Видео

❤

Thank you so much for sharing. I hope you feel better soon

Hi do u have an email? What do u mean by taking mestinon as needed? Do u take it daily? Did u have ur thymectomy immediately after being diagnosed ? Does your fatigue go away after taking mestinon?

Thank you.🙏😘

Warrior Queen.👑🔥🙏😘

How have you been? I’m thinking about getting a thymectomy but kinda nervous. Would love to get an update on your symptoms. Also how long did it take for you to see an improvement post surgery?

Hello, Like to know after these years how you doing now. Any update with MG. Did you able to get rid of . Please update. Thanks;

How are you doing now?

Thank you for sharing your story:)

So I been diagnosed with Myasthenia Gravis back in like April or May and I’m up for thymectomy in September. The only medication I take is Mestinon and I have had two Rituximab infusions and two series of 5 PLEX plasmapheresis. I’m currently waiting on a alternative medication called LDN ( low dose naltrexone. I been told that the chances of my remission is high. I hope I can say I used to have Myasthenia Gravis.

My brother Atson had myasthenia gravis since 2015. He got medically discharged out of the Army, a job he loved well. His heart had 5 myasthenic crises, 3 being severe enough to be ventilated or require CPAP (continuous positive airway pressure) helmet. He have had countless plasma exchanges as his veins are bad. He also needed Hickman lines inserted, he have been on azathioprine, mycophenolate (CellCept), methotrexate and none have worked. He is currently done with his herbal remedy I purchase from totalcureherbsfoundation .com which has totally cured his condition with a surprise after almost four months of their usage, he was discouraged and never thought he would be myasthenia gravis (MG) free ,to me the best to get rid of this condition is totalcureherbsfoundation com treatment because all medications we used never worked include mycophenolate (CellCept)

Have you been having episode of your voice changing ?

I will try & do an update for you guys who follow my channel; I’m in the best of health nowadays. Take care & God Bless you all!!

How many incisions do they make? 3 or 4?

See RUclips.com Myasthenia Gravis symptoms disappear. This MAY be a cure - 90 days - 70% improvement in MG - 90% shrinkage in tumours. "7 X more oxygen/Better Breathing, its free, simple, 2 min. try on phone, call me 905 642 2689 Bill Allen

See RUclips.com Myasthenia Gravis symptoms disappear. This MAY be a cure - 90 days - 70% improvement in MG - 90% shrinkage in tumours. "7 X more oxygen/Better Breathing, its free, simple, 2 min. try on phone, call me 905 642 2689 Bill Allen

The following information is free and may be of great interest to those suffering from Myasthenia. Please see story online “york region bill allen”. When my newspaper story came out online Dec. 6th., I received a call from Anna Abramian who has two cancerous tumours in her breasts, and has Myasthenia Gravis (a muscular disorder). She had started chemotherapy in late Nov., and came to my office on Dec. 8th. With only three high oxygen breaths she got the following relief from Myasthenia symptoms: - her partially paralyzed jaw, tongue and mouth loosened up. - her double vision became crystal clear and droopy eyelids disappeared. - strength, feeling and blood circulation returned to her arms and legs. You cannot imagine the shock and relief she went through. She continues the breathing routine to this date. The blood circulation improved all over her body, from a little extra oxygen and as of this date she estimates that her Myasthenia has improved 70%. The next time she went for her chemotherapy almost all of the usual side effects: nausea, vomiting, sores in mouth and nose, numbness, cramps, pain, paralysis; didn’t occur. Nov. 28th. - 1st. chemo - Lg. tumour 42 sq. cm., sm. tumour - size of finger tip Dec. 19th. - 2nd. chemo Jan. 8th. - 3rd. chemo - Anna lost 6 ½ lbs., tumour 1/3 the size (14 sq. cm.) Jan. 29th. - 4th. chemo - Anna has lost 9 lbs.- Lg. tumour now 8 sq. cm. - Oncologist exclaimed “Wow” - said he had never seen anything like this. This date Oxygen 100%, heart rate 78, blood pressure 117/78 (her B/P was 177/110 in late Nov.) Anna started her next series of chemo this date - Jan. 29th. - The nurse said to expect her finger nails to turn black and her hands would have to be put in ice water for 20 minutes. It wasn’t necessary. Anna has had little or no side effects. Feb. 16th. Tumour is now 1.25 sq. cm - 97% reduction in lg. tumour in 12 wks. small tumour gone - has lost about 17 lbs. Feb. 19th. 5th. chemo - almost no side effects I would be glad to demonstrate over the phone, how you can take these simple breaths that add 10 times the oxygen to your blood and we will see if you get the same results as Anna. Please call me - again it’s free. Bill Allen Info@wholesalehousing.ca Tel. 905 642-2689

How long were the hospital stay after the surgery?

Thanks for the video. If you are interested I will subscribe to your channel if you subscribe to mine. My channel focuses on life, health, education, and living in ketogenic lifestyle. I hope you enjoy, like them and subscribe.

Hi Lauren, Happy New Year. Thank you very much for sharing your experience. May I ask you how you are doing with the symptoms. I have to go for the surgery in March this year. I would like to know if that is going to help my condition. Please let me know.

I just had plasmapheresis for Transverse Myelitis .they put my catheter in my neck and looked crazy . I m still in hospital for rehabilitation now .the condition left me paralysed from waist down .it’ll be 7weeks on Thursday. Hope you are doing well?

THANK U FOR SHARING YOUR STORY

This video was really great and informative. I'm considering plasmapheresis for my mg and was curious what other patients thought of it. I hope you're doing better now! <3

So glad to hear that you are doing well and that you are off of your medications! Continue to stay blessed and share your message!

How is your myasthenia doing? Im thinking of having a thymectomy and kinda scared.

They finally have. 3 shades for WOC. 👍🏾

You go girl, I have a thyme to my, and now I am on prednisones and Lyrica. I'm a little older than you but I believe you must move move move. Kudos to you. Larry Texas

ok I saw the pictures it doesn't match but your skin looks amazing

but they do need more shades

it looks really pretty on you

Blessing to you. Thank God for your continuous healing in advance. ❤❤

I had the same issue but I mixed the foundation with a darker foundation I have from NARS n it works wonders. It's really good makeup. But you still look beautiful dear. Stay blessed.

Thanks for the video. I have a darker skin tone and I don't wear makeup at all, but I was about to try this. I am looking for something natural looking, but I think the rich is a little too light for me. idk, this make up thing is so confusing....

i thought it was pretty on you

But me looking at your face after it's done it looks very pretty and you can see a huge difference I'd like the product I am about to order your tone is glowing right now I guess you just can't see it it looks very pretty and I'm not just saying that the product really do work from the looks of it I think I am about to order

I think if you try it again it might work I think as you put it on with the cloth you're also taking it back off at the same time that's probably why it might not be working for you try using your fingers as you use your fingers it just smooths into your skin as you rub it but using a cloth is like taking the foundation moisturizer back off your face and you're not getting that coverage that you want try using your fingers again Doll

I Love the Real girls! The pictures and the Video were Great! I believe IT will introduce more colors for WOC...

Dermablend and Fashion Fair hands down best for WOC...

my son is only 16 and will be starting this very soon, all the other treatments did not work for him, the surgery, the ivig, oral medications, this is his last result

Did the health insurance cover it without any problems? The IVGs does it also cover it? It's december now have you felt a huge difference by now? if so in which way? I have a niece who has MG and we are thinking about doing it too.

I also deal with Mg , give me a call 806-790-4944

Hi it feels great to see other women with the same condition I was diagnosed with MG when I was 9 yrs of age it's been a rollercoaster I was in remission about 4 yrs after I had my kids and while being pregnant it flared up my youngest is 2 yrs old and it's like my mestine isn't working my kids have Autism my pregnancy was very high risk I'm thankful to god they are here I just hope god keeps me around to at lest see them grow prayers to u and everyone withMG much love

Hey lauren I have Myasthenia Gravis as well and every time I get any treatment I get benadryl and Tylenol. Hope all is well for you.

Hi I also have MG have you tried pyrostigmine med. It works for me.

I Watch your videos and I don't feel alone!!! had my thymectomy in 1998! I sure wish I would've had mine now because I absolutely hate my scars. Cellcept didn't work for me, nor did Imuran. I did plasmapheresis for about 6 months, but I had an unexplained seizure that was stopped immediately after. But IVIG has been the best along with 2 mestinon pills and prednisone (which I seem to not be able to get off of). In the beginning I was on 60mg one day and 40mg the other so weight gain and hair growth have been a really big issue. But as of now I'm doing pretty well considering the journey it took.

hi, im glad hearing that you working out. that's a progress right there. me myself im battling with MG since 2006 together with rheumatoid arthritis, trust me thats a combination nobody wants. ive decided from day 1 after being diagnosed to throw the mestinon away after reading about it. and for my RA pain ive been taking anti inflamatories painkillers. one thing that makes me sad above all the pain and limbness weakness, is my damn droopy eyelids. makes me wear dark shades everywhere i go even at nights. lately ive been studying alot about natural cures for both of my illnesses and i came across cannabis oil which i started using last week. now i must say i dont feel any arthritical pain since the second day i used the cannabis oil. i suggest you to do a research about the oil as they say it heals everything even high level cancers. the other natural remedy i came across is the mineral borax/ boron. i started using a boron supplement for 5 days and i must say im starting to feel way better feeling less weak in my legs and muscles. im looking forward to start using a purer form of borax. i suggest you to read about the borax cure and consider to try it out, before you go ahead and start with the steroids. the steroid use just dont sound right imo. cannabis oil and borax. read about them and give them a try. natural remedies that cures all deseases. god bless you and your family!

im a MG patient combined with RA. i was just wondering whats your update on your MG symptoms. thank you and take care

Lauren, thank you so much for sharing your story. My older brother has Type 2 Diabetes and just 3 months ago was diagnosed with MG. We're trying to research all we can about this disease. He will be starting plasmapheresis tomorrow. Will keep you in my thoughts and prayers ... sending positive vibes your way! :)

Mestinon sucks for me, I have spasms, difficulty speaking, tearing up all the time. MG got so bad with me that I was loosing all body control. Sucks when your dinner lies in front of you on the ground ;) But MG got better and I even started working out and am ripped now, just keep on fighting. Don´t want to do surgery as well.

I am 19 and I have just been diagnosed with MG. You are so strong and I hope this procedure runs your MG into the trash ASAP! Thanks for sharing your experience (not that many videos about thymectomies on here). Much love, God bless you. xoxo