montelukast cystic fibrosis

There are different types of cystic fibrosis mutations in which some are worse than others. Cystic fibrosis has to do with the thickening of the mucous around the lungs, most can't digest their own food, they have trouble breathing and are put on different types of medication. As long as the doctors catch it in time, you shouldn't have a problem. Although there isn't a cure, they can keep it from getting worse or causing death.

My son is a month old now but was diagnosed with cystic fibrosis when he was 2 weeks old. I am so heartbroken. But I want to know what to expect, and what I can do to make his life better. Please don't move this post to the cystic fibrosis forum, as nobody is on there and this is serious to me.

Hi Hun Iam a carrier for Cystic Fibrosis. My baby's father is not so it's not likely my son will have it. & correction she can't be a carrier for it. You can be only be the carrier meaning she may or may not have it.

what is cystic fibrosis. im 30 weeks tmw and found out im a carrier of cystic fibrosis. is this bad? please tell me. this does not help me think im worried and cant think of anything else.

On my twenty week scan it showed an abnormal bowel. Either Side effect of having an Amniocentesis at 13 weeks or cystic fibrosis. I'm absolutely scared stiff. At least two weeks before getting any results. Anyone else been through the same?

Because if baby has cystic fibrosis the drs will need to plan for babies care accordingly. Such as having a nicu team ready and in the room ect. Its not abour knowing for abortion purposes. Also if you know you can start the paperwork for disability. Its always best to know. Then you can join a support group, research and be as prepared as possible.

Yesterday I got told that I am a career of cystic fibrosis should I worry.

I am afraid because I read that this is related to cystic fibrosis and now I think I have it. I also have other symptoms like post nasal drip, seasonal allergies and mucus stuck on my thoath. I also sweat a lot but my sweat is not very salty. My sister also the wrinkling hands. So my question is could I have atypical/cystic fibrosis or at least be a carrier and what is my life expectancy? My doctor says I'm too old to be diagnosed with this, I'm 25 years old.

They saw something that he thinks could be cystic fibrosis. Im not really sure what that is. does anybody have children with this. Does it make it harder. Is it scarey?

- Nasal transepithelial potential difference (NTPD or NPD) testing can be used to assess the function of the cystic fibrosis gene product, a chloride channel called cystic fibrosis transmembrane conductance regulator (CFTR). Certain measurements are characteristic of CF. - Clinical genetic testing for CF looks for mutations in the CFTR gene that cause the condition.

Didn't know about the cystic fibrosis drug. Thanks for the info. Susie wrote:, "By the time the drug gets FDA approval, the bump up is long gone". I have to disagree, how could a company stock not continue to rise if they are making billions off of a new drug?

I just found out that I am a carrier for cystic fibrosis. I will be 24 weeks tomorrow and they suggested having the father tested to see if he is a carrier also. I have two healthy children (with a different man) already and I don't want to stress my boyfriend out with this if its not necessary. Has anyone else had this and if so did your husband/boyfriend get the test done? Am I being careless by not having him tested? I just dont want to stress him out for nothing.

Is there a cystic fibrosis test for baby while you're pregnant? I am 16w and had a dream that my doctor told me baby had it. It's weird cuz I'd never heard of that disease before my dream. I feel calm about it, but I just want to know if my dream is true or not!

My bloodworm came back tgsy I am carrier for cystic fibrosis. Does anyone have experiences with this? My husband goes for testing on Wednesday.

I found out today that I tested positive for genetic cystic fibrosis. My husband got blood work done today to see if we are both carries. I'm so scared that is something wrong with my baby and it's all my fault. Any one else going through this or has with previous pregnancies?

I'm 12 weeks. Last week I found out that I am a carrier for Cystic Fibrosis. I am being referred to a Genetic Specialist so we can do some advanced testing for me and my husband. Just wanted to know if anyone else has had this scare. I'm very nervous.

Read on Cystic Fibrosis. It could be part of HBV complication which shows reddening on the edge of the palm. Ther are many other things connceted to the palm and it could be nothing much. Consult your doctor for professional assistance.

Just found out I'm a carrier for cystic fibrosis. My sister had cystic fibrosis and died from it almost 3 years ago at only 19. Now I have to get my baby's father tested to see if he's a carrier because if he is then there's a 25% chance my daughter can have it.

I hope his test is negative and we can skip amnio. Anyone else did cystic fibrosis test? I never hear anyone discussing this one.

I just had an HIV Antibody Test and an HIV DNA PCR test done. They both came back negative. I have cystic fibrosis and was wondering if the fact that I have CF, can it affect the results of the HIV Antibody Test? Or the HIV DNA PCR test? Also, I was inhaling Pulmicort (a cortcosial steroid), through a nebulizer for my lungs. I was only on it for 5 days and it was about two weeks before I was tested for HIV. Can that affect these tests too? Please let me know. Thank You very much.

Montelukast cystic fibrosis

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