maxmakcMemberMay 2, 2011 at 7:51 pm #171205150901
My experience as a salt room operator:
Your chances of picking up a viral or bacterial infection are very slim because:
1. We ask that people don’t come when they have a fever or during the acute stage of a cold – by far, most clients are treating chronic respiratory or sinus problems, which are not contagious, and many also come to treat sleeping disorders and for stress relief or meditation.
2. Even if someone did attend during the contagious stage of an illness, the chance of the virus or bacteria surviving in the salty environment of the room would be very unlikely. But again, to be on the safe side, we don’t want contagious people – and at the beginning of an illness the body is working hard on its own to fight the illness (with it’s own SALTY solution, of course). Salt therapy is great after that initial stage for clearing the respiratory system to prevent secondary infections.
As for CF, 100% of our clients with CF report the following: A more productive cough, mucous which is more manageable, and feeling better overall. I firmly believe that many medications can be reduced, and often eliminated, which leads to a stronger immune system. The only people who will be hurt include the pharma company that charges outrageous premiums for meds (out of pure greed), your doc, who won’t need to see you as often, and the ER, who likewise won’t be able to bill thousands of $$$ for a few minutes of their time. Sorry, my personal experiences with these three factions has left me more than a little bitter…April 30, 2011 at 9:11 pm #171205150820
LOL!!! I actually have video of Philip trying to eat the big chunks of himalayan salts in Orlando’s salt room. I actually commented on the video…”you know he has CF since he’s trying to eat the salt”….gross 😀April 30, 2011 at 2:13 pm #171205150799
Not yet, though he has had it to try and bring up a sputum culture. He already licks the inside of his mask. Bleah!
Last night I took some friends out for supper and he proceeded to dump a TON of salt on his chicken strips and fries and eat them. Fortunately our friends are used to that.
Parent to a child wcf DDF508hmwMemberApril 30, 2011 at 2:03 pm #171205150798
Hehehe Liza… is Max on hypertonic saline? He’d probably love it. Emily licks the inside of the mask while she does it, and when she ‘checks to see if it’s done’ I catch her tongue-dipping the neb cup. She will outright drink it, given the chance. And to think her dr told us we would likely have to give her a strong-tasting drink to sip on while she nebbed it to help counteract the salty taste.April 30, 2011 at 1:56 pm #171205150797
DS is almost 8 and I wouldn’t trust HIM not to try and eat the salt! I caught him licking the top of our salt shaker the other night, which is why he has his own.
Parent to a child wcf DDF5082girlsMemberApril 29, 2011 at 9:26 pm #171205150777
That’s it, we just need to move to FL – we love it there anyway!! Seriously, thanks for the responses. We did end up going to the St. Louis Salt Room on Monday and it was fine. We were in the room by ourselves – my son sat right in front of me and played with the beach toys. The owner was fully aware of my son having CF and takes extra precautions for people with CF – disinfecting toys, chairs, etc. There is no way they could remove the salt from the floors very often because that would cost them a fortune. This is Halotherapy like Catherine said.
I don’t really know what I expected out of it – it was boring – 45 minutes of trying to keep a 21 month old entertained – not to eat or throw salt was tiny bit of an issue. For the most part, he was very content just playing in the salt. There was no smell, only an occasional taste of salt. All I know is, my son and I slept really good that night and he is having a fabulous week – I don’t know that I can attribute it to the salt room, or just a good week! The idea is to go more consectively for like 10-20 sessions, but we live too far away to do that right now. I am not ruling it out, but I was just more curious than anything.
Our pulmonologist was not opposed to us trying it – he just said there is no research to show it is effective. We also take our son to the chiropractor once a week for adjustments – not sure how effective that is either, but he had a decent winter/spring since we started (minus a 6-day hospitalization because of his weight/and had a bronch done). Maybe if nothing else, we need to discuss starting inhaled saline because we don’t currentlyl do that.giantsfan91MemberApril 23, 2011 at 12:44 am #171205150397
I’d say 21 months is a little young for a salt room only because toddlers tend to touch their faces more than anyone else but once he gets older I’d say give it a try. I know when I spend a week or 2 at the beach I feel better than any other time of the year so I think salt air is the best medication for us. Maybe you could try it out yourself first to see how you like it and if you feel it’s safe for your son.April 22, 2011 at 11:40 pm #171205150396
Actually there have been studies done on the benefits of salt rooms and cystic fibrosis. It was published in the New England Journal of Medicine in 2006. The study was done basically on halotherapy and speleotherapy. Halotherapy is where a generator moves the salt (HyperSal can also be placed in this category). Speleotherapy is where you sit in a salt cave (no movement of salt through the air). Some websites are Salt Caveshttp://www.saltroomorlando.com/salt-caves-respiratory-relief-symptoms/ and Studieshttp://www.saltrooms.com.au/scientific-articles.php. I can’t find the link to the journal. Grr. Anyway, I am certainly not trying to convice someone to go if they are not comfortable. I do know that the one we went to in Orlando was very aware of CF and they santitized the toys between sessions. We also always got the room to ourselves. We were never in contact with anyone else. But, if you aren’t comfortable, certainly don’t go or take your child. Hypertonic saline via nebulizer is cheaper and WONDERFUL. I just speak of the salt rooms, after taking myself and my sick child there and seeing the results. A friend in Australia actually had her CF dr presribe salt therapy (as did ours).Good luck! 😀hmwMemberApril 22, 2011 at 5:11 pm #171205150388
Yeah, I really like the concept of these places, but there are so many hurdles to overcome in the execution. Photos show heaps of salt and salt clinging to the walls, etc at many of these places. I doubt that salt is removed from the room and replaced between patients and it does not remain ‘sterile’ and portions of it becomes airborne with the salt being circulated in the air supply …Salt may have antimicrobial ‘properties’ but there is a difference between that and acting as a disinfectant. We’d never be content with salt acting as the disinfectant between patients at cf clinic or even the pediatrician, and these places are designed to attract sick people.
I think using salt as part of our therapy with cf patients makes a lot of sense (we are loving hypertonic saline for Emily) but doing it in a way where we risk exposure to other people’s germs is taking a risk.LouLouParticipantApril 22, 2011 at 4:03 am #171205150365
FYI Halo NYC was closed. Makes me wonder if it was due to health reasons. I don’t doubt it is helpful but also wonder how they can keep the place clean while attracting sick people galore!April 22, 2011 at 1:49 am #171205150356
IMO, not worth the risk until more research has been done. Would also have to see what DS’ doctor has to say.
Especially seeing how some of the different sites are run as I mentioned above and not sure how they can sanitize the surfaces. Concerns regarding people coughing.
While popular, there have been NO clinical studies regarding salt rooms.
Parent to a child wcf DDF508April 22, 2011 at 1:32 am #171205415270
I am such a huge salt advocate. Salt rooms are absolutely amazing. Make sure they have a halogenerator and that it is actually halotherapy and not speleotherapy. Inhaling salt is naturally antibacterial. The cf clinic in Orlando is actually partnering with a salt room to build one in hospital. Expect this to be huge in the near future. I have experienced them first hand and I also took my son with cf to one when he was sick at 19 months. Ever since we have nebbed hypertonic saline. We are also trying to build one here. Make sure if you take your child, that you tell them about the cf. That way they don’t schedule with other people. Message me if you want more info 😉AleksandraKaczynskaMemberApril 21, 2011 at 11:26 pm #171205150344
We are told to avoid such places as many sick people go there and there are many bacteria and germs around.April 21, 2011 at 6:17 pm #171205150323
I’ve never experienced one, but guess I’d have the same concerns as I would at the hospital, clinic, etc. I would ask if they sanitize the chairs and surfaces between ANY appointments as some germs can live on surfaces not just for hours, but days.
Photos of some of the salt rooms I’ve seen show lawn type chairs and some have plastic toys which tend to remind me of the dreaded waiting room toys.
Parent to a child wcf DDF5082girlsMemberApril 21, 2011 at 6:02 pm #1762750
Wondering if anyone has any experience with Salt Rooms? A new one just opened up in the St. Louis, MO area and I send the info to our pulm to get his reaction. The owners opened because their 9 year old daughter had severa asthma and he told me that they have several individuals with CF who come on a regular basis and are seeing decreased infections, coughing, dr’s visits, and antibiotics.
We are currently not doing any kind of salt treatment with our son who is 21 months, but the winter months are hard as far as infections go – I thought this might be something to check out, but wanted to see if anyone else had any experience. They don’t let 2 individuals with CF in the room at the same time and have a session in between to make sure there is no cross contamination.
If your in the STL area, website is: http://www.mysaltspa.com
You must be logged in to reply to this topic.