MEMBER OF CONGRESS

Lisa Murkowski

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Murkowski’s floor work centers on Alaska-specific legislation—land transfers, Native health and tribal programs, often as the Senate Indian Affairs chair working across the aisle with Democrats like Coons and Schatz—plus bipartisan health measures such as ACT for ALS. Her speeches lean heavily on personal stories, tributes, and anecdotes; she spends far more floor time than most senators on family experiences, thanks to colleagues, and asides, rather than on making reasoned arguments for her positions. When she does argue, it is usually with concrete detail—bill histories, acreages, hearing records—and she rarely claims credit for her side or attacks the other party, instead emphasizing cooperation. On policy asks she is direct about what she wants passed and why, though her case-making often takes second place to storytelling.Written by AI from their statements. Updated .

Average grade
B+
82 / 100 over 7 statements
Signal 63 / 100
Relevance Not scored
Reasoning 95 / 100
Respect 100 / 100
Clarity 99 / 100
Averaged over the 7 of 11 statements graded so far.

In their own words

Statements 11

Senate ·

Als

“The Senate passed a bill to renew funding for ALS research and care. My cousin's husband died from ALS, and my family worked hard for this. I will keep working until we find a cure.”
Official Congressional Record

Mr. President, I am so honored to work alongside colleagues like my friend from Delaware, who has so much heart and so much passion. But it is a reminder to me of how much we have to do on behalf of those who do feel that they do not have a path forward, and they look to us in Congress as they go through some of the most difficult and dark moments as families together. Like Senator Coons, I have been touched by ALS, and my family has. And, in fact, it was through my family that I came to this cause, and it is through my family that I will remain committed to this cause, until such time as we have a full treatment and a cure for this awful and dreaded disease. It was my cousin’s sister, as I call her--it was her husband Pat, who lived with ALS for 8 years. And for 8 years, as a family, we came to understand the impact of the disease, but more than the impact, what it meant to live day by day, hoping--just hoping--that tomorrow was going to bring something that was more positive. And so after Pat left us, my cousin Jenny stayed in the fight. It is pretty hard after you have fought alongside your spouse, and pretty hard when you have come to hate a disease so passionately, and you want to never utter those words, those letters, again. But when ACT for ALS reauthorization passed last night by voice vote, I sent a text to Jenny. And I said: And she sent a note back, late, late last night. And I am just going to share this as my final comments. She said: So, Mr. President, thank you. Thank you for helping us realize this today on behalf of all those who live with ALS and their families. I yield the floor.

“The Senate passed our bill to keep funding ALS research and treatments. This law helps patients try new medicines and keeps scientists working on cures. We must keep this work going without delay, and we still need to pass two more bills to help ALS patients.”
Official Congressional Record

Mr. President, since I am here on the floor and since I have my friend and partner who has worked with me on other matters of great import and impact, I want to take this opportunity to celebrate something that happened last evening when we here in the Senate passed the reauthorization of the ACT for ALS bill. This bill has passed the House, it has now passed the Senate, and it can head to the President for his signature. The path on this one, again, should have been easy. It should have been easy, but it just hasn’t been. It has taken years of work here in the Congress and even more years of work and effort and heartfelt effort from the ALS community, who are amazing men and women--the people who live with ALS and their families, their caregivers, the researchers, the advocates who share their stories and kept pushing us to keep moving this forward. We passed the ACT for ALS in 2021. That was an enormous milestone, and, again, I appreciate my colleague here. But what it meant for those who have been diagnosed with ALS to know that for the first time, there would be this pathway for individuals who have an ALS diagnosis who are not eligible for clinical trials to be able to access these investigational treatments. So we have made good progress. We pushed funding to NIH and to FDA so that we can accelerate the research and we can help move more of these promising treatments from the laboratory to the people who need them. So we have been working with our partners in the House, Senator Coons and I along with Representatives Calvert and Quigley, on this reauthorization--good, strong bipartisan progress in both the House and the Senate. We thought we were cooking. We are going to make this thing happen. We are going to get it across before the September 30 deadline. And then we were literally running out of time. I think my colleague and I would both agree we respect the legislative process. There are times when slowing things down makes good sense, but when it comes to ALS, a slowdown, a lapse in authorization--this is not just a procedural issue; this is disruptive. It causes uncertainty. It causes so much anxiety for those who are already navigating such an unpredictable and such an uncertain disease. Families should simply not have to wonder about whether or not the research infrastructure and the treatment access pathways they are relying on are now going to disappear because a Federal authorization has expired. That is what this reauthorization does. It continues that continuity so that the work that has been built continues and it doesn’t have to stop and restart, because ALS is progressive and not in a positive way. Every day, it is harder and harder. People living with ALS and their families cannot put their lives on hold while they are waiting for the next breakthrough because every single day matters. So what this is about is to see the momentum that has been built over these past 5 years. The ALS community has helped build this momentum, and it is through the research networks, it is through the collaborations, the new pathways. But this reauthorization is about protecting the momentum that has been built. So it is not just about preserving a program; it is preserving the momentum, preserving the options, and preserving the hope because that is what these families are clinging to every day, is that when you are facing a disease that does not wait, that maybe today is going to be the day for that breakthrough. I am so honored to work alongside my colleague Senator Coons. He could not be a better advocate. I am so honored to work with so many ALS advocates and the broader ALS community. We have more work to do. We still have to get the Justice for ALS Act and the ALS Better Care Act. We are going to do that. But I am so enormously grateful for the persistence we have shown, the heart that has been here, and, again, the success that was achieved here in the Congress, and now, moving forward, the hope that will continue with the families and those who live with ALS. With that, I yield to my colleague and partner in all of this, Senator Coons.

Senate ·

The Calendar

“I am asking the Senate to pass these bills together right now.”
Official Congressional Record

I ask unanimous consent that amendments, where applicable, be agreed to; that the bills, as amended, if amended, be considered read a third time and passed en bloc; and that the motions to reconsider be considered made and laid upon the table, all en bloc.

“I am asking the Senate to take up these three bills together right now.”
Official Congressional Record

Mr. President, I ask unanimous consent that the Senate proceed to the immediate consideration of the following bills en bloc: Calendar No. 535, H.R. 3620, the Southcentral Foundation Land Transfer Act of 2025; Calendar No. 459, S. 3383; and Calendar No. 682, S. 3219. There being no objection, the Senate proceeded to consider the bills en bloc, which had been reported from the Committee on Indian Affairs.

Senate ·

Strengthening America's Turning Point Act

“I want the Senate to pass this bill today. It gives about 3.5 acres of federal land in Anchorage to an Alaska Native health group. They run a mental health program there and need to own the land so they can pay to replace an old building.”
  • Speech in the House

    Reasoning 100 of 100

    This statement drew 3 conclusions and gave a reason for each one.

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Official Congressional Record

Mr. President, I have come to the floor this afternoon to seek unanimous consent to pass a bill. This is called the Southcentral Foundation Land Transfer Act. I know that oftentimes, Members come the floor and say: Oh, it is not controversial at all. Let me tell you, this one is pretty straightforward, and it is truly a noncontroversial provision. Senator Sullivan and I have introduced this in the Senate. Congressman Begich is leading the companion legislation in the House. We are seeking to send this bill to the President’s desk before recess because it has become time-sensitive. It is pretty simple. It would convey approximately 3.5 acres--3.5 acres--of Federal land in Anchorage. This is land that is currently owned by the Indian Health Service, and it would be conveyed from IHS to the Southcentral Foundation. The Southcentral Foundation is an Alaskan Native Tribal health organization that provides healthcare services to IHS beneficiaries under a self-governance compact. The Southcentral Foundation has built something pretty special on this property. They call it the Quyana Clubhouse. This is where Alaska Native people can find support, find connection and a path forward when they are dealing with mental health challenges. The program serves adults that are over 21 who are experiencing severe and persistent mental health issues through case management, therapy sessions, health education, tobacco cessation, life skills training--all while integrating Alaska Native culture. Given its success, Southcentral Foundation plans to expand the building as well as the services they provide as they work to support intensive levels of outpatient programming. Right now, Southcentral Foundation is providing these services in one of the oldest buildings in the IHS inventory in Alaska. They were really never intended to provide this kind of patient care. In fact, one of the rooms that is now still being used was once a morgue. So it has been around for a while. As I noted, we are here because this straightforward land transfer has become time-sensitive. Without ownership of the parcel, Southcentral Foundation cannot finance and construct capital improvements and permanent facilities and, in turn, do more to address mental health in Alaska. So this legislation will give Southcentral Foundation the certainty it needs to keep investing in places like Quyana and continue providing these services for the long term. This is a House-passed bill. It can go directly to the President and be signed into law. I would hope that we would agree to do that today because there are no substantive objections to it. Both the House and Senate have had hearings on their prospective versions. Both have been marked up and reported favorably by unanimous consent on the Committee on Indian Affairs. So, really, there is no reason to hold the bill up. We can add to our record of bipartisan legislating at scale. We can address an issue that is important to Alaska Native health and uphold the Federal trust responsibility by passing the Southcentral Foundation Land Transfer Act.

Senate ·

25th Anniversary of the September 11, 2001 Attacks

“We must remember September 11 and teach younger people about the courage and unity shown that day. I want to honor the victims, their families, and the first responders. We should keep supporting our firefighters and emergency workers.”
Official Congressional Record

Mr. President, to the younger generations who know September 11 only through history, we must preserve not only the memory of that day, but also the guiding example set by those who responded. The legacy of September 11 is one of courage over fear, service over self, and unity over division. Today, we honor the individuals whose lives were cut short, the families who continue to bear their loss, and the first responders whose bravery became a lasting testament to the best of America. May we never forget their sacrifice. May we continue to support those who wear the uniform of the fire and emergency services. And may we strive each day to keep building a nation worthy of the courage they displayed on one of our country’s darkest days.

Senate ·

Recognizing the 1960 University of Missouri Tigers Football Team

“Congress just passed a bill to renew a program that helps people with ALS. It funds research and lets patients try new treatments even if they cannot join clinical trials. We need to get it signed into law quickly.”
  • Speech in the House

    Signal 40 of 100

    Much of this statement went to praise, blame, greetings, routine procedure or general stories rather than reasons, requests or specific points.

    See full analysis
  • Speech in the House

    Reasoning 100 of 100

    This statement drew 3 conclusions and gave a reason for each one.

    See full analysis
Official Congressional Record

Mr. President, we go through periods here in the U.S. Senate where there are frustrating issues that we deal with. There are hours of unknown as to what is going to happen. Are we going to be able to make something happen? Are we making a difference? And some days can be particularly discouraging. We have a long way to go before this day is through, but to be here at the midpoint of this day and to be able to, as my colleague and friend from Delaware has stated, to be able to celebrate an accomplishment is a reminder that we do good here. And we don’t do good on our own. It takes teamwork. It takes cooperation and collaboration. It takes advocacy. This is really what makes me just filled with a level of optimism and hope as we are talking about where we are at this moment for the ALS community. The House passed the Accelerating Access to Critical Therapies for ALS Act. We call it ACT for ALS. They passed it a few weeks ago, and then the Senate was able to pass it in wrapup. Yes, that means it passed by unanimous consent here yesterday. We are now in the final step of reauthorizing a program that is making a real difference for people living with ALS. I think it is so important to just take a step back and say ``What does that mean?’’ because we have not found the cure, unfortunately, for ALS. This legislation is not about this magical treatment that has come to be. But what we were able to do working together now 5 years ago when we passed the ACT for ALS Act, we created this pathway for individuals. It is kind of a roadmap. We said: If you are not eligible to participate in clinical trials to access investigational treatments, there is another way here for you. We provided some pretty important funding to NIH and to FDA to accelerate the research, to improve the data sharing, to help speed up the development of new therapies. But what really comes about with ACT for ALS is it gives people who are living with ALS the opportunity to try. Just let me try something. It might not work, but let me try because right now, the diagnosis I am living with offers no hope. So this is something that gives those living with ALS some hope. This is a program that works. So we passed it 5 years ago. What we have now done is a reauthorization that allows us to build on this progress that we have made to ensure that individuals that are living with ALS can continue to access these clinical trials and the programs that continue to meet the needs of the patients and the researchers. Senator Coons has mentioned the advocacy. Those caregivers, those who stand with and are wrapping their arms and their hearts around their loved ones who are dealing with ALS--this is about hope for them as much as those who are living with this dread disease. My friend has acknowledged the names of those he calls friends. Dan Tate--I was able to receive a text message on passage of the reauthorization here saying, you know, ``Go dudes’’ or something like that. I don’t know that I am a dude, but I loved the enthusiasm he had. Brian Wallach has been an extraordinary partner over the years. You mentioned Sandra Abrevaya. Absolutely. Then there is my personal advocate, my cousin Jenny Dwyer. It was through Jenny’s husband Pat that our family learned of ALS, as Pat lived with ALS for 8 years; and as a family, we came to not only understand the disease and the awful progression, but it allowed us to understand some of what families go through who live with the almost daily heartbreak as you are watching your loved one progress through this diagnosis. So to the advocates: Know that your work matters. Know that your stories matter. Know that you have made a difference. So we are pleased to be able to be at this place where we can move to finally get this reauthorization into law. We have to work things through the two bodies here and get it signed in. There is more that we have to do. We are working on some good things as the cochairs of the ALS Caucus--the Justice for ALS Veterans Act, which is a really good one, and the ALS Better Care Act. Again, these address some of the challenges that face individuals with ALS as well as their families when they are trying to access the care and access the benefits after a loved one has passed. We know that for those that are living with ALS, every day matters, every day is precious, and we cannot afford to lose momentum when promising therapies are being studied. I am reminded if not weekly, maybe daily sometimes that people are waiting. People are waiting, and they are counting on us to show up for them. So to all those in the ALS community: Thank you for your advocacy. Thank you for your heart and your passion and your persistence but also your willingness to open your hearts and to share your stories so that we can also become motivated and tenacious on your behalf. I am very grateful for my friend from Delaware. It is hard, as I hear stories of your dear friend and as he goes through these stages of this disease. And know that even though I have not met Jack, he is in my heart as well, as well as the many, many whom we are advocating for. With that, I thank again not only Senator Coons but all Members here in the Senate that have joined us in this effort to end ALS. I yield the floor.

Senate ·

Authority for Committees to Meet

“I am asking permission for four committees to meet today while the Senate is in session. Leaders from both parties agree to this.”
Official Congressional Record

Mr. President, I have four requests for committees to meet during today’s session of the Senate. They have the approval of the Majority and Minority Leaders. Pursuant to rule XXVI, paragraph 5(a), of the Standing Rules of the Senate, the following committees are authorized to meet during today’s session of the Senate: The Committee on Commerce, Science, and Transportation is authorized to meet during the session of the Senate on Thursday, July 30, 2026, at 10 a.m., to conduct a subcommittee hearing. The Committee on Finance is authorized to meet during the session of the Senate on Thursday, July 30, 2026, at 10 a.m., to conduct a hearing. The Committee on Foreign Relations is authorized to meet during the session of the Senate on Thursday, July 30, 2026, at 10:30 a.m., to conduct a hearing on nominations. The Committee on Health, Education, Labor, and Pensions is authorized to meet in executive session during the session of the Senate on Thursday, July 30, 2026, at 9:45 a.m.

Senate ·

AGOA EXTENSION ACT--Motion to Proceed

“I want to congratulate Alaska State Senator Lyman Hoffman on his retirement. He served in our state legislature for nearly 40 years. He worked hard to lower energy costs and help people living in rural Alaska.”
  • Speech on a bill

    Signal 40 of 100

    Much of this statement went to praise, blame, greetings, routine procedure or general stories rather than reasons, requests or specific points.

    See full analysis
Official Congressional Record

Madam President, I come to the floor today to congratulate my friend and former colleague in the Alaska State Legislature. This is an individual for whom I have great respect, Senator Lyman Hoffman. Senator Hoffman is retiring after nearly four decades of service to Alaska. Few legislators leave behind legacies that are measured not only by their years of service but by the generations of lives they have improved. Senator Hoffman--the alltime longest serving member of the Alaska State Legislature--is one of those rare public servants. Throughout his nearly 40 years in office, Lyman has dedicated himself to improving the lives of Alaskans, particularly those in our State’s most remote and underserved communities. It has truly made a difference for them. Everyone who has spent time in the capital city of Juneau knows exactly where the center of gravity has been. It has been with Lyman. We have all come to appreciate and value his experience, his knowledge, and, really, the wisdom the man has. At first, you wouldn’t expect it, as he comes across as kind of a quiet guy with a gruff, deep voice. It is true to say he is a man of not too many words, but he is also a man who knows just exactly the right thing to say and the right time to say it. There have been many a legislator who have found themselves in some pretty tense budget negotiations in the senate finance committee. Senator Hoffman holds the gavel there. And in those settings, he can unnerve the most senior lawmaker just by sitting very quietly through an entire committee meeting before offering just a few choice words. When Lyman does speak, everybody listens because, again, he has this remarkable--almost uncanny--ability to cut through the politics and just focus on what really matters. And that is Lyman. You aren’t going to win a staring contest with him, but he can steer an entire negotiation with just a few carefully chosen words. As the longtime cochair of the senate finance committee, Senator Hoffman has become one of our State’s most influential leaders. Through administrations and periods of economic uncertainty, he has earned bipartisan respect for his careful stewardship of public resources, deep institutional knowledge, and the ability to build practical consensus. And perhaps the accomplishment for which Senator Hoffman will be best remembered is Alaska’s Power Cost Equalization Endowment. He worked, actually alongside, my father Gov. Frank Murkowski, and Lyman secured the long-term future of a program that helps make electricity more affordable in rural Alaska. Out in these regions, costs can be astonishingly high and can take up to half of a household’s budget. But, today, PCE is a major success. Its endowment exceeds over a billion dollars, and it continues to serve families and schools and health clinics and businesses across rural Alaska. Lyman is a little bit predictable, and I say that because I could always--always--count on Lyman Hoffman to ask me the hard questions. And I would give my annual address to the legislature, and Lyman would be sitting in the back of the chamber there. He would raise his hand, and he would say ``What are you doing to make energy cheaper?’’ or ``What are you doing to help rural Alaskans?’’ And I always knew it was coming. I always knew it was coming because Lyman was consistent that way. He was practical and he was purposeful and his clear focus--``What are you doing to help rural Alaskans?’’ ``What are you doing to help lower energy costs?’’--that helped guide me here on my own in the Senate. Because what Senator Hoffman understands is that energy policy is not just kilowatts and price per barrel; it is about whether families can afford to heat their homes, whether elders can stay warm in the wintertime, and whether communities have the opportunity to grow. And, again, this is where Lyman made his mark. As a leading advocate for Alaska’s statewide weatherization program, he helped secure more than $600 million to make homes more efficient for Alaskans. And, again, his work reflected a very simple belief: that every Alaskan, no matter where you live, deserves a safe, warm home. From the days that we served in the State legislature to the present, Lyman Hoffman has represented not only his district--which covers Southwest Alaska and out in the Aleutians--but really he helped all rural Alaska with genuine distinction and giving them voice, giving them hope, and delivering real results. And just as important as those results is the example Lyman has set as a public servant. He has demonstrated that lasting public policy is built through collaboration, rather than division. His influence extended far beyond the bills that he passed, shaping both the great State that he loves, the individuals who have served alongside him, and those that will follow him. And as I speak to Senator Hoffman’s impressive legacy, I also want to acknowledge that no public servant achieves these things alone. Behind every legislative session, every late-night budget negotiation, and every year devoted to serving Alaska, stood some key people--certainly his staff over the years, but always--always--Senator Hoffman’s family. His wife Lillian was always there. His children Trina and Douglas--I know that the family made countless quiet, meaningful sacrifices to make all this work possible. So you too deserve to be recognized. Alaska is stronger because Senator Lyman Hoffman chose to dedicate his life to others, and his work will continue to benefit our State for generations to come. So congratulations, Lyman Hoffman--my friend Lyman. Thank you. At some point--at some point--the special legislative sessions will end, and you will be able to conclude this incredible chapter of service to our State. And when that day arrives and long into the future, Alaskans will remember you. We will celebrate you, and we will remain grateful for all that you have done. I yield the floor. And I thank the Senator from Wyoming for the opportunity to speak.

Senate ·

Privileges of the Floor

“I ask that my summer interns be allowed on the Senate floor in July and August 2026.”
Official Congressional Record

Mr. President, I ask unanimous consent that privileges of the floor be granted to my second-session summer interns Leif Anderson, Bronwyn Brune, Lina Hischer, Victoria Bielefeld, Lydia Wies, Tessa Davis, Ole John Schuldt, Mary Cope, Preston Carter, and Soren Getti for the months of July and August of 2026.

Senate ·

Native Children Commission Implementation Act (Executive Session)

“I introduced a bill to help Native children, and I want my colleagues to support it. It turns recommendations from Native communities into law to improve healthcare, schools, housing, and food programs for these kids.”
  • Speech in the House

    Signal 30 of 100

    Much of this statement went to praise, blame, greetings, routine procedure or general stories rather than reasons, requests or specific points.

    See full analysis
  • Speech in the House

    Reasoning 100 of 100

    This statement drew 5 conclusions and gave a reason for each one.

    See full analysis
Official Congressional Record

Mr. President, I come to the floor this evening to speak about legislation that I have recently introduced as chairman of the Indian Affairs Committee, alongside my friend Vice Chairman Schatz. The bill that we have introduced is the Native Children Commission Implementation Act. Before I get started explaining our legislation, I want to recognize the Tribal leaders, the elders, the youth, the children, and the families who flew in last week for a congressional staff briefing to share their perspectives on the bill and the importance of it but also to help educate members and staff about the importance of the bill. As events turned out, it was unfortunate that I was not here on that day due to my having a family emergency back home, but I was able to tune in virtually. It was 5:45 in the morning Alaska time, and I was able to beam in. I have to say I can’t tell you how proud I was to see the Senate Indian Affairs hearing room. It was packed literally wall to wall, which was a reminder to me of how this legislation has captured the attention of so many people who believe that Native children deserve every opportunity to thrive. I was particularly grateful to the Tribal leaders, to Native youth, to advocates, and to commissioners who traveled from Alaska and across Indian Country all to be there. I really think that their presence, their stories, and their unwavering commitment have really brought this legislation to life. I also want to acknowledge and thank my colleagues Senator Schatz and Senator Smith for joining the event and helping to mark this important milestone. Together, they made it clear that this was more than just the introduction of a bill; it was the continuation of a movement--a movement that has been built on years of partnership, of perseverance, and on hope. I want to take a moment to specifically recognize Gloria O’Neill, who chaired the Alyce Spotted Bear and Walter Soboleff Commission on Native Children. Gloria and her fellow commissioners have devoted years to traveling throughout Indian Country. They have listened to Native families and have brought forward recommendations that are rooted in the voices of the communities themselves, and we owe them a great deal of gratitude for their work. Earlier this year, I joined the Alaska Federation of Natives and Tribal leaders for a gathering to recognize their work behind this effort. We were upstairs in the Hart Building, up on the ninth floor--a big room filled with Native leaders really from across the country--and I was deeply, deeply honored to be gifted the Mandan name ``Ho Hsiihe,’’ meaning ``strong voice.’’ This was gifted to me by Bheri Rose Hallam, who is the granddaughter of Alyce Spotted Bear. I was very humbled--very humbled--to receive the name, and I carry it as a reminder of the responsibility that we all share to continue the work that Alyce Spotted Bear and so many Native leaders began on behalf of Native children and families. That responsibility really is at the heart of why this legislation matters so deeply to me. Thousands of bills, we know, are introduced each Congress, and every bill matters to someone, but this one is particularly important to me. As I look at the Presiding Officer in the chair, I am reminded of his comments at an Energy hearing this morning when he spoke with deep passion and love and care for those children whom he didn’t know-- children who had cancer. All he wanted to do was to be able to help them with a playground--a place to be happy, a place to feel good about being a child. So I know--I know--that he can relate when we talk about the important work we do for our children. The story of how the Native Children’s Commission began didn’t start here in Washington. It began in Tribal communities. It began with parents who wanted better opportunities for their children and with elders who were determined to preserve their languages and their cultures. It began with such a great story. It began with the young people who stood up in front of hundreds of grownups, hundreds of adults, in a convention in Fairbanks years ago, where they had the courage to tell the leaders what they were experiencing. They asked us--they asked us--to do something about it. That, to me, is really where it begins. So more than anything, this bill is about children. Across Indian Country, too many Native children experience challenges that no child should have to face. Some have watched their communities suffer from devastating storms or natural disasters. Some have lost loved ones to violence, to addiction, to suicide. Others have entered foster care. They have struggled to access healthcare or behavioral health services. Or perhaps they have carried the weight of the boarding schools era, which has caused historical trauma that continues to affect families today after subsequent generations. Those experiences are very real, but they are also not the whole story. If there is one lesson that I learned from traveling across my State and meeting with Tribal communities across Indian Country, it is that resilience is every bit as real as hardship. Native communities possess extraordinary strengths, and their strengths include strong families, vibrant cultures, enduring languages, and generations of wisdom that is passed from elders to the children. Time and time again, I have watched grandparents teach language to their grandchildren. I have seen parents work tirelessly to create opportunities for that next generation. I have seen elders reminding young people of exactly who they are and where they come from. That sense of identity and culture is so, so powerful. It gives children confidence. It creates belonging. It fortifies our families. It reminds us that the future of Native children is built not only by overcoming hardship but by building--building--upon the remarkable strengths that have sustained Native communities for generations. That understanding has shaped every part of this legislation whose path began more than a decade ago. I mentioned the Alaska Federation of Natives convention. This was back in 2013. During one of the sessions--again, this is the largest gathering of Native people in our State--a group of young leaders-- kids, kids--from the village of Tanana stood up before Tribal leaders, community members, and elected officials. They stood on stage, and they spoke with an honesty and a bravery about what they were seeing in their community. They spoke of violence. They spoke of substance abuse and suicide. But what struck me most was not the hardship that they described; it was the hope they carried with them. Their message was so simple. It was so clear. It was ``Listen to us.’’ The children were saying ``Listen to us, and then do something,’’ and I have not ever forgotten those words. Last summer, I heard from Natasha Singh. She is a leader from the Tanana region, and she shared that the chiefs there continue to meet with young people every year. They ask: What progress have we made? What challenges remain? What more needs to be done? What more do we need to do to listen to you? And that kind of accountability is really remarkable because it reminds us that leadership is not measured by the promises that we make but whether or not we are willing to answer for them. It also reminded me that if Tribal leaders are willing to answer to their children, then Congress should be willing to do the same. So those young people challenged us more than a decade ago, and this new legislation is part of our answer. That conversation that we had in 2013 ultimately led to bipartisan legislation with my friend and former Senator Heidi Heitkamp, and we established the Alyce Spotted Bear and Walter Soboleff Commission on Native Children. And the commission had a very straightforward but very important mission, and that was travel throughout Indian country, listen to Native children, listen to the families, to the Tribal leaders, to the service providers, the experts, and then come back and tell us here in Congress what is needed to improve outcomes for Native youth. That is exactly what they did. Over several years, the commissioners visited communities across the country, and they heard some pretty tough stories. They heard some heartbreaking stories, but they also witnessed extraordinary examples of resilience, of innovation, and Tribal leadership. They saw communities creating culturally grounded solutions that were then strengthening families and improving health, supporting children, and really restoring hope. And their work culminated in a report that they called ``The Way Forward.’’ But that report was never meant to be the end of the conversation; it was only the end of the beginning. And when the commissioners presented their recommendations to our Committee on Indian Affairs, they urged us; they said: Please, don’t let this work become another report that just sits on the shelf and gathers dust. The families who shared their stories deserved more than that; they deserved action. And so that is when we got to work. Over the last couple of years, we have worked closely with Tribal leaders, Native organizations, youth advocates, Federal Agencies, and Members of Congress on both sides of the aisle. We released draft legislation. We held hearings and roundtables. We invited the criticism. We made changes. We refined provisions, added new ideas, and we remained focused on one goal, and that was honoring what Native communities told us they needed. This bill is stronger because it was built with Native communities, not for them. The Native Children’s Commission Implementation Act reflects a simple idea, and that is: If we want to improve outcomes for Native children, we cannot look at just one issue at a time. And we know when we are talking about kids, you can’t talk about life in separate categories. A child does not experience life in neat, clean, separate categories. Health is connected to education. Education is connected to housing. Behavioral health is connected to family stability. Parents cannot succeed if they can’t find childcare. Children can’t reach their full potential if they are hungry, if they are dealing with untreated trauma or disconnected from language or culture or identity. So our policies should recognize that reality. And we do that within this legislation. It strengthens access to healthcare and behavioral health services. It supports Native education and language revitalization. It improves juvenile justice, public safety, housing, nutrition, workforce development, and research. And, more importantly, it recognized that Tribal communities are best positioned to lead these efforts because they know their children and their families, and they know them better than anyone else. During a hearing earlier this year on a draft legislation, Joan Johnson of the Fort Belknap Indian Community shared a story of a young woman who entered the Tribe’s Tiwahe wellness program, and the Tiwahe Initiative is a pilot program at BIA that assists Tribes in providing holistic services that promote everything from child safety to family stability and Tribal self-determination. And Fort Belknap testified that their wellness program has removed the stigma of intervention by meeting families in their homes and helping them access care. To understand the need to make this initiative permanent, Joan shared the story of a young woman who had struggled with addiction and homelessness. And the young mother shared, she said: And, today, that young woman is sober. She is raising her children. And she is helping build a brighter future for her family. And that transformation doesn’t happen because Washington has all the answers. It happened because a Tribal community invested in one of its own. And we have learned from that, and we are seeking to codify Tiwahe as one important section in our legislation. Councilwoman Johnson also described children who came into the Tiwahe program knowing they were Native, but not knowing their language, not knowing their traditions, or even their own family stories. And elders helped connect those young people with their identity. They learned their Native names. They participated in ceremony. And many of those same young people eventually became mentors for the children who followed them. So healing became leadership; one generation began lifting the next. We heard similar stories from Alaska where the Association of Village Council Presidents redesigned the way that families receive services. So instead of forcing parents in crisis--maybe it is addiction, maybe it is homelessness. But it is hard when you have so many disconnected programs. And so through this initiative, they brought education, employment, childcare, family services all together in one place. And so when you have got a family that is just facing so many big, big, heavy burdens, that kind of coordination can make all of the difference. And these stories, again, remind us that the best ideas rarely begin in Washington. And while I am proud to get to this point, which is our bill introduction, it is also a reminder that our work is just beginning. This legislation represents more than a decade of listening, learning, and working alongside Tribal leaders, Native organizations, families, and young people. And it reflects the belief that lasting change happens when we listen first and legislate second. While this is an important step, what matters is that we keep moving forward because every recommendation in the report which was translated into this bill began with a conversation in a Tribal community. And I am going to keep coming back to those young people from Tanana, because they said--it was more than a decade ago. They asked us to listen. And I hope--I hope--today they can see that we are listening. We are acting. The Native Children’s Commission Implementation Act is not about creating yet one more Federal program or one more report that is going to sit on a shelf somewhere. It is about strengthening what is already working in Native communities. It is about trusting Tribal governments, investing in Native families, and ensuring--ensuring--that every Native child--whether Alaska Native, American Indian, Native Hawaiian--has the opportunity to grow up healthy, to grow up safe, connected to their culture, and confident in who they are. And that is a goal that should unite all of us. So, today, I invite my colleagues--Republicans and Democrats alike-- to join Senator Schatz and me as cosponsors of the Native Children’s Commission Implementation Act. Let’s show that when Tribal communities speak, Congress listens. Let’s turn their recommendations of ``The Way Forward’’ report into meaningful action, and let’s work together to build a future where every Alaska Native, American Indian, and Native Hawaiian child has the opportunity to not only overcome challenges, but to become those leaders of the next generation. So I look forward to working with you and the rest of our colleagues to do just that. With that, I yield the floor. The PRESIDING OFFICER (Mr. Husted). The Senator from Utah.