New Daily Persistent Headache
I was diagnosed with New Daily Persistent Headaches at Johns Hopkins headache clinic in Baltimore last August. I am hoping to find more information on these kinds of headaches. I have found very little actual research information on them, and some of the information I have found is inaccurate.
The first neuro I went to must not have been familiar with this type of headache, as I have all of the symtoms, but he never diagnosed me with NDPH. For those of you unfamiliar with this type of headache, let me tell you what I do know. First of all let me say that I got a headache the first week in June in 2010, and it has never gone away. It does not always hurt in the same place, or in the same way, or to the same extent. That makes it nearly impossible to describe to a doctor because it sounds crazy. I kept apologizing to my first neuro for not being helpful when he asked questions, and I gave him this bizaare set of answers. Finally being correctly diagnosed was huge to me. At least I knew what I had and that there were other people with this type of headache.
The headache pain goes from moderate to severe; I often have migranous headaches but migraine meds do not phase NDPH. NDHP are not migraines. It would be nice to have migraines where at least most people have some type of success with medication. I have easily tried 40 different medications. My doc at Johns Hopkins said that this is the most difficult type of headache to treat; less than half of all sufferers ever find any kind of medication that will ease the pain. For bad and really bad days I have to take oxycodone or apply a fentanyl patch. Not only are these substances highly addictive but they also cause rebound headaches which are far worse than the orginal one was. Most days (and nights) I just try to get through them. I don't really have any options.
I was an English teacher. Last year I had to take 6 months off. I went back this year, but I only made it though the first quarter. I am on short-term disability now with no option to return to my job of 29 years.
I would love to see discussion of this type of headaches on the board! I also wanted to post this in case anyone who reads this may be suffereing from this type of headache. To be classified at NDPH, the headaches must have been continual for at least a 3 month period- no time at all headache free. They say that 80% of people with these headaches can tell you the exact time they began. Have you been give a lot of different medications and none of them phased your pain? It seems like a lot of doctors don't know anything about this headache. Both my GP and my first neuro were clueless. They may need you to educate them.
Interested in more discussions like this? Go to the Chronic Pain Support Group.
@vasaiovic .... Please give your daughter a hug from a stranger. God bless you all. It sounds horrible!
Hello. My husband has suffered from NDPH for 14 months. Like many of the people on this board, he had no prior headache history and can remember the day his headache started. After numerous failed medication trials (and cervical spine facet joint inhections and occicpital nerve blocks) we are trying massage, biofeedback and possibly acupuncture. Your tips for choosing alternative practitioners came at a good time. Thank you.
CiCi
Hello corxdv: My husband has dueling diagnoses: ndph versus cervicogenic (cervical spine) headache. Because his neck MRI and X Rays showed arthritic changes in his neck (bone spurs, swollen facet joints) he was treated with cervical spine steroid infections and nerve blocks by a physical medicine and rehab specialist. The nerve blocs did not work and the physical medicine and rehab doc offered referral to a surgeon for "nerve decompression surgery" of his cervical spine. We are leary of this surgery since the cervical spine nerve blocks did not pinpoint the location of the problem. A neurologst recently diagnosed NDPH on the basis that (1) the cervical spine nerve blocks did not work; (2) he has no neck pain and can move his neck freely; and (3) his history and negative imaging tests are consistet with ndph. Please let us know if your wife had surgery and if she has found relief.
I have had a migraine at least that is what all my Neurologist have told me for the past 6 years non stop, my paid is always high end of the scale and most days I have black and White spots in my eyes, have a very hard time bending over I always feel as though I will vomit. There are some days I do vomit. I have Anti-Phospho-lipid antibody syndrome which I have been told this is a side affect of. I also have sever right foot and back paid, I have had surgery for my back but it comes back. I have actually worn two phyntinal patches at once with no relief. Any suggestions would be great. I have also had 4 strokes as a result of the disease.
My son was diagnosed with NDPH in 2016, when he was 15. He has good luck with pain reduction with amyltriptaline. He takes 40 mg nightly. It provides effective relief but not a complete removal of pain. On a pain scale of 1 - 10, his "normal" is a pain level of 1 to 3.
Thank you so much for the information on NDPH, I have had a migraine/headache for over 7 years not and have had no success in getting any relief from the pain at all. I have had 5 Neuro and 2 GP that did not have a clue how to fix it. I am going to a new Neuro on the 19th and will see what she knows about this type of headache. I hope that she has some kind of idea on what will help because having this kind of pain every day and night non stop is becoming enough to just want to stop trying.
I’m so happy for you and your son. I am one of those unfortunate ppl for whom it seems no medication on earth will work. So many of the drugs I’ve tried have side effects that make me *more* incapacitated than the NDPH. So it’s nice to hear positive outcomes like this.
I can relate. They called my headache migraines at the beginning too and it limited the kind of care I received and the compassion I got from ppl. I’m heading towards the 9 year mark in a few months, and I have had to remind myself that medicine is called a “practice” because going to medical school, specialty training, passing tests and getting a job doesn’t make someone a great doctor. Being proactive in the care of patients is still an individual personality trait. I’ve had numerous neurologists, too. Honestly the last two before my current one shrugged their shoulders and washed their hands of me when they couldn’t help me. You definitely have to be your own advocate on this journey, and it sounds like you are! Don’t give up! Take a rest and regroup if you need it, but then keep going. The one thing you *can* be certain of is that if you don’t try to find answers, no one else will. After every unsuccessful treatment I’ve taken a break and just focused on the basics of eating well exercising and trying to do things I enjoy. Sometimes that’s necessary for my body to detox off whatever crazy drug the docs had me on. Other times it was purely a mental break from the hunt. But always I know that I have a finite amount of mental focus to use, so when I run out of steam in one direction, I need to focus on something else for a while. I’ve learned a lot about how to manage my pain and how to spend time with friends this way. I’m still not able to work or even return to my pre-NDPH social schedule, but I’m a bit happier than I was. Good luck!
I couldn’t agree with you more! I call it the medical rodeo and I too had my orthopedic doctor shrug his shoulders at me! He went to Harvard and guess what, he doesn’t know what’s causing my pain so I’ve decided it’s up to me to figure it out! I sit here in the rheumatologist office while I type this! I will not give up and press forward as my God promises he will never leave me and I believe i will be healed ! Thank u for your help! God bless you !
Amen to that sister! Sending you a great big God Hug from Carol UK x