Help Michael Breathe & Fight Pulmonary Alveolar Proteinosis

For: Michael Thompson
Organizer: Michael's Wife
of $75,000 goal.
Raised by 23 donors
4% Complete
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The Story

Meeting my terminally ill husband online was a beautiful miracle! Now, we're praying for another miracle!

It was in 2009, just seven short years ago, that my dear husband, Michael Thompson, was diagnosed with Pulmonary Alveolar Proteinosis. "I'm sorry to say," said the doctor nervously, "that there is no known cure. PAP is a terminal lung disease. You're probably only going to live for five more years. You'll be lucky to make it to age forty."

It must have felt like a kick in the stomach. Unfortunately, I didn't know him then. I wish I had so we could have gone through it together.

How We Met

Michael and I met through an online dating site in March of 2012. He was very honest and told me in his very first email that we was terminally ill with Pulmonary Alveolar Proteinosis. But I wanted to be Mrs. Thompson, even if it was only for one day! So we met in person on April 7th and were married fourteen days later on April 21st, 2012. We married in haste...and it was the best decision we ever made!

What in the World is PAP?

Well, it's an extremely rare lung disease. So rare, that less than 500 people diagnosed in the United States suffer from it. So rare, that it took the doctors two years to diagnose it.

Basically, it's an auto-immune disease that causes the body to produce extreme amounts of the natural protective protein coating in the lungs. Basically, your fate is to drown to death in your own protein. Michael lives every day with this fate hanging over his head. Any day may be his last.

While suffering from PAP, rheumatoid arthritis, fibromyalgia, spinal stenosis and heart disease, he is still the most cheerful, positive, creative and loving person that I know. And I'm so lucky to have him!

Why YouCaring?

Funds are extremely tight. I'm doing my damnedest to scrimp, save and scratch to make a few bucks from eBay, customized pyrography artwork and freelance writing. But there's no money for anything extra. And Michael has so many extra needs. A travel oxygen concentrator. Dentures to replace the mouthful of beautiful teeth Michael lost due to medication side-effects. A tub so he can soak in hot, hot water when fibro & rheumatoid make his life a misery and the funds to finish installing the On-Demand hot water system we own but couldn't install yet. (We only have a shower with very limited hot water now and he sure misses being able to take a hot bath. Sometimes it's the only thing that eases the pain.)

And eventually, a lung lavage or two (washing out the lungs with warm saline to remove protein build-up.) This procedure costs over $100,000 and is NOT covered by our insurance. And usually more than one lavage is needed.

Please be an angel in our lives and help to ease the burden of these ongoing expenses. 

We thank you very much. God bless you for your help!

If you prefer to mail your donation, please make the check payable to "Help Michael Breathe" and mail to...
Help Michael Breathe
c/o Lenora Thompson
P.O. Box 3
Gully, MN 56646

Like, Share and Follow Michael's journey and battle to breathe at

Fundraiser Updates

Posted on September 30, 2016

Posted on September 30, 2016

Hello Supporters,

I can't believe it's been eight months since our last update. Wow! Where did the time go?

Here's hoping this update finds you all well. I'll be frank. I'm ecstatic that Summer is over. After three years of smiling through gritted teeth, I'm finally admitting that I HATE GARDENING. If it weren't for the heat, bugs and dirt, I wouldn't mind it a bit. ;)

Michael is stable. Of course, he's still hacking, coughing and dry-heaving the excess protein out of his lungs all the time. As long as it comes up and out, we're happy. The hospital bed you helped us afford last year allows him to sleep inclined, which keeps him from laying flat and "drowning" at night. It's also helped his back pain!

Of course, he also suffers from fibro and had a severe rheumatoid flare-up recently. It's days like that when he longs for some kind of tub, wishing he could soak his sore joints and bones in hot, hot water. Alas, we only have a shower. So I decided to do something about it. In addition to my freelance writing, I've launched a pyrography (woodburned) artwork business selling oak plaques and wooden spoons burned with artwork and catchy quotes or cliches. And as Henry David Thoreau said, I've met with "success unexpected in common hours." Literally flying off the shelves. Can't keep 'em in stock! Here's a link to the Gallery. Hopefully, if I sell enough plaques, we can get some kind of tub.

Well, that's about all that's new with us. Oh, a couple of new writing venues have opened up. More details coming in future.

Let us know how you're doing! [email protected]

Thanks again for being there for us. It means more than you'll ever know!

Have a happy Autumn!

~ Lenora Thompson, Michael's wife

Posted on February 5, 2016

Posted on February 5, 2016

Hello Everyone,

A huge "thank you" to the two people who donated this week, one from as far away as the Philippines. I surely appreciate your generosity on behalf of my husband.

YouCaring has a new initiative going for Valentine's Day. It's called #LoveYouCaring. All shares of the URL for this fundraiser, with the hashtag #LoveYouCaring added gives us a chance to be featured on YouCaring's homepage!

They're looking for love stories. And I can't imagine a more unique, a more unusual or a faster love story than Michael and mine.

We met online the first week of March 2012. He told me immediately about his terminal lung illness. Within three weeks, I was head-over-heels in love with Michael. We met on April 7th, got engaged on April 8th and were wed on April 21st, 2012. It all took less than two months! And four years later, Michael's still the best thing that ever happened to me and the best decision I ever made.

Please SHARE to help Michael fight Pulmonary Alveolar Proteinosis so he can stay with me forever.

Just post to Facebook, Twitter and all social media to help get this fundraiser featured!

Thank you!

Mrs. Michael (Lenora) Thompson

Posted on January 23, 2016

Posted on January 23, 2016

Hello Everyone,

How are you? Here's hoping 2016 is treating you well!

Michael's still having a lot of "movement," as he calls it, in his lungs. No sooner does he cough, retch and gag a big wad of protein out of his lungs, to cheers from me, and his lungs plug up again. This is a very weird disease!  And it can be tough watching him suffer. There are millions of other caretakers, like me, out here. So I decided to write about what it's like and give caretakers everywhere a voice. The article is called The Secret Pain of Caretakers. Read it here on the Huffington Post.

In other news, Michael's Facebook page, Help Michael Breathe, is up to 144 likes, which is pretty cool! But we haven't seen any new donations for a while, so please share, share, share this link with your friends, family and social media contacts!

Thank you all again for your support and encouragement. It means more to us than you know!

Have a great weekend!

~ Lenora Thompson, Michael's wife

P.S. Check out my new blog, Narcissism Meets Normalcy, on PsychCentral! Woohoo!

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