Alpha-1 Antitrypsin Deficiency - just been diagnosed
We recently moved to Florida so I've had to find new doctors. I went to a new pulmonary doctor who was very thorough. After reviewing my pulmonary function tests and asking me questions about my family history etc. He suspected that I have something called Alpha 1. They did a blood test and called me ten days later and told me that I the blood work came back indicating that I have Alpha-1. They gave me a brochure with various web sites that I've gone on in an attempt to learn more about the disease. Is there a discussion group here about Alpha-1? I would really like to be able to be in a discussion group with folks who have been diagnosed with Alpha-1 to learn more about it. Thanks!
Interested in more discussions like this? Go to the Lung Health Support Group.
I went to the Gainesville support group, I see Dr Brantly this Wednesday. He will not be the speaker after all at the Orlando group.
I had not seen the response. Thank you for drawing it to my attention!
@nancyjac Hi Nancy! How was the Alpha support group? Were there many people there? Were you able to get more of your questions answered?
@windwalker I met some really nice folks at the Gainesville support group. I learned some new information and the man sitting next to me ended up being my nurse for my infusions that I started last week. I’m looking forward to seeing Dr Brantly tomorrow for the first time.
@nancyjac Hi Nancy! I am so glad you got something out going to the support group. What kind of things did you learn from it? Will you please keep me informed on how the infusions are working for you?
I am diagnosed as mz. Which means I am a carrier.
@windwalker, Terri, in this post you mentioned a low score of 112..... what is that from. The information I got on my alpha 1 test was that I was a MZ and then had a 82? So what does that mean? And my next question is can drs. tell if you copd is caused by smoking or by alpha 1. Is there a difference in the appearance of the lungs on the ct scans...…….. Thank you
@waterboy
@colleen. Do you or anyone know how many conditions have been proven or reseached connected to alpha 1. Do drs ever join any of thes discussions. Just wondering
@sakota, I don't know know how many conditions are related to the alpha 1 gene. I found this resource from the NIH that is a good place to start looking into the most recent research and knowledge. https://ghr.nlm.nih.gov/condition/alpha-1-antitrypsin-deficiency
Connect is an online community, connecting patients with each other. Mayo Clinic experts participate on Connect through the Pages (blogs) and Video Q&As.
- Page Directory: https://connect.mayoclinic.org/pages/
- Video Q&A (upcoming and archived): https://connect.mayoclinic.org/webinars/
You can read more about Connect and its components here: https://connect.mayoclinic.org/page/about-connect/tab/more-about-connect/
I've just been diagnosed with this genetic defect--which certainly explains my situation.
Is there a discussion group here (or elsewhere) for people in the same boat?