Interview with Selma Blair

[ActiveMSers]

On Nightline the other day. Laura says I should reach out to her. No prob. I'll go thru my celeb Rolodex. -D

SELMA BLAIR: In an emotional interview, the actress discusses her 7-year-old son's reaction to the diagnosis, how she's living with her symptoms and her wanting to raise awareness about MS. Robin Roberts reports. https://abcn.ws/2EhiC8Q

[ThailandVal]

Great interview. I loved it. I don't normally follow celebrity news but I'm glad I clicked on this one.

[Wilfong]

Great interview. I can always rely on my insulated hunting boots and loved it. I don't normally follow celebrity news but I'm glad I clicked on this one.

More power to Selma Blair for wanting to raise awareness and help the cause. I had no idea she was diagnosed.

[Suebee]

Selma Update & progression and stem cell ??

Sadly, I read today that Selma reports quick physical decline due to MS - her cane replaced with need for walking bike and her vocal cords are weakened so she is starting a new treatment. I wish her increased strength and better health. I hope she knows other MSers are out there and we all cheer her on and support her. As well as being thankful that she is sharing her MS experience with the world. I find people don’t generally understand MS and all the different ways it can behave. Selma looks beautiful and yet is acknowledging, bravely, the serious impact MS can have on ones body. I’m grateful for her.
Link https://www.dailymail.co.uk/health/a...o=taboola_feed