Introduction

The Gabriella Schopper Hungarian Lupus Group was founded by its denominator in 1993.
Gabriella Schopper had suffered from allergy since her childhood. Later she got steroids due to incipient haemophilia. She was 26 when - in the last period of her problem-free pregnancy - the illness attacked again. Gabriella was living in the United States when it was revealed after approximately one year that behind her accreting complaints there was the SLE. Following the treatments she had become asymptomatic from time to time, while later on periods being full of pains and suffering came. Her marriage got broken because of the illness and finally she made a decision to repatriates to Hungary together with her child. Her American physician recommended to establish a club since all the connection with other patients can help much with bearing the illness in an easier way. She convinced doctors to support them, sought patients, organized meetings, then finally after three years the club formed a group.
It is not an accident that the SLE (Systemic Lupus Erythematosus) patients' domestic group of interest coalesced with her name: Gabriella Schopper led the group until her death in 2006. She organized patient-appointments, conferences where specialists reported about the recent illness-related information and treatment methods. They published leaflets, worked on internet forum and website, built up connections with international organizations.
Since 10 May, 2004 has become the world-day of Lupus, the Hungarian group also connected to this international initiative. The goal of the annual world-programme is not simply the spreading of the illness-related knowledge, but the raising of the lupus-related research's financing, and providing the way to make the SLE a public health topic. We call our one-day meeting also as a family day because the illness affects the patients' close and distant relatives in an indirect way too. The Hungarian Lupus Group attended conventions of Lupus Europe several times, so the European organization of SLE patients and the host of the next congress of Lupus Europe in 2010 going to be Budapest.
Our group has doctor register, leaflet, newspaper, exclusive magazine, DVD release, we maintain good connections with other patient groups, with the media and with some pharmaceutical companies. In autumn 2007, country-wide agencies were established. They are working currently at eleven points in the country. The regional representatives' task is providing information for the patients turning to them in e-mail, through phone or personally.
After the reestablishment in 2007 - with Zoltán Purgel as chair - the work became easier. We got considerable financial support due to successful applications provided by the Ministry of Health and besides of this we could gain support from other applications, such as from little membership fees, and from the support of tax payers who are able to give 1% of their taxes to different non-profit groups like our one. Using this income one of our early dreams came true: our magazine Pillangó, our press "The Most Important Questions and Answers" could be published; and DVDs that contain lectures given by specialists.
All of the information can be found on our websites (www.sle.hu, www.lupusz.hu, www.autoimmun.hu) about the Lupus illness, affections of organs and other autoimmune diseases. All of our publications can be downloaded and viewed in electronic format. Our web page is frequently updated with latest news, information. Our forum receives several comments every day; this is the forum by which autoimmune patients can help each other. We are proud of having a web site where our members can view 30 video movies (lecture) on-line; the length of these is approximately 34 hours.
The group established an award in 2009, which got the name of our vice-chair and international contact person, Krisztina Hevér, who died of Lupus at her age of 34. Our group and the Hungarian autoimmune patients can thank her for working so much for the froup. Krisztina did much for strengthening our international relationships. She helped the Hungarian lupus patients with her civil work. Her eminent work is exemplary for everyone. To give a salute to Her memory, we prepared and published the first Krisztina Hevér Award.
Today, the chair of the group is Zoltán Purgel, vice-chairs are Henrietta Balázs and Gábor Varga. They work together with at least ten active co-operate members who help them with great enthusiasm. We do our job in a disinterested way, without any payments. Today the group has about thousand members for whom we organize patient-meetings and forums four times in a year. According to the opinion of the members, these meetings provide an excellent way for the patients to leave their living rooms, to have fun and to find friends.


Zoltan Purgel
chairman

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Mobile phone:
+36303491100

Postal address:
Magyar Lupus Egyesület
H-6635 Szegvár,
Kórógy u. 69.

My name is Zoltan Purgel.
Presently, I am the chair of the Gabriella Schopper Hungarian Lupus Group.
My illness was diagnosed in 2000. I have been the member of our association since 2002, and I have been taking an active part in the life of this group as its chair since 2007.
When my lupus was revealed, there was no Hungarian information about this disease on the Ínternet. At this time I decided to create a website where all suitable information can be found about lupus. Later on I got to know that in Hungary there was a lupus association led by Gabriella Schopper. I joined this group and I undertook some tasks, e. g. designing their website, the graphic works of their leaflets.
In 2006 I was astonished to hear that Gabriella Schopper, the founder of this group died. I did not know how this association would work on, and I did not want to let „her heritage” loosen. I tried to look for other leaders, but I had no success.
Since there was nobody who would have liked to become the head of the association, we had to congregate a general meeting in 2007 to dissolve its function. In the last moment I offered that if we joined with each other, we could save it. Fortunately, we managed to do it.
We, 12 of us have been maneging the group lately. All of us are working with no payment as a sideline.
Our common aim is to create an associartion with European standard.
 

Download document

 

Prospectus introducing 2010. - page 1.

Prospectus introducing 2010. - page 2.

Poster introducting 2010.

EULAR abstract 2009.

Hungarian survey 2008.

National poster 2008.

National report 2007.

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The Hungarian Lupus Group would be grateful for getting financial donation in order to achieve its goals. All of the offers are spent on giving information to patients (free patients' forum, its Butterfly magazine, webpage, DVDs, leaflets, posters, etc.) and on the costs of medicines for those in need of it.
Please, support the Hungarian Lupus Group by a financial donation of any amount.

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Bank Account Number (IBAN):

HU98 5720 0062 1002 7202 0000 0000

Swift / BIC code:

SZGTHUHB

Bank name:

Szegvár és Vidéke Takarékszövetkezet

Bank address:

H-6635 Szegvár, Szabadság tér 1. Hungary

Hungarian Lupus Group address:

H-6635 Szegvár, Kórógy u. 69. Hungary

 

 

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