Health Boards
As you know I don't like advertising on here and this could be looked at as a publicity stunt*. But I think it's worth showing as the results, (if correct) don't make good reading.
Source: novartis.com
*I should point out, I'm not suggesting the results are fake. I'm just making a personal statement and not one of Psoriasis Club.
#1 A drug manufacturer sponsored survey could be biased.
#2 Online surveys don't always give a true result as people could tick wrong box's or they could be manipulated.
#3 I don't think drug manufacturers should run what looks like a social media site.
Quote:
Novartis presented new findings from the largest global survey to date of people with psoriasis, showing many do not achieve the treatment goal of clear skin or even believe it is a realistic goal. People with the disease also report that they face discrimination, humiliation, and mental illness, according to the research presented at the European Academy of Dermatology and Venereology (EADV) Congress.
While real-world evidence presented at EADV demonstrated that clear skin significantly improves quality of life, the survey found over half (57%) did not achieve clear or almost clear skin, and nearly a third of people (28%) had to wait five years before receiving treatment that resulted in clear or almost clear skin.
"Every patient deserves the opportunity to achieve clear skin, but this research tells us many are not given the chance," said Vasant Narasimhan, Global Head, Drug Development and Chief Medical Officer, Novartis. "Novartis supports the World Health Organization's resolution to make psoriasis a global health priority and help patients overcome the heartbreaking physical, societal and psychological challenges the condition presents."
Over 8,300 people from 31 countries took part in the survey, which aimed to improve the understanding of patients' perspectives on clear skin and, importantly, the impact of not achieving it. This major research initiative represents the largest ever partnership between Novartis and patient organizations, including 25 groups from around the world.
The survey findings reinforce the need for greater education and engagement of healthcare professionals and patients about the achievability of clear or almost clear skin as a treatment goal. In addition, they demonstrate the detrimental impact psoriasis has on patients' lives. The majority of people surveyed (84%) were suffering discrimination and humiliation, while almost half (43%) of patients felt psoriasis had affected their relationships and made it difficult to form intimate relationships.
A third of people (38%) surveyed also reported that they have been diagnosed with a psychological condition due to psoriasis, with one in four diagnosed with anxiety (24%) or depression (25%). Patients with anxiety or depression were also found to suffer more severe disease and worse quality of life in other research presented at EADV, further emphasizing the link between the psychological and physical aspects of the disease.
Source: novartis.com
*I should point out, I'm not suggesting the results are fake. I'm just making a personal statement and not one of Psoriasis Club.
#1 A drug manufacturer sponsored survey could be biased.
#2 Online surveys don't always give a true result as people could tick wrong box's or they could be manipulated.
#3 I don't think drug manufacturers should run what looks like a social media site.