Showing posts with label World PH Day. Show all posts
Showing posts with label World PH Day. Show all posts

Wednesday, May 6, 2015

World PH Day... and Beyond

Today’s blog was co-written by PHA staffers Megan Mallory and Renee Hockaday. They make the point that awareness doesn’t begin and end on World PH Day. It is an everyday necessity if we are to succeed in our efforts to achieve better lives for PH patients and all those living and working with this disease.

Yesterday, on May 5, pulmonary hypertension patients and their loved ones asked their social media friends around the world to join their fight against a life-threatening disease too often dismissed as asthma. Our PH community did this to mark World Pulmonary Hypertension Day, and we joined in a global effort to educate people about PH and bring awareness to this disease.

The fight for awareness does not end after one day. If we are to succeed, awareness-building must continue today and every day. If you missed out on yesterday’s social media blitz, we ask you to join this awareness movement today.

We have designed a World PH Day celebration social media pin with the message, “PH: A disease of many stripes,” to symbolize the diagnostic challenges and how PH comes in different forms, sometimes without a known cause and in other cases, associated with other diseases. Please share this pin with your social media followers to lead them to PHAssociation.org to learn more about PH, find healthcare resources and/or make an online donation.

Please post this social media pin with the following messages on your website, Facebook, Twitter and other social media pages. Or if you want, create a message of your own. Here are our suggested messages:

Facebook:
Pulmonary hypertension may look like asthma. But on average, the survival rate for those untreated is 2.8 years. For World PH Day, share this message and World PH Day pin with 5 people you love. http://owl.li/LVTdB

Twitter:
World PH Day: the other May 5 celebration. http://owl.li/LVTdB @PHAssociation #PHAWorldPHDay #ILovePHA #PHAssociation

Did you know?
Yesterday also marked the beginning of PHA’s Days of Unity. Days of Unity are events and fundraisers hosted by individuals and organizations to raise money to fight PH. The events range from small walks hosted by PH patients to an endurance bike race fundraising effort led by Team PHenomenal Hope, which raised nearly $117,000 for PHA as participants in the endurance bike event Race Across America in 2014. Our 2015 Days of Unity events will conclude on June 20 after Team PHenomenal Hope completes its 860-mile Race Across the West from Oceanside, Calif., to Durango, Colo. Learn more and get involved

An Unexpected Gift for Support Group Leaders
In honor of World PH Day, Pulmonary Hypertension Association support groups got a special delivery. Gerry Fischer, president of PHA Europe, donated books written by his daughter, PH patient Maleen Fischer, to support group leaders. Maleen's book,“Hope Springs Eternal,” is about her PHight with PH. On behalf of all of PHA support group leaders and members, PHA thanks Gerry and Maleen for this thoughtful donation!

Tuesday, May 27, 2014

Around the world in 30 days ... and still going!

As I write this note, three weeks and three days from PHA’s 2014 International PH Conference and Scientific Sessions, I find myself thinking about what Conference years were and what they are now.

It used to be that in even-numbered years (Conference years), volunteers and staff were completely re-directed to manage the thousands of details that make for a successful Conference.

That was then. Today is different.

We are working on so many essential projects beyond Conference that the good of the community requires us to strive for excellence in all.

Here is a snapshot of the 30 days (April 27 to May 26) before I wrote this blog. I hope it will give you a picture of what is being done to accelerate the fight against PH.

PHA opened this 30-day period with news that we had received another four-star rating by Charity Navigator. This is the eleventh time PHA has been rated by the largest online nonprofit reviewer and the eleventh four-star rating they have given this organization. They tell us less that 1 percent of the thousands of charities they rate have received this honor.

As many of you know, one of our goals at PHA is to weave together patients, families and medical professionals across the globe to make sure no good idea is kept in shadows. That concept of cooperation and collaboration has led to the growth of national PH associations with 68 functioning today, up from three in 2000. On May 14, in the context of World PH Day, I blogged about our weeklong trip to Muscat, Oman, and Beijing, China (April 29 – May 6). During that same time, we participated in a Latin America-wide conference of PH leaders. These trips are about much more than visits. They are about strengthening global unity in the fight against PH. For example, one day before the Oman/China trip, we had an April 27 international conference call to agree on the creation of a website that will help PH association leaders more easily find and use resources from all of the PH associations … bringing us one step closer to universally shared best practices for the acceleration of the movement’s growth. This call was an outgrowth of two years of meetings that also resulted in the creation of coordinated PH anxiety and depression studies in Asia, Europe and the U.S.

While I was working with our Chinese PH partners, marking World PH Day on May 5, there was tremendous activity in North America. PHA continues to manage the World PH Day website, which we created last year. Thanks to our friends at PHA Canada, Niagara Falls was lit purple on May 5 in recognition of World PH Day, as were the Peace bridge between Buffalo, New York, and Fort Erie, Ontario, and the CN Tower in Toronto (among other notable sites). In the U.S., besides a number of events, we continued to focus on building PHA’s media blitz, which I blogged about on April 30.

PHA’s media campaign continued to grow rapidly throughout May, with Queen Latifah, Michael Buble, Florence Henderson, (see May 2 entries about Lucas), Laura Dern, Courtney Cox and Diane Ladd helping to get the word out. Reports kept coming in all month about networks playing our public service announcements (PSAs), including in prime time on American Idol. New networks (both English and Spanish) were added to the list agreeing to play our PSAs. Our web pages training those in our community on how to maximize local air play are being visited heavily … as are the web pages for those who are becoming aware of PH by seeing the PSAs on TV or hearing them on the radio.

We spent May refining our formula for success in getting TV and radio play. According to the Benton Foundation, there are 1,744 full-power TV stations in the U.S. Adding low-power and UHF and VHF commercial stations, the number grows to 5,720. There are 14,728 full-power radio stations in the U.S. This month, we had our PSAs sent to the inbox of 4,000 TV stations and the 10,000 most popular radio stations. Through a few easy-to-make phone calls, you can make sure those PSAs are opened by the stations and played. We have never had an opportunity for awareness like this before and, as always, success depends on you and those you can help recruit. You are our only chance to reach in to the community where you live!

On May 8, three of us met PHA co-founders (and sisters) Judy Simpson and Pat Paton at the National Organization for Rare Disorders Gala in Washington, D.C. Pat and Judy (pictured left) were being honored as part of NORD’s Portraits of Courage program. Actelion and Bayer had been selected by NORD for their Innovative Orphan Products Award, with Pat Paton making the presentation to Bayer and me to Actelion.

On May 14, we filled the room at the FDA/PAH patient meeting at FDA headquarters in White Oak, Md. It was a great discussion with the goal of including patient input in the FDA decision-making process. Meetings for only 16 diseases have been scheduled despite requests from hundreds of disease organizations. We feel fortunate to have been able to help make this meeting take place. The webcast of the hearing has already been posted from the FDA PAH Public Hearing page in Part 1 and Part 2.

As we move closer to the launch of PHA’s PH Care Centers accreditation program, the pace of review and final development is accelerating. During the week of May 12, we had four PHCC Committee meetings to discuss the six pilot accreditations that have recently taken place, make necessary adjustments and prepare for the upcoming launch. Much education about the program has already taken place and more is coming.

Between May 16 and 20 – with several other staff – I was at the American Thoracic Society meeting in San Diego. This is the annual meeting attended by more than 16, 000 pulmonologists. When I attended my first ATS meeting in 1999, there was very little about PH … two sessions with attendance at one being 35, the other 50. Now it is one of the most discussed issues at the Conference, with thousands participating in PH sessions.

While at ATS, we had the opportunity to host a three-hour question-and-answer session for patients and their families. Drs. Ron Oudiz, Nick Kim, Jeff Sager and Nurse Practitioner Wendy Hill delivered a great interactive program. PHA’s exhibit was heavily visited with a great deal of interest in both our medical journal – Advances in Pulmonary Hypertension – and the new PH Care Centers accreditation program. Each of us had a number of other responsibilities at the Conference. With PHA's Michael Gray and Briana Rivas-Morello involved in a number of medical committee meetings (Briana also had primary responsibility for the patient question-and-answer program). PHA's Jessica Armstrong held committee meetings and developed new connections for our Early Diagnosis Campaign. She returned with several endorsements and several more pending. Debbie Castro’s schedule was filled as the newly elected Chair-elect of ATS’ Patient Advisory Roundtable (PAR). In two years when she becomes PAR Chair, Debbie will have a seat on the ATS Board. Dr. John Newman, a former PHA Scientific Leadership Council Chair, received the ATS Educator Award. Dr. Val McLaughlin, our current Board Chair received the PAR Award for Excellence – the second time in two years that it has been presented to a PH physician. (Dr. Mike McGoon received the award last year.)

Also, while at the American Thoracic Conference, we learned that we are ATS’ largest research partner … larger than industry or other nonprofits. This speaks to our goal of and success at leveraging our donor’s research support to bring in additional money to support PH research.

There’s something else special about the ATS Conference. Coming as it does every second year a month before PHA’s Conference, it is a time when we are usually discussing options for our Conference’s room blocks, remaining scholarship availability and many other issues. This year was no exception but, fortunately, did not distract too badly from my various meetings with funders, physicians and nonprofit partners. It is a place where we get to connect the dots to accelerate our forward motion.

So, that is a sketch of the past 30 days through one PHA staffer’s experiences. It doesn’t include those of our other employees and volunteers both in the national office and in our Chapter offices. It doesn’t include the glue that keeps our structure together and well governed, monthly meetings with PHA’s executive committee and finance committee, among others. It doesn’t include the time invested by staff and volunteers in support groups, the development and management of our research programs, our advocacy activities, patient and medical education, the creation of a new feedback system related to specialty pharmacies … and a great deal more.

We are truly a busy organization. For those who understand the importance of what we do, for those who can handle the pace, we wouldn’t have it any other way.

Wednesday, May 14, 2014

World PH Day: Pieces of a Brilliant Mosaic

As I've watched it grow and evolve over the past 16 years, I've come to see it as a beautiful mosaic. The power of that beauty flows from people who unite around the common cause of fighting this disease.

First, in 1991, four women sat around a kitchen table in Florida in the United States. Their desire to ease the isolation of living with a disease that was both rare and without treatments drove them to form the first pulmonary hypertension organization in the world, the Pulmonary Hypertension Association.

In 1996, patient associations were organized in France and Germany. 

In 2000, at PHA's International PH Conference in Chicago, we realized that people from other nations had actually come. When we invited them to meet with PHA's Board of Trustees, seven people joined us to begin a conversation that has never stopped. By 2001, PHA-UK and PHA Israel had formed.

When we had a more intentional meeting at our 2002 International Conference, 80 people came. When we asked them what they wanted from us, the message was clear.: PHA has been around longer. Help us to learn. Help us to build.

More national organizations were formed, and by the 2004 Conference, we had staffed a position to help increase communication and collaboration among the patient organizations. We also shared a simple principle that has been adopted by all PH associations: to succeed, we have to stand together – not just patients, not just caregivers, not just researchers, not just medical professionals... but ALL of us.

So now, as we prepare for PHA's 2014 International PH Conference, it remains the same. It has always been equal parts patients, family members and medical professionals. It has always been and will always be homecoming for the PH community

It has also become something more. It is the International Conference and Scientific Sessions. It is the International Conference and Global Leaders Symposium. More than 30 nations are expected to have a presence.

They are part of a global movement that today includes 68 national PH associations.

When our friends in Spain proposed World PH Day three years ago, we were glad to help. Since the Second World PH Day last year, we created and have managed a website for all the associations to share and coordinate activities.

We are also often invited to participate in other World PH Day activities.

This year Julia, who coordinates our international activities, and I were the guests of the Saudi Association for Pulmonary Hypertension. We boarded the plane on April 29 for a 13-hour flight to Muscat, Oman. For seven years, this group of physicians has led the Joint Pulmonary Hypertension Association Assembly of the Eastern Mediterranean Region. As she has with other national organizations, Julia has worked with PHA staff to make our patient and other materials available for translation by SAPH. Last year, she helped organize a call between U.S. and Saudi patients. 

Our visit was a great opportunity for us to meet physicians from throughout the Middle East and share information and discuss possible partnerships. One important conversation is likely to lead to a patient component for the next conference. When we helped Dr. Nick Hill organize a patients component for his medical Symposium at Tufts in Boston more than 10 years ago, we saw that concept spread rapidly to other PH meetings throughout the U.S.  Today it is the rule, not the exception. Our hope is that if Dr. Majdy Idrees and his SAPH leadership group are successful, the concept will spread throughout the region.

After three days on the ground in Muscat, Oman (a beautiful city by the Indian Ocean), it was time to hit the airport. Julia headed back to Washington, D.C., and I headed to a different gate for a nine-hour flight to Beijing, China. (I'm writing this as I wait for a lift to the airport for my trip home.)

ISEEK, the patients’ group in China has been working hard to meet needs in their nation. I had been invited to come to their first Conference. They had brought together more than 150 patients, family members and doctors with government officials to discuss the importance of creating drug availability for PH patients. I was brought in to discuss the multi-part U.S. insurance system (private insurance, Medicare, Medicaid, the Affordable Care Act, pharmaceutical support programs and so on). While there, I had a chance to renew acquaintances with Dr. Cheng, who I had met seven years ago during my last trip. Huan Huang, a young woman who was transplanted two years ago and is now the Director at ISEEK, presented on patient depression issues. It was striking to see the similarities and differences from our own and PHA Europe's depression and anxiety study to this Chinese study.

Following the meeting, about 30 doctors held an open meeting, with press attending, where they discussed positive ways to achieve the same thing every patient group in the world is after: a better life for patients as we continue the march toward a cure. It was good to see the doctors and patient leaders working so well together.

I spent most of the next day with the ISEEK staff. Their executive director, Rong Li, formerly a filmmaker, has built the organization quickly in a country now beginning to accept the value of nonprofits. They remind me so much of PHA's days of early staff history. They have moved four times in the past three years of their existence. Their staff has grown to six. They hire for the same values we do: bright people with commitment to cause and an ability to work well in teams. And they have a refusal to fail.

While Julia and I were traveling, Briana was in Medellin, Colombia, where PHA had been invited to present at the Sociedad Latina de Hipertensión Pulmonar (Latin Society of PH) an umbrella organization similar in structure to PHA Europe. Briana's report will come in a future guest blog.

So, as I wait for my ride to Beijing airport for the long ride home, I continue to catch up with the regular daily and sometimes hourly updates about PHA's World PH Day project, which has generated celebrity interest on Twitter and continues to expand TV and radio play for our public service announcements.

Every day another piece of the mosaic falls into place. Every day we move another step closer to our goal.

It was wonderful to spend time with this enthusiastic and inquisitive group. I know we will hear a lot from them in coming years.

Thursday, May 2, 2013

Heart...

I don't spend a lot of time on Facebook but today I was struck by Mia's World PH Day (May 5) message to her 7 year old brother, Daniel.  Daniel has PH.

The card that Mia is holding is being used by many patients, families and medical professionals around the world to tell their story as part of a Worldwide Photo Mosaic. Watch her video and submit your own photo to be part of the Mosaic.

Tuesday, April 2, 2013

May 5: World PH Day is coming...and www.worldPHday.org is here!

In 2011, Juan Fuertes and Irene Delgado of Asociación Nacional de Hipertensión Pulmonar (ANHP)the Spanish PH association had a big idea.  It was also a big risk. 

Juan and Irene thought that the creation of a World PH Day would help expand awareness of the disease.  However, like all new ideas, it started with very little support.  They worked hard to engage PH associations around the world and to build interest from funders.  On May 5, 2012, they hosted a PH Symposium in Madrid that included about a dozen PH association leaders from Europe, Asia, Latin America, Africa and North America.

Most importantly, they started something that should, could and would grow.

This year, what Irene and Juan began is much easier…everyone is jumping in to help.  Here at PHA,
 
we have accepted the responsibility of establishing the World PH Day website.  Since it went live two weeks ago, World PH Day events and participation from 43 national and international PH associations has been posted…with more coming.  PHA Europe has been working on making a sports event model they have created available to other associations throughout Europe and beyond.  Other groups are planning their own unique activities.


Interest in the website is astonishing.  Custom translations have already been completed for Chinese and Portuguese…and Spanish may well be available by the time you read this.  In addition, Google Translator provides access to the site in 65 languages.

An exciting feature of the website that we hope will grow – and that YOU can participate in – is the Worldwide Photo Mosaic.  Patients, families and friends from around the world are beginning to upload pictures with their own World PH Day message.  There’s even a World PH Day logo that can be printed out and included with the message.  One of my favorites was posted by one of PHA’s founders, Pat Paton. She wrote:

              “I saw 29 doctors about my PH symptoms before I was correctly diagnosed.  That was 26 years ago!”

Another World PH activity that PHA has just launched on our own website is Flames of Hope .  Flames of Hope allows our community to honor or remember a patient, caregiver medical professional or other person who has made a difference in their lives while providing support for current programs.

We hope you will join with us as we establish World PH Day as an important way to expand knowledge and awareness of PH throughout the world.  Awareness is a critical first step in improving the lives of all those who live with PH.

 


 

Monday, May 14, 2012

World PH Day…a first among many

As a community grows, it develops traditions and opportunities.

The First World PH Day – celebrated on May 5, 2012 – offered both of those.  As patient and medical leaders from five continents gathered in Madrid, Spain for the Scientific Session and Celebration, I couldn’t help but think of how far we’ve come in so few years.
The first patient with PH was diagnosed just over 120 years ago, in 1891, by Dr. Ernst von Romberg, a German physician and clinical scientist. 
Sixty years later – in 1951 – after identifying just over 30 cases in the U.S., Dr. David Dresdale gave the disease its name. 
Ninety years later – in 1981 – the National Institutes of Health began a five year registry which enrolled 187 patients across the U.S., providing the first clear picture of the disease.
In January of 1991, 100 years after Dr. Romberg made the first identification of a PH case and forty years after Dr. Dresdale named it, four women sat around a kitchen table in Florida. Three were patients, one was a caregiver and two were also medical professionals (nurses).  Their coming together set in motion the beginning of a PH community and acceleration for change.  Their action led to the first PH association in the world.  Today, there are 58 such national associations throughout the globe.
Five years after PHA was founded, the first disease-specific treatment for PH was approved by the FDA.  Today, there are nine treatments – as many or more than all but two of the 7,000 rare diseases identified in the U.S.  PH association networks are flourishing in Europe  and Latin America.  Asia and North America are active and the South African PH association is a beacon in Africa.
It was great to celebrate with Juan Fuertes and Irene Delgado (who conceived of, organized, fundraised for and inspired the First World PH Day for which we again thank the Spanish PH association, ANHP.  It was an honor to be with leaders like Noriko Murakami who built PHA Japan Cecilia Martinez Ramirez who founded HAP Mexico, Denneys Niemandt, who one by one, told the stories of the 25 patients diagnosed in South Africa, Yvetta and Peter Makovnikova, developers of a Slovakian PH association, Dr. Majdi Idrees, president of the Saudi Association for Pulmonary Hypertension SAPH, Enrique Carazo Minguez, president of the other Spanish association, FCHP, Gerry Fischer, founder of PHA Austria and president of PHA Europe and that network’s vice president Pisana Ferrari who also leads the Italian association, AIPI.  Many others were there including globally recognized PH physicians, such as Drs. Galie, Rubin, and Simmeneau.
There will be many future World PH Days but the traditions began with this one and I have no doubt the opportunities will continue to emerge.  But, as always, we are driven by the stories.  Here’s one to close this blog.  It is a reminder for me why we do what we do... 
A woman came up to me at the World PH Day celebration and said, “I have to thank you.”  When I asked her why, she said that she had been diagnosed before there was a Spanish association and continued, “I came to the PHA website to learn about the disease and how it affected the lives of others like me. Actually, I have to thank you twice.”  When I asked why again, she said, “When I came to PHA's site I didn’t know how to read English.  The information was so important to me that I forced myself to learn to read the language from the site.” 

I regret that I have forgotten her name but I will never forget what she taught me about the importance of the work that we all do.