Eric Dane was seen enjoying a dinner with a lookalike of his estranged wife Rebecca Gayheart after opening up about his battle with ALS. 

The Greys Anatomy star, 52, revealed in April that he’s battling amyotrophic lateral sclerosis, which progressively weakens muscles and affects physical function. There is no cure for the condition.

Eric has been married to actress Rebecca, 53, since 2005 but she filed for divorce in 2018 and the pair have been separated ever since. Rebecca withdrew her divorce petition in March ahead of Eric announcing his diagnosis and has said they co-parent well together as a family. 

But he was spotted out on a date with a mystery woman who bore a striking resemblance to Rebecca on Tuesday.

The pair were seen kissing goodbye as he was picked up by a driver following a dinner date at Chateau Marmont in West Hollywood.

Eric gave an update on his battle with ALS this week, telling Good Morning America on Tuesday: ‘I’m fighting as much as I can. There’s so much about it that’s out of my control.’

Eric Dane was seen enjoying a dinner with a lookalike of his estranged wife Rebecca Gayheart after opening up about his battle with ALS (Pictured)

Eric Dane was seen enjoying a dinner with a lookalike of his estranged wife Rebecca Gayheart after opening up about his battle with ALS (Pictured)

Eric has been married to actress Rebecca, 53, since 2005 but she filed for divorce in 2018 and the pair have been separated ever since (Eric and Rebecca seen in 2017)

Eric has been married to actress Rebecca, 53, since 2005 but she filed for divorce in 2018 and the pair have been separated ever since (Eric and Rebecca seen in 2017)

Eric is currently taking medication to slow the symptoms and he’s also participating in a pioneering research study.

‘I will fly to Germany and eat the head off a rattlesnake if [doctors] told me that that would help,’ Dane stressed. ‘I’ll assume the risk.’

The SAG Award winner was joined by his neurologist Dr. Merit Cudkowicz, who admitted: ‘It’s a hard diagnosis to hear, but I want [patients] to hear that there’s hope. I never want anyone to hear that there’s nothing to do because there’s a lot to do.’

‘That’s what I got from Merit when I met her. There was a sense of hope I didn’t get from other doctors that I met with,’ Eric noted, adding prior doctors were just ‘there to monitor my decline and that’s not very helpful.’

There are currently 5K people diagnosed with ALS annually, according to the CDC.

‘But those numbers are going up moderately fast,’ the Chief of Neurology at Mass General warned.

‘It’s really predicted by, like, 2040 [that] the numbers of people with ALS in the world will be increased by about 40%.’

Dr. Merit listed off some of the ALS risk factors including plastics, bacteria in lakes, head trauma in sports, pesticides, military service, and ‘there’s many more we don’t know about.’

He was spotted out on a date with a mystery woman who bore a striking resemblance to Rebecca on Tuesday

He was spotted out on a date with a mystery woman who bore a striking resemblance to Rebecca on Tuesday

The SAG Award winner was joined by his neurologist Dr. Merit Cudkowicz (L), who admitted: 'It's a hard diagnosis to hear, but I want [patients] to hear that there's hope'

The SAG Award winner was joined by his neurologist Dr. Merit Cudkowicz (L), who admitted: ‘It’s a hard diagnosis to hear, but I want [patients] to hear that there’s hope’

Eric has the love and support of his wife Rebecca (R), who dismissed her divorce petition in March following seven years of estrangement, as well as their 15-year-old daughter Billie (M) and 13-year-old daughter Georgia (L)

Eric has the love and support of his wife Rebecca (R), who dismissed her divorce petition in March following seven years of estrangement, as well as their 15-year-old daughter Billie (M) and 13-year-old daughter Georgia (L)

WHAT IS AMYOTROPHIC LATERAL SCLEROSIS? 

ALS is an acronym for amyotrophic lateral sclerosis.

It is also referred to as motor neurone disease, or Lou Gehrig’s Disease after the US baseball player when he was diagnosed in 1939 at just 36 years old.

The disease is a rare condition that progressively damages parts of the nervous system.

It occurs when specialist nerve cells in the brain and spinal cord called motor neurones stop working properly – known as neurodegeneration.

Life expectancy for about half of those with the condition is three years from the start of symptoms.

However, some people may live for up to 10 years, and in rarer circumstances even longer.

The condition can affect adults of all ages, including teenagers, although this is extremely rare.

It’s usually diagnosed in people over 40, but most people with the condition first develop symptoms in their 60s. It affects slightly more men than women.

There’s currently no cure for motor neurone disease.

Treatment aims to make the person feel comfortable and have the best quality of life possible

It also tries to compensate for the progressive loss of bodily functions such as mobility, communication, swallowing and breathing. 

‘There’s people all over the world working on this,’ the Harvard Medical School professor encouraged.

‘Between artificial intelligence and other imaging technology – to really be able to to subtype people – that’s what gets me excited. That’s all coming in the next, I think, one to two years, if not faster.’

Back in 2014, the viral ice-bucket challenge raised $200million for ALS research ‘in the US alone and it was spent quickly.’

‘I’m very hopeful, yeah, I don’t think this is the end of my story. I’m pretty resilient,’ Eric beamed.

‘I just don’t feel, like in my heart, [that] this is the end of me.’

Eric first experienced weakness in his right hand one year ago, but he ‘thought maybe I’d been texting too much or my hand was fatigued’ until a hand specialist eventually referred him to a neurologist.

‘I have one functioning arm. My left side is functioning. My right side, [which is my dominant side], has completely stopped working,’ the San Francisco-born silver fox revealed Monday.

‘[My left arm] is going. I feel like maybe a couple, a few more months and I won’t have my left hand either. Sobering. I’m worried about my legs.’

Luckily, Eric has the love and support of his wife Rebecca, who dismissed her divorce petition in March following seven years of estrangement, as well as their 15-year-old daughter Billie and 13-year-old daughter Georgia.

‘I talk to her every day,’ Eric emotionally said of the 53-year-old Jawbreaker alum.

‘We have managed to become better friends and better parents. And she is probably my biggest champion and my most stalwart supporter. And I lean on her.’

On average, ALS patients live two to five years following their first symptoms, but FDA-approved medications and physical/speech therapies might slow down the progression of the disorder.

***
Read more at DailyMail.co.uk