You probably don’t give a lot of thought to your olfactory senses day to day, but imagine suddenly losing your ability to taste and enjoy your food. To no longer be able to smell freshly cut grass, delicious cookies baking, or taste fresh blueberries. Smell and taste are senses we take for granted– until they’re gone. I’ve been through this devastating loss and was successfully able to overcome it.
I have spent hours researching how to overcome anosmia (the inability to taste or smell anything) and hyposmia (partial loss of taste and smell). There are few studies and no real cure. But I found a way to help my body heal after suffering from post-viral hyposmia for months. Now I want to share my experience with hyposmia and anosmia in hopes that it will help anyone out there looking to overcome these conditions.
Hyposmia: My Story
Spring 2017 was a very stressful time for me. My mother had just died, and I found myself back and forth between California and Arizona taking care of her and then her estate. I was admittedly not taking very good care of myself at this time and came down with a bad cold (which I’m usually able to ward off with herbs and self care).The cold hit me pretty hard, and with my clogged sinuses I soon lost my ability to taste or smell anything, as sometimes happens when one gets a cold. I tried to push through it, but after a week I felt really bad and stayed in bed a few days. The cold lingered, and I slowly recovered, but I never recovered my sense of smell and taste. I waited patiently until about two weeks had passed and I realized I still couldn’t taste or smell anything– at all.
I contacted my naturopath, who assured me my senses would return. After a few more days, I was catching whiffs of things here and there, but I still couldn’t taste anything. After about a month of no improvement, I went to see an otolaryngologist. There I learned I had postviral hyposmia, the partial loss of taste or smell, caused by an upper respiratory infection where the virus had attacked and killed the olfactory nerves in my nose (who knew they were so delicate?). There was nothing else wrong, no nasal polyps or any other abnormalities. I was told these senses would likely return, probably not 100 percent, and maybe not at all. Damaged olfactory nerve cells can regenerate, but they don’t always reconnect properly in the brain.
I was devastated but optimistic and immediately poured myself into research. I had never heard of this condition and didn’t even know it could happen. Turns out there isn’t much out there on anosmia or hyposmia and even less about how to treat it. There isn’t a cure. There have been very few studies on the prognosis of postviral olfactory dysfunction.
It may be underreported, but it’s thought that olfactory impairment affects approximately one-fifth of the general population, with the highest prevalence observed in older men, especially in individuals who suffer from degenerative diseases such as Parkinson’s disease, dementia, and Alzheimer’s disease (hyposmia and anosmia, when not viral in nature, are actually a harbinger of Alzheimer’s and dementia). Frighteningly enough, olfactory dysfunction predicts a 5 year mortality rate in older adults (source).
Apart from degenerative diseases, the most common causes of olfaction loss are postviral upper respiratory infection (URI), which is what I had; nasal/sinus disease; head trauma/injury, which cuts or damages the olfactory nerve; brain tumors; exposure to toxins/drugs; some meds; and congenital anosmia. Postviral URI is probably the most common cause of olfactory dysfunction observed in ear, nose, and throat clinics (source).
I read story after story online about people who, like me, were totally fine until they got a cold that completely wiped out their ability to taste or smell. Most people, also like me, had no idea this could even happen. Medications such as steroids and antihistamines may be used to calm the inflammation, but nothing was a sure thing. The prognosis is grim: Full recovery rate is 31.7%, but 80 percent of people achieve some recovery within a year (source).
I learned quickly that hyposmia is a safety issue. I had lost the ability to determine if food was fresh by smelling it. I wasn’t able to smell gas that could signal a gas leak. When the dog got sprayed by a skunk, I had no idea until family alerted me that my house and dog reeked of skunk.
What followed was depression, not uncommon in hyposmia sufferers. I was no longer interested in food, nor did I want to cook for people, one of my main joys in life, since I couldn’t taste to correct flavors and seasonings. I spent a lot of time in bed.
Meantime, I also poured over as much info as I could on how to help my body heal. Could olfactory nerves regenerate? Yes, there is evidence they do. With that logic, I researched herbs and supplements to support nerve health and regrowth. I came across a couple studies weakly identifying gingko and alpha lipoic acid as supplements to help hyposmia. I was also doing a lot of immune support.
How I Beat Hyposmia
It took me about four months to regain 90 percent of my ability to taste and smell. The supplements definitely helped (I saw noticeable improvement quickly after starting the protocol), but many people spontaneously recover their senses within six months to a year.
Here’s what I did:
Note: do this protocol for 3-5 months, then reassess. Most herbs are not meant for longterm use and will stop working after a few months.
- Took ginkgo biloba, 3 of these capsules daily. Studies show it helps.
- Took 600-900mg of alpha lipoic acid. Again, studies show it helps, probably because of its antioxidant and nerve regenerative properties.
- Took 60mg of zinc. This is an interesting one. Zinc deficiency correlates with loss of taste, so that’s a no brainer. I thought there was no way I could be deficient in zinc because I take 30 mg daily as part of a multi. But my naturopath told me a severe cold really wipes out your zinc stores. I think the zinc made the biggest difference.
- Added black seed oil because it’s pretty much a cure-all, and I wanted a potent anti-inflammatory.
- Took 1 gram of lion’s mane. I was super impressed with my research on this medicinal mushroom. It encourages nerve regeneration and growth, which is exactly what I needed. It’s also great for brain health and memory. I could tell a difference in cognition taking it.
- I did acupuncture. There is some evidence it helps hyposmia, and it did help me. Interestingly, though, it helped a lot the 24 hours after the treatment, then I’d go back to where I was.
- I got lots of sleep and did basic immune support stuff.
- Smell training, which teaches the brain to recognize smells as nerves are growing.
Here’s what happened:
I noticed great results with acupuncture, but as mentioned, they only lasted for a limited time after the treatment. I did three treatments. I joked that I would eat everything I missed during those 24 hours. The first improvement I noticed after adding the supplements was in my ability to smell most things. Then I could taste the first bite of something but nothing after that (known as taste extinction).
I think the zinc made the biggest difference, followed by the lion’s mane. I noticed the biggest shift after I added zinc. It happened slowly; it’s not like I just woke up one morning and could taste everything. I started to notice after three months or so that I could taste more than just the first bite of something. But then I would regress and have what I called “flares” where I’d go days not being able to taste anything again.
After about four months (where I am today), I can pretty much taste and smell everything and no longer have the flares. Some smells are super distorted, which is very odd, and I can’t really smell certain things, like poop, at all anymore (which I guess is a good thing?). Although I’m not good as new, I’m elated to have recovered as much of my smell and taste as I have.
But most of all, this experience reminded me of the power in our body’s ability to heal if we provide it with the nutrients and boosts it needs. Hyposmia is such an unusual condition, but I discovered many people suffer with it, and there is a sad lack of info about how to treat it. I hope this post helps someone else out there.
One Year Later
I wanted to update you on my success after one year. I did the protocol for about 4 months and then stayed on zinc and ALA a bit longer. I still use Lion’s Mane occasionally, mostly for its aid in cognition! My sense of taste has been fully restored. Sometimes I think I can smell even better than I could before, BUT the smell of poop and urine are still distorted, oddly (though I can smell them). Everything else is normal. I still do get the phantom smoke smell occasionally but rarely. I remain pretty amazed that I had such success from this protocol. I’m very thankful and reminded that our bodies have an amazing capacity to heal when given the right tools.
Good information but isn’t a high percentage of hyposmia age related? Did any of your research relate to that regarding the supplements you listed? Also, I have a vague recollection that zinc overload can be bad for you. Care to comment?
Hi Bill, you’re right, hyposmia and anosmia can be age related, but as I mention in the post, it can also be a warning sign of Alzheimer’s (I linked to the study). I’m mostly discussing post-viral hyposmia. It is of course possible to get too much zinc over time, but that’s not very common. Deficiency is MUCH more common, and as I mention in the article, an illness can wipe our your body’s zinc stores, and supplementation is necessary to replenish. It’s not meant for long term.
About 10 years ago after a particularly difficult upper respiratory illness, I experienced anosmia and was not able to taste Thanksgiving dinner that year. I can certainly understand how depression would result with ongoing symptoms. Thankfully my body gradually healed.
My sympathy to you regarding the loss of your Mom and now as you continue to grieve and move on to life without her. My Mom passed away in July 2017. Even when I was aware of the importance of taking care of myself – it was hard to deal with her terminal illness and death, traveling, eating healthy on the road, and keeping up with everyday life.
Life is very fragile. Just when we think we are strong, we find out that we are one or two steps away from weakness.
Thanks for your comment, Kristin. Glad you were able to recover. Definitely one of the worst things I’ve experienced in my life.
Thank you so much for sharing. It is so difficult to find useful information on this mostly unknown and ignored condition. I have had anosmia for almost 4 years now. My previous doctor didn’t want to refer me to an ENT specialist so I suffered in silence hoping that my smell may come back and that I didn’t have a tumour! Having moved doctors I have now been referred. Luckily my mri came back clear, but the only suggestion I have received is to try a steroid to kickstart my olfactory nerves. I don’t see this as a permanent solution due to the side effects and day 5 in I have not noticed any improvement in smell. I am going to try your suggestions. Fingers crossed it works!
Please report back, Danielle! Sending you healing vibes. Definitely do at least 30 (and more like 60 mg for the first month) of zinc daily. Zinc deficiency can be a cause of anosmia. Believe me, I know exactly how you feel. I’m glad you found my article.
I am so thankful to find this post Mary! There is so little info out there about this condition. I too had a bad cold just before Christmas this year and now have lost my sense of taste. I was very sick for 2 weeks (major sinus issues, cough but no fever.) At one point during the ‘cold’ I lost my sense of smell for about 3-4 days but thought that was normal when so congested. I am pretty sure it turned into a sinus infection as I had a headache and facial pain along with it. I am not one to struggle with sinus issues, this is probably the second time I can remember feeling that way. I went to see the doctor 9 days into the cold and she said I had a viral infection. She gave me antibiotics but said it should clear on it’s own. It did so I didn’t take the antibiotics. 4 days later I was better. I could smell and taste. I remember eating Godiva chocolate cheesecake on Christmas Day and loving it. After a week of being ‘better’ (on New Year’s Day) I noticed I couldn’t taste my soup at lunch and have not had a sense of ‘flavor’ since. I can smell quite well but can’t seem to taste anything. I get hints of sweet, salt, bitter, sour and I think from my sense of smell get a hint of what I am eating. The taste in my mouth is always like a diluted salt water, even when I drink water. I sometimes get very sour and bitter tastes too. Most things taste like cardboard in my mouth. It is all very unsettling and upsetting!
My doctor said that this is not uncommon after having suffered a URI (so it seems this is linked to my upper respiratory infection). She said to give it 1-2 weeks and it should be fine. It is 3 weeks later now. I checked back in with the doc after 10 days, freaking out. My regular doc was out of the office so I consulted with someone new – he said that the issue must be with my nose and not the tongue/mouth as taste and smell come from the same olfactory place and smell is key to taste. He said I need to ‘work on my nose’, that the infection may have cleared from my main nasal passageways but not the smaller ones which can impact taste. I have now been on a regimen of a saline nasal rinse 3x/day and Flonase 2x/day for about 6 days. I also decided to also take the 5 day Z-pack antibiotic in case there is remnants of bacterial infection, today is my last day and no changes so far.
My doctor has also ordered a blood test to look at my Vitamin B and Zinc levels as apparently deficiencies of these vitamins can lead to a loss of taste. My levels came back normal for both vitamins. Everyone seems totally STUMPED by this…especially that I have my sense of smell but not taste. My doc admitted she had never had someone come to her with quite this issue. I think my sense of smell must be impacted by this but I can’t tell how much…I have always had a great sense of smell but it seems unlikely that it would be an issue solely with taste. I also have two kids under 5 still waking up throughout the night, work full time and have a house remodel going on right now. I have known my immune system has been dragging in the gutter for some months because of the current state of my life (lots of wonderful, positive things but all are a heavy load to carry).
Per this post, I am going to add some supplements to my regime. I bought some Alpha Lipoic Acid in a 600mg which I will take and will pick up some additional zinc to boost my Immune support supplement. Any support you can offer Mary would be amazing. This is so depressing, I am a healthy 37 year old Mom 🙁 🙁 🙁
I understand your frustration, Danielle. I would recommend everything I mention in the protocol of the post– the lion’s mane (heals nerve damage), the gingko, the ALA, etc, and especially the zinc. And work on building immune health. Best wishes to you! My smell and taste is almost completely restored, but it took 3-4 months, so don’t give up hope.
Mary, are you still taking the vitamins to help with your situation? And if so how long now have you been on them? I just ordered all the vitamins you suggested, I’m currently going through loss of smell/taste, after having the flu in June 2017. I don’t want to over due it but I do need to hopefully find a cure even if it’s slight.
Cindy, no, I’m not currently doing any support for hyposmia any longer. I did the protocol for 3-4 months until I recovered. Now I’d say I’m at nearly 100%, but it took over 4 months.
Thank you so much for posting your story. You are correct there is not much helpful information on the web. Your story was the only story that gives me some hope. I have never posted before this is my “pay it forward” opportunity.
My story is the same in regards to how it happened even the loss of my parent. I like you have been diligent about nutrition over many years. I’m angry this has happen due to the fact I spend so much time and money making sure I’m healthy.
That being said I’m only 4 weeks into my journey. I had an encouraging visit to my Chiropractor who said my scull was out of alignment. Once adjusted 50% of my taste and smell came back only to leave in a few hours. He recommended I complement his work and give Acupuncture a few sessions.
I strongly feel this is a “energy” imbalance. My Naturopath has muscle tested me for a NES Infoceutical product which will focus on balancing my Immune System. I’m also looking into the “Bemer” Therapy which balances energies. This may sound rather strange to most yet Energy Medicine has been used for years for pain reduction and overall balance.
I have a hard time believing my body is that delicate that it would not only destroy my own cells but not regenerate new cells. The body is so powerful.
Again thank you for your story as it has given me more information to travel my journey of health.
Thanks for your comment, Melissa. I think no doubt it has to do with a compromised immune system. Interesting you had that experience with chiropractic… i had the same with acupuncture. The lion’s mane was truly phenomenal. Best wishes to you.
Thank you so much for this post! I lost my smell/taste, post concussion/head trauma. The loss of taste happened gradually as I remember being able to taste fine when I was at home recovering, immediately after the accident. However about 2-3 weeks later as I was becoming much more functional, and even going to work, I noticed my taste was disappearing! Also different than what you experienced, I have a constant burnt/sweet smell in my nose and everything tastes like this as well. I have researched a bit and it seems as though it is along the lines of Phantosmia, do you know anything more about this? I am honestly just trying to be patient, before going to the doctor, as I have missed too much work as is, and the bills have started coming from all the concussion mess 😐 however I have started taking the supplements that you recommended!! As I mentioned, I am just trying to be patient, as it has only been a week or so that I have been consistently taking the supplements. I was just wondering if you also experienced any of the “phantom” smells and had any insight. Thank you again for your post!! As I think many of these supplements are just good for me recovering from the head trauma as well.
Hi Mariam, I did experience phantom smells as well…. mostly the smell of cigarette smoke, which is not uncommon (also not pleasant). I sometimes still get that even. It comes and goes. The cause in your case is nerve damage, so for head trauma, the lion’s mane especially and the gingko and alpha lipoic acid will all help nerve regeneration. best wishes!
Thank for this valuable post! I’ve always had a very keen sense of smell. I’ve had a chronic sinus condition for the last four months and have just noticed that my sense of smell is diminished – not gone but noticeably less.
I’m going to try your regimen. I have been taking ginkgo, alpha lipoic and zinc for years but not the quantity of zinc. How big are your ginkgo doses?
I just read about Theophylline nasal spray for hyposmia and anosmia. Do you have any thoughts about it? Thanks again for sharing all your research!
Yes, definitely beef on up zinc, which gets quickly depleted with chronic infection in the body. That can make a huge diff. For the gingko, I took 2 of the Gaia capsules per day. I’ve not researched the Theophylline. Glad you found the post helpful!
Hello! I am so excited I came across this article. I have been diagnosed with the same thing after a cold about three months ago. I have the ability to smell but no taste! I am going to start on this regiment and hope that it helps! How much black seed oil did you use? I didn’t see an amount on that. I am starting the zinc today and will get the rest of the items this week. Thanks for your helpful information.
Hi Jennifer, I hope the info helps! I did black seed oil 1 tsp twice daily. Please report back and let us know your progress!
Thanks for the valuable article.i cannot taste anything after taking lefloxazin 500mg and zeos(loratadine 10)mg for 8 days. I accidentally took leflox for the 8 th day . From the 7 th day I ate a kind of Indian spice goraka with cooked fish (goraka is a very sour ingredient) but I didn’t know actually it was with that spice.anyway after eating it I felt I can’t taste anything.then I started eating rice gruel with vegetables ,fish or meat .but it’s so hard.i cannot eat properly .and then after a month I caught a cold .oh then I knock down more .i took clarizromycin for only 6 days .couldn’t continue and stopped it .I have burning sensation in my tongue.sometimes sides pain on my tongue.there are some white thick court on my tongue.oh can’t understand .whats wrong with me.but I have chronic sinusitis .but it’s not harm me at all.once I went to the dentist he mistreated me .that was the start.thank you.
Thank you so much for the article. I had a virus on 27 December 2017. I have no sense of smell and limited taste. I can taste pickled onions and chocolate ice cream. If there is a smell in the air for example bbq my brain interprets it as a biscuity smell. I also have the same taste in my mouth. The specialist told me recently that the senses may never come back. I had lost hope until I read your article. I find it hard that when you tell friends about it nobody seems interested. It has such a huge impact on your life. I will let you know how I get on. Take care x
Hope this helps you, Angela. I felt the same (hopeless), but this worked for me finally! I had phantom smells too, like the constant smell of smoke. It went away eventually.
I have a little different situation that has affected my taste. I went through 4 rounds of chemo (the minimum) in Nov 2016 and lost my taste which is common. What’s NOT common is that it hasn’t come back. My oncologist said I was her “first to have this happen to”, and sent me to an ENT last week who ruled out polyps via a sinus scope. I can smell, but not taste. I have researched this for HOURS and HOURS the past year and have come up with nothing. Hoping this helps. I did the alpha lipoid acid as well as the since but curious to try the other things mentioned.
Pamela, make sure to take the zinc supplement foremost. What you’re describing can indicate zinc deficiency. Zinc is critical for taste and also a very necessary immune builder if you’re fighting cancer. Also see this post: https://www.maryvancenc.com/holistic-cancer-prevention/
Let us know how you’re feeling!
Hi! Did you ever regain 100% of your senses? I can smell things right under my nose and only taste first bite! Can’t smell poop either! Did that ever come back for you? I know it’s a weird question
The ent thinks it’s allergies and has me using Flonase! I don’t notice anything! I am going to get zinc!
Hey Jenn, the exact same thing happened to me. I could only taste the first bite of anything, and oddly enough poop (and urine also) hasn’t smelled the same to me since. Very strange, but I have regained probably 98% of my smell and taste otherwise. It took about 4-5 months to recover.
Thank you SO much, Mary. This is all extremely helpful to know.
Got the flu in Dec. 2017 and that’s when the taste/smell loss occurred. Took Flonase. Nothing. Went to my Chinese Dr., drank the prescribed teas and in one week, noticed a “burst” of flavor. Heaven! Stayed on the teas but it plateaued after a month. Did acupuncture — 7 treatments, taste ebbed and flowed. Then SonicWars30 — homeopathic, did that for 3 months with varying results.
Summary: Have about 35% of my taste/smell. Some days better than others. So will definitely try everything you suggested.
Q: Doesn’t zinc have to be supplemented with copper, since zinc may deplete copper if over-dosed? (Oddly enough, I have a craving for raw oysters — high in zinc!)
Q: Are you on any kind of a maintenance regimen?
Hey Laura, that’s an excellent Q about zinc. Yes, if taken long term it does need to be balanced with copper. I take chlorophyll which has copper in it, so I don’t worry too much about it, and copper is only needed in minuscule amounts. It’s also pretty abundant in our food supply. It’s more common to have too much copper & not enough zinc. And no, I’m not on a maintenance plan (don’t really need it), but I do keep up with the zinc.
Hi Mary
I believe my situation is identical to what you went thru. I have partial taste but very limited and I am going to follow your idea of zinc for now. I also like some of your other ideas, good job, I will keep you posted.
Mary, your response was also very heartening. Thank you for that and for giving us all hope!
Mary, are all of these supplements safe to take together? I don’t want to have any reactions…I also take a small dose of lexapro… how many months did you take the supplements for and you took them everyday? At the same time? Morning? Night?
Jenn, yes, they’re all safe to take together. I don’t know about lexapro; you’d have to ask your doctor or research it. And yes, you have to take them every day. It took 3-4 months.
Do you still take them all? I would be afraid to stop them if they helped that it would come back again…how long have you not taken them for?
Jenn, if you have hyposmia due to nerve damage, which is what I had, when the nerves heal, you’re good. They’re no longer damaged. I can’t speak for other causes.
Hi Mary….I’m so grateful for this post. As others have said, there is so little information on this on the web. And the experience is so distressing that finding your story and protocol gave me hope.
My situation: 1 week ago I got sick with a very bad cold/infection (chest/head cold, bad cough). About day 4 of the illness, when it just seemed to be peaking, my senses of smell and taste completely vanished. I saw the doctor a day after this but don’t think I stressed the complete loss enough (and was there to check about my lungs as I was quite short of breath).
Anyway, missed my opportunity to get a referral to an ENT so started madly researching on my own and found your article.
Can you tell me when you started your protocol? My plan is to start today while I’m still recovering. I was just curious if you thought it would be better to wait to see if it returns or to get started ASAP.
Thanks so much, Mary.
Hi Sandra, I started this a couple months after I’d been struggling with no improvement in sight. I saw very fast results and almost complete reversal within a month or 2. I was also taking very good care of myself otherwise: getting enough sleep, eating well (as usual) supporting immune health, etc. No harm in getting started ASAP. Good luck and let us know how it goes!
I am grateful I happened upon your post while researching black seed oil. My father passed away last October. My family was still reeling from the devastating loss of my brother from suicide in 2016. I have had 3 surgeries in the past year so I think all the above info explains the stress my body has been under both physically & mentally. I caught what I thought was a cold in May & after 8 days decided to see a Dr because I was getting worse. Was given antibiotics & steroids which I took. About the 3rd day of the meds I noticed my sense of smell & taste were gone. I attributed it to the sinus infection & just assumed it would get better when I got better. Wrong! It’s still not better. Normally my sense of smell is very, very acute. I know it’s only been 2 months but I would like to be able to smell & taste again. I will definitely try your protocol. Thanks for posting this info.
I’ve lost my sense of taste since January of this year. In my 7 mo. without it and I’m so down about it. No one seems to understand. I really enjoyed food and drink and my doctor says there’s nothing else he can do. They guess a virus caused it, but I’m wondering if it was the use of Flonase. I have months where I taste nothing, some where everything tastes metallic, others where everything tastes like chemicals and sometimes I just taste one ingredient in something–like I bite a peanut butter cookie and only taste flour or have hummus and only taste garlic. Not one thing has tasted as it should or good in 7 mo. I started taking zinc a month ago and will supplement with some of the things I see here. Brain tumors, swelling and polyps have been ruled out. My doctor is no help. I’m trying to get him to prescribe Theophylline. He hasn’t heard of it, so is looking into it. Has anyone had success with it? Unlike everyone else, I’ve gained 20 lbs. since I’ve gotten this–eating more, trying to regain my sense of satisfaction. No one gets that either!
Jennifer. I also experience the chemical taste. I’m seven months in from losing my sense of smell and taste. I am heartbroken at losing these senses and having the weird chemical taste and smell. I’m guessing it’s my brain trying to fathom out what the taste is and it is distorted. I had a virus in December. I am taking zinc and other things recommended. I am glad I am not alone. XX
Hi, i lost my sense of smell and taste six months ago. Unfortunatelly i never feel hungry or thirsty since i lost my senses. It is very hard to live with it. I did MRI of head and everything seems fine.Please if someone have similar symptoms let me know is there a hope. I will try with Your method. Thanks
Thank you for the post. I have been very frustrated about my sudden loss of smell and taste. Being a “foodie” it is very heart breaking. I tell the family I just eat to survive now since there is nothing else there. Mine started late July I had a sinus infection. So, went to the Dr and he put me on antibiotics, sinus spray, and sinus pills to dry up the moisture. Everyday I was hoping I would start to smell and taste….unfortunately, nothing 🙁 So, I finally made an appointment with an ENT. He looked up my nose, asked several questions and determined that the tissue around the nerves going to the brain may be swollen from the past infection and he put me on Prednisone to shrink the swelling. I have a follow up appt next week with him as that treatment still has not cured me either. After reading your article a light bulb went off and I believe I may have suffered the same thing you did with the nerves being damaged or destroyed. I am going to try everything you suggested in hopes that it will come back soon. You really do not know what it is like not to be able to taste and smell until it is gone. I am grateful for your article! Thank you for posting it!!
Thanks for your comment, Theresa. Please stay in touch and let me know how it goes.
Thank you so much for this post. I’m on the same journey. My story is quite similar yours, a year ago, loss of a parent and a lot of stress . Pneumonia in September 2017. Hysterectomy last Mars. Then viral infection in June with a pneumonia again as a result. After that a total loss of smell and taste. Two months later I could smell some things, others totally out. Starting my own research for cure after a visit to a ENT who informed me that the prognosis was poor. Then I found your post and decided to follow your advices, I had nothing to loose. I started to take Ginkgo Bilopa, Alpha lipoid acid, Zink and vitamin B12 and D and started smell training. Couldn’t get the other stuff (I live in Iceland ). After about 2 weeks I found my smell improving, no change in taste. Then I tried acupuncture and after the first session I could taste something but it lasted only for 24 hours. After the next session I got parosmia, smelling smoked, fat meat in my nose constantly but my taste improved. Now I’m slowly improving. Can smell almost everything (except urin and poop, onion and garlic) getting better for every day now although I still feel abnormal smell for some things (coffee and meat). So now I’m very optimistic that I will regain normal smell and taste. This post really helped, thank you so much!
Halldora, your story does sound remarkably similar to mine. Keep at it! Now, one year later, I’m fully recovered, with the exception of a few quirks. I think the zinc and ALA helped the most.
I just came across your post while looking into alpha lipoic acid for anosmia. I have suffered for five years. Mine is a similar story – lost taste and smell after bad cold; however, the ENT also found polyps. I followed the medical protocol using intranasal sprays and drops, antihistamines, to no avail then oral steroids which did not help followed by steroid injection which also brought me no smell or taste. A course of antibiotics was the final prescription. (Tried homeopathy but didn’t stick strictly to the recommendations). Last medical option was surgery, which I really did not want to do but I was desperate. And it was a complete failure. After seeing yet another ENT who wanted to put me on a horrific cocktail of the meds that didn’t help at all individually, followed by a more aggressive surgery, I walked out the door and began my own journey of healing. I continued my nasal rinses adding in oregano oil and colloidal silver. I took bromelain and quercetin, vitamin D and K, vitamin C, olive leaf extract, listened to Rife frequencies for sinusitis, used a NILI light – within a month and a half I was back to 100%…after four years of anosmia! I was sooo grateful to be able to smell the fragrance of flowers and taste food which is so important to me as one who loves to cook and is a total foodie. I was PROUD of myself for having found the solution. Sadly, although I was in glorious bliss for five months from March through August, hesitantly thinking I had put this nightmare behind me….but now I am back to zero taste or smell. It is so frustrating and I get so sad, but I won’t give up. I’m back on my regimen and adding the alpha lipoic acid in too. Will also get zinc and gingko biloba. Looking into intranasal vitamin A for regeneration as well. Thank you for your post. I hope you stay well.
Thank you so much for this information. Your story sounds a lot like mine with the stressors of caregiving to my mom with dementia and now anosmia. I lost my smell and taste post viral cold/infection back in the beginning of July 2018. I’m really struggling since the ENT wouldn’t even offer any type of treatment except to recommend smell retraining with essential oils. I did the “smell test” in the ENT office and got 15 out of 40 smells and to be honest I think I truly only smelled 3 the other 12 were guesses because there was no option for not smelling anything. It is very depressing and I too love to cook and eat great food. I just started the acupuncture route and am hopeful that it will be successful. I am definitely going to try your regimen and continue to stay hopeful that my smell and taste will return.
Thanks for sharing, Dorene. Keep us posted!