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1961mom last won the day on March 24 2017

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About 1961mom

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  1. Hi 1961Mom,

    I'm trying to find out if there are any Portland/Van/Salem groups that meet in the area. I posted to the Forum and it was suggested by CHFather to IM you.

    Thank you,


  2. And I've put the links into the group's "File" section (no scrolling away). Thank you so much. Your efforts are amazing!
  3. Hey guys! Loved meeting new friends and seeing old pals at the conference last week. I hope all your travels were pain free If you want to join the Facebook group (just to view) let me know your real name in a PM. I"m admin of the group and will add you without going through the "join" process. At this point in time the "Live" video feature does not allow downloads. But, it's fairly new to Facebook and Facebook is famous for changing formats and features regularly. David Nickerson (the member who shot the video) did share how he was able to 'save' them to his device. I'll check with
  4. My experience with the D3 regimen was a Godsend to this [at the time] chronic patient. I watched 100's (honest) of people become pain free using it as written.The most successful are those who begin with getting their baseline 25(OH)D levels done first, then go for it. The only substitution I made was I used honey in place of the Boron. Sticking to it AS WRITTEN is key! D3 test kits available online or most GP's will be glad to send you to their labs. My test came back at <33ng/mL. Cluster patients report relief at <65ng/mL. All the supplements are important, but I think it's
  5. Testing, testing, testing Love the new forums user interface! Can't wait to see you guys in Chicago.
  6. Tyler Mann, CH patient & Documentary Filmmaker Cluster Headache Documentary Film Project Launches Date-Feb. 10th, 2015 Documentary Update #1-March 8th, 2015 Long Term Project Goals https://drive.google.com/file/d/0BwHf09yeneJnM2xwRHEwQXNaMU0/view?usp=sharing
  7. Thanks CHfather, Jeebs & Diamondmaker.... it was a gift from the CH Gods! This treatment may just be gift #2Â Â
  8. Great thread! I'm on my second treatment of 5-MeO DALT...while I had a pf summer, the clusters returned mid October. I'm really excited or interested in the "ghost" attack comments, so thank you par for mentioning. I experienced these too, but didn't count it as attacks, however they were much more than what I normally call 'shadows". I could feel a sort of rolling sensation. I know this sounds odd, but if you've ever experienced sea sickness in your gut and could imagine moving that into your head, then you've got the gist of what I'm talking about. lol. Very strange, but not a sing
  9. I went to book my hotel room online today and got a note: "Not available during your requested days"...... So, I called the hotel, and got a room but was told all the blocked rooms (set aside for the conference) have been booked for the night of 20th & 21st. The hotel still had rooms and will give you the conference rate, when you phone in and explain. Just an FYI.
  10. As Seen on American Academy of Neurology- THIS IS WORKING-IF YOU HAVEN'T WRITTEN, THERE'S STILL TIME EXTENSION! Please Request CMS to Reconsider Oxygen for the Treatment of Cluster Headache http://cqrcengage.com/allianceforheadacheadvocacy/app/write-a-letter?0&engagementId=49273&lp=0 Your Help is Needed! Several years ago the Centers for Medicare and Medicare Services (CMS) decided it would no longer pay for oxygen for the treatment of cluster headache. This is a serious hardship for many of the most disabled headache patients. Headache experts and the American Headache Soc
  11. Thanks CHfather I hope you got my note M'Joe...very exciting that you've already begun a relationship with your representatives. I'll do everything I can to help give you the tools to begin a new conversation with them about cluster headache advocacy work (really all primary headaches). Thanks for reaching out and sharing! Cindy
  12. Thanks for asking Tony, and answering Bob. I went looking for the "Playing Well Together" link just yesterday.
  13. LOL.... ThatHurts...You are so right! I just forgot to add a specific number. Fixed that It's so great to see all the comments on both the Change.org "sign on" letter and the SSA public comments site. I'm reading through the SSA site now...I see AgentOrange (former member here) and CHFather too. YES! And a bunch of the AHDA (The Alliance) Docs too. Good stuff. We're up to 640 comments on the SSA page and 950 signers on the Change.org letter!!!
  14. 1961mom

    CB on TV

    Today, we learned the Kirt Kessler/Dr. Young spot is airing all over the US! Possibly NBC and it's affiliates are running with this today. WIN! ps...MoxieGirl, I totally agree. That's an all inclusive piece for sure!
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