Awareness Day Event: Dr. Bateman

Dr. Bateman is the founder and medical director of Bateman Horne Center. Her speech at the virtual awareness event on May 9th covers research, education, and what we can hope for moving forward.
Learn more about our education and research at batemanhornecenter.org.

[@kathypaup]

Thanks for the update.

[@gloriaharbin1131]

Thank you so much for all you have done Dr. Bateman!

[@beeholtzclaw7935]

Thank you Dr. Bateman , Just think how wonderful it would be to have all doctors and nurses aware of ME/CFS, to feel understood and most important to tell family this is real!

[@Ninjamom4]

❤️❤️❤️Thank you !

[@andeebee2530]

Thank you so much

[@katiestewart1361]

🙏 thank you

[@TheBegleybunch]

One of my dr’s told me that ME/CFS is now considered Fibromyalgia. Doesn’t make sense to me.

[@user-zt5lw4bk1c]

I tried for years to get into your practice! Dr Lewis referred me to you but you never expected me. I have struggled for 22 yrs with Fibromyalgia and Chronic Fatigue, migraines, degenerative discs in my neck and low back, Insomnia, stomach problems ect! I have become disability now and unable to work as a nurse any longer! I would love to have someone contact me about my health. I also struggle with migraine, stomach issues like IBS. I physically cannot hardly get around. I also had Covid, but the Covid Vaccine made me so so so sick! I had 104 fever that would not break and shivering and shaking to were it locked up my back. I have lost so much because of these illnesses! I just want my life back! The Judge that oversaw my social security, disability hearing. Got really upset with me when he asked why I had not seen you? I tried to explain , but was cut off!
When he finally let me speak I explained that Dr Lewis’s office in ogden had sent my records to Dr Bateman to try and get in with her. I was never called back and no one reached out to me to schedule. I am so I’ll and have so many problems I live in terrible pain from all over my body!

[@Truerealism747]

Are you hypermobile?