US$1,158.00Donated So Far
I am raising funds for my son Rayce Low, 12 years old, who has been unable to walk since December 2022.
On that fateful day of 18th April 2018, our family received the heart-wrenching news that our only beloved child, Rayce, a vibrant and lively young boy had been diagnosed with Duchenne Muscular Dystrophy (DMD) at the tender age of seven. DMD is a degenerative muscle-wasting disease for which there is currently no cure. A diagnosis of DMD typically means being confined to a wheelchair by the early teen years, eventually leading to the inability to breathe independently, experiencing problems with the heart, and ultimately having a much shorter life span.
The news of Rayce's diagnosis shattered our family's world. Each day is a battle to hide our own tears and fears from Rayce, who remains blissfully unaware of the severity of his condition. Our hearts bleed as we face the prospect of our once vibrant child being confined to a wheelchair, robbed of his ability to walk and play freely.
Since Rayce's diagnosis in 2018, our family has been on a challenging journey to ensure he receives the best treatments and therapies available. These treatments have not only helped him stay mobile but have also had a positive impact on his heart, lungs, and overall well-being. We have spared no effort in providing him with every opportunity to live a healthy and fulfilling life. Some of the treatments and therapies we've pursued include Nutrient and supplement support, Healthy wave mats (with far infrared, pemf, etc.), Traditional Chinese Medicine (TCM), Physiotherapy, Aqua Therapy, Traditional Chinese Massage, Nature’s Frequencies Patches and Earthing card, Stem Cell Therapy (signaling proteins), Reltec machine therapy, Neufit machine therapy, Energy lights, Peptide therapy and so on.
These interventions have been vital in alleviating Rayce's symptoms and improving his quality of life. Despite our unwavering dedication, the financial burden of these treatments is immense. While there have been advancements in research and therapies, DMD remains a challenging condition with no known cure to date. Hence, ongoing expenses associated with Rayce's care continue to mount.
Rayce's diagnosis caught us blindsided but our family resolves solidified. We are determined to provide Rayce with every possible chance for a better future. The road ahead is uncertain. The challenges are daunting. To slow down the progression of the disease, we embark on a multifaceted approach, combining traditional and non-traditional treatments. Our quest for holistic care led us to explore natural nutrition and therapies that could potentially ease Rayce's journey.
All the treatments that we have done have exerted a very significant financial strain on our family. The costs associated with DMD treatment, especially when considering potential future breakthroughs like Gene therapies, can be overwhelming. Our family is determined to ensure he does not miss out on life-altering treatments due to financial constraints. We hope to secure the necessary resources to give Rayce the best possible chances for a brighter future.
How Can You Help
Your contribution can make a significant difference in Rayce’s life. It can provide the financial support required for his ongoing treatments. Every small effort counts, and together, we can give Rayce the hope and strength to slow down the progression of the disease.
We invite you to join us in this journey of hope by making a donation. Your generosity will be a lifeline for Rayce and his family.
Spread the Word
If you are unable to contribute financially, you can still help by sharing Rayce's story within your network. Your reach and connections might bring more compassionate souls into this mission of hope.
Let's stand together, extend our hearts, and show Rayce that he is not alone in this battle. Your support can bring A Ray of Hope to a young life.
Thank you once more from the bottom of our hearts.
Your kindness matters.
The Low Family
我正在为我 12 岁的儿子卢乐峻筹款，他自 2022 年 12 月开始，无法自主站立行走。
2018 年 4 月 18 日那个决定命运的日子，我们全家收到了令人心痛的消息：我们唯一心爱的孩子乐峻，一个充满活力、活泼的小男孩，在七岁时被诊断出患有杜氏肌营养不良症 (DMD)。 DMD 是一种退化性肌肉消耗性疾病，目前尚无治愈方法。 DMD 的诊断通常意味着在青少年时期就被限制在轮椅上，最终导致无法独立呼吸和出现心脏问题，并最终导致寿命大大缩短。
乐峻确诊的消息震惊了我们一家人。 每一天都是一场向乐峻隐藏自己的眼泪和恐惧的战斗，而乐峻仍然快乐地没有意识到自己病情的严重性。 当我们想到将面对曾经充满活力的孩子被限制在轮椅上，剥夺了他自由行走和玩耍的能力时，我们的心在淌血。
自 2018 年，乐峻确诊以来，我们一家人一直在经历充满挑战的旅程，以确保他得到最好的治疗和疗法。 这些治疗不仅帮助他保持活动能力，还对他的心脏、肺部和整体健康产生了积极影响。 我们不遗余力地为他提供一切机会，让他过上健康和充实的生活。 我们尝试着一切我们所能接触到的治疗方法，包括营养和维生素、健康波垫 (远红外线、脉冲电磁场等）、中医（TCM）、物理疗法、水上物理疗法、中医推拿和拉筋、自然频率贴片和接地卡(Earthing card)， 干细胞疗法(信号蛋白Signaling proteins）、Reltec 机器疗法、Neufit 机器疗法、能量灯和肽疗法 (Peptide therapy) , 等等。
这些治疗措施对于延缓乐峻的症状和改善他的生活质量至关重要。 尽管我们坚定不移地付出，但这些治疗的经济负担是巨大的。 尽管研究和治疗方面取得了进展，但 DMD 仍然是一种具有挑战性的疾病，迄今为止尚无已知的治愈方法。 因此，与乐峻的护理相关的持续费用继续增加。
乐峻的诊断让我们措手不及，但我们家人的决心更加坚定。 我们决心为乐峻提供一切可能的机会，创造更美好的未来。 前方的道路充满不确定性， 挑战是艰巨的。 为了减缓疾病的进展，我们采取多方面的方法，结合传统和非传统治疗。 我们对整体护理的追求促使我们探索天然营养和疗法，以期能缓解乐峻的症状。
我们所做的所有治疗都给我们的家庭带来了非常大的经济压力。 与 DMD 治疗相关的费用是巨大的，尤其是考虑到基因疗法等未来潜在的突破。 我们的家人为了要确保乐峻不会因我们的经济困难而错过改变生命的治疗。 我们希望获得必要的资源，为乐峻提供最好的机会，创造更光明的未来。
您的贡献可以给乐峻的生活带来重大改变。 它可以为他正在进行的治疗提供所需的经济支持。 每一个小小的投入和努力都很重要，只要我们齐心协力，就能给乐峻带来希望和力量，延缓他的疾病的恶化。
- POI SZE TAN
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