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A former US intelligence officer has blown the whistle on the US government by alleging they concealed a programme that has physical evidence of a “non-human origin” craft. David Charles Grusch told The Debrief and NewsNation this week that he confidentially turned over classified information to Congress and the Intelligence Community Inspector General in July 2021 about the programme and possible evidence. According to Mr Grusch, he experienced retaliation when his identity was revealed – something he has filed a formal complaint regarding. But now, Mr Grusch wants the rest of the world to know about some of the information that he believes was being illegally concealed, even if it means putting himself at risk. “I am for real. I am sitting here at great personal risk and obvious professional risk by talking to you today,” Mr Grusch told NewsNation. Here’s what we know about Mr Grusch and the claims he’s making. Who is David Charles Grusch? Mr Grusch is a 36-year-old veteran of the US Air Force as well as the National Geospatial-Intelligence Agency and the National Reconnaissance Office. He is a decorated former combat officer in Afghanistan, according to The Debrief. From 2016 until 2021, Mr Grusch served as a senior intelligence officer with the National Reconnaissance Office. From 2019 until 2021, he was the office’s representative to the Unidentified Aerial Phenomena (UAP) Task Force. From late 2021 until July 2022, he co-led the National Geospatial-Intelligence Agency’s UAP analysis. In total, Mr Grusch has 14 years of intelligence experience. At the National Geospatial-Intelligence Agency, Mr Grusch was a senior intelligence capabilities integration office and had Top Secret / Secret Compartmented Information level clearance. Mr Grusch told The Debrief that he reported to Congress on the existence of a “publicly unknown Cold War for recovered and exploited physical material” that identified UAP [Unidentified Anomalous Phenomena] crashes, landings and retrieved material for “exploitation / reverse engineering to garner asymmetric national defense advantages.” Mr Grusch told NewNation that the UAP task force was refused access to the materials recovery programme. “I thought it was totally nuts and I thought at first I was being deceived, it was a ruse. People started to confide in me. Approach me. I have plenty of senior, former, intelligence officers that came to me, many of which I knew almost my whole career, that confided in me that they were part of a program,” Mr Grusch told NewsNation. What are his claims? Mr Grusch is alleging that the materials recovery programme retrieved, “non-human origin technical vehicles” but kept it hidden from the public. “Call it spacecraft if you will, non-human exotic origin vehicles that have either landed or crashed,” Mr Grusch said to NewsNation. In a separate interview with the Debrief, Mr Grusch described how the government allegedly has evidence of spacecraft created by a “non-human intelligence” of “unknown origin.” “[This assessment is] based on the vehicle morphologies and material science testing and the possession of unique atomic arrangements and radiological signatures,” the former official said. He sounded the alarm to Congress and the Intelligence Community Inspector General in July 2021, confidentially alleging that the materials recovery programme was shielded from proper congressional oversight. However, he claims his identity was somehow disclosed and he suffered retaliation for disclosing the confidential information. “I hope this revelation serves as an ontological shock sociologically and provides a generally uniting issue for nations of the world to re-assess their priorities,” Mr Grusch said to The Debrief. The former defence official said he hadn’t directly witnessed or seen photos of the recovered alien objects himself, but has spoken extensively with colleagues who have. “We’re definitely not alone,” he told NewsNation. “The data points, quite empirically that we’re not alone.” He added that as part of his disclosures to Congress and the inspector general, he turned over verifiable “proof” of his claims. Altogether, Mr Grusch said his experiences have convinced him the US government has been systematically lying to the American people for decades about unidentified aerial phenomena. “There is a sophisticated disinformation campaign targeting the US populace which is extremely unethical and immoral,” Mr Grusch said in his interview with NewsNation. What has the US government said? Sue Gough, a spokesperson for the DOD said in a statement provided to The Independent that to date the All-domain Anomaly Resolution Office (AARO) does not have “any verifiable information to substantiate claims that any programs regarding the possession or reverse-engineering of extraterrestrial materials have existed in the past or exist currently.” The All-domain Anomaly Resolution Office (AARO) investigates unidentified flying objects and other phenomena in the air, sea, land or space. Ms Gough said the AARO is “committed to following the data and its investigation wherever it leads” adding that they are working with the Office of the General Counsel and the Air Force Office of Special Investigations to establish “a safe and secure process for individuals ot come forward with information to aid AARO in it’s congressionally-mandated historical review.” “AARO welcomes the opportunity to speak with any former or current government employee or contractor who believes they have information relevant to the historical review,” Ms Gough added. The Independent has reached out to the Intelligence Community Inspector General for comment regarding the whistleblower complaint. 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Getting married wasn’t “on the books” for London couple Craig Pollard and Alex Herd for a long time. But that changed when Alex got diagnosed with motor neurone disease (MND) in 2021, aged 30. “We decided to get married as a bit of a consequence of Alex’s diagnosis,” explains Pollard, 35. “It wasn’t something that was on the books for us before, especially as being gay, marriage wasn’t available to us when we were younger, so wasn’t necessarily something we’d aspired to. “But then thinking about the legacy we wanted and how much time we had together, we saw it as a good way of bringing our families together and celebrating something really positive in our life.” MND affects nerves in the brain and spinal cord which send signals to muscles. There is currently no cure, so as muscle loss gets worse over time – affecting movement, speech, swallowing and breathing – it eventually leads to death. It’s uncommon and mostly affects people in their 60s and 70s, although as Herd’s diagnosis shows, MND can occur in younger adults too. The charity Challenging MND, which helps people with MND, has the ‘opportunity to create amazing memories’, funded the couple’s big day last year – a fabulous festival-inspired party officiated by drag queen Just May from RuPaul’s Drag Race UK Season 4. They had already been together for a decade, so the wedding was a “celebration of all the things we’ve enjoyed together over the last 10 years”, Pollard notes (plus “lots of glitter and sparkle – it was perfect”). It was also the last time Herd went a full day without using a wheelchair. “So it was the very last moment we possibly could have done that,” adds Herd, now 32. “And we can look back at that as a really special day.” He first started noticing symptoms in early 2021 – muscle twitching then weakness in his hands and arms, before his legs became increasingly affected. Herd used a manual wheelchair for a while but recently switched to an electric one. “That’s changed my life quite a lot,” says Herd. “While I was in the manual wheelchair and Craig was pushing around, I sort of felt like I didn’t really exist anymore, because everyone would interact with him, and I wasn’t responsible for where I was. But now I’m in control of my movement, I feel like I’m more interacting with people myself.” The diagnosis has been challenging on multiple levels, individually and as a couple. MND doesn’t present with exactly the same patterns for everyone – so there is no guidebook as such, and navigating support services relies on a lot of self-advocating. Things such as specialist physiotherapy and occupational therapy can be helpful, along with home adaptations. “Having MND, you have to get used to things changing,” says Herd. “I mean, I can’t necessarily relate at this point to someone who’s been in their wheelchair for their whole life, but because things keep changing, you can’t really get used to it properly. So it’s very difficult for me to kind of keep hold of my identity.” In a recent survey, Challenging MND found 63% of people living with the MND had felt marginalised or ‘othered’ because of their condition, while 51% felt others see MND as their identity. In addition, 80% said they felt isolated, and 69% worry about being a burden to their family. Feeling ‘othered’ is something Alex found himself thinking about while attending Pride London recently. “It’s almost more like something I’m doing, than something other people are doing – because I’m seeing people doing what I would’ve been doing a year ago, it’s still fairly fresh for me, so I’m still comparing the before and after,” he reflects. “At Pride, lots of people get to see themselves represented in the crowds, and that’s nice. But then I realised how much more of a minority people in wheelchairs are. It made us realise how different our situation is now, our priorities and expectations in general.” Music has been an important way for him to stay connected with his identity. “I’ve been making music for over 10 years, so it’s nice I’m still able to do that. I think as much as possible, people in a situation like this need to try and keep doing the things that made them happy before,” he says. While he can no longer play his guitar, Herd made voice recordings to use an instrument and creates tracks on his computer, using foot pedals as he can no longer click the mouse. Since his diagnosis, he’s actually been finishing a lot more songs. “I have less distractions now!” Herd quips. “But using music as a communication tool, that’s definitely become more important to me.” Challenging MND also supported the couple with a trip to Eurovision – “which was really touching and we made great memories”, says Pollard. They’re also grateful to support from the Motor Neurone Disease Association, who provides a local area liaison, and their local St Christopher’s Hospice has been “really helpful”. These things make a huge difference. “Something I’m very conscious of as an able-bodied person is watching Alex have to come to terms with first of all being disabled, then being visibly disabled, and then being disabled in public – there’s been a lot of different elements we’ve had to really tackle,” Pollard reflects, citing navigating public transport as one of the main everyday challenges. There’s an emotional toll too. “My energy levels are a lot lower than they used to be, and my capacity for stress. I feel like I already have this much higher baseline of anxiety about various things, so it feels much easier to become overwhelmed,” says Herd. “I think the only thing we can really do is just try and focus on the next thing, rather than worrying about everything.” As members of the LGBTQ+ community, there are sometimes other nuances to their experiences. They’ve noticed LGBTQ+ events are doing well with accessibility, but representation can be a more subtle matter. “There’s definitely an element of the community who are very mindful of others and very empathetic, which I think has been where I’ve learned a lot about different people’s experiences in my life,” says Pollard. “But when it comes to the overall society of the community, I think there’s still a large proportion of it based on image, based around being cool and trendy. So it’s quite easy for people with accessible requirements to be kind of ignored in that space.” As for their experiences in public, Craig says: “We have struggled to feel like we can take up space. First of all being LGBT, we often don’t feel that safe in certain spaces, public transport we’ve had trouble on once or twice in the past, so you’re always a bit uneasy. With moving into being more visibly disabled and needing more accessible requirements, that’s something we’ve to discuss and manage.” Thanks to Challenging MND, the couple are banking up the joyful times. “They offered to support our wedding, which was really special, and without them we probably wouldn’t have had it,” says Pollard. “That isn’t just a memory for us, it’s a memory for our families and friends too. It was really special.” Challenging MND aims to support and empower those living with MND to create lasting memories for themselves and their families. To date they’ve granted in excess of £1.1million and supported over 100 families.

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