Heart disease remains on the rise in the United States. Most people are aware of common risk factors like high blood pressure and bad cholesterol, but there’s one lesser-known, inherited heart disease risk factor that affects millions and is passed down through families. It’s called lipoprotein(a), (lip-o-pro-teen-a) or Lp(a), (L-P-little A) and experts say having a high level can independently increase the risk of having a heart event such as a heart attack or stroke.

Joining us now is Dr. Icilma (EYE-SIL-MA) Fergus, (Fur-GUS) Professor of Medicine, Director of Cardiovascular Disparities and Clinical Lipidology at Mount Sinai Fuster Heart Hospital, and Lynn, who is living with high L-p(a), to talk about this hidden heart risk and what you should know.

GUEST BIO

Icilma V. Fergus, MD, FACC, FASPC
Professor of Medicine
Director of Cardiovascular Disparities and Clinical Lipidology
Mount Sinai Fuster Heart Hospital at Mount Sinai.
Dr. Fergus is a board-certified professional in Internal Medicine and Cardiology, currently serving as the Director of Clinical Lipidology and Cardiovascular Disparities for the Fuster Heart Hospital at Mount Sinai. Her expertise lies in Preventative Cardiology, specifically focusing on Lipids and Hypertension, Women’s Heart Disease, and Cardiovascular Health Advocacy. She is Professor of Icahn School of Medicine at Mount Sinai.
With an active engagement in professional organizations, Dr. Fergus holds significant roles such as the past President of the Westchester board of the American College of Cardiology and past president of the Association of Black Cardiologists. She is also a past President of the Jack and Jill of America Foundation.
Beyond her professional commitments, Dr. Fergus passionately advocates for health equity and cardiac disease prevention. Her impactful contributions have been recognized through numerous awards, including the Luminary Award from the American Heart Association, the Community Service Award from the Heart Valve Society of America, Young Black & Gifted, and Community award from Delta Sigma Theta in 2023. In addition, she has been featured on numerous publications and broadcasts, including “Here and Now” with Sandra Bookman on ABC

#HeartDisease #LPa #HeartAttack #Stroke #DrIcilmaFergus

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HOWEVER, DESPITE THE POTENTIAL BENEFITS, SOME PATIENTS STILL FEEL EMBARRASSED BY THEIR SKIN. MANY WILL CHOOSE TO COVER UP WITH MORE CLOTHING OR AVOID SOCIAL SITUATIONS ALTOGETHER.

BUT EVERYONE DESERVES TO HAVE FUN IN THE SUN. JOINING US NOW IS HEALTH CARE PROVIDER, MELINDA GREENFIELD, WITH HOW MODERATE-TO-SEVERE PLAQUE PSORIASIS PATIENTS CAN MAKE THE MOST OF WARM WEATHER.

BIO-Dr. Melinda Greenfield Bio

Dr. Melinda Greenfield is a Board Certified Dermatologist in private practice since 1999. She has offices in Ponte Vedra Beach, FL and Albany, GA and has an online Telehealth practice in nine states.

Dr. Greenfield attended The University of Maryland for her undergraduate degree and Nova Southeastern University for Medical School. She completed her internship at Sinai Hospital of Baltimore and her Dermatology residency at St. Barnabas Hospital in the Bronx, NY.

Dr. Greenfield is past president of the Dougherty County Medical Society, the Georgia Osteopathic Medical society and previously served on the Editorial Board of the Journal of the American Osteopathic College of Dermatology.

Dr. Greenfield is a clinical assistant professor at The Georgia Campus of the Philadelphia College of Osteopathic Medicine, The Medical College of Georgia, PCOM South Georgia and The Orlando College of Osteopathic Medicine. She teaches the second-year dermatology curriculum to medical students and has students and residents rotate in her office throughout the year.

Dr. Greenfield has lectured at multiple meetings throughout the years and has authored four publications. She participated in an episode of The Balancing Act on Lifetime TV that highlighted psoriasis and is on the Speaker Board for several pharmaceutical companies.

In her free time, Dr. Greenfield enjoys bike riding, working out in the gym, gardening, cooking and spending time with her family.

IMPORTANT SAFETY INFORMATION

What is the most important information I should know about ILUMYA^® (tildrakizumab-asmn)?

Do not use ILUMYA if you have had a severe allergic reaction to ILUMYA or any of its ingredients.

Get emergency medical help right away if you get any of the following symptoms of a serious allergic reaction:

• feel faint
• trouble breathing or throat tightness
• swelling of your face, eyelids, lips, mouth, tongue or throat
• chest tightness
• skin rash

What is ILUMYA?

ILUMYA is a prescription medicine used to treat adults with moderate to severe plaque psoriasis who may benefit from taking injections, pills (systemic therapy), or phototherapy (treatment using ultraviolet or UV light).

IMPORTANT SAFETY INFORMATION (continued)

ILUMYA is a medicine that may lower the ability of your immune system to fight infections and may increase your risk of infections. Your healthcare provider should check you for infections and tuberculosis (TB) before starting treatment with ILUMYA and may treat you for TB before you begin treatment with ILUMYA if you have a history of TB or have active TB. Your healthcare provider should watch you closely for signs and symptoms of TB during and after treatment with ILUMYA.

Tell your healthcare provider right away if you have an infection or have symptoms of an infection, including:

• fever, sweats, or chills
• muscle aches
• weight loss
• cough
• warm, red, or painful skin or sores on your body different from your psoriasis
• diarrhea or stomach pain
• shortness of breath
• burning when you urinate or urinating more often than normal
• blood in your phlegm (mucus)

Before receiving ILUMYA, tell your healthcare provider about all of your medical conditions, including if you:

• have any of the conditions or symptoms listed in the section “What is the most important information I should know about ILUMYA?”
• have an infection that does not go away or that keeps coming back
• have TB or have been in close contact with someone with TB
• recently received or are scheduled to receive a vaccine (immunization). You should avoid receiving live vaccines during treatment with ILUMYA.
• are pregnant or plan to become pregnant. It is not known if ILUMYA can harm your unborn baby.
• are breastfeeding or plan to breastfeed. It is not known if ILUMYA passes into your breast milk.

Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.

It is not known if ILUMYA is safe and effective in children under 18 years of age.

What are the possible side effects of ILUMYA?

ILUMYA may cause serious side effects. See “What is the most important information I should know about ILUMYA?”

The most common side effects of ILUMYA include: upper respiratory infections, injection site reactions and diarrhea. These are not all of the possible side effects of ILUMYA. Call your doctor for medical advice about side effects.

You are encouraged to report any negative side effects of ILUMYA to FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088. You are also encouraged to report side effects or ADEs (adverse drug events) to our Drug Safety Department at 1-800-406-7984 or drug.safetyUSA@sunpharma.com (preferred) with as much information as available.

Please read the full Prescribing Information and Medication Guide for ILUMYA and discuss any questions with your doctor.

#warmerweather #psoriasis #tips #skin #plaque #symptoms #sunlight #embarrassed #drmelindagreenfield #patients #healthcare #medical #sinaihospital #ilumya #tildrakizumab-asmn

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Celebrated every November, National Family Caregivers Month is a time to recognize and honor caregivers across the US. In a study by the National Alliance for Caregiving, about 50% of 111 cancer caregivers reported feeling “highly stressed” due to the intense and demanding nature of caregiving, and there is growing evidence this could potentially affect the mental health of the patients as well.1,2

In particular, the mental health of patients with blood cancer, including those living with chronic lymphocytic leukemia (CLL) and their caregivers, can be impacted due to the physical, emotional and social effects of the disease.3,4

CLL is the most common leukemia in adults.5 It’s a type of cancer that starts in cells that become certain white blood cells (called lymphocytes) in the bone marrow. 5 The cancer (leukemia) cells start in the bone marrow but then go into the blood.5

As with other illnesses, COVID-19 has exacerbated the mental health impact of blood cancer on patients, as well as placing an added strain on caregivers. In a recent survey of 100 patients with blood cancer, 96% of patients reported their blood cancer has impacted their mental health since the start of the pandemic in 2020, and 72% of patients said they rely most on their family members to provide them with emotional support for their blood cancer.

Hematologist and oncologist Dr. Ken Miller of Sinai Hospital in Baltimore, Maryland, who will discuss the impact of blood cancer, including CLL, on the mental and emotional health of both patients and caregivers, and share resources to help meet this important need.

http://understandbloodcancer.com/

This program is made possible by AstraZeneca.

Dr. Ken Miller is a hematologist and medical oncologist at the Sinai Hospital in Baltimore, Maryland. Dr. Miller has served as the Director of Outpatient Oncology and was a member of the Thoracic Oncology Group at the University of Maryland. He also previously served as the Director of the Yale Cancer Center’s survivorship clinic and the Director of the LiveStrong Survivorship Center of Excellence at the Dana-Farber Cancer Institute. He has authored five books, including: Choices in Breast Cancer, Medical and Psychosocial Care of the Cancer Survivor, Excellent Care of Cancer Survivors, Global Cancer Care, and “The Breast Cancer Book”. Dr. Miller’s wife Joan is a two-time cancer survivor and together they have lectured nationally and internationally on the role of empathy in medicine. They have three children and four grandchildren.

#nationalcaregiversmonth #nationalfamilycaregiversmonth #nationalfamilycaregivers #nationalcaregivers #cancer #lendingsupport #patients #emotionaltoll #bloodcancer #health #physical #social #mental #leukemia #understandbloodcancer #kenmiller #drkenmiller #hematologist #oncologist #sinaihospital

The post November is National Family Caregivers Month, LENDING SUPPORT TO CANCER CAREGIVERS DURING NATIONAL FAMILY CAREGIVERS MONTH AND BEYOND appeared first on Good News!.

Find Out More About this Condition. Capsian Patch, … can be considered. a specific approved product is Qutinza
More than 34 million Americans – just over 1 in 10 – have diabetes1, and neuropathic pain associated with diabetic peripheral neuropathy of the feet, or more commonly referred to as diabetic nerve pain, is one of its most common complications.2
The painful symptoms associated with this nerve damage include numbness, tingling, as well as shooting or stabbing sensations that most often affect the lower extremities.3
Itis a progressive and debilitating complication of diabetes that will affect approximately more than 5 million Americans in 20204 and is expected to double by 2030.5
Joining us now to discuss neuropathic pain associated with diabetic peripheral neuropathy – or diabetic nerve pain – and this newly approved treatment option is Dr. David Simpson, Professor of Neurology at the Icahn School of Medicine at Mount Sinai in New York City.
Key Facts and Figures:
• The lack of effective, innovative treatment options has left many patients with a significant unmet medical need.
• The condition is more common in patients with type 2 diabetes and increases with age and duration of disease.
When you book a window, we’ll provide you with guest bio & suggested questions. The interview is courtesy of Averitas Pharma, Inc.
References:
1. CDC Division of Diabetes Translation, National Diabetes Statistics Report, 2020. https://www.cdc.gov/diabetes/library/features/diabetes-stat-report.html#:~:text=New%20in%202020%2C%20the%20report,1%20in%203%E2%80%94have%20prediabetes. Accessed July 6, 2020
2. University of Chicago Center for Peripheral Neuropathy. Types of peripheral Neuropathy. http://peripheralneuropathycenter.uchicago.edu/learnaboutpn/typesofpn/diabetes/diabetes.shtml. Accessed July 6,2020
3. American Diabetes Association. Peripheral NeuorapthyOverview. https://www.diabetes.org/diabetes/complications/neuropathy/peripheral-neuropathy.Accessed July 17, 2020
4. LTP2020-2030: ADDRESSABLE POPULATIONS BY CONDITION (PDPN, PSNP, PHN, CINP).Company data on file. April 30, 2020.
5. Gore, M., Brandenburg, N. A., Dukes, E., Hoffman, D. L.,Tai, K.-S., & Stacey, B. (2005). Pain Severity in Diabetic Peripheral Neuropathy is Associated with patient Functioning, Symptom Levels of Anxiety and Depression, and Sleep. Journal of Pain and Symptom Management, 30(4),374-385. doi:10.1016/j.jpainsymman.2005.04.009.
https://www.cdc.gov/media/releases/2017/p0718-diabetes-report.html
6. CDC,Behavioral Risk Factor Surveillance System, 2018
7. America’sHealth Rankings. United Health Foundation.https://www.americashealthrankings.org/explore/annual/measure/Diabetes. Accessed July 13, 2020

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Living with ulcerative colitis (UC) can make working, maintaining relationships and juggling family responsibilities difficult. A global survey of 1,254 gastroenterologists and 2,100 adults with a self-reported history of UC revealed both men and women experienced the impact of UC on day-to day life, including emotional wellbeing.1

Now, with the added challenges of navigating the COVID-19 pandemic, focusing on emotional wellbeing is more important than ever.

Laurie Keefer, PhD, who is a psychologist with Mount Sinai Hospital’s IBD Center in New York City who specializes in the psychosocial care of patients with chronic digestive diseases, most notably Crohn’s and ulcerative colitis (UC). Allyson, who has a history of UC, to discuss the emotional impact of UC and share tips for those living with UC on how to have more effective conversations with their healthcare team. Both Dr. Keefer and Allyson have been compensated by Pfizer to appear in this interview today.

Before we start, it is important to note that results from the UC Narrative are not representative of all UC patients, and only reflect responses of those who took the survey. For more information about the survey limitations and methodology, visit talkinguc.com.

BIO: Dr Laurie Keefer is an academic health psychologist and the Director for Psychobehavioral Research within the Division of Gastroenterology. She specializes in the psychosocial care of patients with chronic digestive diseases, specifically inflammatory bowel diseases such as Crohn’s or ulcerative colitis. Dr. Keefer came to Mount Sinai in January 2016 from Chicago, IL to lead a subspecialty medical home for inflammatory bowel diseases (IBD).

The Mount Sinai IBD medical home, known as GRITT-IBD(TM) focuses on gaining resilience through transitions as they occur across the lifespan of patients living with Crohn’s disease and ulcerative colitis. Dr Keefer’s clinical and research interests are in the area of IBD disease self-management, gut-directed hypnotherapy, resilience, the psychosocial care needs of emerging adults with chronic disease and cognitive-behavior therapy. She is a sought after speaker and mentor. She chairs the Division of Psychogastroenterology within the Rome Foundation and is on the Council of the American Neurogastroenterology and Motility Society.

BIO

My name is Allyson and I was diagnosed with Ulcerative Colitis (UC) in 2007 at the age of 29. In hindsight I am certain I had symptoms that went undiagnosed for years, if not back to childhood. My diagnosis and progression of my UC was quite rapid and debilitating, resulting in being bed ridden and hospitalized within less than a month. After 3 years of hospitalizations and a very poor quality of life, I made an emergent decision to have a 3-stage total colectomy. This process had profound impacts of my physical and emotional wellbeing, as well as self-image due to body changes, and I feel strongly about advocating for patients with UC. I feel I often went without a voice until I was able to learn to speak up for myself as I learned more about my UC. As there is no cure, I continue to manage my daily life in often challenging, or what would appear impossible situations to those without UC. I am resilient and strong in a way that I only learned through my UC journey. I live a fulfilling life that may require adjustments, and I am grateful for the opportunities to advocate.

Interview courtesy: Pfizer

#ulcerative #colitis #uc #maintaining #work #relationships #juggling #family #laurie #keefer #allyson #sinai #hospital #new #york #city #nyc #chronic #digestive #diseases #disease #pfizer #covid #19 #covid-19 #covid19 #wellbeing #well #being #coronavirus #pfizer

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Damone, whose smooth baritone led Frank Sinatra to famously declare he “had the best pipes in the business,” died at Mount Sinai Medical Center in Miami Beach, Fla., surrounded by several close relatives.

Damone also received a call from his friend, President Donald Trump, at the hospital in the days before he died, his family said.

Damone starred in several television series, including “The Vic Damone Show” on NBC, and hit movies including “Kismet” and “Rich, Young and Pretty,” but the singer did not consider himself a true crossover star.

“I never thought of myself that way,” Damone wrote in his memoir. “That wasn’t my particular gift. My gift was singing.”

Best known for hits “You’re Breaking My Heart” and “On the Street Where You Live,” with over 2,500 recordings under his belt, Damone was part of the golden age of lounge singers who came to fame after World War II, including Sinatra, Tony Bennett, Dean Martin and Perry Como.

Damone’s first big break came at the age of 14, with Como’s help. Damone was forced to drop out of high school and take a job as an usher at the Paramount Theater in New York City, where he bumped into Como in an elevator. Damone stopped the elevator between floors and started singing.

He asked Como on whether he should continue voice lessons and Como said simply, “Keep singing!”

Fate intervened for Damone again in the summer of 1946, when Sinatra was playing poker at a friend’s Manhattan apartment, and one of Sinatra’s classics, “Night and Day,” came on the radio. Sinatra was astounded when the singer turned out to be Damone, live in the studio. Sinatra phoned the radio station and told Damone: “This is Frank Sinatra, and I want you to stop singing my songs.”

Damone thought he was being pranked and barked back, “Yeah, if you’re Frank Sinatra, then I’m the Pope.”

Months later, Sinatra ended up introducing Damone at a charity fundraiser in Madison Square Garden.

“I’d like to introduce to you Vic Damone,” Sinatra said. “This kid’s a really great singer. He’s got stardust on his shoulders.”

Damone was born Vito Farinola on June 12, 1928, in the Bensonhurst section of Brooklyn to Italian immigrant parents, Rocco and Mamie (Damone) Farinola.

Damone is survived by six grandchildren and two sisters, Elaine Seneca and Terry Sicuso. Two other sisters died before Damone: Sandy Boucher and Pia Romeo.

Damone is also survived by three son-in-laws, William Karant, Michael Woodard, and Joel Brown.

A son named after Perry Como, Perry Farinola Damone, died in 2014.

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For the video featuring Mount Sinai Health System patient testimonials, click here.  

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VPT offers public performances for New Yorkers as well as private shows for under served populations, and they partner with a broad range of local, national and international organizations. Previous clients include New York University, The New School, Mt. Sinai Hospital, and Sing Sing Correctional Facility. Past seasons have included performances for New Yorkers affected by Hurricane Sandy and 9/11, members of the Afghanistan Human Rights and Democracy Organization, and individuals struggling with mental illness and addiction.

The Annual Spring Gala Fundraiser celebrates the end of VPT’s 10th season with food, cocktails, an auction, and an interactive performance from company members. Friends of the company and curious newcomers will have the chance to mix and mingle with artists and experience live theater in a fun and immersive setting.

We have a lot to celebrate but need help with funding. This season we’ve provided performances for audiences struggling with mental illness, addiction and homelessness–people who don’t often have access to the arts.

Additionally, this year marks the launch of VPT’s Open Rehearsals, a popular series of interactive training workshops for actors and non-actors.

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