How is this happening again?

My daughter (15) was decompressed with duraplasty 14 months ago. After 9 months of recovery, I was blissfully happy watching her live fully once again. She was about 75% symptom free and I was fading off a bit, letting her do her thing, cheering from the sidelines.I've not been logging on to this site as CM took a backseat. She had two big sudden painful head attacks in Oct. though that left her struck down for days; both during runs. Since then, she's maybe 45% symptom free and my heart absolutley breaks for her.

Just made an appointment with her NS Dr. Ellenbogan. Take two months to see him. During that time, we'll track her pain to see if the 45% pain free thing holds steady or changes.

Prior to surgery she tried every pill and therapy under the sun. Including the localized shots, biofeedback, and fringe kind of stuff. Home life is stress free, she gave up team sports due to head but is now a varsity and junior olympic runner, eats super well, is an awesome student, watches her sleep, stays away from triggers (concerts, caffeine ,tight schedules,...) etc,…So, emotional or environmental is out the window. She's the best daughter ever, talks openly to me and if I am at a loss, has a nice counselor to help her with CM stuff on occasion.

Lynn has no fevers or swelling. The headaches are back though in varying degrees with no real rhyme or reason.

I've heard of shunts but anybody have one for CM1? Heard scar tissue can fill in that missing vertebrae bone area but nothing could stop that I am thinking, right? Anybody know a DECENT CM KNOWLEDGEABLE NL in the Puget Sound area? All we have now is her NS since everybody else has been so terribly awful or strange or clueless.

Thank you and I hope there's some peace out there for all of us in 2014.

271-IMG_0254.JPG (2.11 MB)

Well here quickly, feeling bad for both of you.

Seattle in October says no Vit D, and that is actually a hormone.. Low levels can cause HA and other malaise. Check out this Video, and see if it convinces you: http://www.youtube.com/watch?v=xF24xmJQK1k

Also see this next link by Mandy, one of our other moderators: http://www.chiarisupport.org/forum/topics/solution-for-headaches-an...

BTW, decent NL that knows CM is probably nonexistent, and it's hard to put those words in one sentence

Hope that helps, wish u well,
Geoff.

Dear GMA,

I hope that you are able to get your daughter HA free again soon. Please keep us posted on your success.

Warmest Regards,

Kim

Thanks. She has been taking D3 for a couple of years now and I thought she was getting enough K in her diet. We could add a supplement though…give it a whirl. Thank you!

Did she have a syrinx by any chance?

Hi GMA,

I am sorry your daughter is having headaches. I live with them daily and know how debilitating they can be. Where are her headaches located? Does medications relieve the pain at all? It will help to know also if her actual skull hurts or eyes hurt. Is there pressure involved? There are many causes for headaches in Chiarians. Did she experience headaches pre op and if so what type did the dr's say she was having? I know this is very heartbreaking for her but there is several treatment options once the NS or pain mgmt. specialist could diagnose her type of headache. I personally haven't found NL or headache specialists that understand Chiari headaches and it's very frustrating. Just be very cautious about medications that may be diagnosed for headaches. They often have negative side effects. I take Fioricet which is an older medication that is proven safe and doesn't have side effects like Topomax and others. I took it as a teenager & have taken it for a couple of years & I am 45 years old. I also have emergency medicatications so I don't have to go to the ER if it gets too bad. I just don't want your daughter to have to deal with side effects when she is doing so great. Please have faith & hope the NS can figure this out. It may be Occipital Neuralgia which can be controlled with major nerve blocks that are effective on most Chiarians. My first blocks lasted 3.5 years before I had to have them again. There are lots of solutions. I know you are both heart broke just please know you aren't alone. Many of us more than understand.

Tracy Z.

Has a connective tissue disorder been ruled out? Often (not always) when decompression is unsuccessful, it can be due to an underlying and undiagnosed connective tissue disorder like Ehlers-Danlos Syndrome. Something that needs to be looked into and checked by a knowlegable geneticist prior to decompression surgeries, and I wish this was a part of all Nsgs protocol!

Hey my 18 yr old son has a Chiari 13mm. I will keep this short cause my story is long. My son was doing great until he got 98% toxic with the Bp Oil dispursements we live on the Gulf in Destin, Fl. He trained in the water everyday. He started having all of these Chiari symptoms headache 24/7, vision, hearing loss, memory loss, brain fog, sinus issues and the list goes on. We did go to Barcelona, Spain for the Chiari and did not have the decompression surgery but he did cut the Fliumn Termanile. My son got a little relief but still had the constant 24/7 headaches and most of the other problems. We had the surgery before we realized he was toxic from the oil. When we finally found out after 30 drs that he was toxic and we detoxed for 6 months getting all of those toxins out of his body he is now 100% BETTER! We live in a toxic world and toxicity causes inflammation which causes the problems. Today we eat nothing but organic and I juice every night. A couple of weeks of ago we walked into a surf shop and there was a smell and we immediately walked out of the store but it caused a headache for about a week. I also clean with no chemicals, no perfume, unscented deodorant and hair spray. We have done a complete life style change and it worked. The number 1 thing to detox is sweating so we will continue to sweat in a sauna a couple times a week and eat extremely healthy. He won a World Champion title jet ski racing that is why he was in the water everyday but this year got his Formula D license car racing. He is now living life to the fullest after being bedridden for almost 2 years. 11racing.com is his website....... I hope this helps you and your daughter:))

GMA, l am so sorry that her success has been slipping. All of the advice sounds like great things look at, but I just want reiterate was Giovanna brought up. If Lynn does have a connective tissue disorder, like hypermobility syndrome/ EDS, she may have a cranial cervical instability, or a cervical instability. These instabilities have the same symptoms as the Chiari. The challenge with getting this diagnosis is that not all Chiari specialists screen for it. The Chiari Institute, Fraser Henderson in MD, Rosner in NC, possible Frim in IL, and possibly Theodore in AZ. I’m there are others that I am not aware of. Give her a hug for me, and one for you too- I know this very hard to go through.

Jenn

My 37 y.o. daughter had Chiari decompression two years ago. All of her original symptoms seemed to improve or go away for about 6 months. She started living life again and was raising her son and all seemed so well. Then the headaches returned and slowly the original symptoms came back. She was told it was just the healing process. She sought a second opinion from Dr. Frim in Chicago. He said there was evidence she was having a rejection to her bovine patch and that she needed to have it replaced with her own skin so it could finally heal. The headaches may be caused by a backup of fluid in the brain due to the swelling inside at the patch. After the patch replacement, she is to wait for healing time and see if things improve. If the headache pressure pain continues, then further testing for CSF buildup and

if needed a shunt would be placed. She has not seen a geneticist for Elhers but certainly has a history of hypermobility of her joints and was told years ago she had connective tissue disorder. She presently has four artificial discs in her neck from disc degeneration besides the upper disc surgery during Chiari decompression, and I feel sure this issue will be re examined when she goes back to see him. She believes she has cranial instability by the increasing of pain and symptoms upon certain movements of her head including dizziness and vision problems. My daughter will be going from Alabama to Chicago for surgery in the next few months. I am sorry to hear of your daughter's problems and hope by sharing our story you might consider palpitating around her patch for pain or having her checked for cranial instability.

All of these issues were discussed with the original doctor, as we had both done much research before surgery. The doctor just ignored our concerns and every time she returned to him with increasing pain and original symptoms he would say "it just hasn't healed yet". We decided to get another opinion. We don't know what the future holds, but my daughter is very glad we sought another opinion on the returning painful headaches, etc. Best wishes to you and your daughter.

Sherry

I was trying to read through to see if anyone mentioned this but just wanted to add in to see if this would help

I had my first decompression last december than suddenly after 10 months symptoms came back (headaches a lot) but got new mri and was told was failed surgery and had fluid build up so I had a 2nd surgery on decemeber 4th still recovering but did have a shunt put in. They told me after it is I believe in my 4th ventricle of my brain and will help drain my large syrinx and if my CSF starts to build up. HOWEVER I found out afterwards the fluid build up in my head was actually a reaction to a type of seal used the first surgery (usually on cardiac patents) that caused this which only discovered after doing surgery again. I wont know more about the shunt exactly until I go in for my MRI to see my NS at the end of this month and if this was the correct fix. Not sure if this helps or not but I will keep you in my thoughts and prayers for your daughter that there are answers soon. It is frustrating but keep having strength and faith and I hope her issues are resolved. Feel free to ask me any more questions and I will try my best to help anyway I can!

Emily

Thankfully, no.

Joalexa said:

Did she have a syrinx by any chance?

So they can do shunts for restricted flow. I had heard they were for syrinx only but of course, three's a ton of varying info out there. THANK YOU!

TracyZ said:

Hi GMA,

I am sorry your daughter is having headaches. I live with them daily and know how debilitating they can be. Where are her headaches located? Does medications relieve the pain at all? It will help to know also if her actual skull hurts or eyes hurt. Is there pressure involved? There are many causes for headaches in Chiarians. Did she experience headaches pre op and if so what type did the dr's say she was having? I know this is very heartbreaking for her but there is several treatment options once the NS or pain mgmt. specialist could diagnose her type of headache. I personally haven't found NL or headache specialists that understand Chiari headaches and it's very frustrating. Just be very cautious about medications that may be diagnosed for headaches. They often have negative side effects. I take Fioricet which is an older medication that is proven safe and doesn't have side effects like Topomax and others. I took it as a teenager & have taken it for a couple of years & I am 45 years old. I also have emergency medicatications so I don't have to go to the ER if it gets too bad. I just don't want your daughter to have to deal with side effects when she is doing so great. Please have faith & hope the NS can figure this out. It may be Occipital Neuralgia which can be controlled with major nerve blocks that are effective on most Chiarians. My first blocks lasted 3.5 years before I had to have them again. There are lots of solutions. I know you are both heart broke just please know you aren't alone. Many of us more than understand.

Tracy Z.

Her headache was 24/7 for two solid years. Pressure, moved all over, worse in back when active or straining. Docs said lots of things from migraine to fibromyalgia to Munchausen (I WAS MAKING HER SICK!). Complete insanity. NS finally agreed it was very likely it was due to severe CSF flow and her CM1 (of course, we thought this all along). Post op she had headache pain less and less until she was 75% better at her high point. Now, the it is back. Not always as severe and not 24/7 but it can get bad. Now she's maybe only 45% better. Yes, pressure and it moves all over her head.

During the two years of trying everything, the pain mngmt people really turned her off to the point that I feel as if she gets stress headaches even discussing it. I don't blame her. NLs gave her lots of scripts and yeah, Topomax had miserable side effects and Fioricet made her high. Neither eased the pain.

Been toying in my mind with re-trying some meds post op to see if they work now but don't know if that's something that could happen or just wishful thinking??

One NL did try nerve blocker shots pre-op and on top of not easing her pain, it ended up being such a bad experience…she doesn't like to think about it or go near that area of town where she had it done. Dark, dark moments…ug.

75% better was just so wonderful and made things seem so normal again: living a happy life without chronic pain. Without the head stuff, life is great: family, trips, school, friends. Lynn has a great passion for life and tries not to let her head stop her. When it does stop her though and she wonders if she can go on…heartbreaking.

Thanks for listening and for your kind words.



TracyZ said:

Hi GMA,

I am sorry your daughter is having headaches. I live with them daily and know how debilitating they can be. Where are her headaches located? Does medications relieve the pain at all? It will help to know also if her actual skull hurts or eyes hurt. Is there pressure involved? There are many causes for headaches in Chiarians. Did she experience headaches pre op and if so what type did the dr's say she was having? I know this is very heartbreaking for her but there is several treatment options once the NS or pain mgmt. specialist could diagnose her type of headache. I personally haven't found NL or headache specialists that understand Chiari headaches and it's very frustrating. Just be very cautious about medications that may be diagnosed for headaches. They often have negative side effects. I take Fioricet which is an older medication that is proven safe and doesn't have side effects like Topomax and others. I took it as a teenager & have taken it for a couple of years & I am 45 years old. I also have emergency medicatications so I don't have to go to the ER if it gets too bad. I just don't want your daughter to have to deal with side effects when she is doing so great. Please have faith & hope the NS can figure this out. It may be Occipital Neuralgia which can be controlled with major nerve blocks that are effective on most Chiarians. My first blocks lasted 3.5 years before I had to have them again. There are lots of solutions. I know you are both heart broke just please know you aren't alone. Many of us more than understand.

Tracy Z.

We are mainly organic and have lived in a "green" kind of place now. We really could look at going 100% organic though. Big thing would be personal products. I clean with vinegar, essential oils, and such but we use regular makes up, toothpaste, shampoo, etc,...

As for environmental, the GA town we lived in while I was pregnant has an old paper mill that is now out of business. Back then people said there were all sorts of problems with them and the EPA so they were going to shut down. Well, we left a million years ago but Lynn happens to have a virtually no enamel on her teeth and a brain malformation. Thus, I've often wondered about that town in GA playing a role.

Sorry your son has suffered. As a mom, I know, we'd try anything to ease their pain. I love that he's racing…we're auto fans and our son races and works on a lemon for lemon type races. Next week, my husband and I will be back at Barrett-Jackson hanging out and gawking!

Thanks for the tips and I will make sure to start looking at detox and sweating. Although, she's and XC runner and runs daily for many miles and is always really sweaty then. Think that works?

Alec Hohnadell said:

Hey my 18 yr old son has a Chiari 13mm. I will keep this short cause my story is long. My son was doing great until he got 98% toxic with the Bp Oil dispursements we live on the Gulf in Destin, Fl. He trained in the water everyday. He started having all of these Chiari symptoms headache 24/7, vision, hearing loss, memory loss, brain fog, sinus issues and the list goes on. We did go to Barcelona, Spain for the Chiari and did not have the decompression surgery but he did cut the Fliumn Termanile. My son got a little relief but still had the constant 24/7 headaches and most of the other problems. We had the surgery before we realized he was toxic from the oil. When we finally found out after 30 drs that he was toxic and we detoxed for 6 months getting all of those toxins out of his body he is now 100% BETTER! We live in a toxic world and toxicity causes inflammation which causes the problems. Today we eat nothing but organic and I juice every night. A couple of weeks of ago we walked into a surf shop and there was a smell and we immediately walked out of the store but it caused a headache for about a week. I also clean with no chemicals, no perfume, unscented deodorant and hair spray. We have done a complete life style change and it worked. The number 1 thing to detox is sweating so we will continue to sweat in a sauna a couple times a week and eat extremely healthy. He won a World Champion title jet ski racing that is why he was in the water everyday but this year got his Formula D license car racing. He is now living life to the fullest after being bedridden for almost 2 years. 11racing.com is his website....... I hope this helps you and your daughter:))

No it has not. She gets headaches ranging in severity and often emanating from the neck/back of head. She gets really exhausted with them and thinking turns a bit fuzzy.

Giovanna said:

Has a connective tissue disorder been ruled out? Often (not always) when decompression is unsuccessful, it can be due to an underlying and undiagnosed connective tissue disorder like Ehlers-Danlos Syndrome. Something that needs to be looked into and checked by a knowlegable geneticist prior to decompression surgeries, and I wish this was a part of all Nsgs protocol!

Oh my gosh…how would the docs even figure it out? Do you have it? Seems so so so complex but of course, I only Googled it for 5 minutes.

jcdemar said:

GMA, l am so sorry that her success has been slipping. All of the advice sounds like great things look at, but I just want reiterate was Giovanna brought up. If Lynn does have a connective tissue disorder, like hypermobility syndrome/ EDS, she may have a cranial cervical instability, or a cervical instability. These instabilities have the same symptoms as the Chiari. The challenge with getting this diagnosis is that not all Chiari specialists screen for it. The Chiari Institute, Fraser Henderson in MD, Rosner in NC, possible Frim in IL, and possibly Theodore in AZ. I'm there are others that I am not aware of. Give her a hug for me, and one for you too- I know this very hard to go through.

Jenn

I know the patch was from higher up on her head but yes, build up there again is something I am wondering about and if they'll consider doing a shunt for that. Guess I have to wait until the new MRI and appt of find out. Somebody else mentioned cranial instability. Did a quick Google search but it seems so frighteningly overwhelming and ug…I am envisioning docs acting as if we're crazy once again and living a medical nightmare all over. Guess I should start researching. Thank you.

SHERRYD51 said:

My 37 y.o. daughter had Chiari decompression two years ago. All of her original symptoms seemed to improve or go away for about 6 months. She started living life again and was raising her son and all seemed so well. Then the headaches returned and slowly the original symptoms came back. She was told it was just the healing process. She sought a second opinion from Dr. Frim in Chicago. He said there was evidence she was having a rejection to her bovine patch and that she needed to have it replaced with her own skin so it could finally heal. The headaches may be caused by a backup of fluid in the brain due to the swelling inside at the patch. After the patch replacement, she is to wait for healing time and see if things improve. If the headache pressure pain continues, then further testing for CSF buildup and

if needed a shunt would be placed. She has not seen a geneticist for Elhers but certainly has a history of hypermobility of her joints and was told years ago she had connective tissue disorder. She presently has four artificial discs in her neck from disc degeneration besides the upper disc surgery during Chiari decompression, and I feel sure this issue will be re examined when she goes back to see him. She believes she has cranial instability by the increasing of pain and symptoms upon certain movements of her head including dizziness and vision problems. My daughter will be going from Alabama to Chicago for surgery in the next few months. I am sorry to hear of your daughter's problems and hope by sharing our story you might consider palpitating around her patch for pain or having her checked for cranial instability.

All of these issues were discussed with the original doctor, as we had both done much research before surgery. The doctor just ignored our concerns and every time she returned to him with increasing pain and original symptoms he would say "it just hasn't healed yet". We decided to get another opinion. We don't know what the future holds, but my daughter is very glad we sought another opinion on the returning painful headaches, etc. Best wishes to you and your daughter.

Sherry

Hey also look at what this lady posted the other day:)))))

Those of you who've been here for a while are probably familiar with the fact that I love to research. I love my children even more than that. So when my 7 year old daughter started getting migraines this year shortly after my Chiari diagnosis, I started searching for answers.

One migraine in April, some leg and back pain before and after, sleeping issues, attention problems, constipation, a couple of "accidents" where she wet her pants, vision problems (blurry, weird shapes or colors), dark circles under her eyes, and constantly dry lips.

In October, while I was in North Carolina seeing a Chiari specialist, she had a bad enough migraine that she threw up. I'm a protective mother in the first place, being across the country and not there while she was in pain about killed me. As soon as I was home, we set up an appointment with our family physician. He's a nice enough guy, and although he thought an MRI was excessive, he agreed to order one. It came back normal, except for a very small pineal cyst. My physician called and left a message, advising the pineal cyst wasn't enough to cause problems. I, of course (now that I've had experience with Chiari and radiologists), took my copy of the MRI home and immediately noticed a problem.

Although my daughter, Jordan, has a small herniation of only about 3mm, and her foramen magnum is mostly open, she has a very sharp clivo-axial angle. The clivo-axial angle is the one at the top of the spine, the clivus is the triangular bone, and the angle it makes with the odontoid (finger shaped bone at the top of the spine) is called the clivo-axial angle, or CXA for short. A normal clivo-axial angle is 165 degrees. Jordan's is 105 degrees. Anything under 135 degrees is considered a sure fail for a posterior fossa decompression (Chiari surgery), and anything under 145 degrees will have some neurological symptoms, to include headaches. Especially headaches in the forehead.

So now I know what the problem is, I go about finding a specialist, and we've found a great one in Phoenix. Only problem is our appointment (we're both seeing him), is in March. So in the meantime my daughter is suffering, and her headaches continue to worsen. At the end, it was a two week headache that just wouldn't go away, although at times it was less painful than others. We tried a cervical collar, not looking down, no extra activities, drinking a lot of water, changing pillows, epsom salt baths, ibuprofen, tylenol, and nothing was working. In the early part of November a friend from this site sent me a video about Vitamin D supplementation. This video changed my life.

http://www.youtube.com/watch?v=xF24xmJQK1k

I would encourage anyone with headaches, or a loved one with headaches, to watch this video. I immediately started supplementing with higher doses of Vitamin D3, and giving my daughter a higher than normal dose as well. After reading two books,

http://www.amazon.com/MIRACULOUS-RESULTS-EXTREMELY-SUNSHINE-EXPERIM...

And

http://www.amazon.com/Vitamin-K2-Calcium-Paradox-Little-Known-ebook...

I realized the Vitamin D3 needed to be combined with Vitamin K2, and that's when the magic started to happen. My pain, for the most part, went away. And even better, my daughter stopped having headaches. For six weeks now, she hasn't had head pain of any kind, no fevers or hot forehead like she used to, no leg or back pain, nothing. Occasionally she'll get a stiff neck or back from sitting in a position for too long, but it's still nothing like we were going through before. No accidents, and the constipation isn't as bad as it used to be (she's going several times a week now)

So if you decide to read the books, although the first one is interesting, the author is not a doctor, and this is his personal experience with high dose Vitamin D supplementation. The second book though, not only discusses the importance of Vitamin D3, it talks about how essential K2 is if you're using higher than normal doses. And, it goes into some very extensive background about diet and nutrition today as compared to that of a hundred years ago.

Basically, there are nutrients only available in specific foods that are typically not eaten in a normal Westernized diet. Vitamin K2 and Vitamin A-Retinol are found in grass fed organ meat (liver, heart, tongue, brain, etc), grass-fed cow milk, pastured chicken eggs (grass fed chickens), and in smaller amounts grass fed meat. Vitamin K2 (MK-4) is also found in Gouda and brie, pate, and fish eggs. Vitamin K2 (MK-7) is found in Natto (fermented soybeans). Vitamin K2 is necessary to move calcium from the bloodstream into the bones, and NOT into the muscles, tendons, and arteries. So if we're not getting Vitamin K2 or Vitamin-A Retinol what happens? Per Dr. Rheume-Bleue, the author of the 2nd book, says we have birth defects, smaller jaws with crowed teeth and high palates, and poorer health altogether. Dr. Weston Price, a dentist back in the 1930's, did research and found traditional populations not exposed to a modernized diet, did not have crowded teeth, and rarely had cavities. Once these populations started eating modernized food, they then had a smaller lowest portion of the skull (possibly a smaller posterior fossa in conjunction with a smaller jaw and crowded mouth), and other health problems not inherent in their parents. There's so much more information, if you can loan the book from the library, or purchase it, I'd highly recommend it.

At any rate, I'm now taking 50,000 IU of Vitamin D3 every morning, with a Vitamin K complex vitamin which has 2000 mcg of K1, 2000 mcg of K2 (MK-4), and 400 mcg of K2 (MK-7). I also take a 25,000 IU Vitamin A-Retinol, but I'm still researching that one, so a smaller dose might be better, at least to start out with. There are some studies out there that attribute high Vitamin A with a variety of problems, so here's a helpful page:

http://ods.od.nih.gov/factsheets/VitaminA-HealthProfessional/

It discusses the Upper limits and recommended dosages, 10,000 IU is the tolerable upper limit for adults using Vitamin-A Retinol.

In reference to the YouTube video, I think proper sleep is essential, and I would suggest everyone get a sleep study. Eighty percent of Chiari patients have sleep apnea. Broken sleep, or lack of REM sleep means the body is not healing at night like it needs to, and pain is the result. Every Chiari patient I've spoken with is also deficient in Vitamin D. So, our system for fixing headaches has been:

1. Getting a sleep study, and wearing a CPAP every night if you have sleep apnea. If you have a lack of REM sleep, you could possibly be having adrenaline spikes from dysautonomia. This video discusses this problem, and the solution is a beta blocker:

http://vimeo.com/35766364

2. Supplementing with a quality high dose Vitamin D3 (I use Solgar) and Vitamin K (I use Life Extension Super K Complex).

3. Supplementing with a chelated magnesium (I just started on Country Life), and using magnesium oil at night on the painful parts (neck, legs, back, arms, etc). Epsom salt baths are helpful as well.

4. Supplementing with Vitamin A-Retinol, at a dosage you're comfortable with.

5. Increasing protein intake. Your body wants to repair itself, and protein is amino acids packaged in a tasty form. Some suggestions are grass-fed whey, organic free range meat, organic pastured eggs, etc. Another option is collagen supplements, gelatin, and supplemental amino acids, although I'm not sure how much those work. If anyone else has suggestions, I'm open to hearing them, we're looking for something easier to give the kids, they don't love meat or eggs unfortunately.

6. Eating more fruits and vegetables. I have a smoothie maker, we make berry banana smoothies for the kids, and I have spinach/banana/berry/carrot smoothies with a scoop of protein powder, cal-mag-citrate powder, and powdered Vitamin C.

There's so much more, and I wish I could just give you all of the information in my head. If you have any questions, please ask. But really, getting sleep, supplementing with nutrients we aren't able to get from food, and increasing protein intake are all good ways to feel better.

As a side note, Vitamin A-Beta carotene from carrots is not absorbed well in humans. It is discussed in the second book by Dr. Rheume-Bleue I believe, but basically humans have adapted to getting nutrients from animal products, and some fruit and vegetable sources are not metabolized as well.

As for my daughter, I give her a chewable D3/K2 (MK-4) in the mornings, and spray magnesium oil in the evenings on her back and legs. I also supplement the chewable with a liquid Vitamin D3, so she is taking 10,000 IU of Vitamin D3 a day and 2000 mcg of Vitamin K2 (MK-4). She also takes an epsom salt bath a couple of times a week. I split a Vitamin A-Retinol 10,000 IU capsule in her and her sister's smoothies twice a week, so her weekly dose is around 9,000 IU, simply because I can't get all of the liquid out of the capsule. I've tried a chewable cal-mag wafer, but they didn't really like it.

The spray magnesium can be itchy/tingly/stingy at first, this is helped greatly with lotion, and if the stinging doesn't go away in a few seconds, I wipe it off with a wet washcloth. On myself I just leave it there, and I've noticed now that I use it consistently, it rarely itches any more. A word of caution, it will dry out your hands if you use it a lot, so you'll want to wash your hands or use a bunch of lotion.

Here are the supplements we use:

http://www.pioneernutritional.com/pioneer-products/d3-k2-spearmint....

http://www.seekinghealth.com/liquid-vitamin-d-drops.html

http://www.solgar.com/SolgarProducts/Vitamin-D3-Cholecalciferol-100...

http://www.lef.org/Vitamins-Supplements/Item01724/Super-K-with-Adva...

http://www.vitaminshoppe.com/p/country-life-chelated-magnesium-250-...

http://www.nowfoods.com/Vitamin-A-25000-IU-100-Softgels.htm (they also make a 10,000 IU version)

http://www.vitaminshoppe.com/p/life-flo-health-care-pure-magnesium-...

Full disclosure, you should talk to your doctor before adding supplements or changing your diet. I am not a medical professional. 50,000 IU Vitamin D3 is much higher than the tolerable upper limit as defined by the USRDA, and high dose Vitamin D has been associated with high levels of calcium in the blood stream. I would suggest reading the book and doing your own research before considering this as a course of action for you or your family. Here's an article from the Vitamin D council regarding supplementation:

http://www.vitamindcouncil.org/about-vitamin-d/am-i-getting-too-muc...

And here's one regarding Vitamin D and Vitamin K2

http://articles.mercola.com/sites/articles/archive/2013/10/19/vitam...

And another:

http://www.lef.org/magazine/mag2008/mar2008_Protecting-Bone-And-Art...

As for the effect, after taking my morning dose of Vitamin D/A/K, I notice a sense of relaxation within 20 minutes.

If anyone decides to do this, I would love to hear the results, I don't think it's a coincidence that my daughter and I both have improved significantly with supplementation.

To finish, here's my daughter's MRI:

Tags: D3, K2, Retinol, Vitamin, apnea, headache, migraine, sleep

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Mandy posted about headaches.....

Not all NSs check for cranial instability. You would have to find one and get an appt. The tests for cranial cervical instability are flexsion extension MRIs and rotational ct scans. I had my decompression done by a reputable Chiari surgeon who missed the instability. Now I am waiting to see Dr Henderson to have it fixed.