It’s great when you meet someone whose mission in life is to help others. Dr. Mac is an inspirational doctor, Mom, and podcast producer. If you have not listened to her show, Housecall with Dr. Mac, you should. The show empowers the listener with up-to-date health information. Dr. Mac is on a mission to help educate others about their bodies so they can live healthier lives. It was an honor and privilege to sit down with Dr. Mac who is full of wisdom and discuss sickle cell disease.Throughout the month of September, I dedicated everyday to help raise awareness about the most common genetic disorder in the world. The conversation about sickle cell disease really is personal for me and my family, I hope as you listen to this episode of Housecall with Dr. Mac you will be empowered with new information and join us to help raise awareness about this genetic disorder.
Interested in learning more about health, subscribe to Dr. Mac’s Podcast. Listen to the podcast below to hear our story.
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You can also find (part 2) here.
@Cleverlychangin thanks for sharing your story #30forSickleCell with our #HouseCall Community http://t.co/BP5sb9cHLt http://t.co/JjAwLeuKfO
— House Call w/Dr. Mac (@realdoc74) October 14, 2014
Please see the post below and Sign the petition to have the Sickle Cell Treatment Act Bill h.R. 5124 passed.
Signatures Needed: Sickle Cell Treatment Act Bill H.R. 5124 #30forSickleCell
Learn more about Sickle Cell from a Obstetrics and Gynecology point of view.
House Calls with Dr. Mac discusses Sickle Cell #30forsicklecell
I think that if you can afford an event planner, you should always use one. I am all for taking the stress off of myself and have the opportunity to enjoy your event. I have given so many parties and wasn’t able to be “present” because I was too busy worrying about everything and everybody else. Great tips.
i know first hand the pain of sickle cell through an ex-boyfriend. He educated me as he had it, and it would break my heart when he would have a sickle cell attack.
My 1 year old niece has sickle cell. Both of her parents passed it on to her. As a result I’ve really been learning more about the disease.
I randomly hear about sickle cell, and I know what an impact it has on those affected by it. This is an important topic, and it’s great that you’re helping educate everyone about the disease.
I admire the way that you handle the challenges of sickle cell, and how committed you are to raising awareness. I have only met one person with it, a child that I taught dance to years ago. Some days were really hard for her, and each time you post about it, I wonder how she is, and how she was able to manage her disease.
I hope she is doing well. There is a lot of advocacy for children, but less for adults. I really hope she has a dynamic support system because it can bring about a lot of emotional issues over time.