In order to ensure proper use of funds, lawyers for special needs planning in Georgia help their clients choose a trustee. This person is put in charge of the special needs trust, and instead of providing money directly to the beneficiary (the child with special needs), the trustee will usually pay directly from the trust to service providers, housing officials, etc. Some trusts are set up with the parents and the special needs planning lawyer in a way that provides payment to the trustee for taking on these responsibilities.
Sometimes, there is no mention of a fee in the trust paperwork, but the trustee is still entitled to payment, if desired. There are several factors that should go into determining an suitable fee, whether it is stipulated in advance by those creating the trust or it is later determined that one is needed. The complexity of the trust is certainly one of those considerations. If there are numerous investments that need to be managed, for example, it would be appropriate to pay the trustee for the time and expertise involved.
The types of services the trustee provides also play into determining the fee. More complex tasks, like the investment management mentioned above, would likely be paid at a higher rate than less complicated ones, such as paying monthly bills. The trustee would be responsible for tracking his or her time, along with the service, in order to determine a fair fee.
Occasionally, a trustee will pay for a good or service from personal money. When that happens, the trustee can expect to be reimbursed out of the special needs trust by providing a receipt for money spent on the beneficiary’s behalf. This type of payment is separate from the trustee’s fee and would not be treated the same. That’s because the trustee’s fee is taxed as income. On the trust’s end of things, the fee is a tax deduction.
Special needs planning lawyers in Georgia are continually looking for the best ways to serve their clients and provide for the future. Having a trustee in place is one method to ensure that funds are being used appropriately, and paying that trustee can be one way to ensure the job gets done right.
Thanks to a new law passed in Congress last month, disabled individuals will no longer have to choose between saving a small nest-egg for future care expenses or preserving long-term eligibility for low-income benefits such as Medicaid or Supplemental Social Security Insurance (SSI).
Under the Achieving a Better Life Experience (ABLE) Act, individuals with disabilities now have the opportunity to begin saving their own money toward future health-care costs, housing expenses, transportation, education, and other needs without jeopardizing eligibility for critical government benefits.
Eligibility under the ABLE Act is limited to those 26 and under, with a $14,000 cap on yearly contributions. A total of $100,000 tax-free can now be accumulated in a special ABLE account, which is limited to one per person.
Prior to the passing of the ABLE Act, individuals with disabilities were unable to have assets totaling more than $2,000 or earn more than $680 per month without forfeiting eligibility for government programs like Medicaid. This was worrisome for families, considering that Medicaid is often the only healthcare option available for those with significant disabilities.
To protect such benefits, then, parents of disabled children would often go to great lengths to avoid putting assets, donations or inheritances their child’s name. But now, under this law, families have new opportunities to help their child save for the future while keeping much-needed government benefits intact.
Additionally, the ABLE Act offers another exciting benefit in that disabled individuals will no longer be deterred from pursing gainful employment opportunities in the local community.
Prior to the passing of this law, individuals who had some capacity to work and contribute to society were often deterred from doing so out of fear of they would cross the income thresholds of their benefits and lose everything. Now, young people with disabilities can take a chance in pursuing meaningful work opportunities without sabotaging their financial future.
As an Atlanta special needs attorney, I feel this is a wonderful law and a positive step forward in empowering disabled children and young adults. An ABLE Account combined with solid planning tools such as Special Needs Trusts now affords families with even more protection and flexibility when saving for the future. A good special needs attorney can help families utilize these tools for maximum savings opportunities and peace of mind.
April is Autism Awareness Month, which seeks to educate the public about the needs and challenges facing those with autism spectrum disorders. Yet despite the observance, Atlanta special needs attorney Steve Worrall warns that many parents of special needs children are still in the dark as to 3 key planning steps designed to protect their child if the unthinkable happens.
Atlanta, GA – April is Autism Awareness Month in the United States.
According to AutismSpeaks.com, the disorder affects one in 110 children in the United States, with boys being four times more likely than girls to be diagnosed on the spectrum. The prevalence of autism has also increased 57 percent from 2002 to 2006, thus prompting The Centers for Disease Control and Prevention to refer to autism a “national public health crisis”.
Yet while autism awareness is at an all time high, Atlanta, Georgia, special needs and estate planning lawyer Steve Worrall warns that many parents are still in the dark as to how to make sure their child is physically and financially cared for if and when death or incapacity occurs.
“As much parents of special needs children hate to think about it, there will come a time when they are physically unable—or perhaps no longer alive—to oversee their child’s care,” warns Worrall. “That’s why long-term care plans must be put in place as soon as a diagnosis is made to ensure the child always stays physically and financially protected if the unthinkable occurs,” he adds.
While Worrall does admit that the options for long-term care planning are broad and depend on the needs of the child, he explains that parents can simplify the process by starting with these 3 key planning steps:
1. Name Guardians– Worrall urges parents to immediately name short and long-term guardians who can oversee their child’s care if something unexpectedly happens to them. Without such designations in place, the child could end up in a lengthy custody battle—or worse—be placed in foster care if the unthinkable happens. Worrall advises parents to think outside the box and focus on finding someone whose love and dedication to the child closely resemble their own. Finally, parents should give copies of their designations to the guardians themselves, as well as the child’s school, babysitters and even the neighbors so everyone knows exactly who to call if a crisis strikes.
2. Set up a Special Needs Trust– A special needs trust is a legal tool that ensures a disabled child’s health care and living needs are taken care of if something happens to mom or dad. Worrall explains that while many parents have good intentions of leaving their child life insurance benefits or other assets in a will if they pass, leaving a child an inheritance outright could void their eligibility for Social Security or Medicaid in the future (which is often the only health care option available!). Instead, a trust helps to ensure that the child receives such financial benefits without actually having assets in their name—thus leaving all government benefits intact.
3. Build a Team of Support- According to Worrall, it’s never too early to begin building a team of trusted caregivers and advisors who can immediately step in and help the child if a crisis occurs. Such team members may include the child’s legal guardians, a trusted doctor, financial advisor, estate planning attorney and dedicated family or friends. Building such a team now also helps to ensure you have the right people in place, as opposed to someone who will prey upon your child’s disability in an emergency.
“Parents of special needs children must go into planning with the mindset that their child will require a lifetime of care,” says Worrall. “Fortunately, by starting with these 3 key steps, parents will make tremendous progress in ensuring their child is physically and financially cared for in their absence.”
FOR MORE INFORMATION, PLEASE ASK FOR OUR SPECIAL NEEDS PLANNING GUIDE AT GeorgiaSpecialNeedsLawyer.com