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Pepcid and 1 month without an 'episode'

Messages
25
By taking Pepcid I've had the first month free of an episode in years. I still have cfs (and with it pem, ibs, pots etc), however for the first time in years I've gone a month without an 'episode' (where I feel like I have the flu and have to sleep for between 3 days to three weeks). Without Pepcid I often have episodes lasting two to three days long (sometimes with only a day or two in between episodes). Up until now, 80 percent of episodes last two to three days, 10 percent of episodes go on about a week, and 7 percent go on two weeks. The longest I had was three weeks of only getting up to pee, hardly eating and dizzy when I do get up, and feeling awful like I have the flu. So I am very thankful for having found Pepcid. I say one month because I just came out of a two day episode. I will track and update the post next month where hopefully I found the same effects!
 
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25
Hi! It is believed Pepcid helps those with cfs as an h2 histamine antagonist, which may give credence to the mast cell activation theorist camp, or at least to those with a subset of cfs experiencing mass cell activation.

H2 receptors are positively coupled to adenylate cyclase, which stimulates the production of cAMP, which then activates protein kinase A (PKA, which also has been singled out as problematic in a lot of cfs research

I have tried hundreds of different supplements, pills, and therapies and only two things have helped, Kratom of the green malay variety and Pepcid. I detail it all on my cfs info page but any time I put a link to the site in a post it gets blocked. Please reply with specific questions, I will do my best to answer and I hope this helps. Thanks, J
 
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25
It's been two weeks since the post and while I haven't had outright episodes, I've slept most of the time since writing it. I'm extremely frustrated. Perhaps it will be more effective at higher doses or taken intermittently, I will experiment. I am certain it has helped and not just as a placebo, as I try many things without expectations. I've tried perhaps 300 supplements medicines and therapies so I would know a placebo effect when I saw it
 
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25
On another forum a user said "It may be working also on lactic acid reduction or even with D-lactate acid. Lactic Acid is also involved in gene MT-ND5 Mitochondria Disease linked to MT-ND4 gene (LHON) Leber Hereditary Optic Neuropathy I have both genes plus Alport Syndrome. Which dose brand did you purchase on Pepcid? Was it a prescription or ever the counter?"
Which gave me the idea to switch back to the generic brand and see if that helps, as that's what I was on for the first 2 successful weeks!!
 

hapl808

Senior Member
Messages
2,313
Which gave me the idea to switch back to the generic brand and see if that helps, as that's what I was on for the first 2 successful weeks!!

Please keep us informed.

As all my crashes usually start with debilitating reflux, an H2 blocker was a normal thing to try. I used Pepcid (I think generic but I'd have to check). I didn't take it for long, though, as it seemed to interfere with my digestion.

How has it been with your digestion, and what dosage and schedule do you take it? Away from meals, after meals, or ?

I've tried stuff like cromolyn, Pepcid, etc - just usually seems to be more negative than positive for me. The most helpful supplements I've taken are things like allicin, andrographis, etc - implying some pathogen or fungus to me, but I don't know. For reflux, things like slippery elm, fenugreek, etc - take the edge off, but don't address the underlying issues.
 
Messages
25
Please keep us informed.

As all my crashes usually start with debilitating reflux, an H2 blocker was a normal thing to try. I used Pepcid (I think generic but I'd have to check). I didn't take it for long, though, as it seemed to interfere with my digestion.

How has it been with your digestion, and what dosage and schedule do you take it? Away from meals, after meals, or ?

I've tried stuff like cromolyn, Pepcid, etc - just usually seems to be more negative than positive for me. The most helpful supplements I've taken are things like allicin, andrographis, etc - implying some pathogen or fungus to me, but I don't know. For reflux, things like slippery elm, fenugreek, etc - take the edge off, but don't address the underlying issues.
Thank you for your input, I used doordash to have a variety of generic pepcid sent to me. Though I'm very thankful to doordash, since discovering it I've hardly left the house. What was delivered wasn't what I ordered, as I allowed alternates, I received a generic famatadine, a Zantec and an Alka Seltzer imitation. After taking all three yesterday I had a drive to leave the house and took my ever patient wife to the park, something I haven't done in 5 months or so. I didn't see the connection until I returned. So, if it's a placebo effect, it's subconscious.
I usually don't eat as it makes me sleepy, so I always take it on an empty stomach, except for coffee and Kratom, my main vices. I've written about Kratom on this site and can add a link if you like, I highly recommend the green malay 'wake up' kind of kratom except that it causes serious constipation
Thank you for the items you mention, I will add those to the retinue as well. I just woke up and took all three again, and I will keep you apprised. Thanks again, J
 
Messages
25
At the other forum site I had some replies to which I said '
@fedbird You have my deepest empathy and sympathies for what you have gone through. I'm similar in that I had a head injury that I believe is at the root of all of this for me at least, and you had concussions. I also was in a moldy house for awhile and am starting to use Itraconozole with nasoneb diffusor to address that. The Oxalate regimen seems intense, I've been a pescadarian that is I was a vegetarian until convinced to eat fish and have been so most my Lfe, so definitely high on oxalate intake. I will do my best to switch and see if it helps, even my supplements are gelatin capsules, I will ask about Ketotifen fumirate. Yes you are super helpful.
@emjo I am concerned about trying an h1 blocker as I read of a user who it made things worse. I wish my follow up was better, but so far since my first post I've been sleeping, the difference has been that I haven't been feverish and achey. Thanks and I will keep aprised '
 
Messages
25
Please keep us informed.

As all my crashes usually start with debilitating reflux, an H2 blocker was a normal thing to try. I used Pepcid (I think generic but I'd have to check). I didn't take it for long, though, as it seemed to interfere with my digestion.

How has it been with your digestion, and what dosage and schedule do you take it? Away from meals, after meals, or ?

I've tried stuff like cromolyn, Pepcid, etc - just usually seems to be more negative than positive for me. The most helpful supplements I've taken are things like allicin, andrographis, etc - implying some pathogen or fungus to me, but I don't know. For reflux, things like slippery elm, fenugreek, etc - take the edge off, but don't address the underlying issues.
For fungus I've started Itraconosole prescription with nasoneb diffusor. So far my nose stopped running for the first time since I got covid 3 years ago.
I was afraid to try andrographis as some users had a strong reaction, for others it was a panacea. I have it, I've just been afraid to try it
 
Messages
25
Theres another similar forum website started by Cort also, but both sites are touchy about placing URL's, so I replied to a user on that site with
10 years ago I stopped taking Cymbalta and that helped immensely, it was my first 'break'. I then extracted myself from a relationship that was a near constant source of stress and that was another 'win'. I found and used Xifaxan which helped with the IBS which in turn made the CFS more bearable (strangely the two are connected, you can't have an official CFS diagnosis without exhibiting IBS as well. I was on fodmaps and after Xifaxan was free to have whatever I wanted, or so I thought. Thanks for the helpful suggestion, I will go back to Fodmaps
 

ChrisD

Senior Member
Messages
489
Location
East Sussex
I've had ME since 2016 but when I got Long Covid in 2021, GERD - POTS was a big factor in me going from housebound to bedbound.

Everything seemed to centre on vagus nerve dysfunction and dysautonomia/POTS. Eventually I found that treating the GERD helped a lot. Firstly by using Famotidine, then D limonene, and now when I have an occasional flare up I use sodium Bicarbonate and separately I chew Mastic gum which has been probably the most powerful intervention.
 
Messages
25
I've had ME since 2016 but when I got Long Covid in 2021, GERD - POTS was a big factor in me going from housebound to bedbound.

Everything seemed to centre on vagus nerve dysfunction and dysautonomia/POTS. Eventually I found that treating the GERD helped a lot. Firstly by using Famotidine, then D limonene, and now when I have an occasional flare up I use sodium Bicarbonate and separately I chew Mastic gum which has been probably the most powerful intervention.
Thank you for your input. As always I send my empathy. You gave us a few items to look into, for instance a prescription Famotidine is preferable, and do I feel better with Alka Seltzer, what is limonene and mastic gum, I will look into, thanks
 
Messages
25
I've been on Mt Toads wild ride when the Pepcid helped incredibly then I decreased other unrelated meds and Pepcid didn't stop chronic fatigue syndrome episodes but made them less achy. So it wasn't a proper test. For the first month, combined with Nasoneb, Itraconozol meds it stopped episodes outright, while for the next month I got frequent episodes but I wasn't feeling as sore or as agitated physically. Mentally I was and am, anxious while the episodes wore on, then when I could spending any waking or lucid moment I'm researching and thinking about or calling for appointments consumed by cfs in another way. Urrg,

Thanks for allowing to vent. Ok thanks for all your input in your replies, and please consider this a hopeful 'back to the drawing board' moment, as I am taking those meds now as well as trying again the Jorgen Sacha which may have cleared the way for the Pepcid positive effects, as well as
stopped taking BetaClucans supplements, in fact the break in my Pepcid stride was when I tried that supplement for a week. That and in the middle of the night I snacked on something that gave me acid reflux and I vomited several times, the episodes started after that . Also I had stopped Acupuncture herbs, while continued with Coffee, Kratom, PYM Attention focus chews, Albuterol and Alvesco

From this experience I can say I started looking more at your replies and considering using specific foods, I used chatgpt to combine food lists combining Keto, Paleo, Low-Oxalate, Pescatarian, FODMAP, and Lectin Avoidance into a shared food list, then the same with adding mycotoxin avoidance, they're attached to the post as word document and pdf file

Taken from 'A patient who recovered from post-COVID myalgic encephalomyelitis/chronic fatigue syndrome: a case report' in her case they used pharmacotherapy including an antihistamine. as stated at https://bpsmedicine.biomedcentral.com/articles/10.1186/s13030-022-00260-3 "Amitriptyline and hochuekkito were prescribed for this patient. Amitriptyline has anxiolytic and sleep-inducing properties and activates the inhibitory nociceptive system as well as acting as an anti-depressant. It also has an antihistaminergic effect"

more on that article 'Although the dose of ascorbic acid the patient ingested was 1.0 g/day, her vegetable-based diet and regular supplementation of ascorbic acid would be helpful for avoiding the potentially harmful effects of oxidative stress and aid in alleviating her symptoms. Recently, the gut microbiota is reported to be associated with the ME/CFS pathophysiology, including neuroinflammation and ME/CFS symptoms [19]. It is also possibile that changes in dietary habits that affected the gut microbiota was responsible for improved symptoms'.'

Also I looked heavily again into FMT, if only I could fake colustrum dificile they would let us try it.

For instance My ME/CFS Expert (Dr. Susan Levine) Said She is Very Excited About This "Future" Treatment (Fecal Microbiota Transplant-FMT) | Phoenix Rising ME/CFS Forums
https://forums.phoenixrising.me/thr...eatment-fecal-microbiota-transplant-fmt.89305

(1) Poo Transplant resolved my ME :) [Deleted] | Health Rising's Chronic Fatigue Syndrome (ME/CFS) and Fibromyalgia Forums
https://www.healthrising.org/forums/threads/poo-transplant-resolved-my-me-deleted.6484

fmt | Phoenix Rising ME/CFS Forums
https://forums.phoenixrising.me/tags/fmt
DIY Fecal Transplant...would you try it? | Phoenix Rising ME/CFS Forums
https://forums.phoenixrising.me/threads/diy-fecal-transplant-would-you-try-it.52562

Faecal microbiota transplantation (FMT) in Norwegian outpatients with mild to severe myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS): protocol for a 12-month randomised double-blind placebo-controlled trial - PubMed
https://pubmed.ncbi.nlm.nih.gov/38858151/

FMT | Phoenix Rising ME/CFS Forums
https://forums.phoenixrising.me/threads/fmt.43733/

Evrensel: Fecal Microbiota Transplantation and Its Usage in Neuropsychiatric Disorders | Page 2 | Phoenix Rising ME/CFS Forums
https://forums.phoenixrising.me/thr...ge-in-neuropsychiatric-disorders.46063/page-2

Episode 19: Fecal Microbiota Transplants - Phoenix Helix
https://www.phoenixhelix.com/episode-19-fecal-microbiota-transplants

So, back to Pepcid, Zantac, Alka Seltzer,
 

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Messages
25
To accommodate Low-Histamine alongside Keto, Paleo, Low-Oxalate, Pescatarian, FODMAP, Lectin Avoidance, and Mycotoxin Avoidance, we need to refine the list further. Histamine is a natural substance found in the body and some foods, and individuals with histamine intolerance need to avoid foods that are high in histamine or that promote histamine release.

Shared Allowed Foods (Low-Histamine):​

These foods are low in histamine and align with all other dietary restrictions.

Proteins (Fish & Seafood):​

  • Fresh-caught Fish (like cod, salmon, and mackerel—must be freshly caught or frozen immediately to avoid histamine build-up)
  • Shrimp (if fresh and frozen immediately)
  • Fresh white fish (like sole or cod)

Vegetables:​

  • Zucchini (low-histamine, low-carb, low oxalate)
  • Cucumber (low-histamine, low-carb)
  • Lettuce (low-histamine, low-carb)
  • Bell Peppers (green) (low-histamine)
  • Carrots (low-histamine)

Fruits:​

  • Coconut (low-histamine)
  • Watermelon (low-histamine)
  • Berries (fresh, especially raspberries and strawberries in small amounts)

Healthy Fats:​

  • Olive Oil (low-histamine)
  • Coconut Oil (low-histamine)

Key Avoidances:​

  • Fermented Foods (e.g., aged cheeses, fermented vegetables)
  • Canned Fish (high in histamine)
  • Vinegar-containing Foods (due to fermentation)
 

Dysfunkion

Senior Member
Messages
352
I've been on Mt Toads wild ride when the Pepcid helped incredibly then I decreased other unrelated meds and Pepcid didn't stop chronic fatigue syndrome episodes but made them less achy. So it wasn't a proper test. For the first month, combined with Nasoneb, Itraconozol meds it stopped episodes outright, while for the next month I got frequent episodes but I wasn't feeling as sore or as agitated physically. Mentally I was and am, anxious while the episodes wore on, then when I could spending any waking or lucid moment I'm researching and thinking about or calling for appointments consumed by cfs in another way. Urrg,

Thanks for allowing to vent. Ok thanks for all your input in your replies, and please consider this a hopeful 'back to the drawing board' moment, as I am taking those meds now as well as trying again the Jorgen Sacha which may have cleared the way for the Pepcid positive effects, as well as
stopped taking BetaClucans supplements, in fact the break in my Pepcid stride was when I tried that supplement for a week. and report in next months

From this experience I can say I started looking more at your replies and considering using specific foods, I used chatgpt to combine food lists combining Keto, Paleo, Low-Oxalate, Pescatarian, FODMAP, and Lectin Avoidance into a shared food list, then the same with adding mycotoxin avoidance, they're attached to the post as word document and pdf file

Taken from 'A patient who recovered from post-COVID myalgic encephalomyelitis/chronic fatigue syndrome: a case report' in her case they used pharmacotherapy including an antihistamine. as stated at https://bpsmedicine.biomedcentral.com/articles/10.1186/s13030-022-00260-3 "Amitriptyline and hochuekkito were prescribed for this patient. Amitriptyline has anxiolytic and sleep-inducing properties and activates the inhibitory nociceptive system as well as acting as an anti-depressant. It also has an antihistaminergic effect"

more on that article 'Although the dose of ascorbic acid the patient ingested was 1.0 g/day, her vegetable-based diet and regular supplementation of ascorbic acid would be helpful for avoiding the potentially harmful effects of oxidative stress and aid in alleviating her symptoms. Recently, the gut microbiota is reported to be associated with the ME/CFS pathophysiology, including neuroinflammation and ME/CFS symptoms [19]. It is also possibile that changes in dietary habits that affected the gut microbiota was responsible for improved symptoms'.'

Also I looked heavily again into FMT, if only I could fake colustrum dificile they would let us try it.

For instance My ME/CFS Expert (Dr. Susan Levine) Said She is Very Excited About This "Future" Treatment (Fecal Microbiota Transplant-FMT) | Phoenix Rising ME/CFS Forums
https://forums.phoenixrising.me/thr...eatment-fecal-microbiota-transplant-fmt.89305

(1) Poo Transplant resolved my ME :) [Deleted] | Health Rising's Chronic Fatigue Syndrome (ME/CFS) and Fibromyalgia Forums
https://www.healthrising.org/forums/threads/poo-transplant-resolved-my-me-deleted.6484

fmt | Phoenix Rising ME/CFS Forums
https://forums.phoenixrising.me/tags/fmt
DIY Fecal Transplant...would you try it? | Phoenix Rising ME/CFS Forums
https://forums.phoenixrising.me/threads/diy-fecal-transplant-would-you-try-it.52562

Faecal microbiota transplantation (FMT) in Norwegian outpatients with mild to severe myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS): protocol for a 12-month randomised double-blind placebo-controlled trial - PubMed
https://pubmed.ncbi.nlm.nih.gov/38858151/

FMT | Phoenix Rising ME/CFS Forums
https://forums.phoenixrising.me/threads/fmt.43733/

Evrensel: Fecal Microbiota Transplantation and Its Usage in Neuropsychiatric Disorders | Page 2 | Phoenix Rising ME/CFS Forums
https://forums.phoenixrising.me/thr...ge-in-neuropsychiatric-disorders.46063/page-2

Episode 19: Fecal Microbiota Transplants - Phoenix Helix
https://www.phoenixhelix.com/episode-19-fecal-microbiota-transplants

How much pepcid were you taking a week? Apparently it's an h2 blocker which only targets the stomach and I'm interested in giving this a go but I don't know whatI should aim for a week if I do in how much pepcid I try. Do you still take it?
 
Messages
25
How much pepcid were you taking a week? Apparently it's an h2 blocker which only targets the stomach and I'm interested in giving this a go but I don't know whatI should aim for a week if I do in how much pepcid I try. Do you still take it?
That's a great question, right now I'm taking 1 pill Pepcid generic famotidin, a Zantac and alka Seltzer once a day, but increased dosage may help. I will try that after working back in Itraconozole and I had stopped Acupuncture herbs, while continued with Coffee, Kratom, PYM Attention focus chews, Albuterol and Alvesco
 

Dysfunkion

Senior Member
Messages
352
That's a great question, right now I'm taking 1 pill Pepcid generic famotidin, a Zantac and alka Seltzer once a day, but increased dosage may help. I will try that after working back in Itraconozole and I had stopped Acupuncture herbs, while continued with Coffee, Kratom, PYM Attention focus chews, Albuterol and Alvesco
That is one complex stack and a unique one at that. I drink coffee daily and used to drink kratom but quit cold turkey last year which was not a good time and I know going back wouldnt benefit me. Interesting that you seem to targeting the immune system through doubling down on the h2 receptor in the stomach, haven't heard of anyone doing that before specifically. I dont think anything can go horribly wrong besides an upset belly if I tried the pepcid and zantac.
 
Messages
25
That is one complex stack and a unique one at that. I drink coffee daily and used to drink kratom but quit cold turkey last year which was not a good time and I know going back wouldnt benefit me. Interesting that you seem to targeting the immune system through doubling down on the h2 receptor in the stomach, haven't heard of anyone doing that before specifically. I dont think anything can go horribly wrong besides an upset belly if I tried the pepcid and zantac.
Thanks for your message :) I drove my fiance' and stepdaughter for a getaway 3 hours away in heavy traffic and slept the next day, however as mentioned earlier I restarted the Itraconozole with nasoneb as well as the 'stack' as you described it. In the afternoon the next day I was able to drive them around sightseeing as well as the day after that. Also at night I was waking up, working 4 or 5 hours, sleeping until the afternoon then driving them around.
This is generally unheard of since my CFS started 13 years ago. I wouldn't have even thought of taking my stepdaughter for a getaway much less doing it. I am happy to check in to say that, knock on wood, this 'stack' is working, and I believe the Itraconozole via Nasoneb is a crucial component of that. You will need a Drs prescription unless you use one of those lenient online pharmacies with Drs that prescribe you just about whatever you want within reason. I will check in again later and let you know, Thanks!
 
Messages
25
The positive roll keeps going! I wouldn't say this 'stack' (Itraconozole, Kratom, Pepcid etc) is a 'Silver Bullet', but it's at least a brass bullet! I drove my fiance and stepdaughter back to their home about 2hrs away and slept. Then instead of sleeping the next day, I woke at 4:45 am and drove to my place again 2hrs away, and instead of sleeping I had one of the most productive days in 13 years. I worked until noon, then napped until 4, got up and worked until sleeping. All the while I was concerned about not pushing myself to avoid pem the next day, so when I walked my guest and his dog instead of the full loop, I did half. Just having a guest was both unusual and a sign of a change in my state of wellbeing and attitude,

To reiterate, Yesterday was amazing, I had driven my fiance' and stepdaughter back to their home in the evening and slept, then instead of sleeping all day the next day I woke at 4:45am and drove, then worked until noon, slept until 4 then was clear to work until the evening. I ordered breakfast, made coffee, did light yardwork, cleaned and sorted my room, showered, shaved, took my medicines, ordered online, then when a guest I had been wanting to collaborate with said he would be nearby, arranged to meet around 5 something I would never have endeavor as I know I loose focus around that time and am asleep by 7, so he arrived, I interviewed him, took his buddee pet Willey for a walk, ordered dinner, picked up dinner, cleaned, emptied dishwasher, and called my fiance.

I was concerned I would have pem today and I did, I slept all through the night got up realised I couldn't work so went to sleep until 4:40pm, though when I got up and now I don't feel achey like the flu. So this week has been a resounding success, I have confidence to take things on I wouldn't have considered such as the vacation and the interview
For the first time in 13 years I have Hope, that's based on observation, a feeling of better not just hopeforhope
Attached are pictures of the Itraconozole I use with Nasoneb, it was prescribed at my request by a private clinic and compounded by Koshlan pharm, contents and direction
CSinusitis (itraconazole 50mg/mupirocin 5mg/EDTA 15mg/Budesonide 0.5mg compounding capsule compounding capsule
Dissolve contents of capsule in 15mL of sterile 0.9% saline. Perfuse each nostril with half the contents of solution 1-2 times per
 

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25
Day two of pem. As I said it's a 'brass' not a 'silver' bullet. Still though, I was well enough to write the post yesterday and today, which as you know with pem it's unlikely I would focus that much, also haven't had a full blown cfs episode since I decided to try strickly adhering to this 'stack'. So I still mark it as a success. Considering doubling the Itraconozole dose and or doing it twice a day instead of once. Also going to look into what else is on Dr Brewer's protocol. There are many supplements and medicines I will like to trial, however, I don't want to interfere with this experiment, I will give it another month or two. I've added pictures of some of the supplements and medicines I will like to audition
 

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