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#food #travel #sports #news #may #monday

May 5th was World Pulmonary Hypertension Day. Get the facts and be aware of how PAH may present. Pulmonary Hypertension occurs in up to 40% of scleroderma patients. Discuss any new symptoms with your physician. #raredisease #pah #scleroderma #findacure #AwarenessMatters #sclerodermaDMV #sclerowarrior #WorldPHDay2024 #WeBreatheUnited #WPHD #pulmonaryhypertension #UnitedToCurePH #UnitedForDiagnosis #awareness #patientcare #patientempowerment #UnitedForCure #PHAEurope Pulmonary Hypertension Association Europe

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5/6/2024, 2:12:10 PM

The Full Time Job of Symptom Management: https://blog.raynaudsscleroderma.co.uk/2017/04/scleroderma-raynauds-rare-disease-full.html Read about scleroderma research Royal Free London NHS Foundation Trust: https://royalfreecharity.org/focus/scleroderma/ https://royalfreecharity.org/news/story/grants-awarded-to-improve-patient-experience/ https://www.royalfree.nhs.uk/services/scleroderma This year, 2024, I will have spent over half of my life, 27 years, living with a scleroderma (systemic sclerosis) and Raynaud's diagnosis, and all that entails. 🤢 Read more: https://royalfreecharity.org/news/fundraising/nicolas-story/ Eternally grateful to Dame Professor Carol Black and Professor Chris Denton Royal Free London NHS Foundation Trust 😇 Please donate to medical research to identify a cure and the cause of scleroderma, at the Scleroderma Unit Royal Free Hospital. Every penny will be used for research purposes. There are several ways as to how you can donate: Via the Royal Free Charity: Donation Page : https://royalfreecharity.org/donate Scroll down to tick box 'your donation will be used where the need is greatest. However please tick this box if you would like to donate to a specific appeal or fund'. Click on the box to reveal 'a where would you like to give to' drop down menu. Scroll down to the Scleroderma and Raynaud's research option and click on this option. Leave a gift in your Will : https://royalfreecharity.org/giftsinwills/ The Royal Free Charity provides a free Will writing service ☝️ Just Giving Page : https://www.justgiving.com/fundraising/sclerodermaunit-royalfree Thank You 🙏 #SclerodermaFreeWorld #RaynaudsFreeWorld #Research #Scleroderma #SystemicSclerosis #Raynauds #Autoimmune #RareDisease #NoCure #UnknownCause #LifeChanging #ConnectiveTissue #DreamSnatcher #Disability #ThickSkin

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5/6/2024, 12:47:06 PM

so so so so grateful for these hands who can still create ❤️‍🩹 #scleroderma #sclerodactyly #sclerococoon

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5/6/2024, 8:38:12 AM

so so so so grateful for these hands who can still create ❤️‍🩹 #scleroderma #sclerodactyly #sclerococoon

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5/6/2024, 8:38:05 AM

IMPORTANT NEWS!!! Scleroderma Australia (@scleroderma_australia) is happy to announce that the Pathways Telehealth Nursing Service is continuing for those living with scleroderma across Australia! The Pathways Telehealth Nursing Service is an Australian innovation that places a trained registered nurse within a patient organisation, to provide specialist care and aid in health system navigation for communities with rare, genetic, and complex conditions! The program was developed by an Australian nurse, Kate Holliday who is a researcher, Chief Executive, and founder of the Centre for Community-Driven Research. The concept for the program comes from leveraging the relationship patient groups have with the community. If they have patients coming to them, it's important to make sure there is a registered nurse there with expertise in their condition to help them navigate the health system! This is a model of care that provides a patient with a holistic care plan and makes the best use of all that is available to them in the Australian health system. It’s a service that anyone can access, regardless of where they live. But it’s also a model that ensures nurses are supported in their role and have guidance in their scope of practice. As part of the training process for the Pathways nurse assigned to Scleroderma Australia, we are asking patients to volunteer to be interviewed and complete an online questionnaire. This will help the Pathways nurse learn more about the unique needs of the community and also be used in the future as part of a report on the experience of people with rare conditions. To register to volunteer for the interview and online questionnaire, see the link in bio. Please note that this Nurse is for Health System Pathways only. . . . . #Scleroderma #SclerodermaAwareness #TelehealthNurse #PathwaysTelehealth #DigitalHealthcare #SclerodermaSupport #Autoimmune #CCDR #AutoimmuneDiseases #SystemicSclerosis #Education #SclerodermaNurse #SclerodermaSurvivors #StandUpToScleroderma #SclerodermaWarrior #SclerodermaFoundation #SclerodermaResearch #SclerodermaStrong #SclerodermaCommunity #SupportUs #NonProfit #HealthSpecialist #Australia

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5/6/2024, 2:23:37 AM

May 5th is World Pulmonary Hypertension Day! World Pulmonary Hypertension Day sheds light on pulmonary hypertension (PH), aiming to increase awareness of this often underdiagnosed and misunderstood condition, while also honouring the lives of those impacted by it. World PH Day serves as a platform to emphasise the importance of enhancing the quality of life and extending the life expectancy of the more than 25 million people worldwide affected by PH. Did you know that individuals with scleroderma have a higher risk of developing several types of pulmonary hypertension? . . . . #StillPHighting #WorldPHDay2024 #WorldPHDay #Scleroderma #SclerodermaAwareness #WorldPHDay2024 #WeBreatheUnited #WPHD #PAH #PulmonaryHypertension #UnitedToCurePH #UnitedForDiagnosis #Awareness #PatientCare #PatientEmpowerment #UnitedForCure

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5/6/2024, 1:07:24 AM

INCREDIBLY GRATEFUL for another year around the sun ☀️ I appreciate you all that have chosen to walk this beautifully broken journey we call life with me. My heart is overflowing with joy from all the support, guidance, friendships, laughter and genuine love. Love to all the beautiful people in my life. I can’t believe I’m still here fighting and kicking all kinds of booty!! AMEN👊🏽🌼❤️ #anotheryearoflife #grateful #thankful #livealifeyoulove #scleroderma #beautiful #bestrong #love #spoonielife #beautifuldestinations #hope #joy #chooseyourself #chronicillnesswarrior

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5/5/2024, 11:06:40 PM

Huge thanks to everyone who came out and supported. What a fun night raising money for a great charity! @sclerodermacan #scleroderma

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5/5/2024, 9:11:46 PM

On this Red Dress Day, we remember the Indigenous women, girls, and Two-Spirit people who have gone missing or been murdered in Canada and around the world. Let's honor their memories, and let's stand in solidarity with their families and communities. It's time to take action to address the systemic issues that have led to this tragedy, and to create a world where every person is valued and protected. Rest in power 🙏🏽🌹 #RedDressDay #MMIWG2S #Solidarity #Justice #Remember #hardwordharderdisease #autoimmune #chronicillness #chronicdisease #sclerodermawarrior #scleroderma

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5/5/2024, 7:30:18 PM

Cold brew Organic Marshmallow Root tea for the esophagus and stomach. I’m hoping it will help with acid reflux, I’d really like to to get off one of my one of my medication. #notyourcupoftea #scleroderma #sclerodermasucks #sclerodermawarrior #acidreflux #healingjourney #tea #coldbrew

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5/5/2024, 6:11:25 PM

World Pulmonary Hypertension Day raises awareness of pulmonary hypertension (PH) and celebrates the strength and resilience of the PH community worldwide. Did you know that people who live with scleroderma are at increased risk for developing several types of pulmonary hypertension? @PHACanada #WorldPHDay #Scleroderma #Sclerodermaawareness

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5/5/2024, 5:16:20 PM

May 5th is World Pulmonary Hypertension Day. Pulmonary Arterial Hypertension can be idiopathic, heritable, developed in association with congenital heart disease or liver disease, induced by drug or toxins such as certain diet pills or methamphetamines, or related to connective tissue diseases such as lupus or scleroderma. Pulmonary hypertension means high blood pressure in the lungs. According to the University of Michigan, "Patients with limited scleroderma have the risk of developing progressive blood vessel narrowing in the lungs frequently in the absence of lung scarring and inflammation. This complication is called pulmonary arterial hypertension. This is an extremely important issue in scleroderma occurring in up to 40% of patients." Pulmonary Hypertension Association #raredisease #pah #scleroderma #findacure #AwarenessMatters #sclerodermaDMV #sclerowarrior #WorldPHDay2024 #WeBreatheUnited #WPHD #pulmonaryhypertension #UnitedToCurePH #UnitedForDiagnosis #awareness #patientcare #patientempowerment #UnitedForCure #PHAEurope

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5/5/2024, 3:46:09 PM

Letters to My Younger Self: Wisdom for Navigating Chronic Illness Living with a chronic illness like fibromyalgia can often feel like navigating uncharted waters. Each day brings its own challenges and learning curves. In this series, "Letters to My Younger Self," we explore heartfelt advice that I wish I could have given to my younger self at the beginning of this journey. From embracing gentle exercise and nourishing meals to understanding the importance of rest and letting go, these letters are a guide to managing your condition with grace and self-compassion. Whether it's finding the strength to take time for yourself or the courage to embark on a holiday, each letter is a reminder that you are not alone, and every step forward is a step toward reclaiming your life ✉️ 💖 🌟

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5/5/2024, 2:09:34 PM

Today is #WorldPHDay. #PulmonaryArterialHypertension #PAH is recognised as high blood pressure in the lungs and can result in right heart failure. Read about scleroderma research Royal Free London NHS Foundation Trust: https://royalfreecharity.org/focus/scleroderma/ https://royalfreecharity.org/news/story/grants-awarded-to-improve-patient-experience/ https://www.royalfree.nhs.uk/services/scleroderma This year, 2024, I will have spent over half of my life, 27 years, living with a scleroderma (systemic sclerosis) and Raynaud's diagnosis, and all that entails. 🤢 Read more: https://royalfreecharity.org/news/fundraising/nicolas-story/ Eternally grateful to Dame Professor Carol Black and Professor Chris Denton Royal Free London NHS Foundation Trust 😇 Please donate to medical research to identify a cure and the cause of scleroderma, at the Scleroderma Unit Royal Free Hospital. Every penny will be used for research purposes. There are several ways as to how you can donate: Via the Royal Free Charity: Donation Page : https://royalfreecharity.org/donate Scroll down to tick box 'your donation will be used where the need is greatest. However please tick this box if you would like to donate to a specific appeal or fund'. Click on the box to reveal 'a where would you like to give to' drop down menu. Scroll down to the Scleroderma and Raynaud's research option and click on this option. Leave a gift in your Will : https://royalfreecharity.org/giftsinwills/ The Royal Free Charity provides a free Will writing service ☝️ Just Giving Page : https://www.justgiving.com/fundraising/sclerodermaunit-royalfree Thank You 🙏 #SclerodermaFreeWorld #RaynaudsFreeWorld #Research #Scleroderma #SystemicSclerosis #Raynauds #Autoimmune #RareDisease #NoCure #UnknownCause #LifeChanging #ConnectiveTissue #DreamSnatcher #Disability #ThickSkin

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5/5/2024, 11:55:10 AM

We’re still here!!🤘 DMM joining a fantastic line up of musicians for a special cause at The Arena! We go on at 8:00pm and play your favorite rock/hard rock covers🎸 Come support local live music and have some fun for a great cause! Food, music, and a good time🥳 #livemusic #rock #hardrock #localartists #805 #bands #scleroderma #sunday #localband #music

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5/5/2024, 4:45:38 AM

“Let’s keep a little optimism here.” - Han Solo, Return of the Jedi #scleroderma #hardwordharderdisease #maythefourthbewithyou #maythefourth #starwars #autoimmune

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5/4/2024, 5:20:18 PM

In preparation for May 5th World Pulmonary Hypertension Day, we are sharing some information to help people live better with scleroderma and PAH. Pulmonary Hypertension occurs in up to 40% of scleroderma patients. #raredisease #pah #scleroderma #findacure #AwarenessMatters #sclerodermaDMV #sclerowarrior #WorldPHDay2024 #WeBreatheUnited #WPHD #pulmonaryhypertension #UnitedToCurePH #UnitedForDiagnosis #awareness #patientcare #patientempowerment #UnitedForCure #PHAEurope Pulmonary Hypertension Association Pulmonary Hypertension Association Europe

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5/4/2024, 4:10:08 PM

Get ready for Scleroderma Awareness Month in June! We are excited to see your post on what you’re doing to raise awareness! The New England Chapter has some exciting ideas to share 🤗 #sclerodermaawareness #scleroderma #nationalsclerodermafoundation

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5/4/2024, 2:11:05 PM

I went to my chiropractor saying “my foot hurt”. She looked at my swollen knee saying “yup! That’s the reason”. I wish that more healthcare providers look into the cause of the problem instead of treating the problem. Pain in foot comes from a slightly twisted knee that causes the foot to stand/walk incorrectly. This is only a small example. It is the same with a lot of things, in some symptoms in scleroderma too. Look a the bigger picture. Find your solution. #scleroderma #chronicillness #sclerowarrior #pain #jointproblems

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5/4/2024, 2:03:08 PM

2 weeks to go, Annual Scleroderma Unit Family Day: https://blog.raynaudsscleroderma.co.uk/2024/04/scleroderma-unit-royal-free-hospital.html Read about scleroderma research Royal Free London NHS Foundation Trust: https://royalfreecharity.org/focus/scleroderma/ https://royalfreecharity.org/news/story/grants-awarded-to-improve-patient-experience/ https://www.royalfree.nhs.uk/services/scleroderma This year, 2024, I will have spent over half of my life, 27 years, living with a scleroderma (systemic sclerosis) and Raynaud's diagnosis, and all that entails. 🤢 Read more: https://royalfreecharity.org/news/fundraising/nicolas-story/ Eternally grateful to Dame Professor Carol Black and Professor Chris Denton Royal Free London NHS Foundation Trust 😇 Please donate to medical research to identify a cure and the cause of scleroderma, at the Scleroderma Unit Royal Free Hospital. Every penny will be used for research purposes. There are several ways as to how you can donate: Via the Royal Free Charity: Donation Page : https://royalfreecharity.org/donate Scroll down to tick box 'your donation will be used where the need is greatest. However please tick this box if you would like to donate to a specific appeal or fund'. Click on the box to reveal 'a where would you like to give to' drop down menu. Scroll down to the Scleroderma and Raynaud's research option and click on this option. Leave a gift in your Will : https://royalfreecharity.org/giftsinwills/ The Royal Free Charity provides a free Will writing service ☝️ Just Giving Page : https://www.justgiving.com/fundraising/sclerodermaunit-royalfree Thank You 🙏 #SclerodermaFreeWorld #RaynaudsFreeWorld #Research #Scleroderma #SystemicSclerosis #Raynauds #Autoimmune #RareDisease #NoCure #UnknownCause #LifeChanging #ConnectiveTissue #DreamSnatcher #Disability #ThickSkin

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5/4/2024, 11:55:08 AM

Collaboration is critical to making research progress. That's why the SRF co-sponsored a recent workshop with the National Institutes of Health (NIH) & other nonprofit organizations to discuss scientific advances in immunotherapies and cellular therapies in systemic sclerosis (SSc) and chronic graft-versus-host disease (cGVHD). Held on April 30 & May 1 at the NIH in Bethesda, Maryland, this workshop brought together more than 100 leaders and investigators in the fields of SSc and cGVHD for a day and a half of discussion and collaboration. The meeting featured topical sessions with Q&A, including a panel that SRF Board Chairman Luke Evnin, PhD served on to share insights about “Novel Approaches to Funding and Infrastructure.“ This workshop created a unique opportunity to better understand mechanisms that contribute to both SSc and cGVHD, the biology of and therapeutic approaches to preventing and treating fibrosis, and to develop and foster collaborations across the fields. The Scleroderma Research Foundation was honored to be one of the co-sponsors of this important workshop, and we look forward to how these discussions will guide future efforts. #srfcure #sayscleroderma #sclerodermaresearch #allinforacure #scleroderma

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5/4/2024, 1:24:16 AM

Now through next Friday, access my online course, 6 Steps To Reversing Disease With Supermarket Foods 100% for FREE at GoodbyeLupus.com! Just click on the free classes on my website and you can see watch all 3 classes, that include my story of reversing lupus almost 19 years ago, the foods that make you sicker, the foods you need for recovery and dozens of studies in reversing many different autoimmune diseases. When you come to my next FREE live coaching Session next Wednesday right HERE on my channel at 12:30pm pacific, I want you to know all the info so you have super good focused questions and I can get your health back, for free! 😊 Many of my followers from around the world have reversed their diseases just from these classes alone, so don’t miss them! Have a watch party with your friends and heal together!! Just go to goodbyelupus.com to watch now. People who bought lifetime access can log into each class separately on my site, but for ease of sharing, the 3 classes are combined into 1 video for free access, so make sure if you need a break, you PAUSE don’t restart! Or click YouTube icon to finish it. Happy learning! For more info, classes, recipes and more click: https://linktr.ee/goodbyelupus #goodbyelupus #goodbyeautoimmunedisease #freeclasses #lupuswarrior #lupusfighter #lupusawareness #rheumatoidarthritis #sjogrens #scleroderma #autoimmunedisease #lupusawarenessmonth

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5/4/2024, 12:43:03 AM

My father laid in his final resting place. Jim D Patrick 03/29/54 - 01/27/24 "Hearts Need Love" - JPGold #scleroderma

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5/4/2024, 12:19:52 AM

🤚Scleroderma is an autoimmune disease that can affect different tissue in the body, but it almost always affects the skin. Skin becomes hard and tight. . 🫁Imagine that happening inside your body too. Not fun. Problems and pain! . ⚡️Mast cell degranulation is found in scleroderma. Those mast cells are busy releasing chemicals that signal an overproduction of collagen, which can be uncomfortable. . ☺️Now imagine how it would feel to calm those mast cells and put a stop to hard tight skin! #mcas #histamineintolerance #histaminehaven #scleroderma

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5/3/2024, 10:18:07 PM

To my silent fighters. I’m there with you. #limitedsclerosis #fighter #lupuswarrior #scleroderma

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5/3/2024, 10:04:31 PM

Repost~ chronically_brave “Chronic Illness isn’t just swallowing some tablets & a few days off work. It’s lost friends, broken relationships, sacrificing of hobbies, forgotten passions, all the while feeling like you have no value or purpose in life. Please consider this before you cast judgement.” Post by @lollyandlupus Edited by me @chronically_brave Using @acolorstory #beautifuldestinations #beautifullybroken #silverlining #simplemoments #scleroderma #pulmomaryfirbrosis #fibromyalgia #type2diabetes #raynuards

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5/3/2024, 9:51:16 PM

Fatigue is a common issue for people living with chronic conditions. A study supported by the Scleroderma Research Foundation found that over 75% of people with scleroderma experienced fatigue, and for 61% of these, it was reported to be one of the most distressing symptoms of the condition. 🌻 . . @scleroderma_australia @sclerodermavictoria @scleroderma_queensland . . #Scleroderma #ShineALightOnScleroderma #SunflowerDay2024 #SclerodermaNurses #ShineLikeASunflower #SunflowerDay #SclerodermaResearch #Donate #SupportUs #NonProfit #Australiafundraising #sclerodermawarrior #invisibleillness #raynauds #multiplesclerosis #fundraisingevent #fibromyalgia #lupuswarrior #spoonielife #sjogrenssyndrome #lupusawareness #chronicfatigue #autoimmunediet #chronicillnesswarrior #pulmonaryfibrosis #mctd #interstitiallungdisease #goodbyelupus #autoimmuneprotocol

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5/3/2024, 9:16:55 PM

Did I mention June is right around the corner? Do you know anyone who suffers from this destructive, incurable autoimmune disease? #scleroderma #juneissclerodermaawarnessmonth

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5/3/2024, 8:05:10 PM

Donate Now to help @sclerostarz with her medical expenses. #scleroderma #tare #autoimmune #give #iviginfusion #medicalbillssuck

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5/3/2024, 7:15:28 PM

Pouring into our community is so important. Join us to support this worthy cause. Hear Dumont resident @sclerodermawarrior speak about her journey and explain ways you can get involved to help! Don’t forget to bring your appetite! #scleroderma #bergencountynj

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5/3/2024, 6:52:25 PM

I love when people pop on to my live sessions to share their success reversing their diseases, without ever meeting me, because of my constant supply of free info and support. It keeps me motivated to keep doing more of the same! If you haven't learned the Goodbye Lupus Protocol yet, which by the way is NOT specific to lupus but rather to optimizing health and cellular repair, the make sure you watch my online classes available NOW until Next Friday at GoodbyeLupus.com! Free live coaching every Wednesday LIVE HERE on my IG at 12:30pm pacific. For more info, classes, resources, click the link in my profile. #goodbyelupus #goodbyeautoimmunedisease #hypernourishment #lupus #lupusawareness #lupusflare #lupuswarrior #lupusproblems #lupusnephritis #lupussucks #lupusfighter #lupusadvocate #autoimmunedisease #autoimmune #sjogrenssyndrome #scleroderma #multiplesclerosis #autoimmuneprotocol #autoimmunediet #mixedconnectivetissuedisease #lupusdiet #psoriasis #greensmoothie #gravesdisease #discoidlupus #hypernourish #rheumatoidarthritis #wellnesswednesday #lupusawarenessmonth

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5/3/2024, 6:48:09 PM

🤸‍♀️ May is #MobilityAwarenessMonth! Mobility is the most common area of disability and one of the many challenges that people with #scleroderma face every day. 🦶 Scleroderma causes a thickening of the skin that makes movement in the wrists, elbows and legs difficult and painful. 📢 Let's raise awareness and ensure mobility is not a limitation!

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5/3/2024, 6:12:46 PM

🤸‍♀️ May is #MobilityAwarenessMonth! Mobility is the most common area of disability, and one of the many challenges that people with #scleroderma face every day. 🦶 Scleroderma causes a thickening of the skin that makes movement in the wrists, elbows and legs difficult and painful. 📢 Let's raise awareness and ensure mobility is not a limitation! #SclerodermaAwareness #MobilityAwareness

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5/3/2024, 5:30:07 PM

Never miss out on a chance to connect. Subscribe to our newsletter for the most up-to-date news, announcements, events, and resources. https://sclerodermadmv.org/newsletters/ #UnitingHearts #SclerodermaAwareness #EndScleroderma #Scleroderma #SclerodermaSupport #SclerodermaDMV #newsletter #sclerowarrior

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5/3/2024, 5:00:46 PM

'Ah Great, Another Day To Spend In Bed' : https://blog.raynaudsscleroderma.co.uk/2017/05/ah-great-another-day-to-spend-in-bed_9.html Read about scleroderma research Royal Free London NHS Foundation Trust: https://royalfreecharity.org/focus/scleroderma/ https://royalfreecharity.org/news/story/grants-awarded-to-improve-patient-experience/ https://www.royalfree.nhs.uk/services/scleroderma This year, 2024, I will have spent over half of my life, 27 years, living with a scleroderma (systemic sclerosis) and Raynaud's diagnosis, and all that entails. 🤢 Read more: https://royalfreecharity.org/news/fundraising/nicolas-story/ Eternally grateful to Dame Professor Carol Black and Professor Chris Denton Royal Free London NHS Foundation Trust 😇 Please donate to medical research to identify a cure and the cause of scleroderma, at the Scleroderma Unit Royal Free Hospital. Every penny will be used for research purposes. There are several ways as to how you can donate: Via the Royal Free Charity: Donation Page : https://royalfreecharity.org/donate Scroll down to tick box 'your donation will be used where the need is greatest. However please tick this box if you would like to donate to a specific appeal or fund'. Click on the box to reveal 'a where would you like to give to' drop down menu. Scroll down to the Scleroderma and Raynaud's research option and click on this option. Leave a gift in your Will : https://royalfreecharity.org/giftsinwills/ The Royal Free Charity provides a free Will writing service ☝️ Just Giving Page : https://www.justgiving.com/fundraising/sclerodermaunit-royalfree Thank You 🙏 #SclerodermaFreeWorld #RaynaudsFreeWorld #Research #Scleroderma #SystemicSclerosis #Raynauds #Autoimmune #RareDisease #NoCure #UnknownCause #LifeChanging #ConnectiveTissue #DreamSnatcher #Disability #ThickSkin

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5/3/2024, 1:39:12 PM

Rheumatoid arthritis Disease OPD Now in Bidar Dr. Rahul Ladda Consultant Rheumatologist 5th May 2024 Place: Bidar Add: Vishwa Healthcare, Opp. KSRTC Depot, Near New Bus stand, Bidar Contact no: 8047182888 Time: 10:00 AM to 12:00 PM Add: Vasu Hospital, 9-8-384, Bvb College Road, New Mailoor Cross, Bidar-585401 Contact no: 9379201341 Time: 12:00 PM - 04:00 PM #rheumatoidarthritis #rheumatologist #rheumatology #kneepain #jointpain #arthritis #arthritisrelief #gout #painrelief #systemiclupuserythematosus #scleroderma #arthritiswarrior #ankylosingspondylitis #osteoarthritis

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5/3/2024, 12:26:31 PM

"Now through next Friday, access my online course, 6 Steps To Reversing Disease With Supermarket Foods 100% for FREE at GoodbyeLupus.com! Just click on the free classes on my website and you can see watch all 3 classes, that include my story of reversing lupus almost 19 years ago, the foods that make you sicker, the foods you need for recovery and dozens of studies in reversing many different autoimmune diseases. When you come to my next FREE live coaching Session next Wednesday right HERE on Instagram, Facebook, & YouTube at 3:30pm eastern, I want you to know all the info so you have super good focused questions and I can get your health back, for free! 😊 Many of my followers from around the world have reversed their diseases just from these classes alone, so don't miss them! Have a watch party with your friends and heal together!! Just go to 6 Steps to Reversing Disease With Supermarket Foods: https://www.goodbyelupus.com/6-steps-to-reversing-disease-with-supermarket-foods-webinar/ to watch now. People who bought lifetime access can log into each class separately on my site, but for ease of sharing, the 3 classes are combined into 1 video for free access, so make sure if you need a break, you PAUSE don't restart! Or click YouTube icon to finish it. Happy learning! For more info, classes, recipes, and more click: https://linktr.ee/goodbyelupus " - L💜VE @goodbyelupus (Dr. G) #goodbyelupus #goodbyeautoimmunedisease #freeclasses #lupuswarrior #lupusfighter #lupusawareness #rheumatoidarthritis #sjogrens #scleroderma #autoimmunedisease #lupusawarenessmonth 📌 Please pin, highlight, & share this... Everyone deserves to know this information, simply to optimize their health & the health of their family!💜💚💝

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5/3/2024, 12:04:10 PM

Siamo felici di partecipare attivamente a questa splendida iniziativa nel chiostro della Chiesa di Sant'Andrea a Cercina, organizzata dal Trentesimo Cercina Pro-loco Sesto Fiorentino, in collaborazione con AIAU ODV - Adozioni Internazionali e con lo squisito menu cucinato dalle Donne del Circolo Arci Cercina... 𝐕𝐢 𝐚𝐬𝐩𝐞𝐭𝐭𝐢𝐚𝐦𝐨 𝐝𝐨𝐦𝐞𝐧𝐢𝐜𝐚 𝟏𝟐 𝐦𝐚𝐠𝐠𝐢𝐨 𝐩𝐞𝐫 𝐮𝐧 𝐩𝐨𝐦𝐞𝐫𝐢𝐠𝐠𝐢𝐨 𝐢𝐧𝐬𝐢𝐞𝐦𝐞! __________ #sclerodermia #scleroderma #malattiefibrosanti #associazione #sclerodermaawareness #cura #ospedale #careggi #volontariato #sclerosisistemica #firenze #terzosettore #nonprofit #nonprofitorganization #careggi #impegno #direttivo #evento #collaborazione

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5/3/2024, 10:03:30 AM

Do I have generic tips for dealing with itchy, blotchy, painful skin conditions? Absolutely. ⚠️Avoid ALL dairy. This means cow, goat sheep buffalo etc This is butter, yoghurt, cheese, milk, ice cream, chocolate. This means reading food labels for any cow’s milk (lactose, whey etc) ⚠️Avoid Gluten This is bread, cakes, biscuits, pasta. ⚠️Avoid refined sugar This is the white stuff. Again, you will need to check labels. ⚠️Avoid Yeast and related foods Yeast, vinegar, Marmite, mushrooms, white potatoes, peanuts, apples. ✅Olives ✅Olive oil ✅Garlic ✅Oregano ✅Oily fish ✅Antioxidants ✅Clean protein ✅Leafy green vegetables Let me tell you about BODY TALK’s approach … ❓Are you a perfectionist? ❓Do you eat gluten? ❓Do you drink cow’s milk? ❓Do you have Asthma? ❓Do you have any siblings? What’s your relationship like with them? ❓How healthy are your teeth? ❓Do you find it impossible to say ‘no’ to people? ❓How well do you sleep? ❓Do you have healthy bowel movement? ❓Do you care what people think about you? ❓Did you go to boarding school? ❓Do you have any tattoos? It’s quite a mix of questions. These are some of the questions I ask clients whilst I start to put the jigsaw of their skin condition together. If you are dealing with a skin condition, you will have tried a lot of approaches. BODY TALK’s approach is DIFFERENT. We look at your - Physical body - Emotional body - Spiritual body We investigate, address, and listen to your body’s talk. Healing your skin won’t happen overnight. It will take time, faith, and commitment. BODY TALK will be with you every step of the way. Body Talk is a bespoke and accountable healing journey. #acne #atopicdermatitis #contactdermatitis #rosacea # #eczema #pempgigus #alopecialtreata #epidermolysisbullosa #scleroderma #vitiligo #hidradenitissuppurativa #ichthyosis #shingles #uticaria #kinesiology #penarth #cardiff #naturalhealth Book a BODY TALK CALL today 📅 [Link in Bio] to find out more

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5/3/2024, 9:00:26 AM