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Has anyone been successful retaining SSI/Medicaid benefits post transplant? We're four years out and although the surgery was successful, my son's is experiencing other complications--diabetes, multiple skin cancers, gall bladder removal, low weight and pulmonary function levels that are stable...
I live in North Texas but have visited San Antonio a few times. Don't know too much about the centers but I'm guessing Houston is the best of the three. Prepare yourself to deal with some very hot weather and a very active allergy season. My son drinks lots of Gatorade in the summer to keep his...
As for the rude nurse...report her, report her, report her. She is there to do her job and not judge you. The remark, "I can see why you can't manage him at home" would have sent me right out the door and looking for the charge nurse.
As for Bill's opinion, ignore it. Even if a person is dealing...
To be on the safe side, I'd also suggest a letter from the doctor. You may not have any trouble at all at one airport and run into problems at another. And be prepared for your child to go through a thorough search. That is what we encountered.
joan
Baylor in Dallas is now doing more transplants with CF patients than in the past. UT Southwestern has a longer history with CF transplants. Children needing lung transplants are sent to Houston. Message me and I'll give you more information.
joan
Baylor in Dallas is now doing more transplants with CF patients than in the past. UT Southwestern has a longer history with CF transplants. Children needing lung transplants are sent to Houston. Message me and I'll give you more information.
joan
In my opinion, it's probably related to the diagnosis and not the disease itself. Hair can fall out from stress. I would go to a dermatologist to rule out anything else then talk to someone to ease your anxiety.
joan
In my opinion, it's probably related to the diagnosis and not the disease itself. Hair can fall out from stress. I would go to a dermatologist to rule out anything else then talk to someone to ease your anxiety.
joan
I wouldn't listen to some of the negative posts here. Some people just live life with the glass half empty and they want everyone else to do the same.
Do what your heart tells you to do. No one is born with a lifetime guarantee or a guarantee of perfect health. Hope for the best. Prepare for the...
I wouldn't listen to some of the negative posts here. Some people just live life with the glass half empty and they want everyone else to do the same.
Do what your heart tells you to do. No one is born with a lifetime guarantee or a guarantee of perfect health. Hope for the best. Prepare for the...
Hopefully, the hospital where the CF center is located has an emergency room. Go there. They have to treat you and if you're sick enough (sounds like you are) they should admit you. I'm sure the ER drs would bring in the CF team at that point.
I wouldn't wait.
Hopefully, the hospital where the CF center is located has an emergency room. Go there. They have to treat you and if you're sick enough (sounds like you are) they should admit you. I'm sure the ER drs would bring in the CF team at that point.
I wouldn't wait.
Yes. Linda is correct. If one of your biological children isn't even a carrier, there is no way you could have CF yourself. If you had CF, you would always pass on the defective gene to offspring. With someone who is a carrier, there's a 50/50 chance of passing on the gene.
joan
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