Ozone ear insufflation ?

Maybe just maybe one day they will have a cure for all the awful diseases of cancer😢. It's a silent killer that kills so many ppl. Just when you fight n beat another form of cancer. Another comes to rob n steal you of blessing n life.

I turned up my volume to the maximum and it is still very hard to hear you. Please fix your audio function on your next presentation.

In January of 2023 Drs found, by chance, a massive meningioma pressing on my frontal lobe. I was life flighted to Shands Neurological Hospital, died twice in the helicopter, for emergency brain surgery. They couldn't get all of it.

I have had a brain tumor on my pituitary gland. I had a cystic component in front of my head. They put a ommaya reservoir to drain off the fluid. I had surgeries in 1989-1990 respectively. My brain tumor cystic component is growing again after 30+ years. I hope i get surgery through the nose, if they ever have to do surgery again. I had the gamma knife to stop the tumor in 1990. Luckily, i was 24 years-old, when I had my brain tumor and I didn't have gianticism.

Nice video! Thanks but I want to know what the hell does treat mean exactly? Does it completely get rid of the tumor or just shrink it? At least eventually? How long does it take best case scenario?

Thank you you’re great ❤

This is amazing, thanks

I loved your Cushing’s moon face impersonation Doc 🤣🤣 ✌️ My son needs to go for an MRI, GP thinks it could be pituitary adenoma!

What would you suggest for a 76-year old woman with 2cm big olfactory groove meningioma with traces of calcification? Thanks!

Interesting

Don't discriminate no matter the circumstances there is always a way out of any situation because with God all things are possible a big thank you to doctor Pius Ozigbe herbal home for helping me get rid of herpes virus and making the world a better places!!🎉❤😮😮

Does anyone knows what side effects will one get after the surgery? Will one have to be on a wheelchair for life after the surgery? Mine is pressing on the optic chaism and currently it's affecting my left vision and slightly on the right also. I'm so afraid of going for the surgery.

I had the same radiotherapy 3- D COMFORMED THERAPY IN RADIOTHERAPY YEARS AGO IN 2015 LINAC THERAPY OF RADIOTHERAPY IS ONE I HAD DONE.

Had gamma knife 20 years ago. AN or VS is now is very small and I've had no negatives from GK in 20 years.

Very insightful thank you

You included a lot of the basic information but you also left out a lot of information. Not everyone goes for extended radiation therapy. Sometimes only one treatment is required. And the brain tumor that's being treated is not the kind that metastasizes. Sometimes the tumor being treated is benign. I have an acoustic neuroma. It only required one radiation treatment. It was a large dose administered all at once. That is the only way to treat an acoustic neuroma. I was hoping that this video would mention side effects but it didn't even get that far. It's very frustrating when your doctor is very vague about side effects. So you don't know whether or not you are healing in a proper manner because everyone's healing process is unique to them. So that makes it harder to know if what you are experiencing is what you should be experiencing. I had my radiation treatment a month ago and I'm still having side effects. And I don't even know if that's normal. Or even if there is a normal in this type of situation. Nobody can give me a straight answer. And it's also going to take a long time to find out if the radiation treatment actually worked. Not until after I have two MRIs that can be compared to each other and that can take the better part of another year. In the meantime I don't have any idea whether or not the tumor is still growing or if it's totally shut down. and there's no way to measure that. I feel totally helpless in this situation.

I had stereotactic radiosurgery for a benign brain tumor but I didn't have any of these types that were shone. I had to have the mask made which held my head in place. The machine moved around me after it was programmed by the doctor and the physicist. So I'm not sure what the type of radiation was called or what kind of machine it was. But the machine was able to do a cat-scan first and then to do the radiation. Whatever part was giving the radiation moved around me and it delivered it in two different times and that took about a total of 5 minutes and that was the only treatment I received. I think it may have been called a photon beam but I'm not sure. It's only been about a week and I'm still having really bad side effects. I haven't even been able to return back to work and I see the oncologist in another week for check-up. And to find out if I'm healing properly. I haven't felt well since the first day. I wasn't even able to take the steroid drugs that were offered to me because I had a bad side effect from those so I had to stop.

What a wonderful doctor he is. I love the way he explained the. I am recently diagnosed as incidental. mine is cavernous sinus 2.5 x 1.7 cm . Thank you so much for great explanation. It helped me.

I was just researching this and Dr Cobbs poped up in my search surprisingly…Hr operated on me September of 2006 at cal pacific in sf…He is a passionate man about what he does and extremely hard working…

I take Bromocriptine for mine, as I couldn't afford Cabergoline. And wow...this tumour difficult to deal with sometimes, hormone wise... I have the rare case of producing testosterone as well. As my Endocrinologist would always check my face and chest for hair growth...fun wow! I am female. I was diagnosed with a prolactinoma...Pituitary micro adenoma. I also have low blood pressure and can find myself in a bit of a pickle with fainting/passing out. Some of my symptoms prior to diagnosis were: Hyperhydrosis/excessive sweating, super intense headaches, peripheral vision loss, breast milk production (long after being pregnant), weight gain from pregnancy (hypothyroidism) and the opposite Hyperthyroidism (weight loss)...been super skinny most of my life...until I became pregnant...then my prolactin levels went through the roof as well... When I first went on Bromocriptine, my weight went back to normal. Now that I am getting older, everything is changing yet again. 🙄🙄🙄 I was told if I did the surgery, through the nasal cavity (left), that the chances of it regrowing were extremely common and that it would. My next option was to have the entire pituitary removed and take synthetic hormones. Anyone with advice or natural supplements to cope with adverse affects would be greatly appreciated. Thank you, Kelly from Ontario Canada

How long do patient has to take the medication to treat functioning prolactin tumor. Do they have side effects? Are the safe for person who has chronic hep B infection? Is surgery better then taking medication if tumor is 6x4 mm. Does surgery has long term effects? Whats the average cost of surgery and medication? Thank you 🙏🏼

I have had been diagnosed with meningioma , but the doctors want a 2nd option to ensure if it was benign and the doctors told me that my meningioma maybe the cause of why im having seizures

I’ve been having severe headaches (migraines?) so they did an MRI. I have one of these buggers, a parafalcine meningioma on the right falx of my brain. I’m having 4-6 severe headaches a week. They’re just too much. The tumor is still small. I do have a history of Neuroendocrine Cancer that originated in my right mainstem bronchus. I’m still waiting to see if the Neurosurgeon is even going to see me. I’m a Medicaid person. 🙄 Sadly I became disabled from all the operations I had to have on my lung, chest wall, and airway. I’m 54. Quite frustrated at the moment, because I feel like the docs just don’t give a 💩. Sorry, just being honest. I feel like if I had traditional insurance I already would have had my consult. I was prescribed Imitrex for the headaches, but that crap was hurting my kidneys. So, at the moment I’m just stuck. You probably won’t see my comment, but your videos have explained so much to me, and I’m so thankful and appreciate you taking the time to do this. God Bless. Sam from Utah. 😊

wonderful video - thank you!

This Dude is riding the Cancer money train like all the rest.

To bad they never bring up the effects of radiating the brain long term with cognitive functions of the brain and long term damage of necrosis caused by radiation.

What are the chances of getting another new mengioma?

I really wanna know what the difference between big tumor and a mass . I just have a MRI done and they found him 12 MM mass on the right side of my brain no one seems to me ever answer me

I'm dizzy as he'll right now ,

I am going to be the one that goes in and comes out cancer free I have no doubt let’s dance bitch

I had my tumorr adenoma removed . The best organic hormone replacements for a female

What are your thoughts on a pituitary tumor that is resistant to cabergoline? My tumor has grown about 1mm per year. It’s about 10mm now. I’ve also had open heart surgery on 2 valves, and I’m sort of leaning towards just removing it. Thanks for your insight!

What happens when the glioblastoma becomes resistant to the Temozolomide?

Mine grew 3mm in 4 years. So watch and wait for me.

I had a pituitary tumor, a spindell cell oncocytoma, but they didn't perform this procedure for removal. For me, the surgeons went in through my skull. I truly wonder why. Maybe it was due to the tumor type. It's been 4 years now and I still have some issues related to the surgery. I still have a "soft spot" and a big scar where they peeled my scalp back to get to my skull. I was off work for 18 months, mostly because my memory was terribly affected in a bad way. I also became diabetic after the surgery.

how do you figure out the growth rate of the Meningiomas tumor Dr. Cobbs referred to in the video? Do you need a small surgery to get part of the tumor out for pathology?

I have the unmethylated glioblastoma. I was told and read chemo wouldn’t work on unmethylated. I took it for a year and my tumors are still gone at 19 months. Why are mine not coming back?

For future watchers, a little bit of hope (I can tell I really need it when I was diagnosed): 6x6x6cm grade 2 meningioma in the frontal top left side, fully removed 4 years ago. No symptoms, no side effects. 100% normal life after the 3rd month after surgery. No recurrence so far. From the UK, the team that managed my case: Dr. Kevin O'Neil & team. I will always be in debt!

For future watchers, a little bit of hope (I can tell I really need it when I was diagnosed): 6x6x6cm grade 2 meningioma in the frontal top left side, fully removed 4 years ago. No symptoms, no side effects. 100% normal life after the 3rd month after surgery. No recurrence so far. From the UK, the team that managed my case: Dr. Kevin O'Neil & team. I will always be in debt!

Hi,,, one year ago have a right perasagital meningioma surgery done ..biopsy report grade 1.now i am pregnant 24 weeks. Plz tell me grade 1 meningioma can regrowth during pregnancy... Plz reply

This was a great watch for me, thank you. You have really explained all of the issues I have with my tumour. I am so very thankful. Sending my kindest regards Claire xxx

IL be having surgery to remove my second pituitary tumor. I've lost vision and now have kidney failure.

thank you for the explanation

My boyfriend had glioblastoma and he was not allergic.

I was just diagnosed with pituitary tumor that was discovered through a MRI Next step is more blood work to determine extent. My testosterone levels are far too low for an adult male is why MRI was advised

Surgery ‘not worth it’ for 80 or 90yr olds……..

In a nutshell: TMZ is more effective if MGMT is inactive. MGMT becomes inactive if its promoter region is methylated.

Can I have your email to send a result of CT scan so as to get what the result is really about ?

Hello Stanford, I have had a pituitary tumor since diagnosed in Rutland Vermont on May 12, 2003. The PC and also Dartmouth neurosurgeons said it was too risky to do transphenoidal and that I would have serious problems. Since living in Burlington Vermont, any time I have complained about the tumor, which is now a macroadenoma, since 2008, noone will do even anything at all here at UVM medical center in Burlington. They have told me not to worry about it, be lucky it has not killed me, or BS that pills will boost sugar levels. I appealed to neurosurgery directly and they had patient advocates call me. Nowhere. THEY WILL NOT DO ANYTHING. I have all types of symptoms in which they said is a mental problem. Lots know here but noone cares or not their problem in Vermont.