One of the notes that inspired us to begin our Together Letters program was one received during our most recent Holiday Hands. Mom Beckie wrote about her son Wyatt, and your response to her desire for connection was overwhelming. “My 8 year old son, Wyatt, is in 2nd grade and is in an LLD classroom for learning disabilities. Over the past year, Wyatt has been struggling with anxiety and depression. Over the past couple of weeks, … he is believing that he is not a good person, worthy of love and friendship. And that there is no hope for him in this world. And that all of the confusion and frustration going on inside cannot be fixed. Would you consider writing a card or letter to Wyatt this holiday season? He needs words & prayers of truth, affirmation, love and encouragement poured into him. He is kind, thoughtful, caring, and funny. I am certain that it would lift his spirits and that Truth and Love can and WILL win in Wyatt.” As you always do, you showed up. Over 140 of you commented, saying you wanted to send love and letters to Wyatt. “I would be absolutely […]
Through your donations, Together Rising meets a variety of physical needs for members of our community. We do this both through our large fundraising events, like Love Flash Mobs and Holiday Hands, and through our year-round giving program. But for many members of this community, money can’t buy what they desperately need – emotional support from their fellow sisters and brothers lifting them up with words of encouragement. In the midst of struggle and pain and loneliness, they need to know that they are not alone. To hear others say – you got this, you are strong, you can survive this, I am here. A few years ago during Holiday Hands we started to receive requests to help meet those needs. Letters for a child who feels lonely, rejected, and sad. Notes of support for kids whose dad is battling cancer. Words of encouragement for a mama of three kiddos with special needs who feels alone. Pen pals for a lonely stay at home mom. The responses have been breathtaking. And since this need doesn’t just creep in around the holidays, Together Rising has started to post them year-round, so that we all have the opportunity […]
Janine and Maggie have been friends for 50 years. At a young age, Janine’s mom and step-dad welcomed Maggie into their family. For Maggie, the child of an alcoholic single mom, Janine’s family has continued to be her second family ever since. Maggie recently wrote to us. She explained that her “sister by life” friend, Janine, had been trying to get on her feet for some time. As life often does, she had encountered several setbacks along the way. Janine has significant learning disabilities which have made it difficult for her to secure a full-time, professional job. She works part-time at Walmart for as many hours as they’ll give her. She struggles to pay her food, car, and housing expenses. Maggie, desperate to give her friend a little breathing room, asked us for help. She said, “Janine is a kind, generous person who would give you her last dime if you asked. She could really use a break.” You sent Janine a gift to cover both her next car payment and a month’s rent. At Together Rising, we believe a little bit of room to breathe and a good friend make a world of difference. If you’d like to donate […]
Jessica and Jenn are friends that share a common bond. They each have a child with a rare disease called FPIES (Food Protein Induced Entrocolitis Syndrome). FPIES is a type of food allergy affecting the gastrointestinal tract. Classic symptoms of FPIES include profound vomiting, diarrhea, and dehydration. These symptoms can lead to severe lethargy, change in body temperature and blood pressure. Unlike typical food allergies, symptoms may not be immediate and do not show up on standard allergy tests. Jessica wrote to us specifically about Jenn’s daughter, Sarah. She said, “Sarah is 11 years old and has FPIES just like my boy Wyatt. She is also on the most severe end of the spectrum of this disease. Basically, this girl lives off of about 8 ingredients and a slew of medicine to survive. You see, when kids like my Wyatt Boy, and sweet Sarah eat food, they have vomit to shock reactions that are life threatening and very scary. They often have poor growth, and many other issues that are results of this disease. There is no cure, no reasoning to why it’s happening, and very few doctors who have even heard of it.” Jessica told us […]
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