Fighting For Your Life | Im Lucky To Be Alive | Pernicious Anemia

[@sarabartel4285]

I was diagnosed in my mid-twenties. I already had several other chronic conditions, and kept ignoring the symptoms because they overlap with my "normal" baseline. But the memory loss was really scary. I was experiencing early dimensa symptoms. The neuropathy, insomnia, paranoia, movement disorder, fatigue, and ulcers were unbearable. I kept getting blood tests for regular anemia with normal results, until a neurologist checked a FULL blood panel. I felt like I was dying, because I was. Injections are the only way to survive and recover. I live a functional life because of shots every other week.

[@JamesonSharp]

I’m glad you found something that works for you. 🙏 JS

[@organicfireorganicfire1236]

@@JamesonSharp what was ur b12 level?

[@JamesonSharp]

@@organicfireorganicfire1236 My Blood B12 was extremely high from experimenting with over the counter tablets. But!!! My intracellular levels of b12 was the problem. My cells were empty. My cells were not accepting the tablet form molecular b12. Injections? I saw major improvement after beginning injections. Hope this is insightful. 🙏

[@organicfireorganicfire1236]

@@JamesonSharp so I need to test for my active b12 to know my intracellular level?

[@JamesonSharp]

@@organicfireorganicfire1236 I honestly do not feel the Blood level B12 test is useful. I was unable to test my intracellular level of b12. So the only explanation I was able to come to? Was my intracellular levels were non existent. Even though my blood levels were high. I would never trust a B12 blood test. You either know your body’s own chemistry. Or you don’t. I hope that helps.

[@ArohaKoe]

I got diagnosed early, at 12 and I've gotten lucky to of gotten diagnosed so early. I'm now 15 and take shots every 3 days. Who knows what could've happened when I got to my 20s and not having it treated. Stories like yours make me feel lucky. You know

[@ArohaKoe]

Btw love from Australia

[@JamesonSharp]

Keep Taking Care Of Yourself-Much Live from Kansas City. 🙏

[@fantaelectro]

I have pernicious anemia too. I went to hospital almost dead 3 years ago. love from Greece.

[@JamesonSharp]

Glad your Alive and Made it. Appreciate ya!! JS

[@b12beyou]

hey vasiliki, i'm so sorry about that. we all need to unite together to overcome this. i have pernicious anemia too. i have improved quite a bit though! how are you feeling now? here is my story in case it helps: kzbin.info/www/bejne/jnvVfpZqjbF4irM

[@nirimalanaidoo4607]

Thank you for this video

[@abovemoon]

Thank you for sharing your story. I 100% understand how you feel. You learn a lot about yourself while working around the complications of pernicious anemia, and I know it can be a blessing in disguise.

[@tracyfreddie7899]

4 years ago I was diagnosed with PERNICIOUS ANEMIA and I have tried everything I could to heal myself, but it was all to no avail, until I saw a post on a health forum about an herbalist preparing herbal medicines to cure everything type of diseases. including PERNICIOUS ANEMIA , at first I doubted it was real, but decided to give it a try, when I contacted this herbalist through his email and he prepared me a herbal cure for PERNICIOUS ANEMIA and sent it to me via the delivery service of UPS from the company, when I received this herbal cure. , gave me step by step instructions on how to apply it, when I applied it according to the instructions I was totally cured of this deadly disease within 2 months of use, I am now PERNICIOUS ANEMIA free, all thanks to Dr. Joshua Ighalo. You can also contact this great herbalist for help by email: [e-mail] or contact Dr. through his whats-app: [phone] They also specialize in the treatment of all kinds of diseases, VIRUS HERPES , HEPATITIS B, CANCER, BRAIN DISEASE, INFERTILITY, DIABETES AND MORE.

[@JamesonSharp]

Abovemoon -Very True, I hope you find continued happiness, and have the stregnth to keep up the good fight. I am in your corner. Seems Like I am late to you comment, however I am so appreciative you felt compelled to share here. Thank you. Let me know if I am able to offer any emotional or morale support in your continued battle.

[@gloriahickey8855]

I have injections every other day, following guidelines in B12 Support Group UK. Unless your getting enough your body won’t heal . When I asked my doctor if I had PA he said not anymore. My levels in Australia iron 9 which is still in the bottom range. I am taking iron every day. This condition is treated so badly by the medical profession. I know if I hadn’t taken control of my own condition I would be in a nursing home by now.

[@JamesonSharp]

I’m very glad to hear you took control of your future and treatment. Your 1000% correct the Medical Professionals are ignorant and do not understand how deadly and progressive this illness is. I’m praying for you. 🙏 Here anytime. ❤️ JS

[@Ellie-qq9zm]

Hi Jameson, I have pernicious anemia as well. I would have had no idea if it wasn’t for my doc randomly testing for it when I was 18 yrs old. I’m now 21 and still dealing with side effects. It’s taken a while to get the right injection schedule, for a while I had 1 injection a month and I wasn’t improving. So now I’m back to 2x per week for a while and then 1x per week and it should help my brain fog and fatigue. It’s not an easy condition to deal with that’s for sure, I also have neuropathic pain from it. After my diagnosis it felt kind of scary having to rely on b12 injections for life. I agree it really makes you think about how important our health is for our quality of life.

[@JamesonSharp]

I’m so happy you got treatment immediately. I agree it does take time and maximizing and listening to your bodies needs to schedule your dosage. My body gives me tell tale signs, like for example my calf muscles will begin cramping and or twitching. My eyes have had difficulty as well. Our health is the only wealth we truly have. If you ever feel I can be helpful by sharing my experiences? You know where to find me. I appreciate your struggle and genuinely Thank you for stopping by. I wish you health and happiness. ❤️🙏🙂 JS

[@nibornnyw3185]

It's so easy for doctors to say that you don't need that. It's like they have no concept of the dark place I would have to go back to.

[@nirimalanaidoo4607]

So glad I got to see your video ..my daughter has it ..sh in hosp ..now and has been admitted over the years ..sh was diagnosed with periconious anemia many years ago ..the Dr told her to take me etformin...not sure why cos she's not a diabetic .. Sh suffered psychiatric issues .. brain fog. .confused. Leg issues .palpitations. eye problems Mouth ulcers ..unable to sleep ..fatigue. Sh can't sleep ..sh gets up in sweats ..serious psychological issues .sh unable to work ..sh gets agitated easily ...has had psychosis ..memory loss ..depression Even though I told the drs at the hosp about her anemia ..they still diagnosed her with bi polar and giving her heavy meds to sedate her .. she's so educated she's a chartered accountant. Unable to even count numbers ..I pray that the doctors can see what I see .and that is she's not a mental person .sh has blood issues ..right now my child is a mess..sh has lost 10 years of her life ..

[@JamesonSharp]

@@nirimalanaidoo4607 I appreciate your comment and story. It is heartbreaking to read. You need to find a Doctor who will listen. It’s a Painful Illness. If a Doctor doesn’t listen? Find one who will. Say “Doctor This is a Matter of life and death!!!” Please no one will listen. This should get you a Doctor who will listen. - I wish you all the Best. And I know things will change for your Daughter. Because you are asking questions and trying new things. That’s all we can do sometimes to find, fix, and Heal our Bodies. Warm Regards, JS

[@jenniferjohnson4677]

I feel bad for you. I know what it's like living with a disability. I have a back problem and sciatic nerve pain. We have to stay strong and keep fighting and make it through day to day. I still support you my friend. Take care!!

[@JamesonSharp]

Thank you Jenn, I am gonna be alright. However Just Have To Keep Fighting. And I advise you do as well. Health and Quality of Life are what you make of it.

[@jenniferjohnson4677]

@@JamesonSharp You're welcome! I'm glad you're doing well. We do have to fight through the rough things in life. I know you are a strong man. If you were strong while being in the military, then you are still strong to fight anything in life especially with your health. I will stay strong and fight too. I am well too.

[@tracyfreddie7899]

@@jenniferjohnson4677 That's so sad to hear you are still suffering from this same situation . Am feeling for you right now, I know of a doctor who can help you get rid of this. He also help me from this same situation , He can also help cure yours permanently

[@karmenr9663]

Thanks for sharing your story. It's certainly very hard when Drs don't seem to know what they're looking for, so the problem just gets worse and worse, and our quality of life goes down the crapper. I'm glad you're on the right path now.

[@seascape1059]

What a beautiful man. We need more people like you in this world. Keep being bold and God bless you! 👌#b12awareness

[@JamesonSharp]

That warms my heart, Thank you for the Compliment. Id love to share the same compliment with you as well. Thank you and be Strong!

[@nibornnyw3185]

It's frustrating when people you confide in think it's trivial because it's so trendy. Weight loss, energy, body building, etc.

[@lisarivers8582]

Your story moved me. I don’t know what was wrong with me I lost the ability to walk pins needles in extremities etc so I have seen a neurologist we are trying to see what is wrong. Brain scan normal. I’m frustrated my methylmalonic acid was really high. Is all I know. I have one more test. eMG so we shall see. But what happened to me was so severe it was shocking. And scary. Thank you for your story.

[@JamesonSharp]

I’m truly happy, any of my mystery and story is impactful to you during your time of great pain. I wish nothing but health and improvement and do reach out if I am able to help answer any questions about this painful disease. Thank you Lisa. 🙏

[@lisarivers8582]

@@JamesonSharp aw thank you so much.

[@osawaruenorense1596]

@@lisarivers8582 hello, what was your diagnose? And how are you feeling now?

[@tyravirkus4322]

What level was your b12 out when you found out ? Mine was at

[@JamesonSharp]

My B12 level in my Blood was High. BUT !!! With that said I knew that something was a miss. I had noticed that taking a B12 supplement was helping just slightly with my nerve symptoms. But still lacking in insufficient. Something in the tablets were causing my Kidneys to feel flank pain. It was weird. So I stopped the tablets. My blood tests B12 results were high. So I had a theory. I recognized even though my blood tests were high, my intracellular levels were non existent. So we tried INJECTIONS. Which made a HUGE difference. I waited along time to get help from a different physician because I was certain I was wrong. Getting that 3rd opinion saved my life. I appreciate you sharing. And stay strong Tyra.

[@tyravirkus4322]

@@JamesonSharp how many shots did you get to begin with ?

[@karmenr9663]

The problem that a lot of people face, and this is where people end up in danger, is that a lot of Drs WILL perform blood tests for vitamin B12 levels... HOWEVER they AREN'T performing the tests for ACTIVE B12. So Drs read the results of the test and say "nope you're fine" and send you on your way. A person can have an astronomical Free B12 level, but it doesn't matter how high that level is, if the ACTIVE B12 level is low, and continues to be low, or continues to get lower over time. That's when the body starts tapping out and produces a LOT of symptoms that can be easily attributed to things other than pernicious anaemia. The amount of drugs, such as antidepressants and whatnot, that are being unnecessarily prescribed to people who don't actually have what they're being diagnosed with, is incredible. Drs need to be made more aware of the importance of requesting ACTIVE B12 instead of, or as well as normal B12.

[@organicfireorganicfire1236]

@@karmenr9663 yup, mine is 267 I think it's too low anyway and I feel like I'm dying , I will test my active b12 now I heard some doctor talking about it too.

[@organicfireorganicfire1236]

How long it took u to get well.

[@nibornnyw3185]

Transdermal magnesium is supposed to help you get b12 into the cells. It helps me in many ways.

[@Justgirliethings6]

thanks for sharing i am a type one diabetic and got my thryoid removed i believe i have this bc of my type one diabetes

[@JamesonSharp]

Take care and do make sure your exercise is up to snuff. Exercise and eating properly do help with the issues. Medication should game planned meticulously to your tolerance. Thank you for sharing. It feels like your being very brave.

[@banzobeans]

8:12 I'd like to hear more about the process of healing and why it was so painful!

[@JamesonSharp]

Sure, when you have a Metabolism, Nutritional Disorder the Nerve fibers are no longer able to generate a coating to cover its fibers. This is very painful and very uncomfortable in certain areas of the body, for me? It was my Emotional state, I can easily seem autistic and become upset. Other areas like your eyes. My eyes have permanent black spots from the fibrers not being covered, my Left leg or thigh area near base of sciatica nerve was damaged. And a few other places of nerves, it’s painful. And it gets better than goes back to being painful. I have accepted this as normal now. And manage with medications here and there. My emotional state is quite difficult sometimes. And my braine’s nerves certainly has been affected. So I do have weird things happen like I will get anxiety for no reason, and sometime I almost fall down because my equilibrium is unsteady. And also if I am exposed to heights I almost fall down from being unable to handle the view of Joe guys in front of me. It’s very strange. It’s a strange illness and it does suck. I hope your pain is not like mine and your life is improving if your Ill. You matter and I’m always here if your sick and need to share. JS

[@banzobeans]

@@JamesonSharp sounds like the pain never left you? Has if gotten better since starting supplementation? I don‘t have much body pain, just neurological dysfunction and psychological symptoms. Lots of weird symptoms as soon as I took my first folate pill two weeks ago. I‘m hoping it's what some call "startup symptoms" and will resolve itself over time.

[@banzobeans]

@@JamesonSharp how long did you have some of these symptoms before starting supplementation?

[@JamesonSharp]

@@banzobeans the truth is this? If you have Pernicious Anemia and are taking Tablet Form b12? You will see a slight difference. However Injections for b12 deficiency are much much much more effective and faster. The illness will take years to treat and stabilize. My pain never left. It only became sporadic. No so constant. I also found I had a folate deficiency. And took tablets to reverse this. It took me 9months to see a big difference in the folate deficiency malfunctions. This is a big life event if you have what I have. And will take you years to get to a place of some normalcy and living with it. I feel it will never be cured. My body tells me I am going to have this illness and never be the same as I was before. I’ve accepted all that comes with this. It’s a terrible situation. However we do what we can and exercise and listen to your body. I’m sorry I am unable to share exact details to cure this illness. I can only share what has been beneficial from my experience. I would probably ask your Doctor to administer Injections. And see how that feels.

[@banzobeans]

@@JamesonSharp Thanks for this! I‘m new to it, will be monitoring from here on. All I know is my folate is low and homocysteine is high and neurological symptoms flared up as soon as I took a small dose of oral methylfolate or folic acid. I therefore assume this is relevant. Currently looking for a doc who might know more about these connections. All the best!

[@caroline8029]

My partner is currently in hospital with his blood levels through the floor. He’s having blood transfusions but his biggest problem is severe chronic pain in his low back which travel down to his knees. Can B12 deficiency cause this much pain? He’s having morphine until they can get to the bottom of the problem.

[@JamesonSharp]

Hello Ms. Caroline, l feel your concern and how understandably upsetting this situation may be to you. I’m sorry their is no easy answers. However if my blood levels were non existent? I would immediately begin administering B12 intramuscular injections 1mcg once a day. If Doctors don’t push this recommendation? I personally wouldn’t listen and do it myself. I have that right. Since Cyanclobalomine is NOT a controlled substance. I hope my opinion on this helps. Much love to your partners struggle. I hope he gets well ASAP. Thank you JS

[@osawaruenorense1596]

Hello, how is your partner? Hope he had gotten it's gotten his diagnosis. Wishing him a quick recovery. Stay blessed.

[@caroline8029]

@@osawaruenorense1596 hello sadly it turned out to be more than a B12 deficiency. It was bone marrow cancer which was crowding out his red blood cells. He spent 6 weeks in hospital but it was an aggressive cancer and he died on 17th September 😞

[@osawaruenorense1596]

@@caroline8029 am so sorry for your loss. Accept my sympathy.

[@TraceyGrainger]

Vit D deficiency causes severe lower back problems...its a very common deficiency world wide

[@dontquestionmyvideos]

Hello sir,what do you mainly eat(Diet),

[@azamqureshi8963]

Since How many month you experiencing eyes issue I have same I issue spots in eyes and light sensitive,

[@JamesonSharp]

Azam, My Eye Symptoms Developed over many months. They did get better. But NOT Entirely. Treatment helped just a little. If you are having problems? Have your Doctor begin Injections right away. That’s the only way to try and stop the downward progression. I genuinely do hope you develop a treatment plan and a Plan moving forward. It’s tough illness. Much love from across the world. Always here if you have questions Good Sir. JS

[@azamqureshi8963]

@@JamesonSharp thanku for your reply, I started inj today, methycobalamin , ur eye issue declining stops or not?

[@JamesonSharp]

@@azamqureshi8963 Azam, Im so happy you start today. That will help absolutely. But everyone is different. Even though MY Experience may be different than yours on the B12 Injection. I can say only my experience. Since you start today with Injections. It may take up to 2 years for recovery. But it wont feel like before. It will be different. IT sucks. Your eyes May begin to stop declining. And may improve. But my experience is My eyes got better only about 5% after injections. But the decline in vision and blackspots stopped spreading to other vision fields. Time will tell with your treatment. Make sure you take up a Physical Activity after treatment and eat healthy. If you don't? You will only have marginal success. I hope this helps Good Sir. I care about you. And I genuinely wish you strength and happiness. Get well soon my friend. JS

[@azamqureshi8963]

@@JamesonSharp thanku.. I facing these issues since 6 month , including kidney issue, like little pain in both side, I study that low b12 can also cause reduce kidney function, so what about your kidneys health after treating

[@JamesonSharp]

@@azamqureshi8963 Yes I had the same problem with Kidneys lower functioning. After about 6months of Injections they get better. However you will likely have permanent damage like me. I have one foot (left foot) that retains water. I also notice my body has electrolyte problems from time to time. If I don’t Drink enough water? My Legs and Calf Muscles get cramps. But after I drink Gatorade or water it gets better. Give treatment of injections time. If needed? I injected myself 1 mcg weekly for 4 weeks. Then I transitioned to 1 mcg injection once a month. And saw massive improvement. I would suggest the same dosage and therapy to you. I hope this helps. 🙏

[@FloopidyMcDoopidy]

OSS!

[@JamesonSharp]

OSSSS BROTHER!!

[@AntarixOfficial]

I am having the same symptoms along with insomnia (muslce twitching and restless legs ). After taking 1500mcg tablets of b12 for a month , my levels were tested and it was 1200 but didn't se any benefit .

[@JamesonSharp]

Doctors often get this Diagnosis wrong. Seek a Doctor who will treat you with a few B12 Shots to see if that corrects your issue. The problem with B12 Tablets over the counter is...They are incredibly hard on your Kidneys. They damaged mine and I could feel flank pain from the Tablets when I took them. Stop taking them. They are not that useful in my opinion. But everyone is different and no one is the same. Your Blood B12 Levels maybe high at the moment. However this is where Doctors get fixated on the blood test even though the blood test is incorrect for metabolizing B12 inside your cells. Even Though your blood test is high in B12, your intracellular is still depleted and possibly having a difficult time reuptaking B12 inside the cells to make them work & function better. This is what happened to me. I needed Injections to stabilize. It took me about 2 years of treatment/injections and continued injections after I was leveled off to get out of the dark hole of being deficient. I would seek a different Doctor share this what I am sharing with you. It may help you. I will also volunteer with you that I do not feel your illness is as progressed as mine. I was having episodes of weird nerve problems and almost passing out. Plus pain in my large nerves in my body and also my vision is permanently affected and so is my mental health. I hope this helps Good Sir. And I hope you keep fighting and do exercise. YOU JUST HAVE TO KEEP FIGHTING!! JS.

[@AntarixOfficial]

@@JamesonSharp ​ @Jameson Sharp Well , I have been having symptoms since October 2021 , which progressively got worse. I got my Vit d and b12 tested back in November , 2021 ( 25th) . Since I was taking 3000 mcg of vit b12 per day , my levels were 1300 but my vit d level was only 6ug/ml ( another culprit lol ) . So on the 2nd of December , I was given a 600,000 IU megadosage of vit d followed by 5000 IU per day for 2 months which im still taking . Some of my vit d deficiency symptoms improved like I no longer have anxiety or palpitations but vit d made my insomnia worse . I started having these weird sinus and cluster headaches along my sinus + eye region . While this was going on , both my legs and left arm became number and as of Jan 24th 2022 , I am struggling to walk . Since its the pandemic , I work from home but since my docs ignored my symptoms and diagnosed me with anxiety and depression , they dont even take me serisouly :( Im 23 years old and I hope that I can recover from this . I shall be having my updated vit b12 and vit D tested but this time I shall get my Homocysteince , CBC , ESR , Liver and kindey tested too. My eyes are super dry and eye sight is getting worse while my face recently started getting numb along with my tongue plus Im finding it difficult to speak :( It feels nice to see people like you fighting and working hard to stay alive and its an honour to speak to you :D Is there any other way where I can contact you ? Like FB or instagram ?

[@karmenr9663]

Make sure they also check your ACTIVE B12 as well as the normal B12 tests. Also, if you're suffering pernicious anaemia, you will find that oral b12 supplements will not help much at all. Although it might help a little. PA sufferers are not able to absorb B12 through the stomach lining, as the stomach doesn't make enough intrinsic factor, which is what binds the B12 so that it can be absorbed through the stomach lining. Injections sort of side-step this problem. Hence, they are more effective at getting, or keeping, the levels up where they need to be.

[@osawaruenorense1596]

@@AntarixOfficial hello, how are you doing now? Hope you are getting better. Prayers for you.

[@reneeraw6927]

@@JamesonSharpThis video just may have saved my life. Neurological symptoms for many months now. Here is my question: If B12 Vitamins are hard on your kidneys then aren’t the B12 shots also hard on your kidneys? What’s the difference?

[@charankumar9685]

Hi iam having similar symptoms like you fatigue black spots in eyes nerve pains shortness of breath forgetfulness but doctors are saying it as depression and pareital cell antibody is positive i went to 20- 25 doctors they are not recomending me b12 injections.

[@JamesonSharp]

Immediately start injections on your own. I would share you should buy it online and buy a syringe and start treating yourself. You have that right. I will share a link I used

[@JamesonSharp]

perniciousanemia.org/b12/injections/buy/

[@charankumar9685]

@@JamesonSharp ok thank you so much

[@JamesonSharp]

I sincerely hope you start feeling better soon. It’s likely going to take years at this point. Nothing but love to you Mr. Kumar. ❤️👍

[@charankumar9685]

@@JamesonSharp can u please tell me how much time does it takes fatigue to go

[@hmtoalharbi3874]

I've had signs of vitamin B12 deficiency since I was 19, now I'm 25 and I think I'm kind of critical. How do I know that my body is not absorbing. Note that supplements help slightly.

[@hmtoalharbi3874]

First, there was amnesia, tremors in the hands and eyes, and premature graying until I reached frequent drops in blood pressure. By 2019 my vision and movements became weak. I have slow reactions and digestive problems such as heartburn, loss of appetite, nausea and constipation

[@hmtoalharbi3874]

after taking 90 days of b12 supplements with b6 and b1 i got my first result as 206

[@hmtoalharbi3874]

They told me, it is possible that you have poor absorption of vitamin B12, and are injections somewhat safe?

[@hmtoalharbi3874]

How do I know that I have poor absorption? I'm curious because I'm confused. How did you diagnose malabsorption? Please Help

[@hmtoalharbi3874]

Note: The supplements was 250mcg only

[@tinyty6570]

Also they said no to pernicious anemia since they did one test for it and was negative

[@JamesonSharp]

Thier is no harm in asking another physician for a second opinion. This thinking and advice saved my life. It may save your as well. Doctors can never agree. Neither should you. 🙏 🙏🇺🇸❤️

[@tinyty6570]

@@JamesonSharp this doctor is my second opinion unfortunately. My insurance seems to give me clinics and people who don’t seem to know about b12.I tried a hematologist but she was really rotten to me and gave me 10 minutes and didn’t even hear my symptoms she didn’t ask just said I deal with iron issues only . I guess I wasted her time

[@theOlLineRebel]

My onc/hemo said it was just as good to use OTC supplements under the tongue. Is this really just as good as shots? (I have tried it for 2 years now and am just this week having terrible symptoms that won’t let up after just letting the supp stop. Since I have no ileum from right hemicolectomy 9 years ago, have high risk.). Since it’s OTC, do we even know if one brand is as good as another?

[@JamesonSharp]

I feel your Pain and Struggle, in my opinion Supplements are not worth the bang. If I found myself in your situation? I’d very much much inject myself once a month Cyanclobalomine 1mcg to see how that feels. I bet that makes a big difference in how you feel. Eat a strict diet of 1 apple a day and exercise 2-3 times a week and your life will improve. I’m very certain of this formula as it works for me. Injections in the Intramuscular are the only way to go in my opinion. 🙏

[@nibornnyw3185]

Laboratory supply sells pure b12 chrystals. Amazon sells sterile saline. Walgreens sells syringes with needles and alcohol swabs.

[@azamqureshi8963]

You have sensitivity to light in your eyes?

[@JamesonSharp]

I did have sensitivity. Now my vision has slightly diminished. Meaning…night time vision is no longer as focused and bright as it once was.

[@azamqureshi8963]

@@JamesonSharp my light sensitivity is worse I drive bike and car comes in front of eyes then very bad light reflects in my eyes, so after the treatment the sensitivity is get improved or not? If I get releive in 50% light sensitivity then I thanks to God, and I completed my 5 injection yesterday and it worses my eye symptoms, light floaters , blur vision and black spots and some time eye pains and corner nerves of eyes is vibrating, I'm very scared of my eyes, getting worse, do you get these effects during treatment, ??

[@JamesonSharp]

@@azamqureshi8963 that will depend on your bodies acceptance of Treatment. Your different than I am. And Honestly you will have symptoms unrelated to mine because metabolism is different in everyone.

[@azamqureshi8963]

@@JamesonSharp ok i will keep trying, it gives relive in fatigue, and mental confusion, depression, confusion I hope it will give relive to others symptoms also. Wish me good health. And what is your age bro, healing depends on age to and one more things I think this injection makes my sugar spike as I noticed something after I eat meals. I think this injection makes me diabetic what your story on this?

[@nibornnyw3185]

B1 helps with the light on your eye thing.

[@Heddyconfetti]

Sorry for your suffering, but you're lucky you only suffered for a year before figuring it out. I am in year 9 of severe neurological issues that have been constant and now progressed to epilepsy. I have trouble walking. Not a single doctor suggested b12/ folate deficiency - they would rather assume I have mental illness. (Until the seizures were finally proven). Also you are lucky your B12 deficiency showed on bloodwork. Sometimes b12 can test normal because it circulates in your blood, but your tissues cannot absorb it. I suspect this deficiency based on the fact I have some genetic mutations that predispose me to impaired metabolism of b12/ folate. It's probably too late to reverse the damage done this past decade.

[@gameage198]

How often are you injecting B12 Now..?

[@JamesonSharp]

Personally I inject once a month. However my regiment is not the standard. When I began injecting Cyanclobalomine it was once a month. But this was not enough. So at about 9months in? I went on a regiment of injecting once a week for almost 4 -1/2 weeks. Then back to one eye a month. That 4 injections lifted me up out of serious nerve damage. But did not cure me or leave me without damage and disability. I struggle daily with my nerve problems and psychiatric changes. Nothing is ever complete. But I have noticed something bizarre. But deadly serious. I must routinely exercise. Or I will die. Meaning my body begins malfunctioning normally and in other crazy metabolic ways. I feel my big toe gets gout if I have NOT exercised or worked out enough. But at least it’s a warning to keep it moving and be vigilant about caring and training my body as a Fighter in MMA activities. I hope this is insightful and I’d be happy to be helpful in any way possible. I wish you the best Good sir. Thank you.🙏

[@MaaikevanBroekhovenIBCLC]

Once a month only???? I need every day!! Try at least 2xweek. Which is the way with neurological damage 2 years. You can do better!!!! B12 methylcobalamin and adenosylcobalamin injections saved my life. I'm on carnivore diet to maybe tackle the autoimmunity or whatever I don't absorb.

[@planetbspace]

I get a shot every day. Once a month is starving

[@JamesonSharp]

I found out Recently my Folate was extremely low. Always have your Doctor check this in Tandem. I’m very Happy your Daily injection is working. 🙌 Cheers to Good Health! 🙌👍 JS

[@tinyty6570]

Hii! Good video! My b12 was only at 58 a few months ago I’m 24 years old they are giving me injections once a month but I’m not feeling better any ideas? They don’t know what caused it as I’m not vegan and they did a endoscopy didn’t see issues … I take folic acid once a day and try to eat potassium rich diet Not feeling any better The lightheaded feeling won’t go away as well as Visual disturbances and energy level . Other symptoms too but those are the top 3 worst With major Brain fog following right behind

[@JamesonSharp]

Good Evening Tyler, Im so sorry your having illness. I can only share from my experiences which were very dire. I feel like from the description you shared you should give the treatment time. I would suggest to your attending personal physicians to try Micronutrient Blood Tests. Id also begin Exercising or finding a activity that keeps you active. Because in all seriousness I had to force myself to train Brazilian Jiu Jitsu in order to get my body's functions moving. It took me literally 1-1/2year to get better to a point where I could tell I had no more arrythmias and attacks related to metabolic panic. I know that is weird sounding but if you are deficient you will have "EPISODES OF PANIC AND WEIRD BLOOD PRESSURE PROBLEMS" Anyways exercise, seek additional help or opinions. BUT LISTEN TO YOUR BODY!! Your quality of life is what you make of it. It's will be painful moving forward. But Commit and FIGHT!!! Much Love To You. And I feel your pain. Here anytime. JS.

[@tinyty6570]

@@JamesonSharp thanks for the quick response wow! I would excersise but it’s dangerous to do so at this point My b12 was critical told me I would of been in a wheelchair or dead if I waited another month to get those results I’m extremely lightheaded every day so I can barely walk and definitely no excersising I been on injections since June of this year Did you feel worse on injections for awhile? I have weird panic and weird times where I am more faint feeling than others and balance gets strange . Vision is very off lately I can’t describe it and I feel in a dream like state almost like I drank alcohol My feet go numb at times , rashes a lot , thrush in mouth , soo lethargic My skin colors changed in face I went to my doctor he wasn’t helpful. I got the injections once a month at least but makes me wonder why this happened and if I’m gettimy enough shots I want to live my life again , I lost my job over this illness I need to start eating better at least and just keep at my injections and seeing doctors I love your positivity though man !

[@JamesonSharp]

@@tinyty6570 Thank you, and Just keep fighting. Here anytime.

[@karmenr9663]

Are you in Australia Tyler ? I'm not too sure about other countries, but I know in Australia you can buy the B12 vials, and syringes required, over the counter at the pharmacy. Maybe give that a try ?? 🤔

[@tinyty6570]

@@karmenr9663 I’m in the US they are very strict can’t do that here My doctor did just increase it though I’m hoping it works

[@prathamrballal1229]

Did u had heart beat issue's

[@JamesonSharp]

I absolutely had a Heart Arrhythmia issue, and because my anemia was so bad I had issues with breathing. And also because my blood was super thin, my hemoglobin was affected. I also had over hydration problems at times. This caused an issue with my Potassium levels and functions. My kidneys were affected and sometimes ached. My arrhythmia episodes lasted for 2 years. My arrhythmia was terrifying it would happen out of nowhere. Please be in tune with your body’s chemistry, educate yourself on the metabolic changes. And do seek parental b12 therapy from your Doctor. If your Doctor doesn’t listen while you explain your illness or keep your future therapy satisfactory for you? Fire THEM and seek a different physicians care. Not medical advice just my course of actions i have taken in my illness. Be STRONG Sri. ❤️

[@prathamrballal1229]

I have so many symptoms like high heart rate after I stand up, maigraine, breathing issues, palpatation, tremors, weekness, anxiety, panic attacks, week legs, bed ridden after covid but in India they give anxiety med nothing else I do have low b12 and pots disease

[@JamesonSharp]

@@prathamrballal1229 I Feel Your Pain. I would find a different Doctor. Do whatever is necessary. I wish you health and improvement. After taking shots you will get better. The symptoms will graudally go away over a year or 2 years. Im so sorry your ill. Warm Regards from USA.

[@prathamrballal1229]

Did u had same symptoms including balance issues while walking?

[@JamesonSharp]

@@prathamrballal1229 "YES" I can make you a Promise that will never be broken. If you grit your teeth find a Doctor to administer B12 Shots to you. You will improve. Its going to be very tough, extremely painful and just terrifying at times. Your body will feel very weird. You will feel completely helpless at times. It will feel uncomfortable, But trust me when I share the light will shine brighter every month.YOU MUST FIGHT!!! Improvements will seem very very slow & Incremental. But keep staying the course and be fierce Sri. I care for your future. You can do it! Remember to do these three things to improve quality of life. -EAT HEALTHY -Eliminate almost all sugars if you can. -EAT GREENS AND MORE GREEN Veggies -EXERCISE find something like Dancing to be active. Its a great workout. I dance from time to time. And surround yourself with health minded friends. -Listen to your bodies chemistry. -Stay Positive don't allow your inner voice become malignant and dark, do not give into your temper. These personality changes may happen where you feel unable to read or process other peoples emotional states. -Medicate yourself with Parental Cyancobolamine IM Injections under a physicians care. Find a Doctor who listens and will give you these. Your life depends on this. If they don't listen? FIND A DOCTOR WHO WILL. Or find the Cyancobolamine yourself. This is all I can give at this time. I believe you will do this and thrive.I am here anytime. :-) JS