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LAOSA Newsletter 2017

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2017 Newsletter

Contents:

  1. Presidents Letter
  2. Meet the 2017 Executive Committee
  3. AGM 2017 Highlights
  4. What’s happening at LAOSA
    • Interesting News
    • Medical Aid updates
    • Support Groups
    • AGM 2018 Planning
  5. Interesting Reading

 

2017 Membership Fees are DUE NOW *PAY R150*

LAOSA:      ABSA Acct # 9280347754       Branch Code 632005

Please send Proof of Payment to info@LAOSA.co.za

Please send email to info@laosa.co.za if you would like your Practice Website to be included on LAOSA Website   Find A Therapist Page

Please note this newsletter is available online:

http://www.laosa.co.za/

VISIT us AND “LIKE” our Facebook page on: https://www.facebook.com/LAOSA.co.za/

 

 

Dear LAOSA Members,

A warm welcome to all of our new members! The Lymphoedema Association of South Africa- LAOSA is looking ahead to the future with a focus on greater Lymphoedema Awareness. Thank you to all of the hard-working members of the Executive Committee who have worked diligently and tirelessly to move the association forward.  We have had a successful year with many projects in the works:

  • Maintaining and updating our laosa.co.za website and responding to email enquiries
  • Keeping and updating a National Practice Register of all certified Lymphoedema Therapists which is shared with Discovery and other Medical Aids
  • Attending conferences, providing FREE LAOSA informational brochures and spreading awareness about LAOSA and Lymphoedema Therapists
  • Newsletters
  • Compiling a South African Lymphoedema Consensus Document-starting with a Position Statement – still being worked on and will require a group effort
  • Your attention, support and commitment will be needed for the upcoming Provincial Therapist Support Group meetings which are planned for end of May in JHB, DBN and CT- please SEE Newsletter BELOW. The focus of meeting will be to work on completing the Position Statement so that we may publish.
  • Discussions with Medical Aids to promote better and fair reimbursement for Lymphoedema Management services in South Africa
  • Compiling questionnaires for Health Care Professionals and patients to collect much needed statistical data about Lymphoedema and awareness about treatment in South Africa
  • VISIT AND “LIKE” our Facebook page on: https://www.facebook.com/LAOSA.co.za/

 

A huge thank for the efforts and hard work of previous EXCO member who is no longer with us in South Africa – Dr Gila Nussbaum has relocated to Israel as of January 2017, as well as Carolyn Hoffman – Treasurer who stepped down in December.

As President, I plan to uphold the LAOSA Vision of “Lymphoedema Care for All”.  I would like to inspire and encourage all of our members to embrace the LAOSA Mission Statement of “To be a Collaborative Association which strives to promote quality Lymphoedema Management, Education, Awareness and Research in South Africa”. 

A multidisciplinary approach throughout South Africa is needed to spread awareness that quality care for Lymphoedema and Oedema related conditions exists.  It is our duty as the specialists in the field of Lymphoedema to share, promote and talk about this relatively unknown and under-diagnosed condition to as many people as possible.  LAOSA is here to support our member’s efforts and to positively impact the quality of lives of those affected with Lymphoedema.  We can achieve greater awareness by educating the medical community, allied health professionals and Lymphoedema patients.

As a group, we need to support each other to promote continuing education and research based therapy techniques.  We should all strive to maintain a high standard of quality care and always work in integrity whether we practice in public or private. Always aim to provide care to patients previously told that “There is nothing that can be done for your swelling condition.”

Thank you for being part of this pioneering association and playing an integral role Lymphoedema Management and Awareness in South Africa.

I look forward to collaborating with each one of you as we expand our professional community and move forward with more Lymphoedema Awareness and research into the future.

 

Warmest Regards

Suzi Davey, OTR/L, CLT-LANA, CLWT

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Meet the Executive Committee for 2017

Please welcome new members to the exco team: Erika van der Mescht, Isabeau Neethling and Maxine Blane. Please see our website for more detailed biographies, contact details and work experience. www.laosa.co.za

 

President: Suzi Davey

Occupational Therapist, based in Cape Town

ILWTI course co-ordinator and lecturer

 

 

Secretary: Nicole van Besouw

Occupational Therapist based in Cape Town

Private Practice Owner

 

 

Vice President: Candice Kuschke

Physiotherapist based in Johannesburg

Private Practice owner

 

Treasurer: Isabeau Neethling

Physiotherapist based in Cape Town

Private Practice Owner

 

Membership: Rogini Pillay

Occupational Therapist based in Cape Town

Head of Groote Schuur OT Dept.

 

 

Education and Marketing: Erika van der Mescht

Physiotherapist based in Pretoria

Private Practice Owner

 

Education and Marketing: Maxine Blane

Nursing Practitioner based in Durban

Private Practice Owner

 

2017 AGM Highlights

The 5th LAOSA AGM 2017 was held in Johannesburg from 3-4 March, at the Rosebank Union Church in Sandton. Many therapists from around the country attended, and we were lucky to have very knowledgeable speakers presenting. In attendance, we had: 9 Physiotherapists, 6 Occupational Therapists, 2 Orthotists, 6 Nurses, 1 Medical Doctor, and 7 exhibitors.

Thank you to all the Exhibitors for your support:  HiTech Therapy, BSN Medical, LEVTRADE, BL Medical, JUMLA Medical, Lymphatic Education Africa/LymphAfrica and Medis Medical.

  • Dr Sarah Nietz (Breast Surgeon) discussed the advances of Breast Surgery over the years. She also discussed the development and progress of her Breast Cancer Clinic at the Charlotte Maxeke Academic Hospital in Johannesburg, as well as statistics of breast cancer in the public sector.
  • Dr Dimitri Liakos (Plastic Surgeon) explained the various surgical options available for the treatment of lymphoedema, including microsurgery, ICG Fluoroscopy, surgical criteria and what options are available to patients in South Africa.
  • Dr Kim Lohlun (Radiation Oncologist) presented research on the incidence of Lymphoedema associated with radiation.
  • Willie Fourie (Physiotherapist) gave us a lecture and workshop in connective tissue release as well as scar tissue management with an excellent review and pictures of anatomy and fascia.
  • Jennifer Blenkinsop (Occupational Therapist) gave a very enlightening talk on medical communication and how it can affect our patient relations and treatment results.
  • Adrian Singh (Orthotist) spoke to therapists and patients on compression garments, and had some very practical tips for all to consider.
  • Suzi Davey (LAOSA President and ILWTI Education Specialist) discussed 20 Steps to Lymphoedema Risk Reduction which encouraged very interesting discussions and debate and all those present contributed some very interesting points.

 

  • We had our First LAOSA Patient Cocktail evening where Lymphoedema patients and family members were invited to attend. Exhibitors displayed different types of compression garments and treatment products that are on the market, and patients mingled with therapists and other patients. This was a very sociable evening that we really hope will grow in the future and become a highlight of the AGM. Big Thank You to Orthotist Adrian Singh who spoke to therapists and patients on compression garments and practical tips.

 

 

LAOSA continues to grow, and it was wonderful to celebrate our 5th Anniversary and NPO status.

 

                            2016 AGM in Cape Town                                   2015 AGM in Durban

What’s Happening at LAOSA

*EXCITING NEWS*

LAOSA has become a member the Cancer Alliance https://www.canceralliance.co.za/  A collective group of Cancer related NPOs and advocates working together to effect change for all South African adults and children affected by Cancer.

We have submitted the paperwork to the ILF-International Lymphoedema Framework  http://www.lympho.org/  to become a National Lymphoedema Framework in South Africa.

The ILF is well established and will be able to assist and guide LAOSA in establishing itself as a well-recognised and highly respected organisation in South Africa.  The ILF Focus Document Guidelines http://www.soffed.co.uk/lymphorg/wp-content/uploads/2016/03/Focus-Frameworks.pdf

 

 

MEDICAL AIDS UPDATE

Currently we are engaging with the Physiofocus group to try and establish what steps to take with regards to improving dialogue with the medical aids in the most effective way. LAOSA is hoping to meet with Discovery to discuss funding problems, and to present a Basket of Care (lymphoedema treatment protocol) for oncology patients with lymphoedema.   We plan to engage with other medical schemes in the near future.  We are working in collaboration with our private practice representatives at Physiofocus who have been very supportive. Unfortunately, it is a slow process, but we will have some news for all therapists soon, and any updates will be emailed to LAOSA members. Please email your medical aid problems or rejected motivation examples to Candice Kuschke: kuschkephysio@gmail.com.    If you do not have the Discovery Lymphoedema Assessment form, please see attached PDF. This is for ALL lymphoedema therapists.

 

 

SUPPORT GROUPS

LAOSA Therapists Support Group. This meeting is for all Lymphoedema Therapists contribute to the Position Statement on Lymphoedema Management in South Africa. We really need as many members of LAOSA to participate and contribute as possible.  As well, this will be your chance to voice your concerns, medical aids issues, discuss difficult cases, present new research or interesting articles and get support, recommendations about products and assistance from other skilled therapists.

PLEASE RSVP to Candice Kuschke: kuschkephysio@gmail.com  For the Johannesburg Support Group on Wed 31 May 2017 @ 18h45. Upon RSVP Email will be sent to confirm venue. 

PLEASE RSVP to Suzi Davey: info@laosa.co.za For the Cape Town Support Group on Friday 26 May 2017  @ 13h00 at  CANSA  37A Main Rd, Mowbray, Cape Town, 7700  Upon RSVP Email will be sent to confirm your attendance.   

PLEASE RSVP to Maxine Blane: max.blane@gmail.com For the Durban Support Group Meeting end of May.  Upon RSVP regarding your interest an Email will be sent to confirm Date, Time and Venue.

 

Questionnaires

We have created 2 Lymphoedema questionnaires to gather information on the prevalence of lymphoedema in SA, referral patterns and what treatment is currently available.  There is one for you as the therapist to fill in for each patient, and one for the patient to complete as well. Please keep an eye on your emails for LAOSA updates as well we will discuss at the Regional Support Group meeting.   WE NEED YOUR HELP!!!

 

 

AGM 2018

We are hoping the 2018 AGM in Durban, March 2018, will be our biggest and most exciting AGM!! The date will be finalised in the next few months. Please send us any suggestions or ideas for presentations/speakers. We will be having an event that patients are invited to attend. Please watch this space!!!

 

INTERESTING READING

Please check out the following links:

 www.laosa.co.za –please check that your details are correct and notify us of any

updates or changes on Find a Therapist Page

Visit AND “LIKE” our Facebook page on: https://www.facebook.com/LAOSA.co.za/ 

PLEASE Share with your patients and on your own Business Facebook Pages

The next BIGOSA conference will be held in Cape Town. Check their

website for updates regarding venue and dates. http://www.bigosa.co.za/conference-2017.html

 

FREE READING:

  1. Lymphatic Mapping and Preoperative imaging in the management of post-mastectomy lymphoedema: http://gs.amegroups.com/article/view/9089/9897
  2. Self-care for management of secondary lymphoedema: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898789/

LAOSA Newsletter 2016

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                                                           NEWSLETTER 2016

Dear LAOSA Members,

Welcome to all of our new LAOSA members in 2016!

I am honoured by the opportunity to lead the way forward and inspire current and future members of the Lymphoedema Association of South Africa- LAOSA. On behalf of LAOSA, I would like to express a debt of gratitude to all of the hard working members of the Executive Committee who have worked diligently to move the association forward to the point it is at today.  A huge thank you to all of the previous EXCO team- Donnee Ness, Isla Muhl, Gillian Freese, Wim de Klerk, Thea van Schoor and Jennifer Blenkinsop.  An exceptional thank you to Rogini Pillay who has been at the helm as President and Secretary over the past 4 years, tirelessly contributing her selfless time and energy to building this Association on the foundation of integrity in fulfilling the LAOSA Vision and Mission.

As President of LAOSA, it is my intention to continue the LAOSA Vision of “Lymphoedema Care for All”.  I would like to inspire and encourage all of our members to embrace the LAOSA Mission Statement of “To be a Collaborative Association which strives to promote quality Lymphoedema Management, Education, Awareness and Research in South Africa”.  We need to spread awareness that there is quality care for Lymphoedema and Oedema related conditions.  It is our duty as the specialists in the field of Lymphology to step out of our comfort zones and share information about this relatively unknown and under-diagnosed condition.  We are here to stay and to positively impact the quality of lives of those affected.  We can do this by educating the medical community, allied health professionals and Lymphoedema patients.

As a group, we need to support each other to promote continuing education and research based therapy techniques.  Through attending Lymphoedema Management Certification training, we can maintain a high standard of care and always work in integrity.  We must provide excellent care to patients previously told that “There is nothing that can be done for this swelling condition.”  Our aim should be to inspire a new generation of practitioners to follow in our footsteps.  Each one of you being part of this association is playing an integral role in pioneering Lymphoedema Management and Awareness in South Africa.  I look forward to collaborating with each one of you as we expand our professional community and move forward with more Lymphoedema Awareness into the future.

Warmest Regards,

Suzi Davey

President of LAOSA

Get to know the executive Committee of LAOSA

suziPRESIDENT

Suzi Davey

 

 

Suzi is an Occupational Therapist residing in Durbanville, Cape Town with her husband, three young children and two dogs. She has always been interested in the Lymphatic System and was working in an Outpatient Rehab department of a hospital in Miami FL when she was approached by an Oncologist to go the Lymphoedema Course and to start a Lymphoedema Program at the Hospital. As soon as she got back from the course she had a whole case load of patients scheduled and LOVED IT as she was making a difference and helping people who had been told that nothing can be done for them. Her credentials include OT HPCSA Registration Exam in South Africa (2015), Lymphoedema Certification Dr. Vodder School Intl (1998), LANA certified (2000), ILWTI Certification (2015). She started Lymphatic Education Africa in October 2015 and ran her first Course in Durban in March 2016. Her areas of expertise involve Lymphoedema, Wound Care, Elastic Taping, Lymphoedema Research, Compression Garments, Devices and Alternative Compression Products. She joined LAOSA in March 2014 as a member, was voted in for Membership at the AGM in March 2015, and Voted in as President at the AGM in 2016. Suzi says her aims for LAOSA are to lead the way forward encouraging and being an example to all members to spread awareness about Lymphoedema Therapy in South Africa.  She is busy with Lymphoedema Certification Courses for 2017 through ILWTI and is developing a course geared toward certifying therapists, nurses and doctors in the Government Healthcare System through a module course program which makes it easier for working professionals to attend. She has made lymphoedema her life’s work and loves it. When she has a rare spare moment she enjoys hiking, sushi and wine farms.
 candice

VICE PRESIDENT

Candice Kuschke

 

 

 

 

 

Candice qualified with a BSc Physiotherapy (Wits). She has also completed training as a CDT therapist (Leduc and FG MLD technique) as well as training through LTA (Lymphoedema Training Academy, UK). She resides in Johannesburg Gauteng but has lived and worked in the UK where she was given the position of Lead Oncology Physiotherapist at the BUPA Cromwell Hospital in London and attended a number of courses specialising in oncology rehabilitation and breast cancer related complications. She is a member of the SASP, British Lymphology Society, LAOSA and HPCSA. She would like to see LAOSA become a well established and recognised association in South Africa and hopes to establish a lymphoedema service in the public sector in Johannesburg. She has a special interest in complications associated with breast cancer treatment and cancer survivorship. She enjoys wild life photography, the Kruger Park and olives.

carolynTREASURER

Carolyn Hoffman

 

 

 

 

Carolyn is a Therapeutic Massage Therapist with a speciality in Lymphoedema Management (CDT trained in Australia). She is located in Claremont, Cape Town. She has been involved with LAOSA from its inception and is a Member of Massage Association of South Africa. She enjoys treating patients with lymphoedema as patients are so grateful to find somebody not only sympathetic to them but also with skills that can help them. The educational aspect is one of the main things she enjoys. She would like to see LAOSA reach a far wider proportion of health professionals and patients, as people really struggle to find suitable therapists. She would like to see more patients being referred BEFORE lymphoedema sets in, ie at-risk-patients being sent for educational purposes. She relaxes by spending time with friends and family and enjoys walking, reading and cooking.

nicoleSECRETARY

Nicole van Besouw

 

 

 

Nicole is an occupational therapist in Claremont, Cape Town. Her expertise include rehabilitation within the realm of Cancer Care/Palliative Care, Hand and Upper limb rehabilitation and Lymphoedema Management. OT philosophy remains the foundation of all her work. She hopes to contribute to the pioneering work of LAOSA in creating awareness about Lymphoedema, networking amongst interested role-players, and together with LAOSA advancing skills through professional development courses and learning from each other. She strives to deliver a holistic service combining OT principles with her Lymphoedema Skills set and hopes to continue being able to help patients who come her way. She enjoys working closely with other therapists, sharing knowledge and growing friendships.  She is a member of OTASA, and has been a member of SASHT.  She is also a member of Vascular Work/Core Group for Limb 4 Life and has been a member of LAOSA since her certification in 2013. She enjoys running the Table Mountain Trails and leisurely Saturday morning breakfasts with her husband.

roginiMEMBERSHIP

Rogini Pillay

 

 

 

Rogini’s qualifications include BSc OT 2000 (UCT), CDT 2010 (Norton School of lymphoedema therapy), MScMedSc (Rehab) 2014 (U. Stellenbosch). She has been involved with LAOSA since its inception first as secretary and then voted into the position of president (but still held secretary) and is now involved in the membership portfolio. She is based in the Western Cape and started the first Lymphoedema service in the public sector at Tygerberg Hospital and took it to Groote Schuur as well. She has already advanced LAOSA for 2016 by getting the organisation registered as an NPO. Her next mission is the SA consensus document/position paper. Provincially, she has also managed to get lymphoedema compression garments on tender.  She is passionate about treating lymphoedema as it is a much needed service, and the patients (there are many!!) seen in the public sector need effective treatment. She feels it should not only be seen as a private service. She also finds the impact effective treatment has on the patient super satisfying. She enjoys family time, reading and watching movies, although her husband is convinced she is a robot who does not know how to relax.

 

gila 

CO-OPTED MEMBER

Dr Gila Nussbaum

 

 

 

 

Gila completed her medical degree at Wits and went on to do her 2-year internship at CMJAH (Johannesburg Hospital) and her 1-year community service at Tambo Memorial Hospital. She then continued working in the public sector in the field of Emergency Medicine as well as in private for Netcare 911’s Aeromedical division. She has completed multiple Emergency Medicine related certifications. She has a qualification in Disability & Medico-legal Assessment (ABIME) and has been working for the last few years in this field. She has a personal interest in Lymphoedema with a particular focus on Primary Lymphoedemas. In May 2016 she completed the ILWTI course and qualified as a lymphoedema therapist. Her aim as a co-opted member of LAOSA is to bring a greater awareness of lymphoedema and the available treatment modalities to the medical fraternity. She would also like to provide medical support and guidance to other therapists while at the same time developing an effective referral network. She is based in Johannesburg with her husband, two young children and two cats. Her favourite past-times are cooking, baking and eating.

 

UPCOMING EVENTS
• BIGOSA (Breast Interest Group of Southern Africa) Scientific Conference, Johannesburg 21-22 October 2016. Go to BIGOSA.co.za for Registration info.
• LAOSA AGM 3, 4, 5 March 2017, to be held in Johannesburg. Venue and programme to be confirmed.
SOME INTERESTING READING
• https://www.cancer.gov/about-cancer/treatment/side-effects/lymphedema/lymphedema-pdq#section/all
• https://www.yahoo.com/news/misery-actress-kathy-bates-gets-walk-fame-star-003859943.html?utm_content=buffera8a4d&utm_medium=social&utm_source=facebook.com&utm_campaign=buffer
• http://lermagazine.com/article/lymphedema-presents-therapeutic-challenges
• http://www.lymphedemablog.com/2016/09/30/reconstructive-surgery-for-the-treatment-of-lymphedema/

Visit our Facebook page on https://www.facebook.com/LAOSA.co.za/
Or find us at www.laosa.co.za or email info@laosa.co.za
Please have a look at our brochure on the website (it is a PDF document on the about us page). The brochure is available to LAOSA members to be printed and stamped with practice details and handed out to patients.

BIGOSA- Scientific Conference Johannesburg 21-22 October 2016

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logo-u1094

PLEASE JOIN LAOSA @

The BIGOSA 2016 Scientific Meeting

 Go to BIGOSA.co.za for Registration info

ONLY R1,540.00 for BIGOSA members

ONLY R1,815.00 for NON-BIGOSA members

 

Bigosa
The Breast Interest Group of Southern Africa (BIGOSA) was formed in 2011 by a group of medical professionals who realized there was a need for standardization in breast health care in southern Africa.

Hyatt Regency

Rosebank

21 and 22 October 2016

Keynote speaker: Professor Philip M.P. Poortmans – ESTRO President and Head: Radiation Oncology, Radboud University Medical Center, Nijmegen, The Netherlands

 Registration for the 2016 BIGOSA Scientific Meeting is now open and delegates can register online with a credit card, or request an invoice. Participation in the Gala Dinner can also be booked at the time of registration.

 Click here for registration

 Please do not hesitate to contact our registration team with any queries:

Email: BIGOSA@africanagendaevents.co.za

Tel: +27 (0)21 910 1913

 Registration Fees

Late Fees (applicable after 26 August 2016)

•             Doctor (Member): R 2,200.00

•             Doctor (Non member): R 2,475.00

•             Registrar/Radiographer/Nurse/Laboratory Technician (Member): R 1,540.00

•             Registrar/Radiographer/Nurse/Laboratory Technician (Non member): R 1,815.00

The registration fees include:

• Entry to the conference, presentations and trade display area

• All lunches and refreshments

• The Gala Dinner on Friday, 21 October 2016

 

Please note that registration fees do not include accommodation or travel costs or BIGOSA membership.

Gala Dinner

DATE: Friday, 21 October

TIME: 19h00 to 22h00

DRESS: Smart casual

LOCATION: Ballroom, Hyatt Regency in Rosebank

 

Delegate: Included in registration fee

Additional Gala Dinner Ticket for a guest: R 100.00

Continuing Professional Development (CPD)

The BIGOSA 2016 Scientific Meeting has been accredited for continuing professional development points. Details thereof will follow shortly.

South African delegates are eligible for these points if they attend the conference. All registered delegates will have to sign the register and will be able to receive a Certificate of Participation at the end of the day.

REGISTRATION TERMS AND CONDITIONS

·         A completed registration will be acknowledged within seven (7) days.

·         A registration will only be valid once full payment of the amount owed is received and

          cleared.

·         All payments must be made payable to BIGOSA.

·         All fees are payable in South African Rand (ZAR) within seven (7) days of invoice.

          Any short payment resulting from bank charges and/or exchange rate fluctuations will

          be charged to the delegate.

·         All cancellations must be made and received in writing by the BIGOSA Meeting

          Secretariat.

·         Cancellation fees will be imposed as follows:

·         Cancellations received 60 days prior to the start of the Meeting (before 23 August

          2016) will receive a full refund less a 15% administration fee.

·        Cancellations received between 59 and 30 days prior to the start of the Meeting

         (before 22 September 2016) will be refunded 50% of registration fees paid; if

         registration fees are outstanding the delegate will be liable for 50% of the amount

         owed.

·        No refunds will be given for cancellations received within 30 days of the start of the

         Meeting, or for no-shows, and the delegate will be liable for full registration fees.

·        A registration is transferable to a delegate not yet registered only if the BIGOSA

         Meeting Secretariat is informed in writing at least 72 hours prior to the start of the

         Meeting.

·         A registration may not be shared, i.e. shared name tags will not be issued and name

         tags may not be shared.

 

BIGOSA- Scientific Conference Durban: 9-10 October 2015

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PLEASE JOIN US–

Donnee Ness-Vice President of LAOSA will be speaking on:

LYMPHOEDEMA-WHAT’S NEW?
By Donnee Ness
Manip. PT
MSc, CLT,VRT,CAMAG
PhD Student UKZN
Overview of presentation:
We will look at definitions of Lymphoedema, challenges with international research methodologies and subsequent variations in prevalence of the problem. I will them move to discuss some of the current work on: Fluoroscopy, Moisture meters for mid line oedema, prospective surveillance using BIS and then explore the concept of genomic expression as a tool to influence pre-morbid risk. The compelling results of Intermittent Pneumatic Compression in Lymphoedema management and finish up with sharing the results of my point prevalence study which is the first study of its kind outlining incidence of BRCA Lymphoedema  in a female breast cancer survivor population in KZN.
We hope to have a video of the talk uploaded onto the website for those not able to attend.

Bigosa
The Breast Interest Group of Southern Africa (BIGOSA) was formed in 2011 by a group of medical professionals who realized there was a need for standardization in breast health care in southern Africa.

 

THE BIGOSA 2015 ULTRASOUND WORKSHOP AND SCIENTIFIC MEETING

BIGOSA 2015 Ultrasound Workshop and Scientific Meeting
Gateway Hotel
Umhlanga, Durban
9 and 10 October 2015

PLEASE visit www.bigosa.co.za for Registration is now open, and delegates can register online

The early registration discount ended on 15 August 2015, but a discount is still offered to all BIGOSA members.

Ultrasound Workshop (9 October)

• Doctor (Member): R 2,000.00
• Doctor (Non member): R 2,250.00
• Registrar/Radiographer (Member): R 1,000.00
• Registrar/Radiographer (Non member): R 1,250.00

Scientific Meeting (10 October)

• Doctor (Member): R 1,800.00
• Doctor (Non member): R 2,050.00
• Registrar/Radiographer (Member): R 1,200.00
• Registrar/Radiographer (Non member): R 1,450.00

Ultrasound Workshop AND Scientific Meeting (9 and 10 October)

• Doctor (Member): R 3,800.00
• Doctor (Non member): R 4,300.00
• Registrar/Radiographer (Member): R 2,200.00
• Registrar/Radiographer (Non member): R 2,700.00
Additional Gala Dinner Ticket for a guest: R 100.00

Additional Gala Dinner Ticket for a guest: R 100.00

CPD Information

The BIGOSA 2015 Ultrasound Workshop and Scientific Meeting have been accredited for 17 clinical continuing professional development points (one point per hour of attendance). Speakers are entitled to a further 10 speaker points. South African delegates are eligible for these points if they attend the conference.

All registered delegates will have to sign the register and will be able to receive a Certificate of Participation at the end of the day.
Please note:

Member fees do not include your 2015 BIGOSA subscription
Non member fees include your 2015 BIGOSA subscription to December 2015
A late registration fee of R200 per person will be charged for registrations received after 15 August 2015. Pre-registration online only, no on-site registration will be accepted.

Registration fees include:
• Entry to the conference, presentations and trade display area on Saturday
• All lunches and refreshments
• The Gala Dinner on Friday, 9 October 2015

Exercise advised for lymphoedema after breast cancer

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Women who suffer swelling following breast cancer treatment should be encouraged to exercise, say experts.

New National Institute for Health and Care Excellence (NICE) guidance says exercise will not make the problem worse and could improve well-being.

One in five people treated for breast cancer will go on to develop lymphoedema in their arm, hand, fingers or chest.

It is a long-term condition that can lead to pain and loss of mobility.

The new NICE guidance, which is subject to consultation, says doctors and nurses should discuss with patients how exercise may improve their quality of life.

They should also stress that the current evidence shows “exercise does not prevent, cause or worsen lymphoedema”.

Clearing ‘confusion’

Many people with breast cancer go on to develop lymphoedema in their arm or chest following surgical or radiotherapy treatment.

It occurs when the body’s lymphatic system becomes damaged and is unable to drain fluid in the normal way.

Prof Mark Baker, director of the NICE centre for clinical practice, said: “For breast cancer patients, lymphoedema may occur as a result of treatment – such as surgery or radiotherapy – or cancer cells blocking the lymph system.

“Some people may be cautious of taking up exercise as they may think it could make their lymphoedema worse or bring it about in the first place.

_73508093_m1220213-coloured_sem_of_a_breast_cancer_cell-spl

“Our proposed new recommendations should clear up any confusion relating to the role that exercise can play for people with or at risk of this condition.”

Jackie Harris, clinical nurse specialist at Breast Cancer Care, said lymphoedema can severely restrict movement and impact lives.

“Lymphoedema can be controlled but will never go away and we know that regular exercise has many benefits for those living with or at risk of lymphoedema,” she said.

“Regular movement in everyday life or work can help keep joints supple and aids lymph drainage and extra exercises can also be useful if swelling restricts movement of the arm.”

 

Published by: www.bbc.com
Link: http://www.bbc.com/news/health-26530269