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April 30, 2012 by bob mason 2 Comments

Benefits Reform Ahead

You have that uneasy feeling that you ought to be doing something . . . just not sure what. Perhaps Mom or Dad has been exhibiting some troubling health symptoms. As the oldest/only/closest child you know that it will be up to you to come up with a solution.

You’ve also been reading the news.

Once the 2012 elections are over and a new Congress is seated, Medicaid rules may likely tighten. It really will not matter which party comes out on top: It will become ever more difficult to qualify for this program as Congress authorizes and directs the states to revise rules.

The Forecast

Social Security, Medicare, and Medicaid are in trouble. Across the political spectrum, from secretaries Geithner and Sebelius to Mitt Romney and Paul Ryan, the alarm is being raised. The only thing the politicos disagree on is what to do. On April 24 the trustees of the Medicare program released their annual report with 3 different sets of numbers (“bleak, bleaker, and bleakest” according to Medscape Medical News).

So desperate is the government getting for money that cuts in Medicare reimbursements to nursing homes, aggravated by Medicaid cuts, will likely cause as much as 35% of nursing homes to reduce staffing – and North Carolina is the third hardest hit state (according to a study by the Alliance for Quality Nursing Home Care).

The financial crisis has set the stage for the problems, but all social programs directed to older population will feel intense pressure from the Boomers “coming of age” and having the nerve to live longer.

Some states are squeezing now. An excellent Wall Street Journal describes this in some detail.

Although the numbers discussed show the programs becoming insolvent at current levels within 10 to 15 years, do not be lulled into complacency:  Action will need to be taken very soon to begin to turn the tide.

While I have real misgivings about the way long term Medicaid is currently designed and believe that there are rational approaches to saving huge amounts, the current program and rules are all I have to use for the benefit of my clients.

So . . . What To Do?

Plan early. When the rules change, they almost always change prospectively, not retroactively. In other words, harsher rules will likely apply to planning strategies implemented after the new rules become effective.

Failure to adequately plan early runs not only the risk of being hit with higher rules hurdles, but leaving a family with fewer options if a parent’s health suddenly declines. There is a medical analogy here: The longer a bothersome problem is left untreated, the more intensive will be the final remedy (if one is even available).

So where does planning start?

Get educated!

Grumpy Guy

Trying To Figure It Out

First, become familiar with Medicaid. There are all sorts of resources online. I have written a “Plain English” guide to North Carolina Nursing Home Medicaid that is available online (fill out the online request form and I’ll even send you a paper copy – which also contains a valuable planning offer).

Learn about trusts. I have a number of informative articles posted on the Mason Law, PC website. There are also hundreds of articles on the web.

If you’re looking for something more comprehensive with planning guides and forms, tryElderLawUniversity. It is not free, but it is not too expensive either. Fair disclosure:ElderLawUniversityis my brainchild.

In May the Friends of the Asheboro Library and I will be hosting a series of three seminars that might get you started on planning. Click HERE for more details on these three seminars.

Get qualified help. Many of the news outlet articles I mentioned above urge people to get the help of a qualified elder law attorney. I know of at least one! On the other hand, there are other sources to find qualified help.

A good elder law attorney need not be certified, but a certified elder law attorney will be good. Check the North Carolina Board of Legal Specialization for board certified elder law attorneys.

The National Academy of Elder Law Attorneys (NAELA) is an organization representing almost all elder law attorneys in the US. The NAELA website has a geographically searchable directory. In fact, if an attorney is not a member of NAELA, he or she likely is not serious about practicing in the elder law specialty.

To recap:

  • Don’t dither!
  • Get educated!
  • Get help!

Filed Under: General, Medicaid, Medicare, Social Security Tagged With: estate planning, Medicaid, Medicaid Planning, Medicare, Social Security

February 28, 2012 by bob mason Leave a Comment

Dog Language: WHAT?Updated April 14, 2017

Recent Question: Bob, is it OK for the trustee of a special needs trust to purchase a $2,000 pure bred spaniel for the trust beneficiary, Edwina?

Recent Answer: Only if Edwina is not planning on eating the dog. I’ll explain. First, you’ll need to understand the SSI income rules and what In Kind Support and Maintenance (ISM) is. Distributions from a special needs trust might be income! The trick is in understanding how income is counted and what it does.

What is SSI?

Supplemental Security Income, or SSI, supplements the income of disabled persons or those aged 65 and over who meet certain low asset tests and have countable income from all sources less than $735 monthly (this article uses 2017 factors and rates). SSI will insure that a person’s countable income from all sources, when combined with an SSI benefit, will equal the Federal Benefit Rate or “FBR” (which for a single person is $735). See the complete FBR chart elsewhere on this website. For example, if a single person’s countable income is $500, then SSI will pay $235.

Usually the amount of SSI is not as important as the fact that someone is eligible to receive any SSI. In most states (including North Carolina and Georgia) receiving even $1 SSI will entitle the person to Medicaid (which for a disabled individual can be a life saver).

How Income Counts in SSI

An SSI eligible individual may not have countable income in excess of the FBR. Countable income will reduce the amount, dollar-for-dollar, that SSI pays. Income includes all amounts received from wages, other public benefits, annuities, gifts (in the month of receipt) and other noncash items such as food and shelter (or payments made for those expenses).

When calculating countable income, the first $20 of income from all sources is disregarded. Thereafter, the first $65 of earned income is disregarded, and after that one-half of earned income in excess of $65.

SSI Earned Income: Can Edwina Work A Little?

Maybe a little. For example, if Edwina, a disabled individual, occasionally answers phones at a local charity and earns $1,200, she will be eligible for $92.50 monthly SSI payments. Let’s do the math: Edwina earns (meaning she works for it) $1,200. Subtract $20 from $1,200 to get $1,180. Subtract the first $65 of earned income from $1,180 to arrive at $1,115. One-half of $1,115 will be the income excluded ($557.50). So, in other words, Edwina’s countable income is $642.50 ($1,200 minus $557.50). Accordingly, Edwina’s SSI benefit is $735 (the maximum SSI benefit) less $642.50 (countable income). She will receive a monthly SSI check equal to $92.50.

SSI Unearned Income: Can Edwina Receive Cash?

Maybe a little . . . a VERY little. Instead of working, say Edwina receives a $1,200 cash distribution from a special needs trust (or even from a well-meaning friend or relative). SSI considers this unearned income (after all, she didn’t earn it). That means there are no earned income exclusions. $1,200 cash distribution, less the general $20 disregard yields $1,180. That is Edwina’s countable income. $735 (maximum SSI benefit) less $1,180 yields . . . TOAST. Edwina is toast! No SSI benefit.

What happens if instead of cash, the trust pays for certain items for Edwina?  Say, for example, the trust pays for clothing, food, computer equipment, prescription drugs or therapy, entertainment, travel . . . or even a pet.

In-kind Support and Maintenance (ISM): Can Edwina Receive “Other Stuff”?

Now to the matter at hand: Can the trustee of the special needs trust buy the fancy dog for Edwina? It depends. Is Edwina planning on Fricasse of Fido (er . . . a feast) or is she planning for the emotional comfort that can only come from the unqualified love of a furry companion? The answer to those questions will determine whether Fido is In-Kind Support and Maintenance or ISM.

Sometimes trusts and other people give a disabled beneficiary certain non-cash items, or pay for non-cash items on behalf of the individual. If such an item is classified as ISM it will reduce SSI benefits. The amount of the reduction may not matter . . . or it could result in the beneficiary losing all SSI (and Medicaid). Of course, if the item is not ISM, it doesn’t matter how much it is worth as long as it is a non-countable asset for SSI purposes.

Items related to food and shelter are ISM. For example, rent or mortgage payments (shelter), utility expenses (shelter), groceries (food), restaurant food certificates (food), property taxes (shelter), or a Christmas gift from Omaha steaks (food) are all ISM. (Interesting side note: Cable, phone, and internet are not ISM).

If Edwina is planning on eating Fido, Fido’s value ($2,000) will be ISM. On the other hand, if Edwina does not intend to eat Fido, he is not ISM.

What Does ISM Do To SSI Benefits?

It depends. One of two rules could apply, depending upon the beneficiary’s living arrangement. If the beneficiary is living in the home of another for at least one continuous month and receiving both food and shelter without contributing her pro rata share of those costs, her SSI benefit is lowered by one-third of the FBR (or $245 in 2017). This is called the “value of the one-third reduction” or “VTR” rule (I have no idea where they get “VTR”).

The problem with the VTR rule is it is “all or nothing.” If the rule applies, the beneficiary’s SSI is reduced $245 regardless of the actual value of the food and shelter received. If someone is receiving $735 SSI, the reduction to $490 might be a good deal (especially if the food and shelter is high quality).

Two conditions must be met for the VTR rule even to apply: (1) living in another’s home rent free, and (2) receiving free food. If those conditions aren’t met, the rule doesn’t apply.

If the VTR rule doesn’t apply, then the “presumed maximum value” or “PMV” rule applies. Under this rule, if the beneficiary receives any ISM during the month, the value of the ISM is “presumed” to be $245. “Presumed” means that if the beneficiary can prove that the ISM wasn’t worth $245, the SSI benefit will be reduced only by the actual value of the ISM. On the other hand, if the ISM is worth more, the value is still “presumed” to be $245 and the SSI will be reduced accordingly.

As For Fido . . .

So . . . if Fido (worth $2,000) is meant for the dinner table (gross), he is ISM. If Edwina’s SSI is more than $245 and she doesn’t have other offsetting earned or unearned income, then she’ll be OK (other than, I presume, a bit of indigestion). On the other hand, if Edwina’s SSI is less than $245 and Fido is ISM (food), she is . . . .

 

FOR FURTHER READING ON TYPES OF SPECIAL NEEDS TRUSTS, SEE A GOOD ARTICLE ON THIS WEBSITE.

Filed Under: General, Social Security, Special Needs Planning Tagged With: In-kind Support and Maintenance, ISM, Medicaid, SNTs, Social Security, special needs trusts, SSI, Supplemental Security Income

January 31, 2012 by bob mason

Originally published in Course & Scope (January 2012) Newsletter of the Workers’ Compensation Section of the North Carolina Bar Association

Your new client Ralph Kramden, 66, comes to you seeking help. He has a $100,000 Medicare Set-aside Arrangement established after a minor 2005 bus accident at work. The MSA includes approximately $60,000 for a spinal cord stimulator, and Ralph reports that his doctor of the past couple of years says that Ralph is not a candidate for spinal cord stimulation (SCS) on account of the pacemaker that Ralph has had since 2002.

Ralph would really like to access some of the MSA funds. Over the years very little of it has been disbursed, and he has had very little pain and never relied on anything stronger than over-the-counter pain relief.

Upon further research you discover that SCS is indeed contraindicated for patients with pacemakers. In fact, a careful review of the 2007 submissions to CMS shows a significant over-allocation to the MSA. Aside from the issue involving the SCS (or lack thereof) it appears that brand name analgesics (notably Duragesic patches) were used.

Duragesic is a fairly powerful opioid patch that Kramden will likely never use. Further Duragesic use can be addictive, and probably should not be used indefinitely. In keeping with what the initial MSA submitters thought to be acceptable practice, the Duragesic was priced in the MSA over Kramden’s life.  Fortunately, the MSA did reference “Duragesic, or acceptable generic.” You have learned that even if Kramden were using anything stronger than OTC analgesics for pain, a Duragesic generic (fentanyl) is now available at less than two-thirds the price of the Duragesic listed in the MSA prescription drug component.

The entire file leaves you wondering whether the CMS staff are still celebrating over the allocations made to Kramden’s MSA. Maybe hindsight is 20-20. Then you begin to wonder if Ralph has any recourse or right to modify the MSA.

What is galling is that while the entire MSA submission process is voluntary (albeit highly recommended if the case falls within MSA workload review thresholds) Kramden’s case would not even be reviewable had the current review thresholds been in place when CMS reviewed Kramden’s MSA back in 2007.[1] The solution then would have been: Fix it and move on.

The CMS Position: Yes, Yes With Limits, No

CMS takes the position that once an MSA has been reviewed and approved no funds should be released from the MSA for any purpose other than the purpose for which the MSA was established unless CMS approves. Upon discovery of such an unauthorized disbursement, future Medicare reimbursement could be denied until an amount equal to the entire settlement (net of reimbursed conditional payments) has been expended on injury-related expenses. Not pleasant, although a denied claimant would have access to the usual Medicare appeals process.

In an April 22, 2003, policy memo[2] CMS announced that if a treating physician concluded that a beneficiary’s medical condition “substantially improved” a written request together with appropriate supporting documentation could be submitted to the appropriate regional office.

Apparently the April 22, 2003, policy unleashed a workflow avalanche. In Q&A 10 of a July 11, 2005, policy memo CMS backtracked and limited review of revised WCMSA proposals to those submitted five or more years after the initial approval letter and justifying a 25% or more reduction in the then outstanding MSA funds. Ralph would have had a reasonably good chance of submitting a revised MSA proposal, less the SCS, and perhaps less the other analgesics (or at least priced at the generic level).

Unfortunately, effective August 25, 2008, CMS rescinded Q&A 10 of the July 11, 2005, policy memo. In effect, CMS is attempting to “freeze” allocations for future medicals at settlement date levels.

Well . . .Maybe

In spite of the air of finality in the August 25, 2008, memo, there may be a glimmer of hope for Kramden.  Q&A 12 of the July 11, 2005, memo remains in force.

Q&A 12, entitled “Additional Information Submission after WCMSA Case Is Closed” might help Ralph out. The policy reminds readers that “[t]here are no appeal rights stemming from a CMS determination of the appropriate amount of a WCMSA” but that there are “several other options available.”

A submitter who believes that there are “obvious mistakes, such as mathematical errors or failure to recognize” previously paid expenses being included in the allocation is invited to contact the Regional Office issuing the final determination for a correction.

A submitter who believes evidence has been misinterpreted or who disagrees “for some other reason” has a couple of options. If a submitter believes additional evidence not previously considered would warrant a change in the MSA amount, the case may be resubmitted “with the additional evidence” and a request for review to the Coordination of Benefits Contractor (COBC). The request will be treated as a new WCMSA submission.

In the case of Ralph Kramden, it may be worthwhile to consider a re-submission under the foregoing policy. The fact that in 2007 he had a pacemaker that would have medically contraindicated the use of a SCS at the time of the WCMSA submission certainly falls under the heading of “additional evidence not considered at the time of the initial submission.”  Had medical evidence been developed much later that pointed to the avoidance of SCS for pacemaker wearers, though not as strong a case, a submission might still be warranted.

With respect to the Duragesic component, two possible arguments could be advanced. First, Duragesic (or a generic equivalent) should not have been priced for Ralph’s life due to its addictive nature; the correct manner would have been limited to a specific duration (be sure to support this contention with medical records or a physician’s statement). Second (and as an alternative argument), now that a less expensive generic is available, any component remaining for the use of this generic should be repriced. With respect to the latter argument, there is no CMS guidance, but it is certainly worth the attempt.

Finally, CMS acknowledges that a claimant has recourse to the usual Medicare appeals route if payment is denied on the basis that the WCMSA has not been properly exhausted. The rights available to a denied Medicare claim are much more extensive, including eventual recourse to the federal courts. The amount involved, however, would have to be significant in order to justify the loss of Medicare during the appeals process, not to mention the direct costs associated with the appeal.

Summary

Unfortunately, there is no longer a procedure for reducing or eliminating an over-allocated MSA. On the other hand, CMS policy indicates a potential for reconsideration in cases of clear error or the development of new or additional evidence. The likelihood of a successful adjustment, however, is far from certain, and the practitioner and client will be required to consider whether the process is worth the time and effort.



[1] As of April 25, 2006, CMS reviewed MSA submissions involving total settlements in excess of $25,000. This was the policy in effect at the time Kramden’s 2007 was prepared. Effective May 11, 2011, CMS announced it would review only those MSA submissions that either (i) involved current Medicare beneficiaries with total settlements in excess of $25,000, or (ii) involved claimants with a “reasonable expectancy” of Medicare enrollment within 30 months and total settlements in excess of $250,000. Had the current policy been in place in 2007, Kramden’s MSA would not have fallen into the review threshold (at age 61 he did not have a reasonable expectation of Medicare enrollment within 30 months).

[2] CMS usually releases administrative practice, guidance and policy in the form of “Regional Administrator” letters from various national office directors.

Filed Under: Medicare Secondary Payer

January 31, 2012 by bob mason

Guest Columnist . . .

Patricia A. Shevlin, MD

Patricia Shevlin, MD

At the beginning of every year, most of us try to get organized, make a few resolutions about what we could do better and start new prescription drug plans. One area that is frequently neglected is the medication list.  In an effort to cut down on medication errors, I offer my recommendations to patients about their medications.

  1. Keep an updated list of your medications with you. Include the prescription and the non-prescription medications. Before your appointments, review the list by comparing it to the bottles that you have at home. If there is a discrepancy, you should adjust your list. If there is an error or suspected error you will be able to get it corrected by calling the office of the physician who wrote the prescription, or ask at the office visit.  At the appointment or when you get home, add any new prescriptions to your list.
  2. Include on the medication list the reason for the medicine, such as diabetes or blood pressure. I think this makes it easier to organize your medications and to realize what to expect if you miss a pill or run out of a medication.
  3. To prevent running out of a medication, I strongly recommend a weekly pill container. When you fill this every Saturday or Sunday, you will know in advance when you need to call for refills. No matter how efficient an office or pharmacy is, delays can occur due to electronic transmission errors, fax machine downtime etc.  The sooner you can request a refill, (within the requirements of your insurance company), the better.
  4. The weekly medication container is NOT an indication of memory impairment.  Most of us are busy and when we have medications we take at the same time day after day, it is easy to think you have taken a medication when you have not. I remind patients all the time that birth control pills have come in packages with the day of the week written on them for this exact reason. It’s not a problem just for the seniors.
  5. Keep the prescription and non prescription medications that you take on an as needed basis separate from the daily medications. The names should be on a separate list or the back of the daily list. The bottles should be in a separate bag. This cuts down on confusion, especially when filling the weekly pill container. It also helps a family member who may be helping you when you are sick and need one of those medications.

You may be asking yourself “Why do I need to do all of this? My doctor has a record of my medications.” First of all, you are the patient and you are responsible for what goes in your body. In addition to your health, it’s also your money that’s at stake here.  Most of us have multiple doctors and all of our medicines are not written in one place. Bringing your list should encourage your physicians to put the entire list into their records. Finally, many patients use multiple drugstores. There are mail order options for daily medications, local drugstores for acute medications and $4 options for some medications.  The possibilities for confusion are endless.  Everybody needs a reliable system.

Dr. Shevlin is a partner in Asheboro Family Physicians of North Carolina, PA

 

 

 

Filed Under: Guest Columns

January 31, 2012 by bob mason

Do not confuse health care powers of attorney with general powers of attorney, financial powers of attorney or durable powers of attorney (by the way, general, financial, and durable are all words to describe essentially the same type of document). As I explain to clients, general, durable or financial powers of attorney are used to appoint someone to take care of your business matters.

A health care power of attorney is used to appoint someone to make decisions regarding your medical treatment if you are unable to do so. A health care power of attorney is not the same as a living will. A living will is a document that can be used to direct health care providers as to the type of treatment someone wants (or does not want) when and if he is unable to make that decision himself.

Health Care Powers of Attorney vs. Living Wills

Usually, if someone has both a health care power of attorney and a living will, the preferences indicated in the living will trump later contrary decisions the health care agent may attempt to make. For that reason, many people lucky enough to have a couple of stable, mature decision makers who understand their health care preferences are content to forego the living will and give the people appointed (a primary and a backup) the flexibility to respond to future circumstances rather than being somewhat “straight-jacketed” by a living will that would over ride some of their decisions.

Of course, some people do not have close family or friends who can be entrusted with that sort of decision-making authority. Perhaps others do not want to saddle an aging spouse or a child with life-or-death decision-making responsibility. And, of course, some people have very firm religious convictions they want to ensure are firmly enshrined in a living will (for example, Jehovah’s Witnesses often wish to ensure that prohibitions against use of blood or blood products are clearly set out in as living will).

The term “advance directive” is a generic term that is applied to both health care powers of attorney and living wills. Both documents are a type of advance directive. To complicate matters, some states have statutory form advance directives that combine the two types of forms into a single document. Georgia is an example of this approach. Other states have form advance directives that are separate. North Carolina is an example.

Simple Forms OK

All states (that I know of) provide that the statutory form is a nonexclusive form that is guaranteed to comply with all the formalities required regarding witnesses and notarization and the like. In other words, people are free to use their own forms as long as those forms hit the minimum state requirements for a valid advance directive. Because the statutory forms are often very confusing and long, many people prefer to have a very simple health care power of attorney (In effect: “I appoint Jane Doe, John Doe if Jane is unavailable, to make all health care decisions for me if I am unable to”).

I have posted a simple for download.

A Walk Through The North Carolina Statutory Form

Amidst much fanfare (and immediately upon the heels of the infamous Terri Schiavo case, North Carolina revised its statutory advance directive forms. The forms have been highly criticized as being too complex. Many attorneys have drafted alternate (and simpler) versions. A couple of sections of the North Carolina Bar Association have begun the work of revisiting these forms to prepare alternatives to the general assembly.

I have posted the North Carolina statutory Health Care Power of Attorney (NCHCPOA) form for download.

The key provisions of the NCHCPOA form are:

  • Section 1:  Appoint an agent and a successor.
  • Section 2:  Usually ignored and left blank, this provision can be used to designate which physician makes a determination to “activate” the NCPOA; left blank and any attending physician may do so.
  • Section 3:  Of course you may revoke your NCHCPOA!
  • Section 4:  This is a broad (very broad) grant of authority to your health care agent to make health care decisions on your behalf. The first clause is key:  “Subject to any restrictions set forth in Section 5 below . . . .” In other words, if you leave Section 5 blank, the authority granted in Section 4 is not limited. If you fill in some or all of the blanks in Section 5, then the Section 4 powers are limited.
  • Section 5:  Subsection A allows limitations on the agent’s ability to order withdrawing artificial nutrition and/or hydration. Subsection B allows other more general limitations on agent authority (this is where, for example, the Jehovah’s Witnesses often specify their specific beliefs regarding use of blood products. Subsection C and Subsection D limit mental health decision making ability. Subsection E places limits on the agent’s ability to order autopsies.
  • Section 6:  This is a specific grant to your agent to order organ donations “to the extent I have not already made valid and enforceable arrangements that have not been revoked.”
  • Section 7:  This provision instructs the Clerk of Court to appoint your health care agent as your guardian of the person if that ever becomes necessary. If you do not agree with that, you should alter that provision.
  • Section 8 and Section 9:  Miscellaneous provisions.

Complicated enough? That’s why I hope it will be revised.

As mentioned, above, North Carolina does an Advance Directive For A Natural Death (“Living Will”). I believe it is a terrible form, extremely confusing, and totally unnecessary if you have health care agents upon whom you can rely (just my opinion). In any event, in the interests of complete disclosure, I have posted that form as well.

A Final Thought

Are advance directives for older people only? Allow me to answer with a pop quiz:

Q:  What did Karen Ann Quinlan, Nancy Cruzan, and Terri Schiavo have in common?

A:  Two things. They became famous (infamous) court cases. All three names belonged to young, healthy women without advance directives.

Filed Under: Advance Directives Tagged With: Advance Directive, Health Care Power of Attorney, living will

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