Njh visit
Hello
I am currently at njh. Great place, glad i came. Have had all kinds of test. Wondering if any of you had a positive sweat test and high anti nuclear score. Have paid for the gene testing for cystic fibrosis. It takes a few weeks for the results. I was shocked to have high levels. Doctor says all the autoimmune test are not back yet but so far they have been normal. Don’t understand why my number is so high. I leave tomorrow after some swallowing test. I had neck cancer so for me this is appropriate.
Any thoughts would be helpful.
Miriam
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
Thank you for this response. Yes, the new options do sound promising if you have the right gene mutation, and from what I was told, the care from the CF Foundation is impeccable. Hoping I and any others receiving a positive sweat test don't have to find out! Again thank you!
Thank you for your response, Tina. Hope we both receive the best news once it comes!
I am still at NJH and received a very high result from my sweat test. I too will have to wait the genetic testing results. Did they send anyone to have a consultation with the CF department here?
Yes, Dr. Lommentzch. I'm not sure if I spelled it right. I loved her!
Hi Tina and Terri
Would you care to share your level on the sweat chloride test? Mine was 52 which is quite elevated ( not the 60 + required for CF diagnosis), but my genetic test was negative for CF, one positive gene for PCD ( Primary Ciliary Dyskinesia). My belief is that there are other mutations for CF that are yet discovered as I have other symptoms consistent with CF. Thanks if you wish to share more.
My level was 89 which is quite high. Just have to wait 2 weeks to get answers.
Please what is NJH? What are sweat tests used for?
Thanks
Sweat tests are for cystic fibrosis or any of the many variants. National Jewish Hospital known for its respiratory research. It is located in Denver
tconz, I see where Tina said they sent someone to have a consultation with the CF department for her, but that was not the case for me. I just got back from there at the end of April. In my case, the plan is talk with the CF dept there on a return trip in a few months if the genetic test comes back confirming the sweat test diagnosis (or at least that was the plan the last time I spoke to my doc). Hope your trip gives you answers and a good treatment plan whether it is tweaking something current or starting over.
They are trying to get me into CF for Consultation before I leave but not sure it will happen. So impressed with everyone here!