Hello, I am a single father, and wished that I had a supportive, loving wife like this gentleman. May the creator of the worlds bless them more. - Muhammad, California.
Thank you for sharing your story. I am the fourth generation diagnosed with Lupus (Mother, Grandmother and Great Grandmother). Molly's Fund has been a great help to me in starting a support group in Terre Haute, Indiana. Thank you!
Hello Chris, my name is Jesse I'm currently 25 years old. I was diagnosed with Lupus at the age of 21, I had health insurance when I was diagnosed with this desease. About 1 year and a half ago I lost my health insurance, insurance became too expensive to afford and ever since I haven't been taking my medication, about a week ago I been having really bad knee and elbows pain. As of today I decided that I was going to declare my self bankrupt because I either take care of my bills or I start taking care of my self. I feel somewhat of failure to my wife, 2 kids and my parent's and to be honest I'm scare of what the future has in-store for me and my family. Thank you for sharing this Video with us Chris and hope one day I get to meet someone like you in person, someone I can relate like the way I did with you Chris
I was just diagnosed after 3 years of being bedridden. My husband got laid off because of my illness and we have a 4 year old and no support. How can I get connected, I’m in MN. Thank you for sharing 🙏🏼🦋
Thanks for sharing your story. 20 years of onset symptoms and my ANA test results were positive after being tested for over 10 years. Mixed Connective Tissue Disorder (Lupus/RA)
Hello there I know this isn't an easy battle for you but I must say I give you so much credit for getting up everyday and striving keep your head up high God is with you everyday above ground is a blessing God bless you brotha wish you all the best 🙏🏻🙏🏻👏🏼👏🏼👍🏼🎗💪🏼
Hello, I’m a New Zealander and I have Lupus. I empathise with the comments. In my country and 40+ others we have Universal healthcare. People with chronic illness go through enough without worrying about healthcare costs. No stress, medical debt, no medical bankruptcies. Our healthcare is not attached to employment or employer. I’ve been following American politics and believe Medicare for all can be your universal healthcare. Bernie Sanders seems to be the only person for these past 40 years fighting for this. Consider voting for Bernie if you can to get this past. Tell your family and friends. Healthcare is a right and not a privilege. Don’t listen to corporate media’s anti M4A propaganda. Who do you think they work for and who are their advertisers. Corporations and pharmaceutical companies don’t care about your bills, suffering or health. It’s their profits. Universal healthcare is successful. It’s works.
The wanting to work and can't part is debilitating. What we "do" defines us as men. Not being able to "do" makes that definition vague, until you can find other ways to make an impact like this husband and father.
![Lp. Сердце Вселенной #60 РОЖДЕНИЕ ЛОЛОЛОШКИ [Финал] • Майнкрафт](http://i.ytimg.com/vi/YoR0pAV9FVQ/mqdefault.jpg)
Hello, I am a single father, and wished that I had a supportive, loving wife like this gentleman. May the creator of the worlds bless them more. - Muhammad, California.
I wish I had a husband who cared After 24 yrs. God bless you
Hey Muhammad am from Algeria and I have lupus too 😊 sending a lot of support and love 💕
This condition can be the worst sometimes prayers InshAllah
Get well soon
Thank you for sharing your story. I have lupus 23 years💜💜. Stay strong and God bless you and your beautiful family💜💟✋🦋
Thank you for sharing your story. I am the fourth generation diagnosed with Lupus (Mother, Grandmother and Great Grandmother). Molly's Fund has been a great help to me in starting a support group in Terre Haute, Indiana.
Thank you!
Gilly Crews my brother has a lupus but not my mother infact no other in my family should I will suffer from lupus
Hello Chris, my name is Jesse I'm currently 25 years old. I was diagnosed with Lupus at the age of 21, I had health insurance when I was diagnosed with this desease. About 1 year and a half ago I lost my health insurance, insurance became too expensive to afford and ever since I haven't been taking my medication, about a week ago I been having really bad knee and elbows pain. As of today I decided that I was going to declare my self bankrupt because I either take care of my bills or I start taking care of my self. I feel somewhat of failure to my wife, 2 kids and my parent's and to be honest I'm scare of what the future has in-store for me and my family. Thank you for sharing this Video with us Chris and hope one day I get to meet someone like you in person, someone I can relate like the way I did with you Chris
may God bless you
God bless you I have that and a 62 yr sister Pancreatic cancer mommy 84. Bad lungs God will help us I feel the same way I'm there helper
What a touching story and such a beautiful family. I wish them the very best❤
I just want to say God bless u all I just found out 2016. But now I'm 58 Thank God but some days I have cement in my knees ankles shoulders the pain.
Thank you and God bless you for this testimony. God bless your family too.
I was just diagnosed after 3 years of being bedridden. My husband got laid off because of my illness and we have a 4 year old and no support. How can I get connected, I’m in MN. Thank you for sharing 🙏🏼🦋
Thanks for sharing your story. 20 years of onset symptoms and my ANA test results were positive after being tested for over 10 years. Mixed Connective Tissue Disorder (Lupus/RA)
Hi, I hope you are doing well! Can I ask you what symptoms were you feeling before your diagnosis?
Omg they told me I have that. What is it. Help God bless you My bones joints fingers all hurt imn58 and feel like omg
Hello there I know this isn't an easy battle for you but I must say I give you so much credit for getting up everyday and striving keep your head up high God is with you everyday above ground is a blessing God bless you brotha wish you all the best 🙏🏻🙏🏻👏🏼👏🏼👍🏼🎗💪🏼
God bless you all. ❤️❤️
Hello, I’m a New Zealander and I have Lupus. I empathise with the comments. In my country and 40+ others we have Universal healthcare. People with chronic illness go through enough without worrying about healthcare costs. No stress, medical debt, no medical bankruptcies. Our healthcare is not attached to employment or employer.
I’ve been following American politics and believe Medicare for all can be your universal healthcare. Bernie Sanders seems to be the only person for these past 40 years fighting for this. Consider voting for Bernie if you can to get this past. Tell your family and friends. Healthcare is a right and not a privilege. Don’t listen to corporate media’s anti M4A propaganda. Who do you think they work for and who are their advertisers. Corporations and pharmaceutical companies don’t care about your bills, suffering or health. It’s their profits.
Universal healthcare is successful. It’s works.
Please i need more info. I have lupus and this is inspirational for me
I am very impressed with this couple. Actually they are fortunate ate, have love. I have a more serious disease and have nobody.
The wanting to work and can't part is debilitating. What we "do" defines us as men. Not being able to "do" makes that definition vague, until you can find other ways to make an impact like this husband and father.
Yes I was always a sick kid. Allergies. Lupus and Sjogrens now. My Mom has autoimmune and 2 of my children.
Hi folks. What about medicare + SSD?
I wonder if they are not considered disabled? That would be sad.
Can you help me I have lupus also.