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Chad Winthrope

Will my disabled adult son continue getting Social Security survivor benefits after age 18 when siblings age out?

I recently lost my husband and our three children (17, 15, and 13) are now receiving survivor benefits because they're under 18. My youngest son has significant vision impairment and cognitive disabilities. I'm trying to plan for the future and have several questions about his benefits. Will he be able to continue receiving Social Security benefits after he turns 18 due to his disabilities? And if so, when his siblings age out of their benefits (at 18), would his monthly payment amount increase since he'd be the only child still collecting? I'm years away from collecting my own retirement benefits and plan to claim on my own record rather than my husband's. What's the best strategy to maximize benefits for both of us in this situation? Any guidance would be appreciated.

Yes, your disabled son can continue receiving survivor benefits beyond age 18 if his disability began before age 22. He would need to qualify under the Adult Child Disability Benefit program (sometimes called Disabled Adult Child or DAC benefits). The process requires a disability determination similar to SSI/SSDI qualification. As for your second question - yes, when your other children age out at 18 (or 19 if still in high school), your disabled son's benefit could increase because of the family maximum calculation. The total amount payable to all survivors in a family is capped, so when there are fewer beneficiaries, each remaining person may receive more.

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Thank you for explaining this! Does he need to apply for this Adult Child Disability Benefit program before he turns 18, or can we wait until closer to that time? His disability has been documented since he was 3 years old.

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You should start the application process about 3-4 months before he turns 18. SSA will need medical records documenting his condition and how it prevents substantial work. Make sure his doctors are documenting his limitations thoroughly. He'll need to meet the same disability criteria as adult SSDI applicants, so gathering comprehensive records now is important. The determination process can take several months, so don't wait until the last minute.

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just want to say i'm sorry about your husband. my kids got survivors benefits too and it was so confusing at first.

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Thank you. It's been overwhelming trying to figure everything out while grieving.

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Regarding maximizing benefits - you might want to consider whether your husband's record would provide a higher spousal benefit than your own retirement benefit. You can actually claim one type and then switch to the other if advantageous. The rules get complicated depending on your age, earnings history, and when you start claiming. For your disabled son, definitely look into the Adult Disabled Child benefits as mentioned above, but also check if he might qualify for SSI in addition to the survivor benefits, especially during the transition to adult benefits. Sometimes people can get both depending on the benefit amounts and other income.

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This is helpful, though honestly all these options make my head spin. Is there a way to get personalized guidance on this from SSA? I've tried calling but never get through to anyone who can give me specific advice about our situation.

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I had the same problem trying to get through to SSA when I needed to discuss my kid's benefits. After wasting hours on hold and getting disconnected repeatedly, I found this service called Claimyr that got me through to an agent in under 10 minutes. Check out their demo at https://youtu.be/Z-BRbJw3puU - it works by holding your place in line and calling you when an agent is ready. Their website is claimyr.com. For complex situations like yours with disabled adult child benefits, speaking to a knowledgeable SSA representative is definitely worth it.

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my daughter has autism and gets DAC benefits after my husband passed she's 26 now. one thing they dont tell you is that your son cant have resources over $2000 and if he ever gets married he loses the benefit completely. they also do reviews every few years to check if he's still disabled. its been a lifesaver for us but theres a lot of rules

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I think you might be confusing SSI with DAC benefits. The $2,000 resource limit applies to Supplemental Security Income (SSI), which is need-based. Disabled Adult Child benefits that continue from survivor benefits don't have asset limits because they're based on the parent's work record, not financial need. You're right about marriage though - marriage does terminate DAC benefits in most cases. The continuing disability reviews (CDRs) are also correct - they typically happen every 3-7 years depending on the nature of the disability.

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Regarding maximizing benefits for both you and your son - I recommend scheduling an appointment with an SSA Claims Specialist specifically. You have several strategic decisions to make, especially considering your own claiming strategy. For your situation, you should know these key points: 1. Your FRA (Full Retirement Age) factors heavily into optimal timing 2. As a widow, you can claim survivor benefits as early as age 60 3. You can switch between your own retirement and widow's benefits at different times to maximize lifetime benefits 4. Your disabled son's benefits will be 75% of your deceased husband's Primary Insurance Amount (PIA) 5. When your other children age out, your son's benefit may increase up to the family maximum For complex cases like yours involving a disabled adult child and widow benefits, getting personalized advice is essential.

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Thank you for breaking this down so clearly. I didn't realize I could claim survivor benefits at 60 and then switch to my own later if that's better. Is there a good worksheet or calculator I can use to compare different scenarios? I'm trying to plan ahead since I have several years before I'm eligible.

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The SSA has a retirement calculator on their website, but it doesn't handle complex scenarios well. For your situation, I recommend using one of the specialized Social Security optimization tools like Open Social Security (free) or Maximize My Social Security (paid). These let you compare different claiming strategies and see the lifetime benefit differences. Since you have the added complexity of survivor benefits and a disabled dependent, you might also consider consulting with a financial advisor who specializes in Social Security claiming strategies.

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One more thing about your son's benefits - if he's receiving survivor benefits now and transitions to Disabled Adult Child benefits, make sure you understand the healthcare implications. Once he's an adult on SSDI (which is what DAC essentially is), he'll qualify for Medicare after a 24-month waiting period. But depending on your state, he might also qualify for Medicaid, which could provide more comprehensive coverage for his specific needs. Some states have special Medicaid waiver programs for people with disabilities that provide additional supports and services beyond medical care.

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I hadn't even thought about the healthcare aspect. He currently has coverage through my employer, but understanding the Medicare/Medicaid options will be important long-term. This is getting so complicated - there are so many different programs and rules to keep track of.

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i feel for u so much. my friend has a disabled daughter and says the whole system is set up to make it as confusing as possible!!!

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TRUTH!!!! i swear they WANT us to mess up so they can deny benefits its so frustrating!!!! took me 14 months to get my sons benefits approved and we had CLEAR documentation of his disability since BIRTH!!!!!

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To summarize the options for your son: 1. He can transition from child survivor benefits to Adult Disabled Child benefits at 18 if his disability began before 22 2. The benefit amount would be the same (75% of your husband's PIA) initially 3. When siblings age out, his benefit could increase up to the family maximum (typically 150-180% of the worker's PIA) 4. The application process should start 3-4 months before he turns 18 5. He'll need comprehensive medical documentation of his disability 6. After approval, he'll get Medicare after 24 months 7. Benefits continue indefinitely as long as he remains disabled and unmarried For yourself, you have flexibility to either claim reduced widow's benefits as early as 60 and switch to your own retirement later, or vice versa depending on which maximizes your lifetime benefits.

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Thank you so much for this clear summary. It helps to see all the options laid out this way. I'll start gathering his medical records and begin preparations well before his 18th birthday. I really appreciate everyone's advice!

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I'm so sorry for your loss, Chad. Navigating all these benefits while grieving must be incredibly overwhelming. One additional resource that might help - many states have disability advocacy organizations that can provide free guidance on transitioning from child to adult benefits. They're often more accessible than SSA directly and can help you understand the specific documentation needed for your son's case. Also, since you mentioned his vision impairment, make sure his eye care records are comprehensive - SSA has specific criteria for visual disabilities that you'll want to ensure are well-documented. The fact that his disabilities have been documented since age 3 should work in your favor for the "disabled before age 22" requirement. You're doing great planning ahead - having this information now gives you time to get everything in order properly.

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Chad, I'm so sorry for your loss. Managing all these benefits while grieving is incredibly difficult. One thing I'd add to the excellent advice already given - make sure to keep detailed records of everything related to your son's disability and benefits. Create a file with all his medical records, correspondence with SSA, and any disability determinations. When it comes time for the Adult Disabled Child application, having everything organized will make the process much smoother. Also, consider reaching out to your local disability rights organization - they often have advocates who specialize in SSA benefits and can help guide you through the process at no cost. The National Disability Rights Network website has a directory to find your local office. You're being so thoughtful planning ahead for your family's future.

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This is such great advice about keeping detailed records - I wish I had started doing this more systematically from the beginning. Between all the doctor visits, therapy sessions, and school evaluations over the years, I have paperwork scattered everywhere. I'll definitely look into our local disability rights organization too. It would be so helpful to have an advocate who really understands the system walk us through this process. Thank you for the resource recommendation!

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Chad, I'm so sorry for your loss. As someone who works with families navigating these transitions, I wanted to add a few practical tips that might help as you prepare for your son's Adult Disabled Child application. First, start collecting not just medical records, but also educational records (IEPs, 504 plans, psychological evaluations) and any vocational assessments - SSA looks at functional limitations across all areas of life, not just medical. Second, ask his current doctors to specifically document how his disabilities limit his ability to work, not just his diagnoses. Phrases like "unable to maintain consistent attendance" or "requires constant supervision" are more helpful than just listing medical conditions. Finally, if your son receives any state disability services, get documentation of those too - it helps establish the severity and consistency of his limitations. The transition from child to adult benefits can be complex, but starting this documentation process now will put you in a strong position when application time comes.

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This is incredibly helpful advice about documenting functional limitations rather than just diagnoses. I never thought about how important the specific wording would be - "unable to maintain consistent attendance" is so much more concrete than just saying he has cognitive disabilities. I'll start reaching out to his teachers and therapists to get statements about his day-to-day limitations and work capacity. The educational records tip is great too - we have years of IEPs that clearly show his need for accommodations and support. Thank you for taking the time to share such detailed guidance!

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Chad, I'm deeply sorry for the loss of your husband. What you're going through is unimaginably difficult, and it's admirable that you're planning ahead for your son's future during such a challenging time. One thing I'd like to add that hasn't been mentioned yet is the importance of understanding how work activity might affect your son's benefits in the future. Even though he has significant disabilities, SSA has work incentive programs like the Trial Work Period and Ticket to Work that allow disabled beneficiaries to test their ability to work without immediately losing benefits. If your son ever wants to try some form of supported employment in the future, these programs can provide a safety net. Also, since he's receiving survivor benefits now, make sure SSA has updated contact information and that you report any changes in his condition or circumstances promptly. The system can be overwhelming, but you're asking all the right questions and getting excellent advice from this community. Take care of yourself too during this difficult journey.

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Thank you for mentioning the work incentive programs - that's something I hadn't considered at all. Right now it's hard to imagine my son being able to work given his current limitations, but you're right that having those safety nets available could be important down the road. I appreciate you reminding me about keeping SSA updated too - with everything going on, it's easy to forget about reporting changes. This whole thread has been so educational. I came here feeling completely overwhelmed by all the rules and options, but everyone has broken it down into manageable pieces. It's reassuring to know there are programs designed to help rather than just barriers to navigate.

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Chad, I'm so sorry for your loss. Reading through this thread, I can see you're getting excellent advice about your son's transition to Adult Disabled Child benefits. One thing I'd like to emphasize that might give you some peace of mind - the fact that his disabilities have been documented since age 3 puts you in a very strong position for the "disabled before age 22" requirement. SSA is looking for evidence that the disability existed and was severe enough to prevent substantial gainful activity before that age, and having 14+ years of medical documentation will be incredibly helpful. Also, don't feel like you need to figure everything out at once. Focus first on preparing for your son's DAC application (starting about 3-4 months before he turns 18), then you can work on optimizing your own claiming strategy later. You have time to make these decisions thoughtfully. The community here has given you a wonderful roadmap - you're going to navigate this successfully.

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Thank you so much, Ryder. You're absolutely right that having 14+ years of documentation should work strongly in our favor - sometimes I get so caught up worrying about all the potential complications that I forget we actually have a lot going for us. Your advice about taking this step by step is exactly what I needed to hear. I've been trying to solve everything at once when really I should just focus on getting his DAC application ready first. This whole conversation has been such a lifeline during what feels like an impossible situation. I'm genuinely grateful for this community and all the knowledge everyone has shared.

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Chad, I'm so sorry for your loss. I wanted to add one more perspective that might be helpful as you navigate this process. Since your son has both vision impairment and cognitive disabilities, make sure his medical team is documenting how these conditions interact and compound each other's effects. SSA evaluates multiple impairments together, not just individually. For example, his cognitive limitations might make it even harder to adapt to or work around his vision impairment. Also, consider reaching out to your state's vocational rehabilitation agency now - they often work closely with SSA and can provide assessments that support disability determinations. They might also have transition services for young adults with disabilities that could be beneficial regardless of the benefit outcome. You're doing an amazing job advocating for your family during such a difficult time.

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This is such an important point about documenting how multiple disabilities interact - I hadn't thought about emphasizing the combined effects rather than just listing each condition separately. You're absolutely right that his cognitive limitations would make adapting to vision loss much more challenging than for someone without those additional barriers. I'll make sure to discuss this with his medical team at our next appointments and ask them to specifically document how his conditions compound each other. The suggestion about vocational rehabilitation is interesting too - even if he's not ready for any kind of work assessment now, having that relationship established could be valuable down the road. Thank you for thinking through all these different angles and resources I might not have considered on my own.

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Chad, my heart goes out to you during this incredibly difficult time. Losing a spouse while trying to navigate complex benefit systems is overwhelming, but you're asking all the right questions and planning ahead thoughtfully. I wanted to add something that hasn't been mentioned yet - consider connecting with your local Independent Living Center (ILC). These centers often have benefits counselors who specialize in Social Security programs and can provide free, personalized guidance throughout the transition process. They understand the nuances of moving from child to adult benefits and can help you prepare the strongest possible application. The Association of Programs for Rural Independent Living website has a directory to find your local center. Also, since your son has significant disabilities, it might be worth exploring Special Needs Trusts now, even before he transitions to adult benefits. This can help protect his eligibility for means-tested programs later while allowing family to provide additional support. You're handling this with such grace and foresight - your son is lucky to have such a dedicated advocate in his corner.

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Thank you for mentioning Independent Living Centers - I had no idea these resources existed! The idea of having a benefits counselor who specializes in Social Security transitions sounds incredibly valuable. I've been feeling like I'm stumbling through this process alone, so having professional guidance specifically for our situation would be such a relief. The Special Needs Trust suggestion is also something I need to research more. I keep hearing about them but haven't fully understood how they work or when to set one up. It sounds like there might be strategic timing considerations there too. I really appreciate you taking the time to share these additional resources - every new option feels like another lifeline during what has been such an overwhelming process.

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Chad, I'm so sorry for the loss of your husband. What you're going through is heartbreaking, and I admire your strength in planning ahead for your son's future during such a difficult time. I wanted to share something that might help with the Adult Disabled Child application process - make sure to request copies of all medical records from his early childhood, especially those vision and cognitive assessments from when he was 3. Sometimes older records get archived or destroyed, so getting them now while you have time to track them down could be crucial for establishing the "disabled before age 22" requirement. Also, if your son has ever had any psychological or neuropsychological testing, those reports are particularly valuable because they often include detailed functional assessments that speak directly to work capacity limitations. The SSA really wants to see how his disabilities affect his daily functioning and ability to work, not just the diagnoses themselves. You're doing such an incredible job advocating for your family - your son is fortunate to have someone fighting so hard for his future security.

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This is excellent advice about requesting early medical records now! I never thought about the possibility of older records being archived or destroyed - that would be devastating to lose that crucial early documentation. I'll start calling his pediatrician's office and early intervention providers from when he was little to request copies of everything. You're also right about the neuropsychological testing being particularly valuable - he had comprehensive evaluations done at ages 5, 8, and 12 that included detailed assessments of his cognitive functioning and adaptive skills. Those reports do focus a lot on daily living limitations rather than just listing diagnoses, so they should be perfect for what SSA is looking for. Thank you for the reminder to be proactive about gathering this documentation while I still have time to track everything down properly.

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Chad, I'm so deeply sorry for the loss of your husband. What you're facing - grieving while trying to navigate these complex benefit systems for your children - is incredibly challenging, and you're handling it with remarkable thoughtfulness and care. I wanted to add something that might help with timing and preparation: when you do start the Adult Disabled Child application process 3-4 months before your son's 18th birthday, consider requesting an in-person appointment at your local SSA office rather than trying to handle it over the phone or online. For complex cases involving multiple disabilities like your son's vision and cognitive impairments, having face-to-face time with a claims specialist can make a huge difference. You can bring all your documentation, ask questions in real time, and ensure they understand the full scope of his limitations. Also, don't hesitate to bring an advocate with you - whether from an Independent Living Center, disability rights organization, or even just a knowledgeable friend. Having support during that appointment can help ensure nothing important gets overlooked. You're doing an amazing job preparing for your family's future during such an unimaginably difficult time.

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This is such valuable advice about requesting an in-person appointment! I hadn't considered that approach, but you're absolutely right that for a complex case like ours, having face-to-face time would be so much better than trying to explain everything over the phone. Being able to bring all the documentation and have real-time discussion about his specific limitations sounds infinitely more effective than the typical phone runaround. The suggestion about bringing an advocate is really smart too - I've been feeling like I need to handle everything myself, but having someone who really understands the system there for support could make all the difference. After reading through all these responses, I'm starting to feel like I actually have a roadmap for navigating this process successfully. Thank you for the encouragement and practical guidance - it means more than you know during this difficult time.

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Amara Eze

Chad, I'm so sorry for your loss. Losing a spouse while trying to navigate these complex systems is overwhelming beyond words. I wanted to mention one resource that might help bridge the gap while you're preparing for your son's Adult Disabled Child application - many states have "Benefits Planning, Assistance and Outreach" (BPAO) programs that provide free counseling specifically for Social Security disability benefits. These counselors can help you understand exactly what documentation you'll need and can even help coordinate with SSA during the application process. You can find your local BPAO through the Social Security Administration's website or by calling their main number. Also, since your son will likely qualify for Medicare after his 24-month waiting period on DAC benefits, it might be worth researching Medicare Supplement plans now so you're prepared for that transition. The combination of Medicare and potentially Medicaid could provide excellent coverage for his ongoing needs. You're being incredibly proactive in planning for his future - that preparation will serve you both well when application time comes.

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Thank you for mentioning the BPAO programs - I had never heard of those before but free counseling specifically for Social Security disability benefits sounds exactly like what I need right now. Having someone who can help coordinate with SSA during the actual application process would be invaluable. I'll definitely look into finding our local program through the SSA website. The Medicare planning tip is also really helpful - I've been so focused on getting through the DAC application that I hadn't thought ahead to the healthcare transitions that will come after approval. It's reassuring to know that the combination of Medicare and Medicaid could provide comprehensive coverage for his needs. This entire thread has opened my eyes to so many resources and programs I didn't know existed. I'm feeling much more confident about navigating this process thanks to everyone's guidance and support.

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