Tuesday, September 28, 2010

HH Out & About!



Heartwood Health attended the first Annual Fall Prevention Walk of Contra Costa County on September 25th.
Jennifer Mountain, Executive Director of the Fall Prevention Program, did an excellent job organizing the program for the day. Seniors from all over Contra Costa enjoyed a leisurely ½ mile walk, entertainment and exposure to a variety of resources in the area. The highlight of the day was the belly dancing performance which included a 96 year young dancer!

Great job Jennifer, we're already looking forward to next year’s event!

Friday, September 24, 2010

Health Reform Changes Go into Effect!

Health Reform key consumer provisions of the Patient Protection and Affordable Care Act (P.L. 111-148) went into effect Thursday, September 23, 2010. These new rules will be applied when an existing group plan is renewed or a new plan is purchased. For instance, if your plan year begins on January 1, then these changes will be part of your policy starting on January 1, 2011. Some of the provisions include:

· End of Lifetime Limits - plans will no longer be able to place lifetime caps on the dollar amount of benefits. If your insurance had a lifetime cap, you will receive notification that the cap has been lifted.

· Annual Limit Minimums Established - the gradual phase - out of the annual limit dollar amount for all group policies and new individual policies begins. For a plan or policy year beginning between September 23, 2010, and September 22, 2011, the minimum annual limit can be no less than $750,000. The minimum annual limit amount will increase in subsequent years until it is eliminated in 2014.

· End of Pre-Existing Condition Exclusions for Children - new individual or existing group plans will have to accept children under the age of 19, regardless of a pre-existing condition. This will extend to all plans and all ages in 2014.

· End of Rescissions and Cancelations - plans can no longer drop a patient's coverage, except in cases of fraud.

· Dependent Coverage Extended - young adults will be able to stay on their parent's health plan until age 26.

Has anyone benefited yet from these changes?

Tuesday, August 17, 2010

Helping Seniors Find Comfort

We were happy to be featured yesterday in Comfort Keepers’ enewsletter with an informative article written by Lisa Gray, RN, one of our Health Advocates. Comfort Keepers is a great, local, non medical home care company that provides in-home services to seniors and others needing assistance. Jessica and her sister are two of the most caring individuals I know. They love their work and their clients and it shows!

It’s informative articles like these that help increase awareness of our emerging field. Health care advocacy has so many applications, and advocacy for seniors is another area that is in great demand. By creating a wide-ranging network of caregivers in the Bay Area, Comfort Keepers serves an important group in our society!

Sunday, August 8, 2010

Advocate for Yourself!

Sometimes, you have to trust your gut instinct. Patti’s niece Nicole recently found out that obtaining a second opinion is not only smart, but necessary!

When visited her regular physician at Kaiser Permanente after injuring her knee, he listened to her explanation of a previous ACL replacement and meniscus tear, and after examining the knee, recommended the usual regimen for a potential meniscus tear; Advil, rest elevation, and so on.

But Nicole had already tried the elevate, rest, ice, rotation of treatment. She had been through knee injury before, and after a month of rest, she knew that the tried and true approach wasn’t helping. Nicole leads a very active life; she plays softball, coaches cheerleading, works fulltime and has three sons, all involved in different activities. She was ready to have an MRI done, to really know the extent of her injury.

Nicole had read that meniscus tears usually do not heal on their own and felt that an MRI would determine if a more aggressive treatment was necessary. But her Dr. resisted, which led to a few awkward silences in the exam room, after which she stated that she wanted a second opinion. He agreed, but the next appointment with the sports MD wasn’t for 2 ½ weeks.
Nicole’s next step was to go directly to Member Services, and unfortunately make a complaint. She was able to get an appointment a week later, and a more specific diagnosis after finally getting an MRI and final diagnosis of a new meniscus tear, she was able to receive treatment and recover more quickly.

Nicole is an informed patient, she had tried the first line treatment and knew the next logical step. By advocating for herself and seeking treatment in that she was satisfied with, Nicole received better care in the long run.
Her belief is that one must be a participant in their health care and her hope is that doctors will “listen “ to their patients, as often they know their body the best.

Monday, July 12, 2010

¡Buenos Dias de Argentina!


Yesterday at the World Federation of Hemophilia in Argentina, I attended a session on the future of hemophilia care. Researchers from China to Germany presented many of the advances that have been made in the care of those afflicted with hemophilia well as the challenges that still exist.

It is hard to believe that in the 1960s many hemophiliacs who did not survive beyond age 20, could live a normal life span today. With treatment, complications of chronic joint disease can be avoided. However, there are still challenges in treatment throughout the world. Affordability and access to the products still make it difficult to receive treatment in many countries.

Here in Buenos Aires, one of the most exciting presentations was the introduction of a long acting product which will allow patients to be treated once weekly instead of the often 3 day per week regime. Can you imagine having to perform an intravenous infusion multiple times a week in your child or yourself? While these patients and their families have no choice now, at some point that may be decreased to once a week!

Even more exciting is the elimination of the disorder completely. One day with gene therapy, patients may no longer have to suffer the pain and complications of internal bleeding. There is still much to be done in the world of hemophilia, and I am extremely grateful to have met so many people from around the world with the same goal of improving care and ultimately the lives of those living with this disorder!

¡Hasta Pronto!

Saturday, July 10, 2010

The Private Sector Works in Argentina!

I am currently in Buenos Aires, Argentina, attending the World Hemophilia Meeting and experiencing another culture's health care system firsthand through the experiences of my friends here. Attending the meeting is a real eye opener. I realized that I did not know what kind of health system Argentines provided to their citizens, but assumed that there was some kind of socialized program.
While having dinner last night with a friend who lives here I learned that the system has 3 sectors. The public sector which is paid via taxes, the private sector, where Argentines who choose this option pay premiums, and the Social Security sector, which I assume are the retirees.

Sound much like our own system? Public sector for Medicaid, private, and the employed, and Social Security for those over 65. There is one major difference: my friend is in her 40s and relatively healthy, except for the all so common bulging disc in her back. She only pays $45.00 per month for her Private Sector Insurance! A similar premium in the US would be $500 - $1000.00. And when she had surgery to correct the disc in her back, she paid near to nothing for the procedure. What a relief to know that one’s health can be taken care of and not bankrupt the citizen. Instead she was able to heal and get back to work as a productive Argentinean citizen.

We have known for a long time that we are the only country that does not provide affordable care. But as I visit Argentina and see a health care system that works effectively for its citizens, it gives me hope that Health Care Reform worldwide is on the right track!

Wednesday, June 23, 2010

Finally, Some Answers about Annual Limits!

Health care reform has so many provisions it has been difficult to keep track of all of them. But one we have been watching closely has been the issue of annual limits. While it has been clear that lifetime limits are going away, annual limits remain an issue for many, especially for those patients with chronic illnesses such as hemophilia.

Yesterday President Obama released a fact sheet: The Affordable Care Acts New Patient Bill of Rights. Included in this is a phase out plan of Annual Limits.

Beginning September 23, 2010, health plans will be allowed to set limits no lower than $750,000. In 2011 the minimum limit will be raised to $1.25 million. In 2012, the amount increases to 2 million and in 2014 annual limits will vanish!

This is great news for all, but my question is, why is it so complicated? What will those individuals who reach their annual limit do in the years before 2014? How will they be able to pay ? It seems to make more sense to eliminate both Annual and Lifetime caps now. What are your thoughts?

Friday, June 18, 2010

Exploring Neuropathies and the NAF


Yesterday in Sacramento, Patti and I attended an informative meeting that was hosted by the Neuropathy Action Foundation, (NAF) a nonprofit organization dedicated to supporting patients with neuropathies, or diseases of the nerves, of which there are many types, including Guillain- Barre Syndrome (GBS), Chronic Inflammatory Demyelinating Ployneuropathy (CIDP), Diabetic Neuropathy and others. While GBS affects approximately 1 person in every 100,000, Diabetic Neuropathy affects close to 60% of all Diabetics.

Diagnosis of neuropathies can be difficult and requires a specialist. Symptoms are often mistaken for other disorders and often include pain, numbness, weakness and balance problems. Patients are often told that their symptoms are psychological and begin to feel isolated and depressed.

The NAF actively supports programs that create public and physician awareness of neuropathy, the use of Intravenous Immunoglobulin (IVIG) and other remedies to improve patient care through NAF activities and services. This organization, though it is only 4 years old, has grown significantly and has the ear of legislatures nationally, joining other organizations to educate and empower patients to advocate for them. For more information look at their website, www.neuropathyactionfoundation.com

Saturday, June 5, 2010

Health Advocate Trisha Torrey


In the last blog post, I mentioned Trisha Torrey (pictured to the left with Patti and I), a well-known health advocate who traveled from her home in New York to attend our advocacy workshop in Oakland on May 19. Trisha gave an engaging and informative presentation on the many layers of health advocacy, and also told her own story.

In 2004, Trisha was diagnosed with a very rare form of cancer. But Trisha didn’t feel as sick as doctors were telling her she should be, and she had the sneaking suspicion that something wasn’t right. She made the decision to follow her instincts and ask questions, research her condition and demand answers to her questions. Even though she had received the same diagnosis from two independent labs, Trisha pushed for more answers. As it turned out, she did not have cancer at all! It was only through advocating for herself and pushing for a third and final diagnosis from the National Institutes of Health in Washington DC, that Trisha was able to save herself from unnecessary chemo treatments which would have been life threatening to her healthy body.

Since then, her m.o. has been to get people to think for themselves and ask questions. It was a terrifying thought that among the millions of other patients who were dealing with the health care system every day, some could be caught in the same ordeal that she had gone through.

Trisha became a health advocate, and now puts advocates and patients in touch nationwide. She is a sought-after national speaker, newspaper columnist and active blogger. Her blog at about.com says that “Trisha is recognized by patients and professionals alike for her ability to translate the challenges patients face into solutions for improved health care.” Trisha also authored You Bet Your Life! The 10 Mistakes Every Patient Makes.

Her Patient Empowerment blog is a great resource for anyone looking into health advocacy. Trisha also created AdvoConnection.com, a website that brings health advocates and patients together.

We hope to have Trisha back again in the future! Check out her website, blog, Facebook and twitter feeds for more on all that she does!

Saturday, May 29, 2010

Advocacy Workshop a Success!

Our second health advocacy workshop, held on May 19th in Oakland, California, was a great success! Forty attendees of various backgrounds, including nurses, social workers and others, gathered to learn about “The Emerging Field of Private Health Advocacy”. The goal of the conference was to give an overview of this important and exciting new field.

The day focused on what health advocates do, why they’re necessary, and how to get into the business of health advocacy. All of the participants had a personal story about dealing with the complexities of the health care system, and were interested in learning how to alleviate those frustrations for others.

We were honored to have Trisha Torrey join us from New York, to tell us of her personal challenges navigating the health care system. Trisha founded AdvoConnection.com, an important website that connecting people with health advocates, around the country. Trisha told the story of how she became a health advocate herself (look for that story in our next post), In addition to speaking about health advocacy, Trisha is an active blogger for about.com and is the author of You Bet Your Life! 10 Mistakes Every Patient Makes.

The workshop offered some basic information about how to get into the business of Private Health Advocacy. The first question to consider was if it is better to work for oneself or an established company.

Each attendee was asked to take a personal inventory, and question whether they were willing to take a risk by stepping out on their own. Some of the questions that posed to attendees were 'are you a critical thinker?' and 'Are you able to find the answer to any problem?' The work of a Private Health Advocate is not always predictable, as each client presents a new and unique challenge.

The industry of Private Health Advocacy is still in its infancy, and beginning a business during this time is very exciting. But with that leap of faith comes a lot of planning and decision making. First and foremost you’ve got to believe in yourself and recognize that you have the skills to assist others in the navigating the complexities of the system. It might sound cliché, but it’s true!

I was very pleased with how the day unfolded, and with everyone’s reaction. Thanks to all that attended and for your positive and constructive feedback. I’m excited about the future Private Health Advocacy and believe that in a few years, everyone will want to have a Health Advocate! And I’m confident that Heartwood Health will make a difference in the lives of the clients we serve as well as contribute to the future growth of the industry. Our next workshop will be October 6th in Oakland, check our website for more details.

Tuesday, May 18, 2010

Could You Be an Advocate?

In anticipation of our workshop tomorrow, ”The Emerging Field of Private Health Advocacy”, A new career for you, - a new resource for your patients, I want to take the time to detail how one can become a health advocate. The complexities of our healthcare system seem to increase daily, as there are new options for treatment almost daily. Medical providers differ on diagnosis regularly and health reform is adding much confusion to the mix.

Patti and I have seen a growing need for a “bridge” between individuals and health care providers, and Health Advocate is increasingly becoming a household word. Also known as a Private Case Manager, a Geriatric Care Manager or Patient Navigator, Health Advocates are there to give peace of mind to their clients as they weave their way through the complexities of the medical system.

A master’s program in Health Advocacy has been in existence at Sarah Lawrence College since 1980, but certification and credentialing for our field is still in its infancy. While there are few training programs located in the US, many companies are now focused on providing this service, which bodes well for the future of health advocacy credentialing. As of now, entering a training program is the best bet for those interested in pursuing a career in health advocacy.

People with previous training and related work in health care are the best health advocate candidates. Their experience naturally gives them a leg up in the field, as working for a hospital or specific disease advocacy group can expose a person to the plethora of ethical and practical issues that health advocates need to be skilled in handling.

Our workshop is intended to give an overview of the field and prepare the participants to look further into a career in this exciting new arena of Private Health Advocacy.

Look for a summary later this week, and announcements on additional workshops later this year…

Friday, May 14, 2010

Advocating for the Deaf Community

As you look around our site or read about health advocacy online, you’ll probably come to realize that advocacy has about as many applications as people have health conditions. An important role of the Health Advocate is to educate and empower our clients. For most of us doing this work, advocating on behalf of a client comes naturally as we have had a personal experience helping family or friends. This is especially true for Patti, my business partner. Her older brother Ralph Jr. received a diagnosis of complete hearing loss over 50 years ago. Growing up before interpreters and programs for the deaf were commonplace, Patti and her family faced challenges in every aspect of Ralph’s life. At that point, signing was not mainstream. Ralph was bussed everyday for more than an hour to a school that taught lip reading. As he reached the age of 13, signing was becoming more common, and during his teen years, he lived on campus at the School for the Deaf in Berkeley, California. During those years, the family learned sign language, and Patti accompanied her brother to most events and family gatherings, becoming his primary interpreter.

Today, Ralph lives in Dublin, CA with his wife Maureen, who is also hearing impaired. Participating in hearing impaired community activities is a way of life for both of them. They often find themselves supporting a friend in need when a family member has become ill or needs assistance in another way. For example, Ralph is an excellent handyman and has replaced new windows or performed minor household repairs for friends and neighbors.   

Ralph has always stood up for his rights, and sought out resources available to him. He is known for his strength and ability to show others how to advocate for themselves. His passion for motivating others is inspiring. Ralph is a huge advocate for the deaf, acting on behalf of his community whenever the need presents itself

Today programs such as the Deaf Counseling Advocacy and Referral Agency (www.dcara.org) are widespread and utilized within the deaf community. DCARA is a nonprofit organization that provides its clients with the resources to make independent decisions. When Heartwood Health works with deaf and hearing impaired clients, they collaborate with DCARA to ensure that services are accessible. It is because of the strong advocacy of the community that being deaf no longer limits those who are affected.

If you have a story about someone who has been successful in improving life for a deaf or hearing impaired person please share it with us!

Monday, April 26, 2010

Upcoming Advocacy Workshop!

Heartwood Health is offering a one day workshop on THE EMERGING FIELD OF PRIVATE HEALTH ADVOCACY, on May 19, 2010 at Jack London Square, in Oakland California.

The program is offered to professionals and laypeople alike to learn about this new field. Continuing education credits are available for nurses.

We are especially honored to have Trisha Torrey, author, patient advocate and founder of Advoconnection( www.Advoconnectin.com) join us as our keynote speaker.

Many are asking, will this prepare me to be an Advocate? What is involved in this profession, is additional training needed? Private Health Advocacy is a new and emerging profession. The workshop will provide the participant with an overview of this new field, including the history of Health Advocacy, current business models and how to become an Advocate. Please join us, network and learn about this exciting new field.

To sign up for the workshop go to: www. Heartwoodhealth.com/advocacy_workshops.html, or call 1 (866) 606-8495

Wednesday, April 14, 2010

Navigating the Medicare Insurance Maze!



Hi there – I’d like to share the story of an old colleague of mine, who is herself a nurse advocate. Her situation illustrates the point that everyone, even nurses themselves, needs an advocate at some time. It was hearing stories like this that inspired Patti and I to form Heartwood Health.
(Names and insurance companies involved in this case have been made anonymous.)


“Back in 2001 my partner put me on her health care insurance. This was a benefit provided by her company and was more cost effective than getting my own policy through my employment. The only thing we had to do was provide a notarized statement that we shared a home and had for several years.

Everything worked very well. When my partner’s division was sold to a private company the insurance benefits traveled with her.

In 2005 I became eligible for Medicare, and I spoke at length with a very nice woman with Social Security. She researched my insurance options at length, made many phone calls, and then told me my best option was to keep what I had, enroll in Medicare Part A, and decline Part B. This was based on a Medicare regulation allowing a retired domestic partner to continue on the employed partner's policy. Medicare A would be the secondary payor.

Last year we changed to a different carrier, and when that new carrier was bought out and became what I’ll call Carrier 2, the fun started. All of a sudden I was informed that Medicare was now primary. For example, this meant that lab work would first be billed to Medicare Part A, would be declined as Part A doesn't cover out-patient procedures, then billed to Carrier 2. As a result I was getting bills from the lab, paying them, then getting a refund eventually, sometimes three months later.

It still was working, but it was very unusual. I did call Medicare (not Social Security ... note well, always call Social Security), and the Medicare rep told me that Medicare was indeed primary.

On January 19, 2010, I received a registered letter, return receipt requested, from Carrier 2 stating that since I had refused Medicare B five years ago, Carrier 2 would only pay that part of any outpatient procedure that would not be covered by Part B if I had it. And this was in effect as of January 15, 2010, four days before I received the notification.

This was very concerning. First I called Carrier 2 to see if they could sort out a mistake, perhaps a computer mis-click. Several more calls ensued, and Carrier 2 continued to deny any responsibility for anything that would have been covered by Medicare Part B. This was made worse because I had a rotator cuff repair scheduled for February 5, less than three weeks away, and my physician does these as an out-patient procedure, no exception, save co-morbidities that I didn't have.

I called Medicare, got a very short, rude response from a woman who answered the phone. She told me that I had done this all wrong five years ago, that I had refused part B, and that I could apply for it but would be subjected to a $50/month penalty in addition to the $100/month (or so) premium. She said she would send me the paperwork to fill out, but to this day I haven’t received it.

In the meantime my partner contacted her company liaison with Carrier 2. This person worked and worked and worked on this. But we still kept getting denial of responsibility from Carrier 2. At first they said it was a regulation that I had to have Part B. I proved that wrong. Then they said that they could require it even if it wasn't a regulation. That was more or less wrong, dependant on the contract they had with my partner's company.

An interesting aside: I had a call from a volunteer for the reelection of Gov. David Patterson of New York. In our conversation I told her about my issues with insurance, domestic partner rights and my current problem. It happened that this woman was an attorney with ERISA (Employee Retirement Income Security Act of 1974), and she was enormously helpful, asked me to contact her if I wasn't successful in the battle with Carrier 2.

The next time I spoke with the Carrier 2 rep, I mentioned ERISA, and I left the impression that I had contacted an attorney from that office, not quite true of course. But hey, we do what we need to do.

Per the advice from the ERISA person, I called Social Security, got someone incredibly knowledgeable and helpful who more or less said "hell no" Medicare can't penalize me if I now elect Part B. I came under a category termed special enrollment, a person who is insured by: 1. Self, 2. Spouse, 3. Someone who lives in the household. I qualified under part 3. This means that even though I declined, not refused, (per advice of Social Security rep) Part B back in 2005, I could enroll in Part B at anytime in the future without penalty.

At this point the company liaison brought the company contract with Carrier 2 to the attention of the Carrier 2 rep. Bingo! The contract explicitly included domestic partners.

I made something like 20 phone calls to Carrier 2, Medicare and Social Security between January 20 and February 1, 2010, managed to refute every argument that Carrier 2 came up with, and on Feb 1, 2010, 4 days before my scheduled surgery, I received a call from a rep at Carrier 2 with an apology. My coverage was in effect as before all this began. I asked her for a letter or even an email stating this, and she "declined" to give it to me, said her supervisor wouldn't allow that. She did tell me that all our conversations including this one were recorded, and that recording was part of the permanent record. Yeah, right.

I did keep careful notes, much of which I have written here. I have applied for Medicare Part B as I am certain Carrier 2 will rewrite their contract with my partner's company when renewal time comes. It is to the benefit of these for profit companies to get people like me off the books as soon as they can.

I am an RN, and believe me I have gone to battle for my patients with insurance companies many times. I am fortunate to know that "no" is not always the final answer and that it takes persistence and fortitude to fight these battles.

I am also certain that most retired people of my age do not have the knowledge to pursue a denial. All need help from an advocate. Most do not have money to hire an attorney. Most attorneys will not take a case like this with no realistic hope of a cash settlement. I am lucky to have a couple or three in the family, and they guided me through my long days of calling and calling and calling, and made sure I was documenting everything. But I am not most people.

Today I am wondering how the new health reform will change all this. I am hopeful, but I am realistic. In the meantime, I thank Heartwood health for providing advocacy. Everyone, and I do mean everyone, will need it at one time or another.”

Tuesday, April 6, 2010

Help for People with Early-Onset Alzheimer's

In case you haven’t heard, in February of this year, the Social Security Administration (SSA) announced that it will streamline the application process and decrease the wait time for benefits for people with early-onset Alzheimer’s disease.

The process for families to receive benefits when family members are disabled with early-onset Alzheimer's is slow and complicated, and many benefits are largely unavailable to people with early-onset as they are under age 65. In an effort to improve the process, and in recognition of early onset Alzheimer’s as a disability, the Social Security Administration (SSA) has added early-onset/younger onset Alzheimer's to the list of conditions under its Compassionate Allowance Initiative, giving those with the disease expedited access to Social Security Disability Insurance (SSDI) and Supplemental Security Income (SSI) for those under age 65.

Finally, Alzheimer's disease is being classified as a disease that causes a disability. Thanks to the Alzheimer’s Association for advocating for patients and their families.
For more information, refer to the Alzheimer’s website at http://www.alz.org

Friday, April 2, 2010

Meet Patti Nieves - the "Other Half" of HH!


Patti Nieves is the other half of Heartwood Health, and an essential half at that. Her skills range from interpreter, to outreach specialist, to hypnotherapist (that’s right!). Patti lives in the Santa Clara area with her partner of nearly 30 years and their two dogs. Hispanic outreach, volunteering, and health care have always been close to her heart.


With her background as a pharmacy technician, Patti started working at Stanford Children’s Hospital in the 1980s when the field was still in its infancy. While working in a sterile environment, compounding various medications, and producing intravenous fluids, Patti became an expert in the field of pharmacy preparation.

Patti moved on to the work that would ultimately define her; working as a unit assistant in a hematology-oncology unit. Spanish is her first language, and Patti soon found herself flip-flopping between her role as a unit assistant and an interpreter when Spanish-speaking families came to the hospital and needed assistance to better understand their disorder, complexities and the medical directions they were given. When a good friend decided to start a company specializing in hemophilia and other chronic disorders, Patti decided to work in the hemophilia industry full time. As her role developed, she began volunteering for the Hemophilia Foundation of Northern California, assisting with the development of outreach and advocacy programs especially within the Hispanic community. It was while volunteering that Patti and I first met and I was immediately struck by her dedication and compassion for the work that she was doing educating, supporting and advocating for those with a chronic illness, while accessing the complexities of the health care system.

Patti worked for her home health company through four different acquisitions, but as it grew bigger and eventually became “corporate America”, she decided to make a change. She didn’t want to be confined by the corporate limitations and impersonal practices. With our shared viewpoint and goals of reaching out to a broader population, Patti and I then ventured on to start Heartwood Health together.

Patti’s immediate goal for Heartwood Health has been and continues to be making sure we are visible to the community that needs us to understand the type of work we do, providing support and guidance as they manage their health. Patti says it best:

“We want people to understand that we’re not just a typical company, that we are really truly here to help individuals and families. It is the most important part of what we do and who we are. We want our clients to understand and be aware that we are the company that really does care.”

Wednesday, March 24, 2010

A Little About Me


I have been a nurse for more than 30 years, and I have always believed that my role is to advocate for my patients and clients. Helping and guiding people has been part of who I am since I can remember. As a young girl I assisted my blind grandmother with many of the challenges she faced. A career in nursing was a natural progression that has allowed me to work in a variety of settings, including pediatrics, geriatrics, home health, emergency room and more. This background has led me to become a health advocate full time and to form an organization that can assist patients and their families with almost any health challenge.

Having witnessed both excellent and subpar care, I have developed a lifelong passion for ensuring that all patients receive the best care possible and are fully educated about their options. When an individual or their family member is faced with a medical issue, it is difficult to remain objective, regardless of their background. Having the peace of mind of knowing that an expert will assist with expediting appointments, problem solving difficult medical situations and interpreting treatment options is a great relief to our clients.

I believe that everyone should have a health advocate, because at some point they or their family member will be faced with accessing the health care system. You can call your attorney for advice; and you can call your mechanic when you have a problem with your car. Why not have a personal health advocate that you can contact at any time with a question about how to navigate the medical system? Health Advocates do not provide hands on care, or in any way replace the advice of a physician. Instead, Heath advocates provide you with information and direction that will assist in making decisions related to the health of you or your family member. We are an integral part of the health care team and will coordinate with the many people involved to assure that you receive the best possible care.

My goal is to make this blog a friendly place for information and stories about health advocacy. Next, I’ll let Patti tell you about herself!

-Michelle



Thursday, March 11, 2010

Heartwood Health – Private Health Advocate Services

Welcome to our inaugural blog post! At Heartwood Health, our mission is to empower our clients to make informed health care decisions through advocacy and education, and support individuals facing health challenges. We hope that this blog will become a useful resource for you in your travels through the health care system.

These days, the health care system can be a vast, and sometimes intimidating, place. By adding our voice to the mix, we’ll strive to become a source you can depend on for the latest news and opinions in this emerging field.

Patient advocate organizations are popping up all over the country. Some offer a specific expertise, while others provide only phone advice. At Heartwood Health we are building a team of professionals of varying expertise, so we are able to provide assistance in any situation. We have specialists in Pediatrics, Geriatrics, health insurance, and more. If we can’t meet your needs we will refer you to someone who can. And since every situation is unique, Heartwood Health will tailor a plan unique to your needs. We believe that everyone should have a private patient advocate to assure the best possible outcome when navigating the healthcare maze. If you are facing elective surgery, dealing with a chronic condition, or helping an aging parent, our experts will support you.

Patti and I have over 35 years of combined hands-on healthcare experience. We’ll tell you more about ourselves soon, but until then, have a look around our site and let us know what you think! And check back here often as this blog grows into another resource for you.