to avoid showing affected areas on the back of her neck

Times when people haven’t wanted to touch her skin, such as a cashier not wanting to take a $20 bill from her hands, during a flare-up

Although Gloria tried a number of treatments to help improve her psoriasis, many of these treatments didn’t give her the results she was looking for — as is often the case among psoriasis patients.

Fortunately, there’s hope. A new, innovative treatment in plaque psoriasis is getting high praise from people like Gloria, as well as the medical community. Following more than 25 years of minimal innovation in the topical psoriasis treatment space, the FDA recently approved a steroid-free, prescription cream for plaque psoriasis in adults — the first in its class in the U.S.

Linda Stein-Gold, MD, Director of Dermatology Clinical Research at Henry Ford Health System and Gloria as they discuss the significant impact plaque psoriasis may have on a person’s life and what this new treatment may mean for those who are suffering with plaque psoriasis as well.

Interview is courtesy: Dermavant Sciences

#plaquepsoriasis #psoriasis #advocate #chronicinflammatorydisease #patchesofskin #itchy #painful #disfiguring #gloria #physicalsymptoms #drlindastein-gold #health #clinical #dermavantsciences

The post The Truth About Living with Plaque Psoriasis And How to Become Your Own Advocate appeared first on Good News!.

PUZZLING SKIN CONDITION AFFECTS MORE THAN MEETS THE EYE
THE HIDDEN REALITY OF LIVING WITH A CHRONIC SKIN DISEASE

Hidradenitis suppurativa (HS) is an under-recognized and chronic inflammatory skin condition caused by an overactive immune system that can often go undiagnosed or misdiagnosed for years. The symptoms of HS include recurrent, painful abscesses and lesions and can have a significant physical, mental and social impact. HS can be progressive and increase in severity over time.

HS also presents itself in sensitive areas like the armpits, groin and under the breasts and buttocks, so it may be hidden by clothing – leaving many to suffer in silence. Further, the lack of awareness around this disease may lead to patients going undiagnosed or misdiagnosed for seven or more years. Patients may visit a number of doctors before finding a dermatologist with experience in managing HS to confirm diagnosis and determine a plan that best fits their specific needs.

Dr. Joslyn Kirby, a dermatologist with Penn State University, will bring greater understanding about HS by sharing how it’s more than just an inflammatory skin disease. Dr. Kirby will also discuss the importance for HS patients – along with their caregivers – to advocate for their care and seek out a dermatologist with experience treating HS who can help patients to receive an accurate diagnosis and appropriate treatment options.

Interview courtesy: AbbVie Inc.

#november #healthy #skin #month #condition #meets #eyes #eye #chronic #disease #hidradenitis #suppurativa #hs #inflammatory #overactive #immune #system #undiagnosed #misdiagnosed #symptoms #recurrent #painful #abscesses #lesions #physical #mental #social #impact #increase #dermatologist #penn #state #university #psu #caregivers #treatment

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