No one should have to stop their treatment due to cost—but for many with psoriatic disease, this is the harsh reality. The time to act is now. The psoriatic disease community needs better care and resources today. Your gift can make an immediate difference, breaking down barriers and ensuring that millions can treat their disease without delay. on #InternationalDayofCharity give the gift of hope: https://ow.ly/ZRui50T3nZz
National Psoriasis Foundation’s Post
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The preparation of a UVB home phototherapy device represents a prudent approach to mitigating treatment costs for individuals affected by psoriasis. #psoriasis #Skincurex #UVBtherapy
No one should have to stop their treatment due to cost—but for many with psoriatic disease, this is the harsh reality. The time to act is now. The psoriatic disease community needs better care and resources today. Your gift can make an immediate difference, breaking down barriers and ensuring that millions can treat their disease without delay. on #InternationalDayofCharity give the gift of hope: https://ow.ly/ZRui50T3nZz
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Never lose hope! You're not crazy—it's not in your head. After 27 years of undiagnosed Lyme, I became a practitioner who can help you find answers and healing. Don't give up; the solution may be just around the corner.
🌿 How do you talk to yourself? Sometimes, the fight is invisible. May is Lyme Disease Awareness Month, and it's time to shed light on the silent struggles many face every day. Those affected by Lyme disease might not show it outwardly, but are fighting hard internally. 🍃 Go to my website. The link is in my bio to learn more💚 #LymeDiseaseAwareness #InvisibleIllness #FightLyme #LymeWarrior #TickTalk #HealthAwareness #SpreadAwareness #LymeSupport #TickPrevention #thelymeboss #thereishope #youarenotalone
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May is ALS Awareness Month! 🎗️ It's a time when we strive to shed light on this rare yet devastating disease, known as Lou Gehrig's disease. Let's use this time to raise awareness, advocate for research 🧪and support those living with ALS. 🤝#FightALS #CureALS #ALSAwarenessMonth #VisitingAngels
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It’s #NationalKidneyMonth and we are doing our best to help our #OPO and #Transplant partners to utilize as many precious gifts of life as possible. #Organ procurement organizations have worked with record numbers of families to offer them an opportunity to make meaning from tragedy. In that process more transplants were done last year than ever before. Still, it is no secret that while OPOs have offered the opportunity to #donate more successfully than ever, there has been a corresponding trend in increased kidney discards/non-utilization. At #BuckeyeTransplantServices we are coming up with #innovative and #data driven #solutions for our partners. As proud members of the #OPTN we are working toward a better tomorrow where everyone who needs a transplant gets one. The best tomorrow starts today and today on the first day of national kidney month we promise to do our best day in and day out to be the change we seek! Come see what we are all about at www.buckeyetransplant.com and be part of a team/family that is making a difference! #BuckeyeTransplant #Buckeye #BTS #DonateLife
March is #NationalKidneyMonth where we shine a light on the 37 million Americans affected by kidney disease, all of whom should have access to high-quality, patient-centered kidney care. Visit KidneyEquityforAll.org to learn more about our mission. #KIDNEYEQUITYFORALL
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Today is World Scleroderma Day which highlights the need to increase awareness of scleroderma and to advocate for those affected by this life-threatening disease. It's a day to recognize the bravery of those who live with scleroderma, and to demand equal treatment and equal care. Learn more here: https://hubs.li/Q02D2Jt20
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As medical students, we are taught to keep a "rare disease" diagnosis at the bottom of the list of differentials. During my professional journey as a Clinical Geneticist, I have realised that the adjective "Rare" restricts due attention from healthcare providers, researchers, and policymakers. Awareness, support, and sensitivity on these fronts will definitely bring hope in the lives of millions of individuals affected with #raredisease worldwide. Bringing comprehensive care for #raredisease under one roof @ Yashoda Hospital & Research Centre, Nehru Nagar, Ghaziabad, Genestring Lab, Seeds of Innocens IVF & Fertility Centres #rarediseaseawareness #rarediseaseday2024
On this Rare Disease Day, we are raising awareness among the people and committed to provide quality care to our patients and help the families to navigate the disease complexities and problems. #rarediseaseday2024
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Never lose hope! You're not crazy—it's not in your head. After 27 years of undiagnosed Lyme, I became a practitioner who can help you find answers and healing. Don't give up; the solution may be just around the corner.
🌿 This May, as we observe Lyme Disease Awareness Month, let's spread the word that not all battles are visible. While we may look just like anyone else on the outside, the fight against Lyme disease is a daily reality for many. 💚 🔍 Lyme disease can be silent but debilitating, affecting countless lives around the world. Yet, with support and awareness, there is hope. ✨ Don't lose heart. If you or someone you know is struggling, you're not alone. Visit the link in bio to learn more and join us in spreading awareness and understanding. Together, we can make a difference. 💪 #LymeDiseaseAwareness #InvisibleIllness #FightLyme #thelymeboss
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What does 50 years of impact look like for those affected by Crohn’s disease and ulcerative colitis? It’s Crohn’s and Colitis Canada’s 50th anniversary! Learn more about the difference we’ve made – together: bit.ly/50yearsimpact
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The countdown to #RareDiseaseDay is on, but for those living with a #RareDisease, every day is Rare Disease Day. To learn more about how you can support the rare disease community, visit RareDiseaseDay.com.
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Did you know more than 11 million Americans have #HeartValveDisease (HVD)? Today is #ValveDiseaseDay, and we invite you to join us in spreading awareness of symptoms, prevention and support for those battling #HeartDisease. Learn more about HVD and how you can inform your patients of this potentially disabling and deadly disease here: https://lnkd.in/f3fYg4F
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18mHello, my name is Hamida and I can help you to treat psoriasis patients definitively. My medicinal solution consists of 5 types of plants.🙏🏼🩷