MyFox
 

newsdoctor's Blog

by newsdoctor from St. Louis

Last Post 8 days, 4 hours Ago


 

That's what doctors wish they could get.. more attention for sickle cell disease. It's a disorder of the red blood cells that carry oxygen to the body and it can be devastating. It can hit people from Latin America, the Middle East or the Mediterranean, but it mostly strikes African-Americans. If both parents carry the gene, they have a one-in-four chance of having a child with some type of sickle cell disease. About one-in-400 African American babies are born with the disorder. The irregular cells clog up blood vessels and cause pain, infections, organ damage and strokes.

Penicillin has helped hold down infections that used to kill many of these children before age 5. But doctors say the average life span for sickle cell patients is around 40-45.

I did a story with a couple that lost their wonderful 25-year old daughter to sickle cell. Miki Hudson suffered a stroke in grade school and had to be home-schooled. Miki's parents, Mike and Stephanie Hudson, and her three sisters would all help massage her limbs when she would suffer excruciating pain. The pain was often so intense that she had to be hospitalized. She had to have frequent blood transfusions. Colds would often turn into pneumonia. Yet she worked in the family business, drew strength from taking care of her nieces and nephews and developed a social life. But a major stroke last May would prove to be too much. Miki had to enter a nursing home. She got the flu.. which turned into pneumonia.. and she died on Valentine's Day of this year.

Doctors need more money for more studies for more and better treatments. Some patients lose their insurance and can't afford the care that's available. In the meantime, Miki's parents say getting educated about the disease can help others avoid the heartache they suffered from Miki's struggle and her death.

8 Comments |  Add a Comment

Member Comments Total Comments: 8
Page 1 of 1
kurkel read my blog view my photos
Apr 28, 2008 | 1:00 PM

it is a horrible and painful illness that we see in the ICU when they have a sickel cell crisis. Very hard on all....

Flaglady read my blog view my photos
Apr 28, 2008 | 1:06 PM

I remember hearing about sickle cell when I was in school, grade and high school. Now that I think about it I heard it alot through those years. Now that I care what is or is not in the news, I don't recall hear anything about sickle cell. I assumed it was cured.

kurkel read my blog view my photos
Apr 28, 2008 | 2:07 PM

no....not even close. They have come up with better treatments for the symptoms...sort of

but really havent made much progress, I dont think..

IbKat read my blog view my photos
Apr 28, 2008 | 2:49 PM

We lost a dear friend to sickel cell - she was in her early 40s and left behind 3 children .
Its a horrible disease there needs to be more awareness about the disease more research.
The crisis and pain they suffer is unbelievable.

mr_wildflower read my blog view my photos
Apr 28, 2008 | 5:38 PM

Hopefully someday someway they can come up with better treatments for this.....

TheShan2007 read my blog
Apr 28, 2008 | 6:45 PM

"but it mostly strikes African-Americans"

Not true. It has nothing to do with being African-American. You don't have to be American or African to be afflicted.

It does however effect the black race mostly. If you're a white African-American, you are just as likely not to have it as all other Caucations. This disease doesn't discriminate based on your nationality. It strikes predominately the black race regardless of whether or not they are African, American, French, Canadian, etc.


You can't assume all black people are African OR American. And not all African-Americans are black. That's just a term of birth origin or nationality.

suzseeq read my blog view my photos
Apr 29, 2008 | 2:38 AM

one of my children carries the sickle cell trait but does not have the disease. She is now 20 and the last time I heard about this was when she was born. They said she wouldn't suffer any affects; just being a carrier...so I'm ashamed to say; that I never looked further into it and completely forgotten about it. Def. needs to be more attention surrounding it. I need to at least worn her of her chances of producing an offspring that WILL have the disease. Thank you so much for this blog!

Patch_W_Adams read my blog
Apr 30, 2008 | 8:40 PM

Gee, we can clone dogs but can't find a cure for this...? Someone has their priorities screwed up...

Page 1 of 1


Write your comment below:




newsdoctor

I anchor the 5pm and 9pm news at Fox 2. This is the career I chose when my dreams of playing professional baseball faded into reality. Should I coach or go into the news business? I made the right choice. But I have played sports all my life and remain an avid sports fan. When I'm not working, I enjoy working out, riding my motorcycle, playing golf and doing a little fishing.

Member Since: 9/13/2006