DPO&Co. - DPO Consulting and Investing, LLC的动态

Click on the link below to join my American Heart Association Heart Walk Team!!

We are 10 days away from Expunge Colorado's 7th annual record sealing clinic! It has been 7 years of putting on a record sealing event in Denver, free to the community, where we literally change people's lives for the better. Expunge Colorado's mission is to enable people to move forward from their criminal records. We do this through our 3 pillars of service: education, advocacy and offering pro bono record sealing services. What's different about this year compared to the other years is for the first time our application for clinic opened and closed within 24 hours. Our capacity was reached in 24 hours! In 72 hours, we had 100+ people on a waitlist to be notified for the next record sealing event in 2025. This proves that our pro bono legal services for petition-based record sealing is at an all-time high. Expunge Colorado provides an essential service to people who are in need of jobs, housing and a chance to move forward with dignity from their past. We cannot do this work without the help of sponsors and donors. If you believe in criminal justice reform, reparative justice, and social equity and are in a position to donate, please consider our local 501c3 nonprofit. The funds will go towards food, supplies and the work that continues weeks after the clinic. We have a crowdsourcing campaign with a goal to reach 5K: https://lnkd.in/gqVw2Zsi I'll leave you with a few testimonials from our Intake application: “This would help me regain dignity in all aspects of my life. I just want to thank all the professionals willing to help us get our lives back!” “I really hope you can help me and i look forward to moving in a brighter future for myself and my family!” “Thank you very much for your assistance in this process.? I very much appreciate it, and it will have a dramatic impact on my life.” #ExpungeColorado #criminaljusticereform #secondchances #recordsealing #expungement #Coloradononprofit #nonprofit

Legacy Treatment Center is proud to sponsor the 2025 Recovery Open! We believe recovery is about more than healing—it’s about helping clients reconnect with adventure, sport, and community. These experiences are essential for building a sense of purpose, meaning, and belonging. At Legacy, we see firsthand how moments of connection can inspire change. Sponsoring the Recovery Open is our way of supporting the same values we encourage in our clients: finding joy, building relationships, and feeling part of something bigger. We’re honored to be part of this event, knowing that every swing, every partnership, and every moment shared brings us closer to what matters most—helping people live meaningful lives. #RecoveryOpen2025 #PurposeAndConnection #AdventureInRecovery #CommunityHealing #BackToAdventure #RecoveryThroughSport #BehavioralHealthcare #MentalHealthMatters #ConnectionIsHealing #PurposeDrivenCare #ReconnectingThroughRecovery #LegacyTreatmentCenter #HealingInAction #SportsAndRecovery #RecoveryCommunity #BuildingBrighterFutures #rxoffthecouch https://recoveryopen.com/

#SUDEPActionDay2024 1 out of every 150 people with poorly controlled seizures or epilepsy die from SUDEP. Before April 7, 2024, I was unaware of SUDEP (Sudden Unexpected Death from Epilepsy). It wasn't until my brother passed away in his sleep that we learned seizures can lead to this risk. If you know anyone with seizures or epilepsy, please inform them about SUDEP and discuss it with their neurologist. Taking proactive steps can reduce risks and potentially save lives. There are resources out there, it’s a matter of having a conversation first. While it's too late for Jaaden, we can all help others avoid a similar fate. In honor of Jaaden Steward and others who have passed from SUDEP, the Steward family will be hosting a kickball fundraising event on Nov. 16th. We invite all who can to participate. All proceeds will be donated to the Epilepsy Foundation. Information can be found on the website listed below. https://lnkd.in/ewh-Sfua

Are you familiar with Axial spondyloarthritis (axial SpA)? Most aren’t, as it works silently. Axial SpA is an inflammatory arthritis where the main symptom is back pain. It mainly affects the spine but can also affect other joints, tendons and ligaments. 1 in 200 of the adult population in the UK have axial SpA (AS). That's twice as many as multiple sclerosis and Parkinson's disease. National Axial Spondyloarthritis Society(NASS) exists to transform the diagnosis and care of people living with axial SpA. Create your own fundraiser and support here ???https://hubs.ly/Q02GkK4s0 #Fundraising #UKCharity #UKFundraising #UKNonprofit

Today is?#ClinicalTrialsDay. In a world where more and more information are, presumably, obtained through all sorts of tech solutions,?#machinelearning,?#bigdata?#AI, there is still a need for "old fashion" trials. I have seen several times before where data driven analysis do actually produce interesting hypotheses, but how can we trust them? Clinical trials quantifies the?#scientific?procedure that is needed to find out IF there actaually is a real effect or just a coincidence. Good clinical trials also requires good data handling, data manipulation, analysis plans, procedures for analysis and reporting. #statistics #science

Arjan's spirit is unstoppable. Even with bladder cancer trying to throw him off, he keeps showing up with grit and humour that remind us all what resilience really means. But here’s the deal: he’s facing some major medical bills, and this next treatment is his best shot at getting his life back. It's not a small cost, but that’s where we can come in to lift him up! What if, together, we could make this easier? Imagine Arjan, post-treatment, getting back to his friends, family, and daily life without the constant cloud of medical expenses over him. We can help make this happen by coming together. Here's how: ?? Chip in what you can! A little from everyone makes a huge difference. ?? Share his story with others who may want to help. ?? Send some positive vibes his way! Let’s get Arjan back to living his best life. For more details and to lend a hand, here’s the link --> https://lnkd.in/ez4vCZPz

Preparing for The 36th Annual Peak Challenge - Sponsor a team or sponsor a child; or both. Learn more here: https://ow.ly/Wk0050S7QV2 #peakchallenge #elevatesuccess #hikeformentalhealth #griffithcenters #hopeandhealingstartshere

For the 2nd year, I am supporting individuals and families affected by CACNA1A by participating in the 3rd Annual CACNA1A 5K Run, Walk, and Roll. This cause is near and dear to me, as our daughter Barri, has been diagnosed with this rare disorder at 13 months old. We are asking for your support by making a donation to assist with research for Barri and others affected. The CACNA1A Foundation is dedicated to improving the lives of those affected by CACNA1A-related diseases and accelerating research to find a cure. 100%of the funds go directly to the foundation! Last year we crushed our goal, and this year we hope to exceed our $7k goal! Sign-up here: https://lnkd.in/e-MXYe9p If you plan to walk with us on Sunday, May 19th at Anacostia Park- please register for the walk and order the swag bag, which contains the Tshirt we will be wearing. You can register now through may, however in order to receive the Tshirt, you must order by March 7. If you are not in the area, but still want to donate, please support by giving to my personal fundraising page: https://lnkd.in/ebQDtQxv What is CACNA1A? CACNA1A is a gene that plays a vital role in the communication between neurons in the brain. CACNA1A-related disorders are rare and lifelong conditions that affect the brain. People who have brain differences due to CACNA1A can have a wide range of symptoms or features, but they are united by the fact that their symptoms all are due to differences within the CACNA1A gene. These symptoms significantly impact the lives of the people who live with this disorder and their families. Current options for treating CACNA1A-related disorders are limited to managing and/or treating symptoms. There is no known cure for CACNA1A Why Participate? Individuals and families are affected by challenging symptoms related to CACNA1A every day, including uncontrolled seizures, hemiplegic migraines, cerebellar atrophy and more. There are very limited treatments and no cure. The clock is ticking.

The latest Spinal Network News is heading out in to the world - with a focus on the Paris Paralympics, this one is pure gold. Wondering where your copy is? It's only $30 for an annual subscription and you'll not only get three issues each year direct to your mailbox, you'll be supporting our work - win/win! If you would like to subscribe, support our mahi and get some actual mail instead of bills in your mailbox, the link is here. #nzst #sci #spinaltrustnews