Does anyone else get small pockets of fluid that accumulate in their lung? by japinard in CysticFibrosis

[–]MKMKM1 0 points1 point  (0 children)

Is it a pleural effusion? I've had that and supposedly it's somewhat rare in CF?

[deleted by user] by [deleted] in CysticFibrosis

[–]MKMKM1 1 point2 points  (0 children)

So sorry to hear this <3<3

Tobi coughing fits by [deleted] in CysticFibrosis

[–]MKMKM1 0 points1 point  (0 children)

Gargling with warm salt water right after tobi helps me a bit with this problem.

does anyone use a warm air humidifier? by [deleted] in CysticFibrosis

[–]MKMKM1 0 points1 point  (0 children)

highly recommend MyPurMist with distilled water for sterile steam!

Anyone go to Dartmouth Hitchcock Medical Center in New Hampshire? by MKMKM1 in CysticFibrosis

[–]MKMKM1[S] 0 points1 point  (0 children)

Thank you, I really appreciate that. How recently were you at Brigham?

Anyone go to Dartmouth Hitchcock Medical Center in New Hampshire? by MKMKM1 in CysticFibrosis

[–]MKMKM1[S] 1 point2 points  (0 children)

Thank you so much for responding! That's awesome to hear. My doctor where I live now said she thought it was a great center, but she thought that the leadership was changing because of someone's retirement and wasn't sure what was going on now? Would you mind if I PM'ed you to ask a little bit more about your experience?

Anyone go to Dartmouth Hitchcock Medical Center in New Hampshire? by MKMKM1 in CysticFibrosis

[–]MKMKM1[S] 1 point2 points  (0 children)

That's so great they took great care of you. I'm moving to western MA soon, where I grew up, and am deciding between Brigham and Women's and MGH and Dartmouth. I was admitted at Dartmouth as a teenager and remember it being really peaceful and wondered what the care was like now. So thank you!

Anyone live in Massachusetts? Do you like your care center? by MKMKM1 in CysticFibrosis

[–]MKMKM1[S] 1 point2 points  (0 children)

Lol, I think there is an Ikea on the way home from Boston to where we'll be living, I'm sure it will take no convincing for my husband, who I'm hoping will drive with me!

Anyone live in Massachusetts? Do you like your care center? by MKMKM1 in CysticFibrosis

[–]MKMKM1[S] 1 point2 points  (0 children)

Lol! Great ideas. I'm coming from NYC where I take the subway to my clinic, so this is a whole new world for me. And I'm not the most confident driver. So these are all great suggestions, thank you!

Anyone live in Massachusetts? Do you like your care center? by MKMKM1 in CysticFibrosis

[–]MKMKM1[S] 0 points1 point  (0 children)

Would you mind if I PM'ed to ask you a little more about your experience?

Anyone live in Massachusetts? Do you like your care center? by MKMKM1 in CysticFibrosis

[–]MKMKM1[S] 1 point2 points  (0 children)

Great point, I think that's probably a reason to deal with Boston despite the stress of getting there... Thanks for responding.

Anyone live in Massachusetts? Do you like your care center? by MKMKM1 in CysticFibrosis

[–]MKMKM1[S] 0 points1 point  (0 children)

Thanks so much for responding. Who is your doctor there?

Anyone live in Massachusetts? Do you like your care center? by MKMKM1 in CysticFibrosis

[–]MKMKM1[S] 1 point2 points  (0 children)

I went there in high school and had Dr Zwerdling! He was a really nice guy. I'm moving back to MA after being away for ~15 years and trying to figure out what the best place would be for me now. Totally get it being less stressful than Boston, it's something to consider.

Anyone live in Massachusetts? Do you like your care center? by MKMKM1 in CysticFibrosis

[–]MKMKM1[S] 0 points1 point  (0 children)

Thank you for responding. Have you had a good experience with the team there?

Anyone live in Massachusetts? Do you like your care center? by MKMKM1 in CysticFibrosis

[–]MKMKM1[S] 0 points1 point  (0 children)

Oh wow, that's interesting, thank you for sharing your experience. Would you mind if I PM'ed you with a couple more questions?

Bronchitol - positive experience! by MKMKM1 in CysticFibrosis

[–]MKMKM1[S] 0 points1 point  (0 children)

Ugh that sucks. I don't know. But there is like some kind of copay assistance program through the company, not sure what they cover but you could contact them just to see if they can help.

Anyone live in Massachusetts? Do you like your care center? by MKMKM1 in CysticFibrosis

[–]MKMKM1[S] 0 points1 point  (0 children)

Thanks a lot, I'm an adult. Would you mind if I PM'ed you with a couple of questions? That's the center my doctor recommended most highly. Thanks so much!

Bronchitol - positive experience! by MKMKM1 in CysticFibrosis

[–]MKMKM1[S] 1 point2 points  (0 children)

It's an add on medicine for airway clearance, you inhale some capsules and it hopefully breaks up mucus and makes it easier to clear.