Tuesday 20 October 2015

Homoeopathy in Hemophilia

 


http://homoeopathyinhaemophilia.com/

Prof. (Dr.) Tapas Kumar Kundu

B.H.M.S (Cal), P.G.D.P.C., M.S. (Ibms)
Professor of Medicine
Motiwala Homoeopathic.Medical College and Hospital, Nashik, Maharashtra, India.
  • Recipient of Rajiv Gandhi Vidya Gold Award-2012
  • Recipient of Best Teacher Award of MUHS-2013.
Consulting Homoeopath and Psychological Counsellor
HIH Nashik (Chapter):- 1-A, Sairaj Apartment, Behind Ichchhamani Lawns, Upnagar, Nashik (Maha)- 422006, India.
Camp: - First Sunday of Every Month
Time: - 10 a.m. – 2 p.m.
Cell: +91-9373908112
E-mail: dr_kundu2002@yahoo.co.in



Wednesday 14 October 2015

A Letter From A Hemophiliac: Dear Lady Gaga, I've Never Drank Blood In My Life


Broadcast Journalism Student at Hampton University

 


"I'll have a cheeseburger with a cup of blood on the side," said no hemophiliac, ever. Let me start this off by saying I am not writing out of anger or spite. During your recent interview on The Tonight Show Starring Jimmy Fallon when asked about your character on American Horror Story: Hotel, you said, "Mine in particular is a hemophiliac or "vampire," so I need to drink blood in order to survive." I understand that you meant no harm by this comment, but hear me out. I was born with this bleeding disorder and have never seen fangs in my mouth or have drank blood. I've come to understand that the only people that will truly comprehend the extent of hemophilia, are people living with it, so please don't feel singled out.
Hemophilia is a genetic disorder caused by missing or defective clotting protein within the blood. According to the US Centers for Disease Control and Prevention, Hemophilia occurs in approximately 1 in 5,000 live births. Currently, the exact number of people living with hemophilia in the US is not known. However, the CDC estimates there to be about 20,000 males with Hemophilia within the United States based on expected births and deaths since 1994. I have been an active member of the Hemophilia community for 20 years, attending conferences and seminars, and have seen zero pairs of fangs.
When we have any form of physical trauma, we have a risk of profuse internal and or external bleeding. The main medication used to treat the various forms of Hemophilia is a medication we call Factor. This medicine is administered intravenously, through a vein. My fellow hemophiliacs and I practice a routine regimen called prophylaxis, pushing us to take this medicine three times a week. Let me reiterate, we don't have to drink blood, we have to take shots of our clotting Factor, to survive.

Although our medicine is advanced today, the road to clean and reliable medicine was not easy. There was a time in which the demand for our hemophiliac product was so high it overpowered the quality of it. According to the CDC, until 1992, all factor replacement products were made from human plasma. Within B.L. Evatt's, World Federation Of Hemophilia's publication of, " The Tragic History Of Aids In The Hemophilia Population, 1982-1984," it is highlighted that our medicine was once infected with blood-borne diseases, due to unsuccessful screenings of the collected blood. This crisis unconsciously affected many innocent hemophiliacs, who wanted nothing more than to be healthy. I personally have never had a chance to meet my hemophiliac grandfather, who I was named after, because he died as a result of being effected by this crisis.

As I've said before, I'm not writing this out of anger or spite. The way Hemophilia is perpetrated within the media, school textbooks, medical world, etc. is very skewed. Gaga, I will always support you as an artist and overall person. It is understood that you spoke on Hemophilia the best way you could. Hopefully this will give you some insight to Hemophilia, our lack of fangs, and treatment for the disorder. The next time I take my clotting Factor, I'll be sure to throw my paws up.

Tuesday 6 October 2015

2015 Reno and Las Vegas Hemophilia Walks Raise Record Funds! October 5, 2015 By Mitch Truswell


Walks and 5Ks held in Reno and Las Vegas brought in a record $61,000 in donations to the Nevada Chapter of the National Hemophilia Foundation.


LAS VEGAS - Walkers and runners in Reno and Las Vegas in September raised a record amount of donations for the Nevada Chapter of the National Hemophilia Foundation, surpassing last year’s record amount.
More than $61,000 was raised through the efforts of walk participants and supporters for Nevada’s only nonprofit organization advocating on behalf of the inherited bleeding disorders community.
The majority of the funds will allow the chapter to continue efforts to send 150 kids with inherited bleeding disorders, along with their siblings, to a special medically supervised summer camp at no cost to them.
There is no cure for hemophilia or von Willebrand Disease, meaning those affected rely on life saving medicine, called factor, to prevent bleeds. While extremely effective, factor medication is expensive. The Chapter will also use walk funds to help clients without medical insurance, or without the financial ability, to get their needed medication.
“The support we continue to receive from across Nevada is absolutely humbling,” said Kelli Walters, Executive Director of the Nevada Chapter of the National Hemophilia Foundation. “We cannot continue our efforts to improve the lives of those with inherited bleeding disorders without the community’s involvement and help!”
The Reno Hemophilia Walk & 5K event was held September 12, 2015 at Virginia Lake Park. The Las Vegas Hemophilia Walk & 5K was held September 26, 2015 at Floyd Lamb Park at Tule Springs. Both walks were sponsored by the Hemophilia Treatment Center of Nevada which provides diagnosis, treatment, medical referrals and comprehensive clinics to all people with inherited bleeding and clotting disorders in Las Vegas, Reno and throughout the state. It is the only federally recognized hemophilia treatment center (HTC) in the state.

About Nevada Chapter of the National Hemophilia Foundation
NHF Nevada was founded in 1990 and helps meet the vast education and support needs of the bleeding disorders community in Nevada. There are approximately 20,000 people living with Hemophilia in the United States. It is an expensive disease where life-long management of Hemophilia places a large financial burden on individuals and families. Additionally, NHF Nevada provides services to those affected by von Willebrand disease, and clotting disorders such as Thrombophilia, which causes the blood to clot excessively. Every dollar raised at this event will help the bleeding disorder community in Nevada.
Filed Under: Press Release Wire