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DTSTART;VALUE=DATE:20260701
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SUMMARY:Group B Strep Support (GBSS) Awareness Month 2026
DESCRIPTION:Each July\, families\, health professionals\, and campaigners across the UK come together to raise awareness of group B Strep – a common yet often misunderstood bacterium that can have life-threatening consequences for newborns. Group B Strep Support Awareness Month is a time to educate\, empower\, and advocate for better testing\, treatment\, and understanding of this preventable infection. In 2026\, the campaign is more urgent than ever\, as families continue to push for policy change and greater public awareness. \nWhat is Group B Strep Support Awareness Month?\nThis awareness month\, led by the UK charity Group B Strep Support (GBSS)\, shines a spotlight on group B Streptococcus (GBS) – the most common cause of severe infection in newborns in the UK. It aims to educate expectant parents and health professionals about how GBS is carried\, how it can be transmitted during childbirth\, and what steps can be taken to reduce the risk. \nAwareness Month also honours the families affected by GBS and highlights the stories of those who’ve experienced loss or trauma due to late diagnosis or missed opportunities for prevention. \nWhen is Group B Strep Support Awareness Month 2026?\nGroup B Strep Support Awareness Month takes place throughout the month of July 2026. It is observed annually across the UK and supported by hospitals\, midwives\, campaigners\, and community groups. Events and campaigns run all month long\, including webinars\, fundraising efforts\, personal story sharing\, and calls for action. \nWhy Group B Strep Support Awareness Month Matters\nGroup B Strep is carried by around 1 in 4 adults\, usually harmlessly. But during childbirth\, it can be passed to babies – and in rare cases\, lead to serious complications like sepsis\, pneumonia\, or meningitis. On average\, two babies a day in the UK develop group B Strep infection. One baby a week dies\, and another is left with life-changing disability. \nWhat makes this especially heartbreaking is that most group B Strep infections are preventable. With better awareness\, routine testing\, and timely antibiotics during labour\, the risk can be significantly reduced. This month helps put that life-saving information into more hands – especially among new and expectant parents. \nHow to Get Involved in Group B Strep Support Awareness Month\nWhether you’re a parent\, health worker\, or supporter\, there are powerful ways to make a difference: \n\nLearn the Facts: Visit the GBSS website to understand what group B Strep is and how it’s prevented.\nShare Your Story: If you’ve been affected by group B Strep\, your experience could help raise awareness and save lives.\nRaise Funds: Organise a sponsored walk\, bake sale\, or community event to support GBSS’s campaigning and support work.\nCampaign for Change: Contact your MP to support routine testing for GBS during pregnancy\, or sign the latest petition.\nUse Your Platform: Share GBSS content\, infographics\, or personal messages using the campaign hashtags.\n\nHistory of Group B Strep Support Awareness Month\nThe awareness month is organised by Group B Strep Support\, founded in 1996 by Jane Plumb MBE and Robert Plumb MBE after their son Theo died from GBS infection shortly after birth. Since then\, GBSS has grown into the UK’s leading voice for group B Strep awareness\, working closely with health professionals\, researchers\, and families to improve information and change policy. \nGBSS Awareness Month was established to give greater visibility to the cause\, push for wider testing availability\, and unite people in sharing knowledge and support each July. \nNoteworthy Facts About Group B Strep\n\nGroup B Strep is the most common cause of severe infection in newborn babies in the UK.\nRoutine testing is standard in countries like the US\, Canada\, and Germany – but not yet in the UK.\nA simple ECM (enriched culture medium) test at 35–37 weeks of pregnancy can identify carriers with over 90% accuracy.\nMost babies exposed to GBS are born healthy\, but a small number develop serious infection\, often within hours of birth.\nGBSS provides free information booklets to hospitals\, clinics\, and families across the UK.\n\nHashtags\n#GBSAwarenessMonth\, #GBS2026\, #GroupBStrep\, #TestForGBS \nLinks\n\nGroup B Strep Support – Official Website\nGBSS Awareness Month Campaign Page\nGBS Testing Information
URL:https://www.awarenessdays.com/awareness-days-calendar/group-b-strep-support-gbss-awareness-month/
LOCATION:International
CATEGORIES:Health & Wellbeing Awareness
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SUMMARY:National Fragile X Awareness Month
DESCRIPTION:National Fragile X Awareness Month takes place throughout July every year\, running from 1 to 31 July 2026. The observance raises awareness of Fragile X syndrome\, the most common inherited cause of intellectual disability\, and supports the individuals and families living with the condition. It is led by the National Fragile X Foundation and marked by organisations and advocates around the world. \nWhat is National Fragile X Awareness Month?\nNational Fragile X Awareness Month is a month-long health observance dedicated to Fragile X syndrome and related FMR1 gene conditions. The National Fragile X Foundation co-ordinates the month to educate the public\, encourage early diagnosis\, raise funds for research\, and celebrate the families and carers who support loved ones with Fragile X. It builds on National Fragile X Awareness Day\, which falls on 22 July\, expanding awareness across the whole month. \nWhen is National Fragile X Awareness Month?\nNational Fragile X Awareness Month is observed every July\, running from 1 to 31 July. In 2026 it begins on Wednesday\, 1 July and ends on Friday\, 31 July. National Fragile X Awareness Day falls within the month on Wednesday\, 22 July 2026. The dates are fixed to the calendar month\, so they remain the same each year. \nWhy National Fragile X Awareness Month Matters\nFragile X syndrome is the most common inherited form of intellectual disability and the most common known single-gene cause of autism. It affects roughly 1 in 4\,000 males and 1 in 8\,000 females\, yet awareness of the condition remains low\, which can delay diagnosis and support. Raising the profile of Fragile X helps families access earlier intervention\, connects them with support networks\, and drives the research needed to improve treatments and quality of life. \nHow to Get Involved in National Fragile X Awareness Month\nThere are many meaningful ways to support the month\, whether you are personally affected or simply want to help. \n\nLearn the facts – Read up on Fragile X syndrome from trusted sources such as the National Fragile X Foundation so you can recognise the condition and share accurate information.\nWear teal – Teal is the colour associated with Fragile X awareness. Wearing it\, especially on 22 July\, helps start conversations and show solidarity.\nShare on social media – Post facts\, personal stories\, and resources to help spread awareness to people who may never have heard of the condition.\nDonate to research – Organisations such as the National Fragile X Foundation and FRAXA Research Foundation fund vital research and family support. A donation makes a direct difference.\nSupport affected families – Offer practical help\, understanding\, and inclusion to families you know who are living with Fragile X.\nAttend or host an event – Join a walk\, webinar\, or fundraiser\, or organise your own to bring your community together for the cause.\nEncourage genetic awareness – Since Fragile X is inherited\, raising awareness of genetic carrier testing can help families make informed decisions.\nAdvocate for inclusion – Champion accessible\, inclusive practices in your school\, workplace\, or community so people with Fragile X are fully supported.\n\nHistory of National Fragile X Awareness Month\nThe roots of the observance lie in advocacy work carried out in Washington\, DC at the turn of the millennium. In July 2000\, the United States Senate passed a resolution designating 22 July as National Fragile X Awareness Day\, and the following year the House of Representatives passed a resolution in support. The 106th Congress thereby gave national recognition to a condition that had previously received little public attention. \nThe campaign was driven in large part by the FRAXA Research Foundation and advocate David Busby\, a Washington lawyer whose two adult sons lived with Fragile X syndrome. His political connections and personal commitment helped secure the resolution that established the awareness day. \nThe National Fragile X Foundation later expanded the single day into a full month\, designating July as National Fragile X Awareness Month. Today the month is marked by fundraising drives\, informational events\, and community activities both in the United States and internationally\, all working to improve the lives of those affected. The broader awareness movement sits alongside related observances such as Autistic Pride Day\, reflecting the close links between Fragile X and autism. \nNoteworthy Facts About National Fragile X Awareness Month\n\nFragile X syndrome is caused by an expansion of the CGG repeat in the FMR1 gene on the X chromosome\, which silences the gene and reduces the FMRP protein needed for healthy neural connections.\nIt affects approximately 1 in 4\,000 males and 1 in 8\,000 females.\nIt is the most common known single-gene cause of autism\, accounting for an estimated 2 to 3 per cent of all autism cases.\nNational Fragile X Awareness Day was designated by the US Senate in July 2000 and falls on 22 July.\nTeal is the recognised colour of Fragile X awareness.\nBecause the condition is inherited\, multiple members of a single family can be affected or be carriers.\n\nFrequently Asked Questions\nWhat is National Fragile X Awareness Month?\nIt is a month-long observance in July that raises awareness of Fragile X syndrome\, supports affected families\, and promotes research\, co-ordinated by the National Fragile X Foundation. \nWhen is National Fragile X Awareness Month in 2026?\nIt runs throughout July\, from Wednesday\, 1 July to Friday\, 31 July 2026\, with National Fragile X Awareness Day on Wednesday\, 22 July. \nWhat is Fragile X syndrome?\nFragile X syndrome is a genetic condition caused by a change in the FMR1 gene. It is the most common inherited form of intellectual disability and the most common single-gene cause of autism\, and it can affect learning\, behaviour\, and development. \nSpread the Word\nHelp raise awareness by sharing National Fragile X Awareness Month with your friends\, family\, and followers. Use the hashtags #FragileXAwareness and #FragileXAwareness2026 on social media. The more people who understand Fragile X\, the better the support for those who live with it. \nRelated Awareness Days\n\nAutistic Pride Day – Closely linked\, since Fragile X is the most common single-gene cause of autism.\nNational NonSpeaking/Nonverbal Awareness Day – Supports people with communication differences\, including some affected by Fragile X.\nMakaton International Awareness Day – Promotes a communication system that helps many people with learning and developmental conditions.\n\nLinks\n\nVisit the National Fragile X Foundation awareness page\nExplore more awareness days at AwarenessDays.com
URL:https://www.awarenessdays.com/awareness-days-calendar/national-fragile-x-awareness-month/
LOCATION:United States\, United States
CATEGORIES:Health & Wellbeing Awareness,July Awareness Days,United States
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