<span fr-original-style="color: rgb(34, 34, 34); font-family: Roboto; font-size: 14px; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; white-space: normal; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; background-color: rgb(255, 255, 255); text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial; float: none; display: inline !important;" style="color:rgb(34, 34, 34);font-family:Roboto;font-size:14px;font-style:normal;font-variant-ligatures:normal;font-variant-caps:normal;font-weight:400;letter-spacing:normal;orphans:2;text-align:start;text-indent:0px;text-transform:none;white-space:normal;widows:2;word-spacing:0px;-webkit-text-stroke-width:0px;background-color:rgb(255, 255, 255);text-decoration-thickness:initial;text-decoration-style:initial;text-decoration-color:initial;float:none;display:inline !important;box-sizing:inherit">Please visit our full website at <a href="https://www.dylans6pdreamteam.com/" style="text-decoration-color:currentcolor;user-select:auto;box-sizing:inherit;color:inherit">https://www.dylans6pdreamteam.com/</a> for more information. <span fr-original-style="color: rgb(34, 34, 34); font-family: Roboto; font-size: 14px; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; white-space: normal; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; background-color: rgb(255, 255, 255); text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial; float: none; display: inline !important;" style="color:rgb(34, 34, 34);font-family:Roboto;font-size:14px;font-style:normal;font-variant-ligatures:normal;font-variant-caps:normal;font-weight:400;letter-spacing:normal;orphans:2;text-align:start;text-indent:0px;text-transform:none;white-space:normal;widows:2;word-spacing:0px;-webkit-text-stroke-width:0px;background-color:rgb(255, 255, 255);text-decoration-thickness:initial;text-decoration-style:initial;text-decoration-color:initial;float:none;display:inline !important;box-sizing:inherit">Dylan’s Rare Chromosome Dream Team Inc. is a tax-exempt charitable organization under Section 501 (c) (3) of the Internal Revenue Code. <span fr-original-style="color: rgb(34, 34, 34); font-family: Roboto; font-size: 14px; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; white-space: normal; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; background-color: rgb(255, 255, 255); text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial; float: none; display: inline !important;" style="color:rgb(34, 34, 34);font-family:Roboto;font-size:14px;font-style:normal;font-variant-ligatures:normal;font-variant-caps:normal;font-weight:400;letter-spacing:normal;orphans:2;text-align:start;text-indent:0px;text-transform:none;white-space:normal;widows:2;word-spacing:0px;-webkit-text-stroke-width:0px;background-color:rgb(255, 255, 255);text-decoration-thickness:initial;text-decoration-style:initial;text-decoration-color:initial;float:none;display:inline !important;box-sizing:inherit">We are raising funds to both further the research of and increase awareness of Rare Chromosome and Gene Disorders. This organization was started on behalf of Dylan Nikol. Dylan, who turned 3 in October, has a rare chromosome disorder called 6p duplication (or partial trisomy 6). Essentially instead of having 2 copies of chromosome 6, he has 2.5 copies. There's only about 50 reported cases of this, and probably only a handful of his exact duplication. Since it's so rare, there's very little out there in the literature, and a lot is unknown. At this point, he has some motor and speech delays, but overall he’s doing great with the help of Physical Therapy, Speech Therapy, and Occupational Therapy. He’s making progress everyday, and as we have learned, he just goes at his own pace. Thank you to everyone that has supported us thus far and helped to make our 1st annual fundraiser so incredibly successful! We will be hosting our 2nd annual fundraiser event on Thursday, June 19, 2025 at the Piermont in Babylon, NY. Ticket sales will open in early 2025. Stay tuned for more details.  Any size donation makes an impact, and we greatly appreciate your support!

Dear <span contenteditable="false" data-custom-variable="{{firstname}}" fr-original-class="fr-deletable styled-tag-chip" fr-original-style style="background-color:rgb(248, 248, 255);border:1px solid rgb(191, 191, 255);border-radius:4px;color:rgb(42, 42, 196);padding:1px 8px;font-size:11px;display:inline-block;margin:0px;overflow-wrap:anywhere;user-select:none;box-sizing:inherit">First name <span contenteditable="false" data-custom-variable="{{lastname}}" fr-original-class="fr-deletable styled-tag-chip" fr-original-style style="background-color:rgb(248, 248, 255);border:1px solid rgb(191, 191, 255);border-radius:4px;color:rgb(42, 42, 196);padding:1px 8px;font-size:11px;display:inline-block;margin:0px;overflow-wrap:anywhere;user-select:none;box-sizing:inherit">Last name , Thank you so much for your generous donation to Dylan’s Rare Chromosome Dream Team Inc. The two main organizations we are currently supporting are <a href="http://rarechromo.org" style="text-decoration-color:initial;user-select:auto;box-sizing:inherit">Unique </a>and <a href="http://rarediseases.org" style="text-decoration-color:initial;user-select:auto;box-sizing:inherit">NORD</a>. We are working with NORD to create a research grant specifically for rare chromosome disorders (stay tuned for more info!). Our Second Annual Fundraiser Event will be held on Thursday, June 19, 2025 at the Piermont in Babylon, NY. The event will take place from 6:30PM – 10:30PM. Be sure to mark your calendars, ticket sales will be opening very soon! Please follow and like us on social media and help spread the word to inform others about our mission! Sincerely, THANK YOU for your support!  Love,Dylan’s Rare Chromosome Dream Team <img src="https://res.cloudinary.com/hxn9dbuhd/image/upload/v1737751204/qzuxpodpufooamlrd8z5.png" style="width:100px;display:inline-block;vertical-align:bottom;margin-right:5px;margin-left:5px;text-align:center;max-width:calc(100% - 10px);position:relative;cursor:pointer;padding:0px 1px;user-select:none;box-sizing:inherit" />Dylan's Rare Chromosome Dream TeamEmail: <a href="mailto:dylans6Pdreamteam@gmail.com" style="text-decoration-color:initial;user-select:auto;box-sizing:inherit">dylans6Pdreamteam@gmail.com </a>Facebook: <a href="https://www.facebook.com/Dylans6PDreamTeam" style="text-decoration-color:initial;user-select:auto;box-sizing:inherit">@Dylans6pdreamteam</a>Instagram: <a href="https://www.instagram.com/dylans6pdreamteam/" style="text-decoration-color:initial;user-select:auto;box-sizing:inherit">@Dylans6pdreamteam</a>Website: <a href="https://www.dylans6pdreamteam.com/" style="text-decoration-color:initial;user-select:auto;box-sizing:inherit">www.dylans6Pdreamteam.com</a>

Thank you for fundraising with us this year again! Here is more information.

Please visit our full website at <a href="https://www.dylans6pdreamteam.com/">https://www.dylans6pdreamteam.com/</a> for more information. Dylan’s Rare Chromosome Dream Team Inc. is a tax-exempt charitable organization under Section 501 (c) (3) of the Internal Revenue Code. We are raising funds to both further the research of and increase awareness of Rare Chromosome and Gene Disorders. This organization was started on behalf of Dylan Nikol. Dylan, who turned 3 in October, has a rare chromosome disorder called 6p duplication (or partial trisomy 6). Essentially instead of having 2 copies of chromosome 6, he has 2.5 copies. There's only about 50 reported cases of this, and probably only a handful of his exact duplication. Since it's so rare, there's very little out there in the literature, and a lot is unknown. At this point, he has some motor and speech delays, but overall he’s doing great with the help of Physical Therapy, Speech Therapy, and Occupational Therapy. He’s making progress everyday, and as we have learned, he just goes at his own pace. Thank you to everyone that has supported us thus far and helped to make our 1st annual fundraiser so incredibly successful! We will be hosting our 2nd annual fundraiser event on Thursday, June 19, 2025 at the Piermont in Babylon, NY. Ticket sales will open in early 2025. Stay tuned for more details.  Any size donation makes an impact, and we greatly appreciate your support!

2024 Donate to Dylan's Dream Team

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Dylan’s Rare Chromosome Dream Team Inc.

### Context Profile for Dylan’s Rare Chromosome Dream Team Inc.

#### 1. Organization Mission & Cause
Dylan’s Rare Chromosome Dream Team Inc. is dedicated to raising funds and increasing awareness for rare chromosome and gene disorders, particularly focusing on the condition known as 6p duplication (or partial trisomy 6), which affects their namesake, Dylan Nikol. The organization aims to support research and provide resources for families affected by similar rare disorders, as there is limited literature and understanding of these conditions.

#### 2. Type of Activities
- **Fundraising Events**: The organization hosts annual fundraising events, with the next scheduled for June 19, 2025, at the Piermont in Babylon, NY.
- **Awareness Campaigns**: They engage in campaigns to educate the public about rare chromosome disorders.
- **Community Support**: They provide resources and support for families dealing with rare genetic conditions.

#### 3. Tone of Voice
The tone of voice used by Dylan’s Rare Chromosome Dream Team is **friendly, supportive, and inspiring**. The language is straightforward and heartfelt, aiming to connect with families and supporters on a personal level. The organization expresses gratitude and emphasizes community and progress, particularly in relation to Dylan's journey and the impact of therapies.

#### 4. Emoji Usage
The website and email communications do not prominently feature emojis. The tone remains professional and heartfelt without relying on emojis to convey emotion or engagement.

#### 5. Key Facts
- **Founding Information**: The organization was founded to support Dylan Nikol, who has a rare chromosome disorder.
- **Scale**: They have conducted at least two fundraising campaigns and have sent out 14 email campaigns.
- **Impact Metrics**: Specific metrics are not detailed on the website, but the organization emphasizes the importance of donations and community support.
- **Volunteer Information**: There is no specific information about volunteer opportunities available on the website.

#### 6. Writing Guidelines
- **Style**: Use clear, accessible language that conveys warmth and gratitude. Avoid overly technical jargon, especially when discussing medical conditions, to ensure inclusivity.
- **Structure**: Keep paragraphs short and focused. Use bullet points for lists when appropriate to enhance readability.
- **Engagement**: Incorporate personal stories or testimonials where possible to create an emotional connection with the audience.
- **Call to Action**: Always include a clear call to action, whether it’s to donate, attend an event, or share information about rare chromosome disorders.

This context profile provides a comprehensive overview of Dylan’s Rare Chromosome Dream Team Inc., enabling AI assistants to generate personalized and effective content that aligns with the organization's mission and values.

Dylan’s Rare Chromosome Dream Team Inc.

2024 Donate to Dylan's Dream Team

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