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Senology department moves from Hôpital Erasme to Institut Jules Bordet
This women's imaging clinic will now be located in the Centre de Sénologie at the Institut Jules Bordet.  Big news: Imedia's senology clinic is moving to the Institut Jules Bordet from August 19, 2024. This women's imaging clinic will now be located in the Centre de Sénologie at the Institut Jules Bordet. Patients will benefit from new facilities. The teams at Erasme Hospital and the Institut will work together to continue to offer patients excellent care and positive, reassuring treatment.  The possibility of performing a biopsy directly after imaging remains open, for a faster diagnosis and fewer constraints for patients.If you have any questions, please contact our team on 02 555 45 34.To book a senology appointment, click here.
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In September, let's talk about blood diseases
Hematology experts from the H.U.B. are on hand to talk to patients about various blood diseases. Discover our program. Blood diseases still little known to the general public Every year thousands of people are diagnosed with a blood cancer, while the general public   often remains unaware of the different forms these cancers can take.  In September, during Blood Cancer Awareness Month, we put the spotlight on these diseases to promote increased understanding and support for persons affected. Blood diseases awareness: program at H.U.B. To increase public awareness of blood cancers, the H.U.B.’s Department of Haematology is organising a number of events throughout the month of September:  On Friday 6, 13 and 20 September: Join us on for seminars dedicated to patients and their families. An opportunity to talk to haematology experts   and to better understand the implications of blood cancers. On 18 September: a giant red blood cell will be displayed in the lobby of the Jules Bordet Institute. Come and discover this interactive and educational installation and gain a better understanding of how red blood cells work and the vital role they play in our body.   From 9 to 30 September: the "Blood for 100" exhibition which highlights diversity and the importance of giving blood for treating patients with blood diseases and for helping achieve progress in research. Discover the exhibition at the Erasmus Hospital between 19 and 25 September and then between 25 and 30 September at the Jules Bordet Institute. A project organised in cooperation with the Red Cross and Abbvie.   On 29 September, teams from the Queen Fabiola University Children's Hospital (HUDERF) will be taking part in the “Run to Kick”, a solidarity race organized in Brussels to support research into pediatric cancer. The event will bring together thousands of participants, including HUDERF's “Wakili” team of doctors, nurses, psychologists and other healthcare professionals. By running, the “Wakili” team aims not only to support its young patients, but also to raise public awareness of the importance of pediatric cancer research.  Expertise in Haematology at H.U.B Our mission is to provide specialised and personalised care for each patient. To discover our specialities and our care units in:General Haematology (Erasme), click here.Haemato-Oncology (Jules Bordet Institute), click here.paediatric haemato-oncology (HUDERF), click here.If you do not yet have a precise diagnosis you can make an appointment with general haematology after which you will be directed to one of our experts 
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Services
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Sharing data and file access
If you want to share your medical data and access your file. The hospital is a member of the Brussels Health Network, an information sharing network that links up all Brussels and Belgian hospitals with GPs and brings together certain medical records. By agreeing to share the file on your child you allow doctors to have immediate access to his or her medical records and to ensure a quality follow up. For all information about access to your health data, visit: MaSanté.be. If you are already a member of the network, you can consult your medical records or the medical records of your underage child at any time by connecting to the same platform.  Visit MaSanté.be Discover the Brussels Health Network
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Shops / cafés
The Erasmus Hospital has many shops, cafés  and restaurants: On floor -1 (route 701), a self-service restaurant is open on every working day between 11.30 am and 2 pm. On the hospital ground floor you will find a florist, bookshop, travel agency and restaurant-caterer. In the shopping arcade there is a bookshop with a BPost service, a supermarket, a perfumery, a drugstore, a chocolate shop, a mutual health insurance agency, a clothes shop, a copy shop with telecom services, a restaurant-caterer and several snack bars and bakeries.  The Erasmus Hospital has many shops, cafés and restaurants:
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SICKEL CELL DISEASE AWARNESS DAY
JUNE 19, 2024 | 12:00 PM - 2:00 PM H.U.B is proud to support the SICKEL CELL DISEASE AWARNESS DAY On this occasion, we are pleased to present: The first unit for adolescent and adult hospitalization Videos and testimonials An overview of the latest innovations for this rare disease Join us on June 19 at 12:00 PM at Auditorium Tagnon The presentation will be followed by a luncheon cocktail Registration Open Date and Time: June 19, 2024, beginning at 12 pm Location: Tagnon Auditorium, Jules Bordet Institute (H.U.B) Address: Rue Meylemeersch 90, 1070 Brussels The session will conclude with a networking luncheon. For further details, please contact us via email at secretariat [dot] hematologie [at] hubruxelles [dot] be (secretariat[dot]hematologie[at]hubruxelles[dot]be)
Article
Sickle cell disease: the H.U.B is campaigning for rare blood donations and against received ideas
On the occasion of World Sickle Cell Day on 19 June, the Erasmus Hospital and the HUDERF, national and European reference centres for sickle cell disease within the Brussels University Hospital (H.U.B), are focusing on the disease. Among care staff as well as the general public, received ideas regarding this disease, its symptoms and its complications fuel a series of prejudices resulting in social exclusion as well as difficulty in stimulating the blood donations needed to transfuse these patients. In Belgium almost 90% of sickle cell disease patients require regular blood transfusions.   Sickle cell disease: combating received ideas to encourage access to specialised care Sickle cell disease is a genetic disease of the blood that affects 1 child for every 2,329 births. Particularly frequent among populations of Caribbean, African and Mediterranean origin, it is the commonest genetic disease in Belgium. It is characterised by a deformation of the red blood cells that results in severe anaemia, a local obstruction in the blood circulation and a reduction in the oxygen supply to several vital organs. A child with sickle cell disease has episodes of extreme pain, periods of acute anaemia and is much more prone to serious infections. Complications of this rare multisystemic disease can affect the brain, heart, lungs, kidneys, bones and eyes. These become established over time, increase in frequency in adulthood and have a major impact on comorbidities and mortality. Since January 2023 sickle cell disease has been one of the diseases detected by the Guthrie test in the Wallonia-Brussels Region, this making it possible to identify and treat patients at an early stage of the disease within a reference centre. Hydroxyurea, chronic transfusion and bone marrow transplants are at present the only treatments available in Belgium that modify the symptoms of the disease to reduce complications and improve the quality of life of patients. The sole curative option is to transplant stem cells (bone marrow) but its applications are limited. Two reference centres and expert professions within the H.U.B to support the sickle cell patient This rare and complex disease requires treatment at specialised centres such as the HUDERF and Erasmus Hospital, both recognised as reference centres for rare diseases of the red blood cell at national and European level since 2017. More than a third of patients on the sickle cell disease register in Belgium are being followed up by the H.U.B for the treatment by multidisciplinary teams of the various aspects of this disease. Our haematologists are central to the clinical biological follow-up, treatment and prevention of complications. The referring nurses, essential links in ensuring awareness and an effective response to a patient's needs, coordinate the care and the professionals who provide it. Our biologists play a major role in screening and boosting awareness of the risk of transmission to children. Finally, our psychologists, dietitians and social workers pay special attention to pain management, emotional support, well-being and diet. For children and adolescents, supporting the child in his or her psychological, social, school and family reality is a central element of care in encouraging the development of autonomy despite the illness as well as adherence to treatment and knowledge of the disease. It is essential to help the child to acquire the awareness and know-how to continue to look after themselves throughout their life, with the solid support of medical teams in an adult environment. Rare blood donation and the search for new drugs are the top priorities Most sickle cell patients will need a blood transfusion at some point. Some of them will need regular transfusions throughout their life. Hence the supply problems. The transfused blood must match as closely as possible that of the sickle cell patients who have blood groups that can be rare in Belgium. At present we regularly face shortages and that is particularly true for the blood groups found predominantly among non-Caucasian populations. Treating sickle cell patents is a daily battle and it is essential to continue research into developing new treatments. A number of clinical trials involving medicines are proposed for both adults and children and especially in the field of cell therapy, with gene therapy a promising avenue for curing rare diseases of the red blood cell. Make a blood donation To assist sickle cell patients, a campaign for rare blood donations focusing on sickle cell disease is being launched by our teams within the hospital and on social networks. To give blood, please go to the Erasmus Hospital Blood Donation Centre or donate via any Red Cross blood donation center. Save the date! Festival Drépanocyt’OSE from 17 to 19 June at Tour & Taxis During the weekend of 17 June 2023, associations active in the field of combating sickle cell disease are organising a festival to increase public awareness of the disease. Experts from the Erasmus Hospital and the Children's Hospital will also be there to represent professionals from the H.U.B. Saturday 18 June from 1 pm to 5 pm at our stand at Tour et Taxis Monday 19 June, World Sickle Cell Day, during the conference at Tour & Taxis For more information: https://www.festival-drepanocytose.com