What are the opening hours?

Monday 11am - 7pm Tuesday 11am - 7pm Wednesday 9am - 5pm Thursday 9am - 5pm Friday 9am - 7pm

https://www.facebook.com/100697434776323/

Power In Me Foundation, laxminagar, Delhi (2026)

11/05/2026

Beyond the Diagnosis: Building a Lifetime of Dignity 🎗️

When dealing with rare diseases like Hemophilia, medical treatment is only the beginning of the story.

At Power In Me Foundation, we believe that "management" isn't enough. A "Standard NGO Model" often focuses on short-term crisis intervention. While vital, it leaves a gap in the years that follow. What about education? What about financial independence? What about a life lived with dignity?

As part of our 'Year of Rare' 2026 initiative, we are championing a 7-Step Holistic Journey that moves from clinical care to complete social integration:

Sensitization & Pre-Counseling: Preparing families for the journey ahead.

Genetic Counseling: Deepening the understanding of impact.

Clinical Treatment: Essential factor replacement and care.

Government Advocacy: Navigating RPWD Act benefits and state support.

Education: Ensuring "Rare Warriors" never have to drop out.

Livelihood: Building skills for economic empowerment.

Longitudinal Monitoring: Preventing disability through lifelong follow-up.

We invite you to be a part of this transformation.

The transition from a "Short-Term View" to a "Holistic View" requires sustainable resources. Your support directly funds the bridge between clinical survival and a thriving life.

How you can help:

🤝 Partner with us: For CSR opportunities and strategic collaborations.

📢 Advocate: Share this post to help us reach "Rare Warriors" who need this ecosystem.

💳 Support the Cause: Scan the QR code in the image below or use the details provided to contribute to our mission.

Together, we aren't just managing diseases—we are empowering lives.

Reg. No. 1109 (Delhi/NCT) | Certifications: CSR1, 80G & 12A

HolisticHealing SocialImpact InclusionMatters

11/05/2026

✍️ Empowering the Next Generation of Indian Literature!

We are thrilled to announce the official launch of the **'Sponsor A Writer'** program by the **Power In Me Foundation**, unveiled on May 10th, 2026, at the vibrant Singrauli Open Mic.

India is brimming with untapped literary talent, but many powerful voices remain unheard due to a lack of resources and guidance. Our Pan-India initiative aims to bridge this gap by transforming your contributions into life-changing **scholarships** for deserving writers.

📖 How the Program Works
When you choose to sponsor a writer, your support provides a comprehensive ecosystem for growth:

* **Professional Mentorship:** One-on-one guidance into professional writing career.

* **Skill Enhancement:** Training in creative writing, editing, and storytelling.

* **Path to Publication:** Full support in getting their manuscript published.

* **Strategic Promotion:** Marketing and platform-building to ensure their voice reaches a global audience.

🤝 Join the Movement: Support the Arts
We invite **Individual Donors** and **Corporate Partners (CSR)** to invest in the future of Indian literature. Your donation isn't just a gift; it’s a scholarship that empowers a storyteller to change the world.

**"Every great book starts with a writer who was given a chance."**

**How to contribute:**
1. **Scan the QR code** in the image above.
2. **UPI ID:** 123612459003375@cnrb
3. **Visit our website:** www.powerinme.org

Let’s ensure that no story goes untold. Sponsor a writer today!

09/05/2026

we are thankful to Dainik Bhaskar for supporting our cause and Voices for ground level challenges for Rare diseases community. Here is the detail of our Thalassemia day Special program for Thalassemia & Hemophilia patients in Singrauli. Key issues were raised by patients & existing support programs by government were explained during this program.

You can read Article online at https://epaper.bhaskarhindi.com/c/79826335

08/05/2026

🎗️ Transforming Rare Disease Management in Singrauli: World Thalassemia Day 2026

Knowledge is the most powerful tool in managing chronic blood disorders. On World Thalassemia Day, Power In Me Foundation, in collaboration with the District Hospital Singrauli, organized a high-impact Information Sharing Session under the Madhya Pradesh Government’s ‘Rare Disease Management' initiative.
Despite the extreme heat, the spirit of the community remained unshaken. While young warriors (under 5) were advised to stay safe at home, their dedicated guardians attended to ensure no critical health information was missed.

🔑 Key Highlights from the Session:

Clinical Excellence: Dr. Rajesh Vaish (District Nodal Officer) provided a roadmap for Thalassemia & Hemophilia management, emphasizing the critical need for regular follow-ups and the utilization of UDID/Disability certifications available right here at the District Hospital.

Government Support: Bharti Singh (RBSK) detailed how the Rashtriya Bal Swasthya Karyakram covers 32 diseases for children up to 18 years. She highlighted the life-changing Bone Marrow Transplantation (BMT) initiative in association with NHM Bhopal, Medanta Gurugram, and Coal India.

Innovation & Advocacy: Our National President, Manoj Kumar Singh, shared his personal journey with severe Hemophilia. He discussed the future of treatment—from Hemlibra & Fitusuran to the global landscape of Gene Therapy.

A Regional Vision: We proposed a "Blood Disorders Association for Madhya Pradesh & Chhattisgarh" to bridge the gap between patients and doctors across state lines, ensuring seamless information sharing.

💡 The Road Ahead
The session concluded with a vibrant Q&A and the distribution of our specialized information pamphlets. Our message was clear: Awareness today leads to a healthier, independent tomorrow. From local Anganwadis to AIIMS Bhopal, the network of care is expanding.

We urge all eligible patients to expedite their document submissions for BMT and other advanced treatments. Together, we are moving from "managing" a condition to "thriving" despite it.

06/05/2026

8 मई, 2026 को विश्व थैलासीमिया दिवस पर सिंगरौली के समस्त हीमोफिलिया और थैलासीमिया के मरीज एवं उनके परिवार जन, ज़िला अस्पताल सिंगरौली ज़रूर आवें और विशेषज्ञों से जानकारी प्राप्त करें । प्रातः 11 बजे। अगर अपके जानकारी मे कोई इन बिमारी का मरीज है तो उसे ज़रूर सूचित करें और इस काम मे अपना सहयोग दें।

https://epaper.bhaskarhindi.com/c/79802470

05/05/2026

On 8th May, 2026 we are celebrating & creating awareness about Hemophilia & Thalassemia A District Hospital & Trauma Centre. Every Hemophilia patient & thalassemia patient with family is invited.

**कार्यक्रम का मुख्य उद्देश्य**
हीमोफिलिया और थैलेसीमिया आनुवंशिक बीमारियाँ हैं। जहाँ हीमोफिलिया में चोट लगने पर रक्त का थक्का नहीं जमता और जोड़ों में दर्द व सूजन (Joint Bleeding) जैसी समस्याएं होती हैं, वहीं थैलेसीमिया में शरीर में हीमोग्लोबिन की भारी कमी हो जाती है, जिससे मरीज को बार-बार रक्त चढ़ाने की आवश्यकता पड़ती है और शरीर में अत्यधिक कमजोरी व हड्डियों की विकृति जैसे लक्षण दिखाई देते हैं।
# # # **प्रमुख चर्चा के विषय**
इस जानकारीपूर्ण सत्र में प्रतिष्ठित विशेषज्ञों (Eminent Speakers) द्वारा निम्नलिखित महत्वपूर्ण विषयों पर विस्तार से जानकारी साझा की जाएगी:
* **सटीक निदान (Diagnosis) और आधुनिक उपचार:** बीमारी की जल्द पहचान और सही प्रबंधन।
* **दिव्यांगता प्रमाण पत्र (Disability Certificate):** शासन द्वारा निर्धारित प्रक्रिया और इसके लाभ।
* **दिव्यांगता पेंशन:** पात्र रोगियों के लिए आर्थिक सहायता और पेंशन योजनाओं की जानकारी।
* **बोन मैरो ट्रांसप्लांटेशन (BMT):** थैलेसीमिया के स्थाई इलाज की संभावनाओं पर चर्चा।
* **NHM-भोपाल की नई पहल:** राष्ट्रीय स्वास्थ्य मिशन (NHM), एवं RBSY मध्य प्रदेश द्वारा इन बीमारियों के लिए शुरू की गई नई सुविधाओं और सहायता कार्यक्रमों का विवरण।

Also inviting sponsors who would like to sponsor patients food/snacks packet. DM for info.

04/05/2026

Ink Your Healing: The Neuroscience of the Writing Brain ✍️🧠

Can a pen and paper actually rewire your mind? The science says yes.

At Power In Me Foundation, as part of our 'Circle of Care' and 'Year of Rare' 2026 initiatives, we are exploring the profound link between expressive writing and neurological health. Already done research highlights how reflective writing acts as a "cognitive reset" for the brain.

The Scientific Impact of Writing:

Cognitive Powerhouse: Handwriting forces summarization, leading to better data retention and enhanced working memory.
Emotional Regulation: It strengthens the Prefrontal-Amygdala connectivity, creating a functional link between logic and emotion—essential for trauma processing.

Psychological Healing: Techniques like "Affect Labeling" decrease amygdala activity (the brain's fear center) by simply naming feelings on paper.

Biological Recovery: Expressive writing is linked to lower cortisol levels and improved immune system markers, facilitating faster physical healing after trauma.

A Call to Action for CSR Partners 🤝
Mental health is the backbone of a productive society, yet it remains one of the most underserved sectors. We are looking for Corporate Social Responsibility (CSR) partners to help us scale our therapeutic writing workshops and digital mental health toolkits.

By directing your CSR funds to Power In Me Foundation, you support:

Marham - Ink Your Healing Workshops: Evidence-based writing therapy for rare disease patients and caregivers.

Cognitive Research: Continuing our study into neuroplasticity and reflective functions.
Community Reach: Bringing these low-cost, high-impact mental health tools to vulnerable populations across India.
Let’s transform "Brain Dump" into "Brain Power" together.

Invest in a future where mental equilibrium is accessible to all. Reach out to us today to discuss how your organization can drive this groundbreaking initiative.

🔗 Visit us: www.powerinme.org

📱 Scan the QR code in the image to contribute.

Reg No. 1109 under section 60 Delhi/NCT | Certifications: CSR1, 80G & 12A

03/05/2026

Who Cares for the Caregivers?

Behind every patient fighting a rare or chronic disease is a caregiver fighting a silent battle of their own.

The data is startling: 72% of caregivers report anxiety and depression, while 68.5% face PTSD symptoms. The "Diagnostic Odyssey"—marked by prolonged uncertainty and a lack of specialized knowledge—places an immense multidimensional burden on those providing care.

Breaking the Cycle of Burnout
Through the 'Circle Of Care', Power In Me Foundation is addressing this crisis head-on. We believe that to sustain the patient, we must first support the caregiver.

Our 'Year of Rare' 2026 initiative focuses on:
Respite & Support: Implementing innovative programs to reduce social isolation.
Specialized Training: Filling the 81% gap in formal training for chronic care management.

Systemic Advocacy: Pushing for financial aid and counseling to alleviate the 50% struggle with financial strain.

Mental Health Resilience: Providing genetic counseling and therapeutic pathways to manage anticipatory grief.

Your Contribution Creates the Circle
We cannot do this alone. To provide formal respite care and mental health resources for these "unsung heroes," we need your support.

How you can help:

Donate: Funds go directly toward mental health workshops and caregiver respite programs.

Partner: We are looking for corporate CSR partners to help us scale our 'Systemic Financial Aid' models.

Volunteer: Share your expertise in counseling or specialized healthcare training.

Don’t let the caregiver be the forgotten patient. Join us in building a stronger, more resilient support system. Every contribution helps turn the 'Diagnostic Odyssey' into a journey of shared strength.

🔗 Support our mission: www.powerinme.org

📱 Scan the QR code in the image to donate directly.

Power In Me Foundation | Reg No. 1109 Delhi/NCT | CSR1, 80G & 12A Certified

02/05/2026

Community is the Best Medicine: Healing Beyond the Individual

Science confirms what we’ve always felt: we aren't built to heal in isolation.

The 'Circle of Care' by Power In Me Foundation highlights a powerful truth: the "Solo Situation" isn't just lonely—it’s a physiological hazard. Chronic isolation triggers systemic inflammation and accelerates disease progression. Conversely, being part of a supportive community acts as a biological buffer, strengthening our immune systems and fostering neuroplasticity.

Why Your Support Matters
At Power In Me Foundation, we are bridging the gap between isolation and recovery. Through our 'Year of Rare' 2026 initiative, we are building infrastructure that transforms lives by:

Reducing Systemic Inflammation: Moving from high-stress "hazard" zones to supportive community circles.

Boosting Cardiovascular Health: Lowering strain and blood pressure through consistent social connection.
Enhancing Neuroplasticity: Stimulating new neural connections and oxytocin release through meaningful interaction.

Extending Longevity: Reducing cognitive decline and promoting faster recovery from mental health conditions.

Join Our Mission
Healing is a collective effort. To expand our reach and provide these vital 'Circles of Care' to those navigating their darkest hours, we need your partnership.

Your contribution directly funds:

Support group infrastructure for rare conditions and mental health.

Community-driven wellness programs and awareness workshops.

Resources for active recovery and long-term wellbeing.

Invest in the Science of Connection.

Support the Power In Me Foundation today and help us turn isolation into impact.

🔗 Donate/Partner with us: www.powerinme.org
📍 Reg No. 1109 under section 60 Delhi/NCT | Certifications: CSR1, 80G & 12A

01/05/2026

The Economic Paradox of Hemophilia: Reactive vs. Proactive Policy 🩸💼

Following up on our discussion about timely intervention, let’s look at the specific impact of policy on Hemophilia. The difference between "On-Demand" treatment and "Prophylaxis" isn't just medical—it's a massive socioeconomic divide.

The Power In Me Foundation is highlighting the "Cost-Concentration Fallacy." When government policy only reacts to pain, it inadvertently creates permanent disability.

🚫 The Reactive Cycle (On-Demand Only)
The Path: Internal bleeds → Cartilage erosion → Full joint destruction → Wheelchair dependency.

The Economic Hit: Parents must withdraw from the workforce for 24/7 care. The state faces higher lifelong costs through disability pensions and frequent surgeries.

✅ The Proactive Cycle (Prophylaxis Policy)
The Path: Early screening + preventative factor treatment = Preserved joint health.

The Economic Win: Individuals remain productive, families stay financially active, and the "Life-Course Approach" leads to significant long-term savings for the GDP.

🤝 Calling All CSR Leaders
Corporate Social Responsibility is the bridge between policy and impact. By supporting the Power In Me Foundation, your organization can:

Fund Preventative Care: Help us provide the "Factor" therapy that acts as a bridge to independence.
Support Skill Training: Ensuring those with rare conditions have the tools to remain economically active.

Drive Policy Change: Join us in advocating for Prophylaxis as the standard of care in 2026.
Investing in Prophylaxis isn't just a donation; it's an investment in a dynamic, resilient workforce. Let’s shift the narrative from "Managing Disability" to "Fostering Autonomy."

How can your CSR wing help change a life today?
📍 Donate: Scan the QR code below
📞 Collaborate: 8851537816
📱 Instagram:

SocialImpact CorporateResponsibility ProphylaxisSaveLives EconomicGrowth

30/04/2026

Early Intervention Isn’t Just Healthcare—It’s Economic Strategy 📉💡

When we ignore the early signs of progressive health conditions, we aren't just failing individuals; we are creating a cycle of "Permanent Disability" that exhausts families and strains the state.

The Power In Me Foundation highlights two very different paths for our society in 2026:

🔴 The Cost of Inaction

Progressive Decline: Manageable symptoms turn into full functional loss.

Family Dependency: Caregivers are forced out of the workforce to provide 24/7 support.

State Burden: Depleted family resources lead to high, lifelong state dependency costs.

🟢 The Power of Timely Intervention

Early Screening: Catching conditions before they escalate.

Independent Living: Maximizing personal autonomy and productivity.

Sustainable Lives: Families remain economically active, leading to significant long-term savings for the government.

The Bottom Line: Higher initial investment in rare disease support leads to a more resilient workforce and a lower societal cost.

Let's move from managing disability to fostering independence.

📍 Support the Movement: Scan the QR code in the image to donate. Companies can support through CSR funds too.

📞 Connect: 8851537816
📱 Follow:

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Monday	11am - 7pm
Tuesday	11am - 7pm
Wednesday	9am - 5pm
Thursday	9am - 5pm
Friday	9am - 7pm