Zhino Maanavi’s Post

Epilepsy is a scary and painful condition that people suffer from. It’s not just the person with the condition but also the family. Amyn’s condition shook the world for my whole family. All of the crying and all of the praying was worth it. To all of the families loving someone with epilepsy 💜💜💜 You are very special. We were designed to here for them. I pray for comfort and healing to the families affected by epilepsy! I would like to share two facts with you. 💜According to Healthline.com 1 in 26 ppl will develop epilepsy at some point in their lives. Doesn’t this number make it sound like globally we should be more aware of this condition. Spread awareness today! 💜1/3 of people with epilepsy experience depression and anxiety- the most common comorbidity of the disease. #nationalepilepsyawarenessweek #epilepsyawareness #epilepsy #shareinfo #amynking #statistics #numberscount #share

Join us in supporting #PurpleDay! Epilepsy affects millions worldwide. Let's raise awareness and build a more inclusive community by wearing purple and learning more about it. Our epilepsy awareness course offers comprehensive insights into epilepsy, covering its causes, symptoms, and treatments. Join us in spreading awareness and understanding of epilepsy 👇 https://ow.ly/RXkE50R0Q2L #epilepsy

Today, on International Epilepsy Day, let's shed light on the meaning, causes, prevention, and more. Let's raise awareness and support those living with epilepsy worldwide. #EpilepsyAwareness #InternationalEpilepsyDay #EndTheStigma #SupportEpilepsy #HealthAwareness

Every year March 26 is observed as the 'Purple Day For Epilepsy'💜 across the world to raise awareness around the causes, symptoms, and treatment of Epilepsy. Don't believe in the Myths, Trust in Care.💜 #WorldPurpleDay #WorldPurpleDay2024 #EpilepsyAwareness #Epilepsy #PurpleDay #Purple #EpilepsyAwarenessDay #epilepsy

Feb 12 is World Epilepsy Day. Epilepsy impacts millions but there is an huge awareness & treatment gap. There is also irrational stigma associated with it. What can you do to help ? Watch this video to learn more. www.epilepsymumbai.org.

Have you ever considered what life would be like if you were diagnosed with an untreatable condition? A condition where you've exhausted everything the NHS can provide, leaving you to suffer daily. Now imagine a new treatment is available but unattainable, a treatment your sister is able to access abroad, but unavailable to you. A treatment you've seen change your sisters life. How would that make you feel? Sisters Interrupted : A transparent and open film of the reality of living with severe treatment resistant epilepsy in the UK. If you're working in the field of epilepsy treatments we urge you to take an hour to watch. https://lnkd.in/eGu_PvBH

Infantile Spasms are characterized by sudden, repetitive movements and can be challenging to recognize. These spasms, often occurring in infants between 3 to 12 months, demand our attention and collective effort. That’s why awareness is crucial. By fostering a deeper understanding of this rare epilepsy syndrome, we pave the way for early detection and intervention. Our mission extends beyond knowledge – it’s a call to action. Let’s amplify our voices to ensure that infants affected by spasms receive timely support and medical attention. Share your stories, spread awareness, and let’s make a lasting impact on the lives of these tiny warriors and their families. 💜 #ISAW2023 #InfantileSpasmsAwareness #infantilespasms #nevergiveup #epilepsy #epilepsywarrior #epilepsyawareness #ketodiet #vnstherapy #anightforIS #purpleday #corpuscallosotomy

Learn more about our Epilepsy Deaths Register for #NationalEpilepsyWeek Every epilepsy death that is reported to the register contributes to vital research into understanding SUDEP. By learning lessons from those who have died, we hope that we can save future lives. To know more, go to: https://lnkd.in/dzRCmMC #epilepsy #SUDEP

⏰ New ToxTime Incoming! ⏰ Fetal Alcohol Spectrum Disorders are not rare. In fact, they are more prevalent than either autism or Down Syndrome, but they are rarely diagnosed, denying services to those who need them to address immediate developmental concerns and mitigate lifelong damage caused by prenatal alcohol exposure. Statistics indicate that about 5% of the population has an FASD…that’s more than one child in every classroom…but diagnoses are lagging. On Thursday, August 22 at 1 PM CT, join Guida Brown for a ToxTime presentation all about FASDs. Learn how YOU can be part of the solution for nearly four million children in the US who live with an FASD. Register now: https://zurl.co/bNZq

Embracing National Epilepsy Week from May 26th to June 2nd! Join us in spreading awareness about epilepsy, a condition characterized by unpredictable seizures. Recognizing symptoms such as sudden jerking movements, loss of awareness, or temporary confusion is key. Let's also shine a light on progress: with advancements in treatment and support, there's hope for improved management and quality of life. Together, let's raise awareness, share knowledge, and foster understanding.  Praveen Sikri , Bharat Sikri , Dr Priyanka S Wadhwa , Akanksha Singh #NationalEpilepsyWeek #EpilepsyAwareness #HopeForACure #SeizureRecognition #EpilepsySupport #EndEpilepsy #KnowTheSigns #EpilepsyCommunity #HopeForACure #EpilepsyResearch #SpreadAwareness #ikrispharmanetwork