Health
“My class is really excited about readathon .. They were really surprised to find out that I have MS
All the kids loved the story and reading wasn’t that important. With a pandemic, we are all very welcome to suspend our normal lives and escape into the fantasy world.
And with Annual MS Readathon In progress this month MS Ireland Adults also want to participate in the campaign. “MS Readathon is Ireland’s largest sponsored reading initiative to raise funds for key services for young readers to help people with multiple sclerosis in their communities,” he said. Ava battle, MS CEO Ireland..
“Originally Roald Dahl It has grown since 1988, and this year the economic impact of Covid-19 is expected to reduce funding revenue by 38% year-on-year. That’s why we invite “adult” readers to join us. And rediscover their love for reading. “
Last year, about 10,000 children participated in the campaign, each with an average of nine sponsors. However, this year’s health and safety guidelines require that Readathon be “rethought” and the event will be held online for the first time in 33 years.
“Our amazing new website allows kids to review and record their books, create avatars, download resources, participate in contests and win stars and prizes.” Says Battles. “All fundraising activities are done online, so you don’t have to visit other households with your dog’s ear sponsor card. Family members from remote parts of the world can now join, so go online. You can now cast much wider.
“We also decided to make it easier and faster for teachers to attend school and involve large children in the action, so adults can participate as solo leaders or as part of a team. We ask people of all ages and all reading abilities (audiobooks also work) to participate in the 2020 MS Readathon. “
Debilitate
Maggie Greene She is not only a reader and teacher, but also has MS and knows how debilitating her condition can be, so she is fully engaged in the program.
“I was diagnosed four years ago after a doctor initially thought that his nerves were trapped and experienced numbness and tingling,” he married Danny McFadden and married Abigail (10) and Connor. Says a 39-year-old who has two children. (8). “But my symptoms got worse and I felt like I was walking in the water. After being sent to an MRI, I was referred to a consultant, where I was diagnosed and took medication.”
Maggie Greene
The· Donegal The woman currently has an annual schedule to monitor her condition, but thankfully she manages well with her current treatment.
“So far, I’ve been lucky,” she says. “I was gradually regaining my senses and feeling tired, but I was able to lead a daily life. My family was wonderful and my diagnosis shocked all of us, but they all got together. Helped me – I woke up with a lot of pain, my vision was blurred, I was exhausted and I still have days to rest. At first I tended to pierce, but now it is. It turns out that does not bring me any benefit and ultimately interferes with the proper care of my children.
“But overall, my life is really good. I have two great kids, a great, supportive husband, an intimate and caring family. Teach great classes and do what you love. I’m studying, so life is good. “
Two mothers teaching senior autism spectrum disorders (ASD) classes at Letter Kenny Educate together According to the national school, MS hasn’t affected her work, but it can be a difficult day if you’re in pain. But she rarely misses a day, and her students looking forward to a reunion say they didn’t know their teacher was in that state.
“My class was really excited about the reunion and when I showed them Video I made They were really surprised to find out that I actually have an MS, as MS Ireland advertised it, “she says. “They have a lot of questions and are very enthusiastic about raising as much as possible for MS Ireland. My kids and their classes are also in attendance and I did it myself as a kid. I remember that, so I’m glad that two of them are participating this year.
“MS Ireland offers an invaluable service and requires significant funding raised by readathon to do this. It’s a very easy and fun fundraising activity to participate in, regardless of age or gender. We encourage you to pick up and read books. We hope that teachers across Ireland will join the class and school community.
“I didn’t expect MS to appear in my life. I’m very happy that MS Ireland was there when I needed it. And I’m glad that the money raised was for others who were diagnosed with MS. I know it makes it possible to be there for. “
Isolation and anxiety
While many report isolation and anxiety, Ava Battles states that pandemics have had a significant impact on people living in this condition, and delays in service and support also create additional stress. I will.
“Some community members were afraid of home health care workers bringing the virus home, which caused problems early in the pandemic,” she says. “Family Carers Ireland recently announced Caring through Covid, which has chosen to temporarily suspend support for 14% of homes that normally use home care services to reduce the risk of infection. It is a report.
“In some cases this meant that the individual did without assistance, and in other cases the family was able to support the need for care, but this puts additional strain on the family and individuals. It resulted in a loss of income for some who had to prioritize the care of their loved ones over their employment.
“Just because you have multiple sclerosis does not mean that you are susceptible to the virus, but taking certain medications or having a severe disability increases this risk and increases the risk of the community. Many of the members are advised to make cocoons. This was a problem for some people, including those who might have had to return to work in public, so they were advised by cocoons. Nevertheless, I faced the reality of returning to work to support myself and my family.
“The Covid-19 pandemic has had a huge impact on the lives of people with multiple sclerosis, but it doesn’t stop during the pandemic, so the needs of our community continue.”
About MS
– Multiple sclerosis is the most common debilitating neurological condition affecting young Irish adults.
– 9,000 people live in Ireland with this disease.
– It affects the body’s motor, sensory and cognitive functions and is usually diagnosed between the ages of 20 and 40.
– The impact of MS on individuals, their families, and communities can undermine the resilience needed to keep individuals purposeful and in control of their lives.
– Three times as many women as men are diagnosed with MS.
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