Chemical sensitivity affecting throat/chest
Posted , 34 users are following.
Hi, I am a regular on here as some of you will know. I am still battling, esophagitis/gerd/hh/reflux which was diagnosed by scope earlier this year. I refused PPI and doc gave me 150mg Zantac to take am and pm. I also take mastic gum and seemed to be getting better. I also cut out spices, way down on alcohol, onions, garlic, fizzy drinks, citrus, most meat and anything that hurt my tum. I feel better for weeks then something sets me off again and I start again.
However, I have developed a sensitivity to smells like: perfume, after shave, deodorant, toilet cleansers, diesel and even the normally lovely smell of passing a log fire if it is smoking. This is making my life a nightmare (we have a log fire at home). Within seconds my throat and chest start burning and can last for hours. I have had this for the last couple of months and my hubs scratches his head and can't understand why I won't let him use body cologne any more.
No one has heard of it just says - you are weird!!!!!!!
Before I go back to my doc with this and no doubt she will say she has never heard of it, can I have any thoughts from you guys. I actually think you will know more than my doc anyway. Other than that, I will google all day tomorrow to find something or someone who has this flippin horrible complaint.
Thanks to you all.
G.
3 likes, 69 replies
penny35478 gwen45436
Edited
I've been diagnosed with LPR / Silent Reflux and Oesohagitis back in July and I was really suffering with strong smells - like petrol (my husband has to fill my car up). I couldn't stand the smell of cleaning products, especially dishwasher tablets. I've also had to tell my teenage son he couldn't use his deodorant spray. It's eased a bit, but was really troubling me for a while.
gwen45436 penny35478
Edited
Oh my, you are the first person to say the same as me. Yes petrol is a nightmare. We have both petrol and diesel and both kill me. Also exhaust fumes. And now the log fire - when will this stop. I find people don't believe me. Did you talk to your doc about it?
penny35478 gwen45436
Edited
I've joined the LPR / Silent Reflux Facebook support group, and seems this has happened to other sufferers. Maybe due to acid reflux or vapours going as high up as the nostrils, and perhaps causing damage to the smell receptors. I've also had problems with the roof of my mouth and ear pain, plus sinus problems, thick mucus, hoarseness and tightness round throat.
cheryl06050 gwen45436
Edited
gwen45436 penny35478
Posted
Hi Penny, I would join but don't wish to let my friends know. Do your friends see your posts also or can you arrange that they don't. I would really like to join. Thanks G.
gwen45436 cheryl06050
Edited
Well Chery I sure thought I was. My hubs does not believe me I am sure. I clean the loo with a mask on. Laquer/perfume/after shave is out. But now the fumes from our log fire. I was also out shopping the other day and a lady in front of me had perfume on and I had to get the hell out of the shop.
I have not spoken to my doc about this new symptom as I don't really know what she can do for me. I refused PPI's but my Zantac is not reducing the reflux nor the Mastic Gum. Diet is well toned down. How long have you had this and do you think you can ever get shut of it? I cannot imagine life like this. I am turning down having a get together with my mates in the early evening for a catch up because I am worried about their perfume, not to mention what I can and can't eat or drink and will it get stuck with reflux and I need to go to the loo to get it up.
Any hints appreciated......................Hate this so much...............G.
cheryl06050 gwen45436
Posted
I don't like taking medications because of side effects, however, in this case, I will gladly take them if they will help and they do help me. I just can't imagine feeling nauseous the rest of my life. That is the only solution I have found for this miserable affliction. When I feel better the smells don't bother me as much. But there have been times especially if someone decides to smoke even if they are outside I just have to leave it affects me so severely.
Are you nauseous all the time?
penny35478 gwen45436
Posted
You can create a secondary Facebook account and keep your primary account for your friends and family. That's what my husband set up for me, as I also didn't want to share. I access my secondary account through my iPad and my primary through my iPhone, but expect it's possible to switch to your different accounts on the same device. Do a Google search on how to set up a secondary Facebook account. And then search for the LPR and GERD Support Group, requesting to become a member.
gwen45436 cheryl06050
Posted
gwen45436 penny35478
Posted
Or just send your hubs to me lol lol - I'm a bid of a nerd on computers. It's a flippin wonder I found this site - but very glad I did.
cheryl06050 gwen45436
Posted
gwen45436 cheryl06050
Posted
Can I ask what meds your doc gives you?
vero14915 cheryl06050
Posted
mary67468 gwen45436
Posted
Yes I have same prob.
Can't deal with any smells.
And wander why they promote perfumes etc
Cleaning supplies yes Petri etc
And the worst cannibus smoke
And never know when a smell
Body odors on buses etc
Food smells OK so far
Thanks
susan26882 gwen45436
Edited
I am concerned that everyone on here has found that they are just expected to live with these symptoms- I have just booked to see a private specialist in the hope of speeding up some procedure, but now feeling very disheartened reading posts on LPR as you all seem to have been allowed to get worse than I am currently. Not a bright outlook for us all.
susan26882
Posted
Please ignore 'room' in my post it was supposed to 'to' -
gwen45436 susan26882
Posted
jane47175 gwen45436
Edited
It’s awful, isn’t it. I’ve been suffering from reaction to chemicals, exhaust fumes, burning wood, mould and dust for a while now. A new bathroom was fitted in my flat and I still can’t use it months later owing to the strong glue and Lino used in an unventilated area. My throat is in intense pain, mouth, lips and ears burn, chest, Esophagitis (spelling) pain, sweating, nerve pain in face, etc. Ive had to stay away from my home for ages. I’ve developed acid reflux recently too - wondering if it was linked. My doctor thinks I’m imagining it. Although I feel so sorry for others suffering from this, i at least realise I’m not going completely mad! How should I deal with this, please? Thanks folks
gwen45436 jane47175
Posted
Hi Jane - my sympathies. I had all these very same symptoms which came out of the blue. I had HH/GERD/Esophagitis confirmed and took Ranitidine and Mastic Gum plus Pepsin. It eased the reflux a lot then I got this darn sensitivity. I have an open log fire and that was a nightmare. Whereas for years I loved the smell, all of a sudden, it caused pain. Hair laquer and deodorant were out and colognes and toilet cleaners etc. Petrol and fumes hurt, underground carp parks and exhaust fumes, I had to run from.
I researched and came across Kinesiology - I had heard of it but not for what I had. I contacted the lady that did it and she assured me she had helped people before with it. I was desperate and had a session. It lasted 2 hours and was very reasonable in price. She could feel inflammation in my body via my hand muscles. 4 days later the symptoms started to go. I had another two sessions and that was over a year ago and I am still free of this sensitivity.
When desperate, we to have a go at anything coz this sensitivity is a nightmare.
Hope that helps you a little. Good luck.
p.s. My doc actually smiled when I said I had this problem and just said "how strange, never heard of it before" - hence me doing my own research. People don't believe you, I know my hubs did not
G.
jane47175 gwen45436
Posted
I will try Kinesiology - it’s making my life unbearable.
I’m glad you found a cure and can enjoy your fire again x
jane47175
Posted
I saw a kinesilogisy here but it was no help - she advocated a complete diet change, which I have done and my sensitivities are just getting worse. Nail varnish and diedorant are starting to make my throat swell now and they didn’t before. I’m guessing you are UK based. May I ask you who you saw and where they are, please?
Many thanks
gwen45436 jane47175
Posted
Gwen (Manchester)
jane47175 gwen45436
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norma04599 susan26882
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There is a Dr Michael Vaezi from Vanderbilt Hospital in America that has a special interest in LPR. I think he has done some research. From what I have read he doesn't appear to have cracked any further treatments. Not sure if anyone has been to see him? I live in Sydney, Australia so, out of the question for me! If anyone wants to investigate him who might live in that area? Maybe if they do, they can refer him to this blog. Most of us I'm sure would support him in his research in whatever way we could, or able to do. I had the fundoplication surgery in May 2017, it helped with the discomfort after eating (middle of the chest pain/discomfort) but, unfortunately not with the LPR. The surgeon mentioned Dr Vaezi's name when discussing the interest in the medical profession of LPR. The surgeon put me on 3day steroid treatment for the treatment of voice problems, but said not to use for long period because of the side effects. But I do try this for 3 day spells until the bottle runs out, that how desperate I get at times.
nicola76456 jane47175
Posted
Dear Jane and Gwen, Please would one of you mind passing me on the details of the kinesiologist - I am really desperate for help with this. Its so severe right now. Please help me. Thanks