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  2. just to follow up- oxygen worked much better last night- stopped the first hit in about 10 minutes and the second hit in about 20. The third hit took more like 35 minutes but if nothing else, even if the last one took a bit longer to work the pain never got too bad.
  3. Today
  4. @DanP, it is commonly found that O2 is less effective when tanks have less oxygen in them. This can happen when the tanks are as much as half full, and it seems to be very common at 1/3 full or less. If you can vary the flow rate of your regulator, people say that increasing it as the tank becomes less full is one way to cope with this situation, before resorting to a new tank. I hope this is the issue for you, since it's pretty easily fixable.
  5. Yep yep, nice and informative Cant complain pain wise. Hope all is well with you 2!
  6. thanks for all the info Shaun! I am on the D3 regimen now and did it the last couple of times I was in a cycle- seemed to help. Haven't tried busting yet but would like to- I'll look into it some more. Have a good holiday!
  7. Was that quite well enough @BoscoPikosorry took time to replay on holiday in Bulgaria hope you well and pain free at present
  8. @DanPit's great that your only using once a day. but temptation is always there to use more as the relief from the pain is so fast, triptans can cause really bad rebound attacks that can be alot worse than your initial attacks, plus triptans can prolong your cycle, you only need 2mg to abort with triptans so consider splitting your injection (easily done) I've been down the dark rabbit hole with triptans, I got to a state where I was using up to 5 injections a day, prolonged my cycle by around 3months with headbanging attack day and night, my body became so weak and after each injection I'd feel like I was going to have a heart attack, so please be really careful with them, don't get me wrong I still carry them with me if I out in public or go on holiday because it's not great to get an attack in public, but I never use them at home anymore I'd rather ride the pain if my O2 doesn't work but I'm lucky at present as O2 works for me, I do change my breathing techniques know and again, have you ever tried busting? And get on D3 ragime it really help alot of use
  9. As much as I want to reply to this I'm going to wait for @Shaun brearley because he explains it quite well.
  10. thanks for the replys! Hopefully last night was an anomaly and it will work as it normally does tonight. Shaun- why do you say that triptans are a nightmare? I've heard that before, but they do work- at least for me- are the side effects really bad? I haven't noticed anything but have always been careful to not use more than once a day.
  11. I haven't read anything about triptan use reducing the effectiveness of O2. Are you using the same provider? My first thought tends to want to lean toward a bunk tank or possible wear and tear of your existing set up? I'm sure you know the basics of O2 usage (suggested LPM's/mask type & breathing techniques etc.) but maybe it's time to change up your intake method? I've had many discouraging and maddening experiences with O2. Some that included me being convinced it just didn't work anymore and some where I was sure it caused the attack to ramp up. In the end I discovered a few things, some of which you mentioned (the sooner the better), the breathing technique that worked last time is not guaranteed to work this time and a quick gulp of something caffeinated prior goes a long way.
  12. Yesterday
  13. Triptans are a nightmare my friend, O2 works so well for many of use, what's your routine with O2?
  14. Hey everyone, I am in the 3rd week of a cycle- haven't had one for almost 2 1/2 years. First week I was traveling so just had to power through- the first weeks headaches tend to be fairly mild for me, then start to ramp up in intensity. Second week I was aborting with imitrex injections . They really worked well but I only did them once a day. Just got O2 yesterday and had two attacks last night and one this morning- the normal routine for me once the cluster really kicks in- and the oxygen doesn't seem to be working. In the past, if I got on the O2 soon enough it would knock them out within 10-20 minutes but last night, nothing. Ive been dealing with clusters for 30 years now and using O2 successfully for about 20 so I know how to do it, it just didn't seem to have any effect. Curious if anyone thinks this might have something to do with using Imitrex injections first and that for some reason is making the O2 less effective? thanks!
  15. Last week
  16. I keep them in the car, the office and any other place I might be going to. I even take them on vacation with me. I figure they do enough work for me they deserve a little vacation too.
  17. Hey all, relativley new here! Got diagnosed four years ago and have loosely followed the website since then and learned some excellent info about oxygen treatment. It has helped a ton! I finally feel comfortable enough to reach out somewhat so, here I am. Thank you.

  18. Just completed survey
  19. Again, thank you all! Some updates — O2 concentrators, while not ideal, are DEFINITELY aborting my headaches. Used 7 times with 100% success rate after ~10-15mins of use. Half of these were headaches I woke up to mid-sleep, not onsets. Haven’t used for a “monster attack” yet, just standard CHs. Intensity may matter considering sumatriptan nasal spray failed for my worst “monster.” (I have 3mg injectables in place of nasal spray, now, but have not used them). To repeat a common CH phrase: “best thing since sliced bread.” Really. I’m sure this is common, but now that I have a taste of O2 and sumatriptan, my tolerance of untreated attacks has gone way, way down. Haven’t had to use the 100%-O2 canisters yet but will be taking your advice and asking for larger canisters nonetheless.
  20. I appreciate i am very late to this conversation but I just want to drop in that red bull is now a key part of my armoury the moment the dreaded knock kicks in. I will post a detailed synoptic of my experience in coming days but for anyone suffering right now, seriously consider taurine. To me it's a life saver but I do have to say we are all different and some of us have intolerances and other complications so do be conscious of your personal needs. But if you don't have an issue with caffeine and taurine give it a go. Pour on lots of ice and gulp it freezing cold so it hits the back of your throat which is the nearest you can get to your pituitary gland without poking a hole in yourself. The cold soothes the brain and the taurine does some magic and at least dulls the agony. X
  21. I was a management consultant for many years. As I said to a former colleague the other day, ChatGPT is a better consultant than I ever was -- in less than a minute, and for free. I don't have grandchildren, but Chat is becoming like my grandkid, where I keep saying to others, "You'll never believe what Chat did today! Isn't this fantastic!?!" Still a bit of a jokester, though. I had it colorize an old black-and-white photo of my father the other day. Everything looked right, except that it was someone else's face! I pointed this out, and Chat said "Oh, gosh, you are right. Let's try that again." It did. A different face, still not my father's.
  22. I'm loving my AI tools for web dev. My image assets, logo's and scripts are better than ever. You have to move with the tools because everybody else is...
  23. Earlier
  24. Double barrel meow meows!!! All is rt with the world now
  25. Sod off @jon019your mad as a hatter
  26. ....well, it's a given Shaun is quite batty, but as for myself...i am perfectly normal since the transplant...
  27. @Craigoonly speaking the true my friend, we have to be mad to put up with this
  28. Welcome, sorry you had to find us but glad you found CB. I had a chuckle at Shaun’s comment but I would agree we are a lovely but mad bunch. I am sure you’ll get the support you need here. I’d be another of the replies to encourage you to investigate the vitamin D3 anti-inflammatory regimen; has worked beautifully for me with eCH.
  29. Hi all. I saw a post recently from a fellow CH warrior that designed and built a CH tracker app. Heres the link: https://clusterheadachetracker.com I believe it may be in beta test mode but love the ingenuity and skill in our amazing community.
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