During the Pandemic various online webinars were given about the Psycho-Social Impacts of COVID-19 on Patients with Chronic Skin Conditions. Generally they showed that:

Patients with chronic skin conditions (auto-immune disease related) using HQC have no higher risk of getting Covid. When using immune suppressants, patients should be more careful. When infected with Covid, consult your doctor whether to go on with the prescribed medication. People with autoimmune diseases of the skin do not have a greater risk of getting infected with Covid-19. There is no proof that Covid will have a worse effect on patients with autoimmune diseases of the skin.

In general anxiety and mood related complaints are the most common complaints of patients with skin conditions during the pandemic. When getting Covid, stigmatization and feeling rejected are also present.

About 20-40% of Chronic Skin patients experience a psycho-social impact of Covid-19.

Two webinars can be found at:

https://youtu.be/3bvWIwDAIHE (Impacts of Covid-19 on Autoimmune Diseases & Immune Suppressed Patients)

https://youtu.be/5FJQWqpJ2fs (The Psycho-Social Impacts of COVID-19 on Patients with Chronic Skin Conditions)

 

By Annemarie Sluijmers[/vc_column_text][/vc_column][/vc_row]

Live Facebook Feed

Comments Box SVG iconsUsed for the like, share, comment, and reaction icons
4 days ago

♦️ Few days left to fill the Living With Lupus in 2024 survey!

✍🏻Doe mee aan de enquête.

🔊Deel met uw gemeenschap.

🙏 Help us and NVLE achieve more answers to ensure that the Dutch population is represented in the results

buff.ly/3xGBU6T
... See MoreSee Less

5 days ago

♦️ Few days left to fill the Living With Lupus in 2024 survey!

✍🏻Deltag i undersøgelsen.

🔊Del med dit fællesskab.

👨🏼⚕Hvis du er sundhedsprofessionel og behandler patienter med lupus i Europa, ville vi sætte stor pris på, at du informerer dine patienter.

🙏 Help us and Sle-Lupus- info achieve more answers to ensure that the Danish population is represented in the results

s.surveylegend.com/-NqmjTjyUXHGLMmAu5qS
... See MoreSee Less

6 days ago

♦️ Few days left to fill the Living With Lupus in 2024 survey!

✍🏻Dalyvaukite apklausoje.

🔊Dalinkitės savo bendruomenėje

👨🏼⚕Jeigu esate sveikatos priežiūros specialistas ir gydote vilklige sergančius pacientus Europoje, būtume labai dėkingi, jei informuotumėte savo pacientus.

🙏 Help us and Lupus Lt achieve more answers to ensure that the Lithuanian population is represented in the results

s.surveylegend.com/-NqwWcQ0UhyMxDtCBYRD
... See MoreSee Less

1 week ago

✍🏻Doe mee aan de enquête.

🔊Deel met uw gemeenschap.

👨🏼‍⚕Bent u een gezondheidsmedewerker en behandelt u lupuspatiënten in Europa, dan waarderen we het zeer als u uw patiënten deze informatie verstrekt.

s.surveylegend.com/-NqgyeOSaTVcd7gBoK15
... See MoreSee Less

✍🏻Doe mee aan de enquête.

🔊Deel met uw gemeenschap.

👨🏼‍⚕Bent u een gezondheidsmedewerker en behandelt u lupuspatiënten in Europa, dan waarderen we het zeer als u uw patiënten deze informatie verstrekt.

https://s.surveylegend.com/-NqgyeOSaTVcd7gBoK15

1 CommentComment on Facebook

💪💪💪

LUPUS EUROPE Uniting people with Lupus throughout Europe
Send