Latest news with #MND
Straits Times
an hour ago
- Politics
- Straits Times
Two new town councils formed in Jalan Kayu, Punggol after GE2025, total 19 TCs
Two new town councils formed in Jalan Kayu, Punggol after GE2025, total 19 TCs SINGAPORE – Two new town councils have been formed in Jalan Kayu and Punggol after the 2025 general election. The Ministry of National Development (MND) issued an order under the Town Councils Act on May 30 to put into effect the formation of a total of 19 town councils, which were set up at the requests of the MPs. There were 17 town councils previously. The Jalan Kayu town council will comprise only the single member constituency that was won by PAP's Ng Chee Meng at the recent polls against the Workers' Party's Andre Low. Mr Ng will chair the town council. The Punggol town council covers the corresponding group member constituency. The last time a town council was formed with just one SMC was after the 2011 general election when Potong Pasir was won back by PAP candidate Sitoh Yih Pin from the Singapore People's Party. Goh Yan Han is political correspondent at The Straits Times. She writes Unpacked, a weekly newsletter on Singapore politics and policy. Join ST's WhatsApp Channel and get the latest news and must-reads.
Time of India
a day ago
- Politics
- Time of India
China ramps up naval incursions around Taiwan
Taiwan's Ministry of National Defense (MND) on Thursday reported Chinese military presence around Taiwan, with eight vessels from the People's Liberation Army Navy (PLAN), and one official ship detected operating in the region. The MND did not detect any flight operations by the PLA during this timeframe. In a post on X, the MND said, "8 PLAN ships and 1 official ship operating around Taiwan were detected as of 6 a.m. (UTC+8) today. Illustration of flight path is not provided due to no PLA aircraft operating around Taiwan were detected during this timeframe." by Taboola by Taboola Sponsored Links Sponsored Links Promoted Links Promoted Links You May Like One of the Most Successful Investors of All Time, Warren Buffett, Recommends: 5 Books for Turning... Blinkist: Warren Buffett's Reading List Click Here Undo "At 01:31 (UTC+8) today, China launched satellites from XSLC, with the flight path over central Taiwan toward the Western Pacific. The altitude is beyond the atmosphere, posing no threat. ROC Armed Forces monitored the process and remain ready to respond accordingly," Taiwan's MND added. — MoNDefense (@MoNDefense) Live Events Earlier on Wednesday, MND reported a military presence around Taiwan, with 31 aircraft from the People's Liberation Army (PLA), nine vessels from the People's Liberation Army Navy (PLAN), and one official ship detected operating in the region. Sharing a post on X, MND wrote, "31 PLA aircraft, 9 PLAN vessels and 1 official ship operating around Taiwan were detected up until 6 a.m. (UTC+8) today. 22 sorties crossed the median line and entered Taiwan's northern, central, southwestern and eastern ADIZ. We have monitored the situation and responded." — MoNDefense (@MoNDefense) Meanwhile, Taiwan's Mainland Affairs Council (MAC) criticised China on Wednesday for organising two summits for Taiwanese participants later this week, claiming these gatherings aim to "lecture" rather than promote authentic exchanges across the Taiwan Strait, as reported by Focus Taiwan. The MAC stated that the upcoming summits are "conducted under the guise of cultural and media exchanges aimed at summoning Taiwanese media and cultural figures to Beijing for lecturing and instruction." The council emphasised that these events do not embody the essence of true cross-strait cultural and educational exchanges and are "not supported by the Taiwanese government". The council remarked that the Chinese Communist Party's (CCP) utilisation of various forms of exchanges as tools for united front work does little to bridge differences across the Taiwan Strait and will not earn the acceptance of Taiwanese society, as highlighted by the Focus Taiwan report.
Scoop
a day ago
- Health
- Scoop
National Campaign Returns This June—Raising Awareness And Support For New Zealanders Living With Motor Neurone Disease
Press Release – Motor Neurone Disease Association NZ Throughout June, the campaign will spotlight real stories from people living with MND and their whnau highlighting the urgency of timely equipment, the emotional and physical load carried by carers, and the courage of those navigating the unknown. Motor Neurone Disease NZ is calling on New Zealanders to tip a bucket or pour a brew this June — and join the movement to make time count for those living with motor neurone disease (MND). MND Action Month 2025 brings together two powerful fundraising strands — the iconic Ice Bucket Challenge and the heartfelt Cuppa Tea for MND. Together, they shine a light on the daily realities of life with MND, a rapidly progressing and terminal condition that affects more than 400 people across Aotearoa at any given time. 'Motor neurone disease turns life upside down — not just for the person diagnosed, but for everyone around them,' says Mark Leggett, Chief Executive of Motor Neurone Disease NZ. 'This June, we're asking people to take action. Whether you tip a bucket or pour a cuppa, your support helps people with MND access the care, support, equipment, and connection they urgently need — and brings hope to everyone affected.' Throughout June, the campaign will spotlight real stories from people living with MND and their whānau — highlighting the urgency of timely equipment, the emotional and physical load carried by carers, and the courage of those navigating the unknown. The Ice Bucket Challenge injects energy and visibility — challenging participants to take the plunge in support of people facing even colder truths: system delays, limited access to care, and inconsistent support.1 Meanwhile, the Cuppa Tea for MND strand invites reflection, connection, and conversation — a moment to honour someone you love, share their story, and support the journey. All funds raised during MND Action Month will support Motor Neurone Disease NZ's vital work — including support services, advocacy, information provision, and research. 'Behind every statistic is a person, a whānau, a community,' says Leggett. 'We can't yet stop the disease, but we can change the experience of living with it. That's what MND Action Month is all about.' New Zealand has one of the highest incidence rates of MND in the world — and while its causes remain unknown, the need for action is clear. To get involved, register your event, or make a donation, visit Join the movement: #MNDActionMonth | #TipOrPour | #IceBucketChallenge | #CuppaTeaforMND Notes: About MND • Motor neurone disease (MND) is a fatal, rapidly progressing neurodegenerative disease that robs people of their ability to move, talk, and eventually breathe. • Often known as amyotrophic lateral sclerosis (ALS) or Lou Gehrig's disease, MND is a group of conditions, with ALS being by far the most significant proportion. All have roughly the same pathway and always the same outcome. • Little is understood about the causes of MND. There are currently very few treatment options available, and no cure. • The average life expectancy is two to three years after diagnosis. Around 50% of people die within 30 months of symptom onset, and only about 20% survive longer than five years. • Around 400 people are living with MND in NZ at any given time, with on average two people dying each week and two people receiving a diagnosis. • The incidence rate of MND in NZ is higher than the rest of the world – researchers are trying to find out why, so we can change it. • MND can affect adults at any age, though most diagnoses occur after the age of 40, with the highest incidence between 50 and 70. About MND NZ • Motor Neurone Disease NZ is the only charity focused on improving the quality of life, funding research and campaigning for people affected by MND in NZ. • We provide personal, wraparound support through our nationwide team of community based Support Advisors — travelling alongside people with MND and their whānau from diagnosis onwards.2 • Our mission is to make time count — because for people with MND and their loved ones, time is precious. • We focus on five key areas: • Support – emotional and practical help tailored to each person's needs. • Advocacy – championing timely and equitable access to care and support. • Education – providing clear, relevant, plain-language information to individuals, families, and health professionals. • Research – funding New Zealand-based studies and connecting to global developments. • Awareness – sharing real stories from the MND community to build understanding and empathy. • We receive minimal government funding and rely on donations, grants, and community fundraising to deliver our vital services.
Time of India
a day ago
- Politics
- Time of India
KN Puttegowda, Bengaluru civic agency's legal bulwark for 40 years, dies
Bengaluru: Senior advocate KN Puttegowda, the man behind BBMP's successful legal defence of public assets worth crores, passed away at his Bengaluru residence after a long battle with motor neuron disease (MND). Tired of too many ads? go ad free now He was 69. As per his wishes, his family has decided to donate his body to Adichunchanagiri Hospital for medical research and to aid the visually impaired. For nearly four decades, Puttegowda was BBMP's legal bulwark, handling over 8,000 cases since 1986, many involving high-stakes public interest litigations and lake encroachments. His courtroom advocacy helped BBMP retain key parcels of land across Bengaluru, including the Dasarahalli Lake near Magadi Road (now Dr Ambedkar Stadium), 8 acres in Milk Colony (Malleswaram), Byrasandra Lake, and open spaces at BTM Layout and Coffee Board Layout. Many of these lands were later turned into public parks. In the final chapter of his life, Puttegowda fought a different kind of battle—against silence and apathy. Diagnosed with MND in 2022, he gradually lost his ability to speak and move, surviving on supplements, round-the-clock nursing care, and Rs 2 lakh per month in medical expenses. Yet BBMP, to whom he dedicated his legal acumen for 38 years, failed to pay Rs 35 lakh in dues pending since 2014. Despite appeals to DyCM DK Shivakumar and the then BBMP chief commissioner Tushar Giri Nath, there was no response—except for a one-time Rs 10 lakh payment when he was hospitalised. Puttegowda used to charge a modest: Rs 15,000 per case, totalling Rs 35 lakh. When his health deteriorated, he appealed to the BBMP: "The govt gives Rs 25 lakh compensation to suicide victims. I protected public lands worth crores. My health declined due to overwork. Tired of too many ads? go ad free now My case deserves special consideration." A champion of public causes, Puttegowda also took bold stances outside the courtroom. In 2008, as president of the Advocates Association, he led a boycott against the chief justice of the state high court over corruption allegations—an act of rare defiance that led to the chief justice's transfer and resignation, following a Supreme Court intervention. Former law minister Suresh Kumar, his ex-classmate and close friend since 1981, recalled: "One of us became a minister, the other became the greatest advocate the city has ever seen. Bengaluru owes a great deal to him." His autobiography, Mareyuva Munna' (before forgetting), details his life's work, legal victories, and his commitment to justice. He raised his daughters with discipline and self-reliance. "Even if he gave us Rs 10, he asked for Re 1 back," said his daughter Kavya. His wife added, "We barely went on vacations. He was always working, outside home, fighting someone's battle." MSID:: 121469293 413 |
Scoop
a day ago
- Health
- Scoop
National Campaign Returns This June—Raising Awareness And Support For New Zealanders Living With Motor Neurone Disease
Motor Neurone Disease NZ is calling on New Zealanders to tip a bucket or pour a brew this June — and join the movement to make time count for those living with motor neurone disease (MND). MND Action Month 2025 brings together two powerful fundraising strands — the iconic Ice Bucket Challenge and the heartfelt Cuppa Tea for MND. Together, they shine a light on the daily realities of life with MND, a rapidly progressing and terminal condition that affects more than 400 people across Aotearoa at any given time. 'Motor neurone disease turns life upside down — not just for the person diagnosed, but for everyone around them,' says Mark Leggett, Chief Executive of Motor Neurone Disease NZ. 'This June, we're asking people to take action. Whether you tip a bucket or pour a cuppa, your support helps people with MND access the care, support, equipment, and connection they urgently need — and brings hope to everyone affected.' Throughout June, the campaign will spotlight real stories from people living with MND and their whānau — highlighting the urgency of timely equipment, the emotional and physical load carried by carers, and the courage of those navigating the unknown. The Ice Bucket Challenge injects energy and visibility — challenging participants to take the plunge in support of people facing even colder truths: system delays, limited access to care, and inconsistent support.1 Meanwhile, the Cuppa Tea for MND strand invites reflection, connection, and conversation — a moment to honour someone you love, share their story, and support the journey. All funds raised during MND Action Month will support Motor Neurone Disease NZ's vital work — including support services, advocacy, information provision, and research. 'Behind every statistic is a person, a whānau, a community,' says Leggett. 'We can't yet stop the disease, but we can change the experience of living with it. That's what MND Action Month is all about.' New Zealand has one of the highest incidence rates of MND in the world — and while its causes remain unknown, the need for action is clear. To get involved, register your event, or make a donation, visit Join the movement: #MNDActionMonth | #TipOrPour | #IceBucketChallenge | #CuppaTeaforMND Notes: About MND • Motor neurone disease (MND) is a fatal, rapidly progressing neurodegenerative disease that robs people of their ability to move, talk, and eventually breathe. • Often known as amyotrophic lateral sclerosis (ALS) or Lou Gehrig's disease, MND is a group of conditions, with ALS being by far the most significant proportion. All have roughly the same pathway and always the same outcome. • Little is understood about the causes of MND. There are currently very few treatment options available, and no cure. • The average life expectancy is two to three years after diagnosis. Around 50% of people die within 30 months of symptom onset, and only about 20% survive longer than five years. • Around 400 people are living with MND in NZ at any given time, with on average two people dying each week and two people receiving a diagnosis. • The incidence rate of MND in NZ is higher than the rest of the world - researchers are trying to find out why, so we can change it. • MND can affect adults at any age, though most diagnoses occur after the age of 40, with the highest incidence between 50 and 70. About MND NZ • Motor Neurone Disease NZ is the only charity focused on improving the quality of life, funding research and campaigning for people affected by MND in NZ. • We provide personal, wraparound support through our nationwide team of community based Support Advisors — travelling alongside people with MND and their whānau from diagnosis onwards.2 • Our mission is to make time count — because for people with MND and their loved ones, time is precious. • We focus on five key areas: • Support – emotional and practical help tailored to each person's needs. • Advocacy – championing timely and equitable access to care and support. • Education – providing clear, relevant, plain-language information to individuals, families, and health professionals. • Research – funding New Zealand-based studies and connecting to global developments. • Awareness – sharing real stories from the MND community to build understanding and empathy. • We receive minimal government funding and rely on donations, grants, and community fundraising to deliver our vital services.
