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BEGIN:VEVENT
DTSTART;TZID=America/Halifax:20201101T110000
DTEND;TZID=America/Halifax:20201101T150000
DTSTAMP:20260403T213833
CREATED:20201007T164848Z
LAST-MODIFIED:20201021T172215Z
UID:2603-1604228400-1604242800@cystinosis.org
SUMMARY:Mulligans Fore Morgan
DESCRIPTION:Join us for our first Mulligans Fore Morgan event at TopGolf in Cleveland on Sunday\, November 1st at 11:00 AM. \nRegistration is $75 per player for 3 hours of unlimited play. Each golf bay will hold teams of 6.  An “All-American” lunch is included. Guests will pay individually for alcoholic beverages. \n \n  \n2020 has brought Morgan Peachman a new kidney\, and a new lease on life. After turning 13 this summer\, and hitting her six month kidney-versary last month\, she’s been cleared for most normal activities. And she’ll be hitting the day’s ceremonial first tee shot! \nWhile nothing feels normal this year\, The Peachman Family is keeping with the theme of changing times by bringing their family’s annual fall fundraising event to TopGolf in Cleveland to ensure social distancing! \nWhether you’re an avid golfer\, playing for fun\, or have never hit a golf ball in your life\, our tournament style format will hit all the marks. Competitive\, lots of fun and in support of a good cause\, we hope you’ll join us November 1st! If you can’t attend\, donations are welcomed and sponsorship opportunities are available. Contact Jen Peachman at jennifer.peachman@gmail.com for details or register using the form below.
URL:https://cystinosis.org/event/morgan/
LOCATION:5820 Rockside Woods Blvd N\, 5820 Rockside Woods Blvd N\, Independence\, OH\, 44131\, United States
CATEGORIES:Fundraising Events
ATTACH;FMTTYPE=image/png:https://cystinosis.org/wp-content/uploads/2020/10/Mulligans-Fore-Morgan-Logo.png
ORGANIZER;CN="Jen Peachman":MAILTO:jennifer.peachman@gmail.com
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20201101
DTEND;VALUE=DATE:20201102
DTSTAMP:20260403T213833
CREATED:20201021T184456Z
LAST-MODIFIED:20201021T202417Z
UID:2705-1604188800-1604275199@cystinosis.org
SUMMARY:LLLFF Virtual 5K
DESCRIPTION:On the one year anniversary of Laura McGinnis’ passing\, the Live Like Laura Fun Fund (LLLFF) was launched. Laura lived life in pursuit of adventure\, making memories every step of the way. We’d like to keep her spirit alive by fulfilling as many “fun” requests for the cystinosis community as possible. To grow our funding\, we are hosting a virtual 5k on November 1\, 2020.\n\nWe invite friends\, family\, and anyone who has been touched by her story and/or cystinosis to take part. It doesn’t matter if you walk\, jog\, stroll\, bike\, or scooter; let’s take this time to move our bodies and reflect.\n\nHosting a virtual 5k means you can participate from anywhere in the world! We’ve got in-person teams meeting on November 1st from Pennsylvania to Kauai. \n\n\n\nOnline registration is $25 per person. As a small token of gratitude\, you’ll receive a commemorative “Live Like Laura” ornament. For any questions\, contact Frankie McGinnis at frankiemcginnis@gmail.com.
URL:https://cystinosis.org/event/lllff-virtual-5k/
CATEGORIES:Fundraising Events
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20201014T190000
DTEND;TZID=UTC:20201014T203000
DTSTAMP:20260403T213833
CREATED:20200917T162806Z
LAST-MODIFIED:20200917T162806Z
UID:2579-1602702000-1602707400@cystinosis.org
SUMMARY:Cystinosis Gene Therapy & Research Updates: Virtual Meetup
DESCRIPTION:Learn more about gene therapy as it relates to the cystinosis community. Dr. Paul Grimm from from Stanford University School of Medicine and Fernanda Copeland\, MS\, RD. Head\, Global Patient Advocacy & Engagement\, AVROBIO are our guest speakers. \n  \nRegister today to reserve your space at https://us02web.zoom.us/webinar/register/WN_PQZeGL2GT5W1MythBHbDzA. \nFREE welcome kits are here – availability is limited.
URL:https://cystinosis.org/event/cystinosis-gene-therapy-research-updates-virtual-meetup/
CATEGORIES:Gatherings/Conferences
ATTACH;FMTTYPE=image/png:https://cystinosis.org/wp-content/uploads/2020/09/research.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20201006T190000
DTEND;TZID=UTC:20201006T203000
DTSTAMP:20260403T213833
CREATED:20200917T153750Z
LAST-MODIFIED:20200917T153750Z
UID:2576-1602010800-1602016200@cystinosis.org
SUMMARY:Cystinosis & Mental Health: Virtual Meetup
DESCRIPTION:Let’s have an open discussion on mental health and living with cystinosis. Everyone within the community is invited! Licensed psychologist\, Dr. Cortney Taylor Zimmerman will guide the meetup. \nRegister today at https://us02web.zoom.us/webinar/register/WN_Gw1Wxj3oQkCi00OpR2WFPQ. \nWelcome kits are here – with limited availability.
URL:https://cystinosis.org/event/cystinosis-mental-health-virtual-meetup/
CATEGORIES:Gatherings/Conferences
ATTACH;FMTTYPE=image/png:https://cystinosis.org/wp-content/uploads/2020/09/mentalhealth.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20201003T120000
DTEND;TZID=UTC:20201003T133000
DTSTAMP:20260403T213833
CREATED:20201001T143243Z
LAST-MODIFIED:20201001T143243Z
UID:2601-1601726400-1601731800@cystinosis.org
SUMMARY:Cystinosis Sessions: Alternative Therapies\, Exercise & Activities
DESCRIPTION:Join hosts from the Adult Leadership Advisory Board (ALAB) for the Cystinosis Sessions video conference series – LIVE- on Saturday\, October 3 at 12:00 pm ET. This open discussion will include alternative therapies\, exercise and activities. \nJoin Zoom Meeting\nhttps://zoom.us/j/2663523786\nMeeting ID: 266 352 3786 \nHere are instructions to help with downloading Zoom. We recommend completing these steps prior to the call. \n\nSecure access to a mobile device (PC\, Apple\, Android)\, desktop or laptop computer\nEnsure reliable internet connection\nDownload Zoom Cloud Meetings here or through your device’s app store\nClick on the link https://zoom.us/j/2663523786\nHave the Meeting ID ready: 266 352 3786. If you use the link provided\, the meeting ID is not needed.\n\nAdd the meeting to your calendar by clicking one of the buttons below.
URL:https://cystinosis.org/event/cystinosis-sessions-alternative-therapies-exercise-activities/
CATEGORIES:Gatherings/Conferences
ATTACH;FMTTYPE=image/png:https://cystinosis.org/wp-content/uploads/2020/03/Logo_Header.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20200929T190000
DTEND;TZID=UTC:20200929T203000
DTSTAMP:20260403T213833
CREATED:20200917T152803Z
LAST-MODIFIED:20200917T153022Z
UID:2573-1601406000-1601411400@cystinosis.org
SUMMARY:Cystinosis Basics: Virtual Meetups
DESCRIPTION:Learn more about the fundamentals of cystinosis during our Cystinosis Basics video meetup. Dr. Larry Greenbaum\, Emory School of Medicine is our expert speaker. Join us by registering today at https://us02web.zoom.us/webinar/register/WN_HU0G6SQuR4W_G8mmFr3bog.\n\nFREE welcome kits – limited availability.\nWe hope you can join us!
URL:https://cystinosis.org/event/cystinosis-basics-virtual-meetups/
CATEGORIES:Gatherings/Conferences
ATTACH;FMTTYPE=image/png:https://cystinosis.org/wp-content/uploads/2020/09/CystinosisBasics.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20200919T170000
DTEND;TZID=UTC:20200919T183000
DTSTAMP:20260403T213833
CREATED:20200917T152146Z
LAST-MODIFIED:20200917T152146Z
UID:2570-1600534800-1600540200@cystinosis.org
SUMMARY:Caregivers Connect: Virtual Meetup
DESCRIPTION:Caregivers of children with cystinosis under 18 years old are invited.\nJoin us for a video conference to connect with other caregivers. This is a free networking opportunity. Register at https://us02web.zoom.us/meeting/register/tZUpde2tqj8uH9yGl5nmGG6v1TvprXaLgtOV.\n\nFREE welcome kits – limited availability.\nWe hope to see you there!
URL:https://cystinosis.org/event/caregivers-connect-virtual-meetup/
ATTACH;FMTTYPE=image/png:https://cystinosis.org/wp-content/uploads/2020/09/Caregivers_18condensed.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20200905T160000
DTEND;TZID=UTC:20200905T173000
DTSTAMP:20260403T213833
CREATED:20200903T150208Z
LAST-MODIFIED:20201001T142405Z
UID:2564-1599321600-1599327000@cystinosis.org
SUMMARY:Cystinosis Sessions: Open Discussion
DESCRIPTION:This installment of the Cystinosis Sessions video conference series is live on Saturday\, September 5 at 4:00 pm ET. Our September session will be an open forum to discuss the topics on the minds of our fellow cystinosis warriors.  We hope you can join us! \nJoin Zoom Meeting\nhttps://zoom.us/j/2663523786\nMeeting ID: 266 352 3786 \nCystinosis Sessions were created and are hosted by the Adult Leadership Advisory Board (ALAB). Here are instructions to help with downloading Zoom. We recommend completing these steps prior to the call. \n\nSecure access to a mobile device (PC\, Apple\, Android)\, desktop or laptop computer\nEnsure reliable internet connection\nDownload Zoom Cloud Meetings here or through your device’s app store\nClick on the link https://zoom.us/j/2663523786\nHave the Meeting ID ready: 266 352 3786. If you use the link provided\, the meeting ID is not needed.\n\nAdd the meeting to your calendar by clicking one of the buttons below.
URL:https://cystinosis.org/event/cystinosis-session-open-discussion/
CATEGORIES:Gatherings/Conferences
ATTACH;FMTTYPE=image/png:https://cystinosis.org/wp-content/uploads/2020/03/Logo_Header.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20200822
DTEND;VALUE=DATE:20200823
DTSTAMP:20260403T213833
CREATED:20200806T065610Z
LAST-MODIFIED:20200807T034601Z
UID:2499-1598054400-1598140799@cystinosis.org
SUMMARY:Podcast: Youth to Adult Transition (part 2)
DESCRIPTION:Youth to Adult Transition Part 2- Q &A Panel with Adults Living with Cystinosis \nPart two of the youth to adult transition discussion is focused on personal experiences of adults living with cystinosis. Joining our panel on behalf of the adult community are Serena Scott (via mum Sue Scott)\, Kevin McCalla\, Ashley Abedini\, and Joe Rumney. \nHosts from the Adult Leadership Advisory Board (ALAB) are Jana Healy\, Sara Healy\, Steve Schleuder\, Cheryl Simoens. \nPlease check back. Link to podcast coming soon.
URL:https://cystinosis.org/event/podcast-youth-to-adult-transition-part-2/
ATTACH;FMTTYPE=image/png:https://cystinosis.org/wp-content/uploads/2020/02/Website_Header.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20200815
DTEND;VALUE=DATE:20200816
DTSTAMP:20260403T213833
CREATED:20200806T065341Z
LAST-MODIFIED:20200814T184450Z
UID:2496-1597449600-1597535999@cystinosis.org
SUMMARY:Podcast: Youth to Adult Transition (part 1)
DESCRIPTION:Youth to Adult Transition Part 1- Discussion with Medical Professionals \nThe third podcast from the ALAB will focus on transitioning from youth to adult medical care. Part one of the youth to adult transition conversation begins with the healthcare professional opinion. Join us and special guests Dr. Paul Grimm from Lucile Packard Children’s Hospital and Stanford University of Medicine and Dori Rivera\, PAM (Patient Access Manager) from Horizon Therapeutics. \nHosts from the Adult Leadership Advisory Board (ALAB) are Jana Healy\, Sara Healy\, Steve Schleuder\, Cheryl Simoens. \nBeginning August 15\,2020 at 9am ET\, this link will go live and connect you to the podcast via YouTube: https://youtu.be/zEMdQmxR0UU. \nThank you for your interest.
URL:https://cystinosis.org/event/podcast-youth-to-adult-transition-part-1/
ATTACH;FMTTYPE=image/png:https://cystinosis.org/wp-content/uploads/2020/02/Website_Header.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20200801T120000
DTEND;TZID=UTC:20200801T133000
DTSTAMP:20260403T213833
CREATED:20200729T053416Z
LAST-MODIFIED:20200729T053416Z
UID:2490-1596283200-1596288600@cystinosis.org
SUMMARY:Cystinosis Sessions: Exercise
DESCRIPTION:The Cystinosis Sessions live video series continues on Saturday\, August 1st from 12:00pm – 1:30pm ET. The Adult Leadership Advisory Board (ALAB) will lead the discussion open to all community members. \nCystinosis Sessions: Exercise \n\nImportance of exercise\nTypes of exercise\n\nStrength training\nAerobics\nStretching\nBalance training\nModerate vs Intense exercise\n\n\nAnd more\n\nPlease download the Zoom app prior to the meeting. \nJoin Zoom Meeting\nhttps://zoom.us/j/2663523786\nMeeting ID: 266 352 3786\nClick on the above and have the Meeting ID ready\, if you use the link provided\, the meeting ID is not needed.
URL:https://cystinosis.org/event/cystinosis-sessions-exercise/
CATEGORIES:Gatherings/Conferences
ATTACH;FMTTYPE=image/png:https://cystinosis.org/wp-content/uploads/2020/03/Logo_Header.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20200711T160000
DTEND;TZID=UTC:20200711T173000
DTSTAMP:20260403T213833
CREATED:20200711T133417Z
LAST-MODIFIED:20200711T133417Z
UID:2484-1594483200-1594488600@cystinosis.org
SUMMARY:Cystinosis Sessions: Mental Health
DESCRIPTION:The forth live video conference hosted by the Adult Leadership Advisory Board (ALAB) will discuss Mental Health\, Anxiety\, Depression\, and Coping. Our featured guest is Maya Doyle\, MSW\, PhD\, LCSW. We look forward to seeing you at 4pm ET on July 11th. \nJoin Zoom Meeting\nhttps://zoom.us/j/2663523786 \nMeeting ID: 266 352 3786 \nZoom Meetings Instructions \nDesktop\, laptop or mobile device (PC\, Apple\, Android)\nReliable internet\nDownload Zoom Cloud Meetings Here or your devices app store\nClick on the above and have the Meeting ID ready\, if you use the link provided\, the meeting ID is not needed.
URL:https://cystinosis.org/event/cystinosis-sessions-mental-health/
CATEGORIES:Gatherings/Conferences
ATTACH;FMTTYPE=image/png:https://cystinosis.org/wp-content/uploads/2020/03/Logo_Header.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20200606T120000
DTEND;TZID=UTC:20200606T133000
DTSTAMP:20260403T213833
CREATED:20200521T050942Z
LAST-MODIFIED:20200521T051344Z
UID:2430-1591444800-1591450200@cystinosis.org
SUMMARY:Cystinosis Sessions: Overcoming Limitations & Goal Setting
DESCRIPTION:The third live video conference takes place June 6 at 12:00 pm ET. The Adult Leadership Advisory Board (adults living with cystinosis) will host the event. Topics will include: \n\nFacing challenges\nPeer pressure\nLimitations & how to overcome them\nGoal setting\n\nDownloading Zoom/Video Conference Prep \n\nSecure access to a mobile device (PC\, Apple\, Android)\, desktop or laptop computer\nEnsure reliable internet connection\nDownload Zoom Cloud Meetings here or through your device’s app store\nClick on the link https://zoom.us/j/2663523786\nHave the Meeting ID ready: 266 352 3786. If you use the link provided\, the meeting ID is not needed.\n\nJoin Zoom Meeting\nhttps://zoom.us/j/2663523786\nMeeting ID: 266 352 3786 \nAdd the meeting to your calendar by clicking one of the buttons below. We look forward to “seeing” you and hearing you on June 6th!
URL:https://cystinosis.org/event/cystinosis-sessions-overcoming-limitations-goal-setting/
CATEGORIES:Gatherings/Conferences
ATTACH;FMTTYPE=image/png:https://cystinosis.org/wp-content/uploads/2020/03/Logo_Header.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20200507
DTEND;VALUE=DATE:20200508
DTSTAMP:20260403T213833
CREATED:20200415T000234Z
LAST-MODIFIED:20200415T001744Z
UID:2400-1588809600-1588895999@cystinosis.org
SUMMARY:Podcast Discussion: Coping with Loss & Grief
DESCRIPTION:The next topic in the Adult Leadership Advisory Board’s (ALAB’s) podcast series focuses on coping with loss and grief. This is the second installment of the series – Cystinosis Rare: A Journey into the Unknown. \nThe podcast will be published on YouTube on Cystinosis Awareness Day\, May 7th. \nOur featured guest and episode leader is Maya Doyle.\nPartnering with the cystinosis community for over a decade\, Maya is a professor and certified social worker (CSW) specializing in nephrology. Her unique background and set of experiences will make this a conversation you do not want to miss! \nIn preparation for the podcast recording\, please send any questions for Maya or thoughts you’d like to add by emailing Jana at jana_healy752@hotmail.com. Emails will be accepted through April 15th. Your names will be kept confidential and will not be mentioned during the episode. \nSubscribe to our YouTube page and receive an email alert when the podcast is available: http://bit.ly/2Y28tsx on Thursday\, May 7th. We hope you tune in!
URL:https://cystinosis.org/event/lossgrief/
CATEGORIES:Gatherings/Conferences
ATTACH;FMTTYPE=image/png:https://cystinosis.org/wp-content/uploads/2020/02/Website_Header.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20200507
DTEND;VALUE=DATE:20200508
DTSTAMP:20260403T213833
CREATED:20191130T062559Z
LAST-MODIFIED:20200504T182950Z
UID:2313-1588809600-1588895999@cystinosis.org
SUMMARY:Cystinosis Awareness Day - 3rd Annual
DESCRIPTION:Cystinosis Awareness Day is recognized as May 7th for the most commonly linked cystinosis mutation\, the 57-kb deletion. This marks the third year we’ve come together on this day to support education\, awareness\, research\, and fundraising for our rare disease. \nMonths of planning go into Cystinosis Awareness Day. In-person events like 57 Miles for Cystinosis or Miles for Moose require training\, sponsors\, team coordination\, and consume a massive amount of time and dedication. With the latest COVID-19 restrictions\, this year’s events have been canceled\, postponed or re-imagined. We thank the entire community for your unwavering support – now more than ever. \nIt’s like our CRN President says\, “Cystinosis doesn’t stop. Until there is a cure\, neither will we.” \nCystinosis does not ease up during a worldwide pandemic; it does not understand quarantine. Not for one single day\, not for one hour\, not for one second do bodies living with cystinosis get a break. And we thank you for enduring this ongoing battle with us. \nHere are a few ways to help us in this fight: \n\nLike & share our awareness video\nUpdate your Facebook profile frame\nShare your cystinosis experience with a friend\, neighbor\, or colleague (in compliance with your local COVID-19 guidelines)\nRead inspiring cystinosis stories\nDonate\nStart a fundraiser by emailing info@cystinosis.org\n\nIf you’d like to learn more about cystinosis resources and research\, click here. We are proud to be one of the only organizations to provide comprehensive support\, education\, awareness\, and research relevant to each point in the cystinosis journey. \nThank you!
URL:https://cystinosis.org/event/cystinosis-awareness-day-3rd-annual/
CATEGORIES:Fundraising Events
ORGANIZER;CN="Cystinosis Research Network":MAILTO:info@cystinosis.org
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200502T160000
DTEND;TZID=America/New_York:20200502T173000
DTSTAMP:20260403T213833
CREATED:20200414T234814Z
LAST-MODIFIED:20200414T235101Z
UID:2399-1588435200-1588440600@cystinosis.org
SUMMARY:Live Video Conference: Dependence\, Education & Employment
DESCRIPTION:Join the Cystinosis Sessions video conference series hosted by the Adult Leadership Advisory Board (ALAB). Starting May 2nd at 4:00 pm ET\, the ALAB welcomes anyone impacted by cystinosis. This “session” will focus on: \n\nEducation\nEmployment\nImportance of Being Self-Reliant vs Being Dependent\nEssential Needs & Medication\nGeneral conversation as time allows\n\nTo join the meeting: \nhttps://zoom.us/j/2663523786 \nMeeting ID: 266 352 3786 \nDownloading Zoom/Video Conference Preparation \n\nSecure access to a mobile device (PC\, Apple\, Android)\, desktop or laptop computer\nEnsure reliable internet connection\nDownload Zoom Cloud Meetings here or through your device’s app store\nClick on the link https://zoom.us/j/2663523786\nHave the Meeting ID ready: 266 352 3786. If you use the link provided\, the meeting ID is not needed.
URL:https://cystinosis.org/event/live-video-conference-dependence-education-employment/
CATEGORIES:Gatherings/Conferences
ATTACH;FMTTYPE=image/png:https://cystinosis.org/wp-content/uploads/2020/03/Logo_Header.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20200502
DTEND;VALUE=DATE:20200503
DTSTAMP:20260403T213833
CREATED:20200221T065804Z
LAST-MODIFIED:20200414T221034Z
UID:2368-1588377600-1588463999@cystinosis.org
SUMMARY:57 Miles for Cystinosis
DESCRIPTION:
URL:https://cystinosis.org/event/57-miles-for-cystinosis-2020/
LOCATION:DE\, United States
CATEGORIES:Fundraising Events
ATTACH;FMTTYPE=image/png:https://cystinosis.org/wp-content/uploads/2020/02/Website_Header-1.png
ORGANIZER;CN="Clinton Moore":MAILTO:Clintonmoore1@aol.com
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200425T070000
DTEND;TZID=America/New_York:20200425T150000
DTSTAMP:20260403T213833
CREATED:20190910T193640Z
LAST-MODIFIED:20200408T044503Z
UID:1685-1587798000-1587826800@cystinosis.org
SUMMARY:Virtual: Cystinosis Network Europe 2020 International Conference
DESCRIPTION:Following much consideration\, Cystinosis Network Europe (CNE) and Cystinosis Ireland have decided to cancel the in-person International Cystinosis Conference planned for Dublin in July 2020 due the ongoing situation with COVID-19. \nThe International Cystinosis Family Conference is now taking place online! \nOn April 25th from 7am to 3pm ET you will have access to this free event. Available in you own home anywhere in the world\, you can now watch cystinosis world experts (with translation) presenting the latest information on managing cystinosis; educational issues; bones and muscles; eyes and possible new treatments; kidneys – pre and post transplant and keeping well; the latest research in gene therapy and other new treatments; pregnancy and male fertility; the impact of COVID-19; and maintaining your mental health. \nConfirmed speakers include Prof Elena Levtchenko (Chair)\, Prof Atif Awan\, Dr Rachel Bishop\, Prof Don Cairns\, Dr Anuj Chauhan\, Dr Stephanie Cherqui\, Prof Paul Goodyer\, Prof Paul Grimm\, Dr Patrick Harrison\, Prof Craig Langman\, Dr Herbie Newell\, Dr Joyce Senior\, and more. \nRegister Now. To secure your place and notify the group of translation preferences. \nAbout CNE \nCystinosis Network Europe (CNE) which comprises members from patient organizations across Europe and further afield. Eight European organisations come together to support people with cystinosis and promote research and form a network. We have a number of projects ongoing to support people living with cystinosis and their families; an international conference every two years; and the development of a Community Advisory Board in Cystinosis\, with the support of EURORDIS.
URL:https://cystinosis.org/event/cystinosis-network-europe-2020-international-conference/
CATEGORIES:Gatherings/Conferences
ATTACH;FMTTYPE=image/jpeg:https://cystinosis.org/wp-content/uploads/2019/09/CNE.jpg
ORGANIZER;CN="Cystinosis Network Europe":MAILTO:denise.dunne@cystinosis-europe.eu
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20200325
DTEND;VALUE=DATE:20200330
DTSTAMP:20260403T213833
CREATED:20190911T155801Z
LAST-MODIFIED:20200320T001329Z
UID:1697-1585094400-1585526399@cystinosis.org
SUMMARY:National Kidney Foundation (NKF) Spring Clinical Meeting
DESCRIPTION:*Update* March 10\, 2020 \nOver the weekend\, the Centers for Disease Control and Prevention (CDC) updated its recommendations for older adults and people with kidney disease or other severe chronic medical conditions. They note that these groups appear to be at higher risk for experiencing more serious COVID-19 illness. Out of an abundance of caution to protect your health\, and the health of the patients you care for\, NKF is changing the NKF 2020 Spring Clinical Meetings (SCM) to a Live-Virtual Meeting.   \nAdditional information on the logistics for live-virtual participation will be provided. Because the NKF is providing the conference as a live-virtual meeting\, no general registration fees will be waived.  However\, attendees who purchased lunch workshops or pre-conference course tickets will be reimbursed\, please look for additional information on this over the coming weeks. \n  \n 
URL:https://cystinosis.org/event/national-kidney-foundation-nkf-spring-clinical-meeting/
LOCATION:LA\, United States
CATEGORIES:Gatherings/Conferences
ORGANIZER;CN="NKF":MAILTO:clinicalmeetings@kidney.org
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20200321T160000
DTEND;TZID=UTC:20200321T173000
DTSTAMP:20260403T213833
CREATED:20200317T212213Z
LAST-MODIFIED:20200319T190233Z
UID:2378-1584806400-1584811800@cystinosis.org
SUMMARY:Cystinosis Sessions: Coronavirus\, Medication
DESCRIPTION:Welcome to Cystinosis Sessions\, a series created by the Adult Leadership Advisory Board (ALAB). These video conferences aim to help adults living with cystinosis and hope to inform stakeholders beyond our patient community about life with this rare disease. \nYou are invited to ALAB’s very first video conference – Saturday\, March 21 at 4pm ET.\nTopic: Medication ***UPDATE*** Given the current Coronavirus/COVID-19 climate\, we are adding time to discuss questions and concerns with the ALAB team and Registered Nurse and mom of 2 with cystinosis: Anna Pruitt. \nBelow you will find a draft agenda and Zoom (video conference provider) log in instructions. Please download Zoom prior to the 4pm ET start time. We hope to see you then! \nDraft Agenda: \n\nCoronavirus/COVID-19\nProcysbi: Advantages & Disadvantages\nMedicine containers\nTravel tips/hospital visits with Procysbi\, Cystagon and/or eyedrops (Cystaran)\nMedication odor tips\nPersonal experiences (time permitting)\n\nDownloading Zoom/Video Conference Prep \n\nSecure access to a mobile device (PC\, Apple\, Android)\, desktop or laptop computer\nEnsure reliable internet connection\nDownload Zoom Cloud Meetings here or through your device’s app store\nClick on the link https://zoom.us/j/2663523786\nHave the Meeting ID ready: 266 352 3786. If you use the link provided\, the meeting ID is not needed.\n\nJoin Zoom Meeting\nhttps://zoom.us/j/2663523786\nMeeting ID: 266 352 3786 \nOne tap mobile\n+16465588656\,\,2663523786# US (New York)\n+16699009128\,\,2663523786# US (San Jose) \nDial by your location\n+1 646 558 8656 US (New York)\n+1 669 900 9128 US (San Jose)\nMeeting ID: 266 352 3786\nFind your local number: https://zoom.us/u/a9v2YRNtU
URL:https://cystinosis.org/event/cystinosis-sessions-medication/
CATEGORIES:Gatherings/Conferences
ATTACH;FMTTYPE=image/png:https://cystinosis.org/wp-content/uploads/2020/03/Logo_Header.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20200229
DTEND;VALUE=DATE:20200301
DTSTAMP:20260403T213833
CREATED:20200218T151504Z
LAST-MODIFIED:20200220T161841Z
UID:2358-1582934400-1583020799@cystinosis.org
SUMMARY:Podcast: Staying Positive while living with Cystinosis
DESCRIPTION:Welcome to our podcast series – Cystinosis Rare: A Journey into the Unknown. \nLead by the Adult Leadership Advisory Board (ALAB)\, this series will focus on issues specific to our rare disease. \nThe initial podcast episode launches on Rare Disease Day – February 29\, 2020. \nThis episode focuses on positive aspects and inspiring stories of adults living with cystinosis. There will be two featured guests: William Brink and Shannon Keizer. William (Bill) will discuss his journey and how his brother inspired him to start weightlifting. Shannon will share her experience from overcoming low mental health to working towards a nursing degree. \nALAB hosts will be Jana Healy\, Sara Healy\, Steve Scheudler\, and Cheryl Simoens. All four are adults living with cystinosis. \nThe episode will be approximately 1 hour in length. \nSubscribe to our YouTube page and receive an email alert when the podcast is available: http://bit.ly/2Y28tsx on Saturday\, February 29th. We hope you tune in!
URL:https://cystinosis.org/event/podcast-staying-positive-while-living-with-cystinosis/
CATEGORIES:Gatherings/Conferences
ATTACH;FMTTYPE=image/png:https://cystinosis.org/wp-content/uploads/2020/02/Website_Header.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20191203
DTEND;VALUE=DATE:20191204
DTSTAMP:20260403T213833
CREATED:20191120T162128Z
LAST-MODIFIED:20191222T124032Z
UID:2254-1575331200-1575417599@cystinosis.org
SUMMARY:Giving Tuesday
DESCRIPTION:The CRN is a proud participant in Giving Tuesday – a global movement encouraging people to “do good.” This is our fifth year celebrating the event that has inspired millions to give\, collaborate\, and celebrate generosity. The Tuesday after U.S. Thanksgiving has been designated as the global day for giving back. It was created in response to the shopping frenzy surrounding Black Friday and Cyber Monday. \nHere’s a glimpse of the overall impact from 2018’s Giving Tuesday: \n\n150+ countries participated\n110+ community coalitions involved\n$440M+ dollars raised online\n\nGiving Tuesday – December 3rd\, 2019 \n#GreatGivers Campaign \nThis year we’ve asked community members to reflect on those who’ve helped along the cystinosis journey. Leading up to Giving Tuesday\, we are sharing some of those experiences to recognize the sacrifice\, generosity\, and selflessness many of us have been fortunate to benefit from. A nod to those #GreatGivers. Click on their stories below. \n\nAna\nCheryl\nGail\nIna\nJana\nJenn\nSara\nSteve\n\nWays to Help  \nYour online donation will benefit our cystinosis community as we continue to provide grassroots research\, meaningful support and educational programs. However\, there are many ways to “give” beyond monetary donations. Visit our How to Help page. \nUPDATE: Our #GreatGivers campaign surpassed an online fundraising goal of $5\,000! \nA special thank you to each person who has supported the CRN in our quest for improved treatments and ultimately\, a cure for cystinosis. \nHappy Holidays!
URL:https://cystinosis.org/event/giving-tuesday/
CATEGORIES:Fundraising Events
ATTACH;FMTTYPE=image/jpeg:https://cystinosis.org/wp-content/uploads/2019/11/GivingTues2019.jpg
ORGANIZER;CN="Cystinosis Research Network":MAILTO:info@cystinosis.org
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20191105
DTEND;VALUE=DATE:20191111
DTSTAMP:20260403T213833
CREATED:20190910T194605Z
LAST-MODIFIED:20190910T194605Z
UID:1688-1572912000-1573430399@cystinosis.org
SUMMARY:American Society of Nephrology – Kidney Week
DESCRIPTION:CRN will join the American Society for Nephrology (ASN) and more than 13\,000 other kidney professionals from across the globe at Kidney Week 2019 in Washington\, DC. The world’s premier nephrology meeting\, Kidney Week provides participants exciting and challenging opportunities to exchange knowledge\, learn the latest scientific and medical advances\, and listen to engaging and provocative discussions with leading experts in the field.
URL:https://cystinosis.org/event/american-society-of-nephrology-kidney-week/
LOCATION:Walter E. Washington Convention Center\, Washington\, DC\, USA\, 801 Mt Vernon Pl NW\, Washington\, 20001\, United States
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20191101
DTEND;VALUE=DATE:20191104
DTSTAMP:20260403T213833
CREATED:20190911T154809Z
LAST-MODIFIED:20190911T154925Z
UID:1695-1572566400-1572825599@cystinosis.org
SUMMARY:Community Advisory Board (CAB) Meeting
DESCRIPTION:The Community Advisory Board (CAB) was created to establish a worldwide cystinosis committee under the mentorship of Eurordis\, the representative body for rare diseases in Europe. \nThe key objective of CABs is to engage with pharmaceutical companies in order to bring the patient perspective to clinical trials and other areas. \nMembers of the CAB receive extensive education and training in all aspects of clinical trials/treatment development so that they become patient experts. The Cystinosis CAB has expanded its remit to engage at all stages of research development\, including at the early research stage\, and to provide advice and the patient perspective to ensure more effective clinical trials and more efficient and speedy market access. \nMore information on CABs can be found on the EURORDIS website.
URL:https://cystinosis.org/event/community-advisory-board-cab-meeting/
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20190918
DTEND;VALUE=DATE:20190921
DTSTAMP:20260403T213833
CREATED:20190904T170703Z
LAST-MODIFIED:20190904T171910Z
UID:1676-1568764800-1569023999@cystinosis.org
SUMMARY:Global Genes: Rare Patient Advocacy Summit
DESCRIPTION:On behalf of the cystinosis community\, CRN advocates will attend this rare disease summit to absorb information on the latest therapies and research and participate in collaborative workshops. \nGlobal Genes has more information on their website and FAQs page. “As the largest gathering of rare disease patients\, caregivers\, thought leaders and other rare disease stakeholders in the world\, the RARE Patient Advocacy Summit is an unparalleled opportunity to forge meaningful connections with other rare advocates and take home actionable strategies and tools to accelerate change.” \n \nAbove: Clinton Moore (left) and Katie Morrison (right) at the 2018 Rare Patient Advocacy Summit. \n  \n  \n 
URL:https://cystinosis.org/event/global-genes-rare-patient-advocacy-summit/
LOCATION:Sheraton San Diego Hotel & Marina\, 1380 Harbor Island Drive\, San Diego\, CA\, 92101\, United States
CATEGORIES:Gatherings/Conferences
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20190909
DTEND;VALUE=DATE:20190910
DTSTAMP:20260403T213833
CREATED:20191010T153425Z
LAST-MODIFIED:20191010T153553Z
UID:2141-1567987200-1568073599@cystinosis.org
SUMMARY:Seed-Balls for Cystinosis
DESCRIPTION:(Left) Carter'(s last boat ride before G-J tube insertion. (Right) Look who turned 2!  \nOver the last few years\, Carter’s family has taken a strong interest in monarch butterflies. Post diagnosis\, Grandmom (Carrie) knew she wanted to create an event to honor his resilient spirit. To celebrate Carter’s second birthday and new found love for butterflies\, they’ve partnered with Seed-Balls. This fundraiser sells clay\, compost\, and wildflower seeds to support pollinators AND proceeds benefit the Cystinosis Research Network. \n  \nUPDATE: Seed-Balls orders are now closed. If you are still interestd in supporting Carter and the cystinosis community\, you can make a secure donation here. \nThank you for your support!
URL:https://cystinosis.org/event/seed-balls-for-cystinosis/
CATEGORIES:Fundraising Events
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20190718
DTEND;VALUE=DATE:20190721
DTSTAMP:20260403T213833
CREATED:20190124T211427Z
LAST-MODIFIED:20190711T143440Z
UID:1144-1563408000-1563667199@cystinosis.org
SUMMARY:2019 CRN Family Conference
DESCRIPTION:Ring in the future with us at the 2019 Family Conference. The weekend is filled with research updates from clinicians and international cystinosis organizations\, opportunities to meet and renew friendships\, participate in studies\, and interact with expert health care professionals. Browse the draft agenda here. \nThe 2019 Family Conference is July 18 – 20\, 2019 at the Hilton Philadelphia at Penn’s Landing. The Hilton Philadelphia at Penn’s Landing is the only hotel on Philadelphia’s beautiful waterfront in the historic district. They offer an indoor pool\, lobby bar\, 24-hour coffee shop and waterfront dining at Keating’s Rope & Anchor\, Bar + Kitchen. Walk to Philadelphia attractions including the Liberty Bell\, Independence Hall\, Museum of the American Revolution and Blue Cross Riverrink Summerfest. For more information on the hotel please visit their website.
URL:https://cystinosis.org/event/2019-crn-family-conference/
LOCATION:Hilton at Penns Landing\, 201 South Christopher Columbus Blvd\, Philadelphia\, PA\, 19106
CATEGORIES:Gatherings/Conferences
ATTACH;FMTTYPE=image/jpeg:https://cystinosis.org/wp-content/uploads/2019/01/Design-41.jpeg
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20190507
DTEND;VALUE=DATE:20190508
DTSTAMP:20260403T213833
CREATED:20190503T052931Z
LAST-MODIFIED:20190507T074552Z
UID:1594-1557187200-1557273599@cystinosis.org
SUMMARY:Cystinosis Awareness Day 2019
DESCRIPTION:
URL:https://cystinosis.org/event/cystinosis-awareness-day-2019/
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20190504T120000
DTEND;TZID=UTC:20190505T120000
DTSTAMP:20260403T213833
CREATED:20190417T185926Z
LAST-MODIFIED:20190503T184057Z
UID:1532-1556971200-1557057600@cystinosis.org
SUMMARY:2nd Annual 57 Miles for Cystinosis
DESCRIPTION:
URL:https://cystinosis.org/event/57-miles/
LOCATION:Sussex Central High School\, 26026 Patriots Way\, Georgetown\, DE\, 19947\, United States
CATEGORIES:Fundraising Events
ATTACH;FMTTYPE=image/png:https://cystinosis.org/wp-content/uploads/2019/04/57miles_Website.png
ORGANIZER;CN="Clinton Moore":MAILTO:Clintonmoore1@aol.com
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20190427
DTEND;VALUE=DATE:20190501
DTSTAMP:20260403T213833
CREATED:20190125T185348Z
LAST-MODIFIED:20190307T173615Z
UID:1166-1556323200-1556668799@cystinosis.org
SUMMARY:Pediatric Academic Societies (PAS) Annual Meeting
DESCRIPTION:The PAS Meeting brings together thousands of pediatricians and other health care providers united by a common mission: improve the health and well-being of children worldwide. \nEvery one of the top 10 children’s hospitals support the Pediatric Academic Societies (PAS) Meeting as the CRN has for years. We look forward to working with the providers and attendees once again in 2019. \nThe Patient Congress is focused on incorporating the patient voice across the entire product lifecycle. This international gathering includes researchers\, academics\, as well as clinical care providers and community practitioners. Presentations cover issues of interest to generalists as well as topics critical to a wide array of specialty and sub-specialty areas. \nEVENT INFORMATION \n\nRegister via the PAS website\nView the PAS Program\nIf you are interested in becoming involved in cystinosis advocacy and awareness\, contact Aimee at adelmann.aimee@gmail.com.
URL:https://cystinosis.org/event/pediatric-academic-societies-pas-annual-meeting/
LOCATION:Baltimore Convention Center
ATTACH;FMTTYPE=image/jpeg:https://cystinosis.org/wp-content/uploads/2019/01/Design-34.jpeg
END:VEVENT
END:VCALENDAR