Stop by and see us at booth 5653 to learn more about our recently launched NBX-HEK293. The first 50 people to visit the booth will receive tickets to the C14 Charity event! #BIO #BIO2024 #genetherapy #viralvectors #HEK293
NewBiologix’s Post
More Relevant Posts
-
Mark your calendars for Saturday, October 5! That is when we’ll hold our 2024 Cure the Cycle Challenge. In-person and virtual ride options available. More info coming soon. #worldbicycleday #curethecyclechallenge #curethecycle #fundraising #nucdf #nationalureacycledisordersfoundation #ureacycle #ureacycledisorders #ucdresearch #raredisease #rarediseases #metabolic #metabolicdisorder #geneticdisorder #genetic
To view or add a comment, sign in
-
⛳Case study: Nurture Fundraising Activity Year Round Scramble for Sight is an annual golf tournament, dinner and auction that has been running annually for twenty years. Scott Burt & Sherri Kroonenberg have been chairing the event since it’s inception. In that time the money raised has gone directly into research to fight blindness. Scott is happy to proclaim “We are winning”. The very first genetic treatment approved by the FDA was because of research funded by the Foundation Fighting Blindness. Vision can be restored with one injection in each eye for patients suffering blindness due to a particular gene mutation. The fight is not over though, there are still many retinal degenerative diseases that still need to be cured. The Scramble for Sight golf tournament is a one-day event starting with golfer registration, exciting tournament activities on the course then coming together for an open air dinner, silent & live auction. In 20 years the event has raised over two million dollars and even more exciting the millions has been used to fund research, treatments and cures for blindness. This year's event https://lnkd.in/eE8mHbVj With all this fundraising success Scott’s best tip for event fundraising is short on explanation but long on implementation. Nurture ALL participants in the golf tournament, doing so will multiply the efforts and amplify the message. Read case study: https://lnkd.in/egcnQ6ax #GolfTournament #GolfEvents #NonprofitGolf #FundraisingCaseStudy
To view or add a comment, sign in
-
⛳Case study: Nurture Fundraising Activity Year Round Scramble for Sight is an annual golf tournament, dinner and auction that has been running annually for twenty years. Scott Burt & Sherri Kroonenberg have been chairing the event since it’s inception. In that time the money raised has gone directly into research to fight blindness. Scott is happy to proclaim “We are winning”. The very first genetic treatment approved by the FDA was because of research funded by the Foundation Fighting Blindness. Vision can be restored with one injection in each eye for patients suffering blindness due to a particular gene mutation. The fight is not over though, there are still many retinal degenerative diseases that still need to be cured. The Scramble for Sight golf tournament is a one-day event starting with golfer registration, exciting tournament activities on the course then coming together for an open air dinner, silent & live auction. In 20 years the event has raised over two million dollars and even more exciting the millions has been used to fund research, treatments and cures for blindness. This year's event https://lnkd.in/eE8mHbVj With all this fundraising success Scott’s best tip for event fundraising is short on explanation but long on implementation. Nurture ALL participants in the golf tournament, doing so will multiply the efforts and amplify the message. Read case study: https://lnkd.in/egcnQ6ax #GolfTournament #GolfEvents #NonprofitGolf #FundraisingCaseStudy
To view or add a comment, sign in
-
Since the inception of the Mectizan Donation Program in 1987, an astounding 12 billion tablets have been generously donated for the treatment of onchocerciasis (river blindness) and lymphatic filariasis (LF). But the question remains: How do these life-changing tablets reach the hands of those who need them? It's a complex journey, orchestrated through the collaborative efforts of numerous stakeholders. From pharmaceutical companies to non-profits, governments to local communities, each plays a vital role in ensuring the success of this ambitious mission. Experience the journey through with this video from Mectizan Donation Program, as they unravel the intricate process behind getting these tablets to the heart of affected communities. They will be delving into the pillars of success for eliminating river blindness and lymphatic filariasis with Mectizan. Available in both English: bit.ly/3tnAigJ and French: bit.ly/3RspWEl 🌐 OPC's recent Oncho-FL activities in Chad (Q1 2023) and Democratic Republic of Congo (2021) have marked significant milestones in our commitment to this cause. As we reflect on these accomplishments, our eyes are set on the future, with a shared aspiration to expand our efforts and make an even greater impact. Stay tuned for insights, stories of success, and a deeper understanding of the collaborative spirit driving the fight against onchocerciasis and LF. Together, we're making strides toward a world free from the burden of these debilitating diseases. 💙 #MectizanImpact #GlobalHealth #OnchoFLElimination
To view or add a comment, sign in
-
Brain Cancer Survivor || Founder of "Hemp it Forward" || Medical Cannabis Breeder || Consultant || Speaker || linktr.ee/ccodyguy
We're not "wishing and hoping" that plant-based cannabis molecules will fight the disease when we know that our natural internal cannabis molecules perform the same actions. Because there are similar compounds, namely phytocannabinoids, that effect the same system, the endocannabinoid system, we've deemed them as "cannabimimetic." Our #501c3nonprofit #donates #hempproducts #cancerpatients #qualityoflife #casestudies #like #follow #share #subscribe #donate #GotCancer #Apply #ApplyOnline #hempitforward.org
To view or add a comment, sign in
-
Rare Disease KOL, Educator & Advocate for people with Multiple System Atrophy & Atypical Parkinson’s
DONATE TO THE MSA DRUG REPURPOSING EXPLORATORY FUND: www.defeatmsa.org/donate ~ Choose the MSA Drug Repurposing Fund - Thank You for the Donation! #defeatmsa #kickmsa #msawarriors #newdrugs #clinical #msaresearch #clinicalresearch #repurposing #drugs ~ About the Cure Parkinson’s UK iLCT Program, a pioneering drug repurposing program for Parkinson’s - explained by Dr Patrik Brundin: https://lnkd.in/gMW86-7f
To view or add a comment, sign in
-
*** Fundraising News *** Today we are highlighting Mikes bike ride for research into NF2 related Schwannomatosis (NF2). Mike is one of our trio of fundraisers who did the epic Pennine Way trek for NF2 last September and he's decided he's not resting on his laurels for too long to raise more funds this year. Mike says:- "I am aiming to raise £500 for NF2 Bio solutions UK. Their support in research for Neurofibromatosis Type 2 (NF2) is amazing. Anything we can do to aid them is certainly worthwhile. Research into finding a cure for a rare genetic condition, NF2-related schwannomatosis - NF2 for short. My reason for doing this is that In 2019, my friend Andy’s daughter Rebecca, now 35, was diagnosed with NF2. In the same year, my other friend Noel’s daughter Hayley, now 34, was diagnosed with Schwannomatosis. My ride will take me 6 days, from... Bognor to Lyndhurst Lyndhurst to Wareham Wareham to Monkton Wyld Monkton Wyld to Exeter Exeter to Launceston Launceston to Bodmin" We are delighted to have you along Mike, and we thankyou for your support. If you are able to support Mike's bike ride you can do here: https://lnkd.in/exdz8Kcm #endNF2 #NF2awareness #NF2Schwannomatosis #schwannomatosis #NF2support #nf2 #nf2family #nf2warrior #LetstalkNF2 #nf2charity #nf2cure #nf2treatment #nf2gene #nf2chromosome22 #nf2trials #nf2diagnosis #nf2lifeexpectancy #nf2prognosis #nf2research #nf2ismyteam #nf2awarenessday #nf2journey #StrongerTogetherAgainstNF2 Reading real life stories about how NF2 affects people help others to understand why we need better treatments. Please help us to make that happen by donating to research, sharing your story & raising awareness.
To view or add a comment, sign in
-
Until midday 5th December, one donation 👉 https://lnkd.in/e76aj8s4 = TWICE the impact as part of @BigGive #ChristmasChallenge Donations will help to fund #geneediting research. The ability to correct the genetic faults that lead to epidermolysis bullosa would mark a major breakthrough in progress toward permanently treating EB. #CureEB #ResearchtheCure #BigGive #EpidermolysisBullosa #GeneEditing #Research
To view or add a comment, sign in
-
Here are some common misconceptions about donating plasma — share this post if you've heard these too. ❌ Plasma donation is risky ✅ Plasma donation is low-risk to donors, comparable to blood donation ❌ Compensation encourages frequent donations, posing risks ✅ Donors follow safe donation limits set by each EU country. ❌ Compensation affects the quality of plasma ✅ Donors are verified, screened, checked & plasma is tested (RTTIs). ❌ Compensation conflicts with the voluntary unpaid donation principle ✅ EU countries vary in compensating donors; all are aligned with VUD. ❌ Compensating plasma donors reduces whole blood donation. ✅ Whole blood & plasma donors belong to separate donor groups. ❌ Plasma gathered by the public sector alone can meet patients need. ✅ 46% of EU plasma originates from the private sector in just 4 countries. Don't get caught out by misconceptions about plasma donation. 𝐊𝐞𝐲 𝐟𝐚𝐜𝐭𝐬 𝐚𝐛𝐨𝐮𝐭 𝐩𝐥𝐚𝐬𝐦𝐚 𝐝𝐨𝐧𝐚𝐭𝐢𝐨𝐧 ↳ https://lnkd.in/ePUpiQHK 𝐊𝐞𝐲 𝐟𝐚𝐜𝐭𝐬 𝐨𝐧 𝐩𝐥𝐚𝐬𝐦𝐚 𝐝𝐨𝐧𝐚𝐭𝐢𝐨𝐧 𝐚𝐧𝐝 𝐜𝐨𝐦𝐩𝐞𝐧𝐬𝐚𝐭𝐢𝐨𝐧 ↳ https://lnkd.in/ejdnTNmt 𝐏𝐫𝐢𝐯𝐚𝐭𝐞 𝐬𝐞𝐜𝐭𝐨𝐫’𝐬 𝐜𝐨𝐧𝐭𝐫𝐢𝐛𝐮𝐭𝐢𝐨𝐧 𝐭𝐨 𝐩𝐥𝐚𝐬𝐦𝐚 𝐜𝐨𝐥𝐥𝐞𝐜𝐭𝐢𝐨𝐧 𝐢𝐧 𝐭𝐡𝐞 𝐄𝐔 ↳ https://lnkd.in/e2R4z2gR #EUNeedsMorePlasma
To view or add a comment, sign in
-
🚨 Exciting News! 🚨 I am thrilled to share that I have been selected as an honoree to support the Cystic Fibrosis Foundation in their vital fundraising efforts. This opportunity means a lot to me, and I am committed to making a significant impact in the fight against cystic fibrosis. Cystic fibrosis is a life-threatening genetic disease that affects thousands of people, particularly children and young adults. The foundation's work is crucial in funding research, providing support, and improving the quality of life for those affected by this condition. Exciting Research: The Cystic Fibrosis Foundation is at the forefront of groundbreaking research into genetic mutations that cause cystic fibrosis. This research focuses on understanding these mutations and developing therapies to correct them, offering hope for better treatments and, ultimately, a cure. Your donations directly support these innovative scientific endeavors that are making real progress in the fight against cystic fibrosis. How You Can Help: 🔹 Donate: Every contribution, no matter how small, brings us one step closer to a cure. You can donate an amount of your liking. 🔹 Sponsor: There are opportunities for event sponsorships ranging from $1,000 to $7,000, which are largely tax-deductible. We are seeking sponsors for the Acadiana's Finest event taking place on July 18, 2024. 🔹 Share: Spread the word by sharing this post with your network. 🔹 Get Involved: Join me in supporting this cause by participating in events and activities organized by the foundation. Your generosity and support can make a real difference in the lives of those living with cystic fibrosis. Together, we can help ensure a brighter future for everyone impacted by this disease. Please consider donating or becoming a sponsor through the link below and be a part of this incredible journey. Thank you for your kindness and support! Donation link https://lnkd.in/gXj5VGKw Sponsorship link https://lnkd.in/gPTCKg5Q #CysticFibrosisFoundation #Fundraising #Support #Charity #GiveBack #FightCF #GeneticResearch
To view or add a comment, sign in
2,394 followers