[{"id":4962,"link":"https:\/\/www.kidphysical.com\/resource\/two-angels-foundation\/","name":"two-angels-foundation","thumbnail":{"url":"https:\/\/www.kidphysical.com\/wp-content\/uploads\/2025\/11\/twoangels-logo.png","alt":""},"title":"Two Angels Foundation","postMeta":{"omnipress_post_type_fonts":["a:0:{}"],"_edit_lock":["1764547053:2"],"_thumbnail_id":["4963"],"_et_pb_use_builder":[""],"_et_pb_old_content":[""],"_et_gb_content_width":[""],"_jetpack_post_was_ever_published":[""],"footnotes":[""],"_edit_last":["2"],"resource_title":["Two Angels Foundation"],"_resource_title":["field_63be1374dcc9e"],"resource_description":["Our Reason for Being\r\nTwo Angels Foundation, Inc. was organized in the memory of Allyson and Rachel Mohatt. Both girls were diagnosed with Nemaline Myopathy, a rare form of Muscular Dystrophy. Providing them with the most normal life possible was their family\u2019s primary goal. After long, brave battles, they both passed away at the age of five. Because Allyson and Rachel touched so many lives, friends and family have come together to form the Two Angels Foundation in their memory.\r\n\r\nObtaining funding for adaptive equipment can be a financial burden for many families and in many cases is not covered by health insurance. The Two Angels Foundation will help purchase adaptive recreational equipment including bikes for children living in Colorado. Both Allyson and Rachel were able to attend their neighborhood preschools and it was a very positive experience. This was possible because of the adaptive equipment that was available to them. We want to provide similar opportunities for kids with special needs.\r\n\r\nTwo Angels: Allyson and Rachel's Story\r\nAllyson was born April 12, 1995 and appeared to be healthy and vibrant at birth. She was a dream come true for her loving family. At a two month check-up she was not physically progressing and at one year a muscle biopsy revealed Nemaline Myopathy, a rare form of Muscular Dystrophy. Since neither parent had any history of muscular disease, doctors advised that the chances of having another child with this disease were very slim. Unfortunately, that was not the case.\r\n\r\nRachel was born on April 8, 1999 and at four months old was diagnosed with the same disease. While both girls had big hearts and active minds, the disease made them extremely weak. Both girls relied on the use of special walkers and both needed custom wheelchairs. The lack of muscular development made such routine sicknesses as the common cold a life threatening ailment.\r\n\r\nThough both Allyson and Rachel had numerous hospital stays, weekly therapy sessions and scores of medical appointments, they were happy and vibrant little girls. Providing them with the most normal life possible was their family\u2019s primary goal. Both girls loved preschool and playing with other kids. After long, brave battles they both passed away at the age of 5. Because Allyson and Rachel touched so many lives, friends and family have come together to form the Two Angels Foundation.\r\n\r\nOur Mission\r\nThe mission of the Two Angels Foundation is increasing the recreational opportunities for children with physical disabilities, inspiring them to lead the most inclusive and active lives possible."],"_resource_description":["field_63be1588a0b78"],"resource_link":["https:\/\/twoangelsfoundation.org"],"_resource_link":["field_63be1406dcc9f"],"resource_image":[""],"_resource_image":["field_63be1414dcca0"],"resource_file":[""],"_resource_file":["field_63be150ea0b76"],"category":[""],"_category":["field_63be156ca0b77"],"organization":[""],"_organization":["field_63be15f7aeef7"],"featured":["0"],"_featured":["field_64360123c3257"],"_et_builder_dynamic_assets_loading_attr_threshold":["2"],"_et_dynamic_cached_shortcodes":["a:7:{i:0;s:13:\"et_pb_section\";i:1;s:9:\"et_pb_row\";i:2;s:12:\"et_pb_column\";i:10;s:12:\"et_pb_button\";i:31;s:11:\"et_pb_image\";i:39;s:16:\"et_pb_post_title\";i:50;s:10:\"et_pb_text\";}"],"_et_dynamic_cached_attributes":["a:0:{}"],"et_enqueued_post_fonts":["a:3:{s:6:\"family\";a:1:{s:11:\"et-gf-rubik\";s:104:\"Rubik:300,regular,500,600,700,800,900,300italic,italic,500italic,600italic,700italic,800italic,900italic\";}s:6:\"subset\";a:2:{i:0;s:5:\"latin\";i:1;s:9:\"latin-ext\";}s:9:\"cache_key\";s:73:\"{\"gph\":-1,\"divi\":\"4.27.5\",\"wp\":\"6.9\",\"enable_all_character_sets\":\"false\"}\";}"]},"author":{"name":"Kristy Miller","link":"https:\/\/www.kidphysical.com\/author\/kristy\/"},"date":"Nov 30, 2025","dateGMT":"2025-11-30 23:32:35","modifiedDate":"2025-11-30 16:57:30","modifiedDateGMT":"2025-11-30 23:57:30","commentCount":"0","commentStatus":"closed","categories":{"coma":"","space":""},"taxonomies":{"res_cat":"<a href='https:\/\/www.kidphysical.com\/res_cat\/community-support\/' rel='res_cat'>Community Support<\/a><a href='https:\/\/www.kidphysical.com\/res_cat\/equipment-technology\/' rel='res_cat'>Equipment & Technology<\/a><a href='https:\/\/www.kidphysical.com\/res_cat\/financial-funding\/' rel='res_cat'>Financial & Funding<\/a><a href='https:\/\/www.kidphysical.com\/res_cat\/recreation\/' rel='res_cat'>Recreation<\/a>"},"readTime":{"min":0,"sec":0},"status":"publish","excerpt":""},{"id":4942,"link":"https:\/\/www.kidphysical.com\/resource\/sharing-hunters-voice\/","name":"sharing-hunters-voice","thumbnail":{"url":"https:\/\/www.kidphysical.com\/wp-content\/uploads\/2025\/11\/Screenshot-2025-11-25-at-6.08.59-AM.png","alt":""},"title":"Sharing Hunter's Voice","postMeta":{"omnipress_post_type_fonts":["a:0:{}"],"_edit_lock":["1764076416:2"],"_thumbnail_id":["4943"],"_et_pb_use_builder":[""],"_et_pb_old_content":[""],"_et_gb_content_width":[""],"_jetpack_post_was_ever_published":[""],"footnotes":[""],"_edit_last":["2"],"resource_title":["Sharing Hunter's Voice"],"_resource_title":["field_63be1374dcc9e"],"resource_description":["MISSION\r\nSharing Hunter's Voice is a registered 501(c)3 non-profit organization that aims to help families who have been denied a Speech Generating Device (SGD) for their nonverbal children. 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Hunter would rather eat the picture or throw them around the room.  It wasn't an effective way for Hunter to communicate his wants and needs.  Hunter was having daily meltdowns that included head banging due to not being able to communicate.  Hunter continued with speech for six months, with very little progress, so the decision was made to stop outpatient speech and look into Early Intervention speech through Hunter's local county. \r\n \r\nDuring this time Hunter's mom spoke with the AAC specialist at her work about introducing a Speech Generating Device (SGD).  This speech therapist agreed it could help.  Hunter's mother began bringing home loaner devices on the weekends.  Hunter's family saw a shift in Hunter.  He was using the device to request preferred movies and snacks.  Hunter's family was seeing a decrease in his meltdowns.  Hunter's mom then requested a formal evaluation in order to submit a funding request for an SGD for Hunter.  When Hunter was 19 moths old he was approved funding, and received his device!\r\n\u200b\r\nThings didn't end there.  Through Early Intervention therapy Hunter had a few therapists who didn't understand how to use a communication device for someone that young.  Some therapists wanted Hunter to sign and ignored the device; however, due to Hunter's motor planning issues he was unable to use sign.  Another wanted his family to force Hunter's hand to use the device if they wanted him to say something.  Hunter's family believes in bodily autonomy, so this didn't work for them. Hunter was then sent Danielle.\r\n\u200b\r\nDanielle quickly gained Hunter's affection and his mother's respect.  Danielle worked hard with Hunter and his family for over a year to see his speech system grow from 15 buttons, to 42, and finally to 60.  During this time, Danielle and Hunter's mom quickly formed a bond and were able to discuss the pitfalls in the system when it comes to funding SGDs for children, especially under 3.  Hunter's mom had the idea for a non-profit and Danielle jumped on board!\r\n \r\n***\r\n\u200b\r\nWhile this is Hunter's story to getting funding approved and receiving a device, Hunter's mom, Kendra, realized this isn't everyone's story.  Due to Kendra's background as a COTA in pediatrics, she has seen first hand families be denied funding for devices for various reasons and\/or have extremely high deductibles to meet.  Danielle has also shared her own stories of client families being denied and having to find ways to give her client's voices. 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