I suffer from secondary Sjogren's overlapping rheumatoid arthritis and lupus. My POTS symptoms have caused me to be unable to function without constantly needing to lay down and catch my breath. Heart palpitations, migrain head aches, diarrhea, vomiting, gas, sciatica, fibromyalgia, brain fog. I have not worked in more than 6 months, I live alone and do not have any financial support. I am being evicted and can't pack my house or pay for all my medications. I recently filed for SSDI. it is taking a long time to be awarded. I don't sleep well. It is after 3AM. THIS video was an answered prayer!!!!!
Oh wow, appreciate you sharing this here Jonna for watching our video! We have some many resources about these issues - trainings and case studies. Do make sure to join our group if you're on Facebook for more info www.drmaggieyu.com/transform and send us a message too m.me/maggieyumd?ref=w14110934
For the POTS, if you haven't already, try wearing compression socks even while sitting. That way when you stand, it helps reduce the effects. And also squeeze your hands or a stress ball for at least 20 secs before standing each time. These have both helped me a lot. It also helps to have other electrolytes, not just salt. Ex: cucumbers with lemon and salt, salt and vinegar is better than just salt alone (just a note, these can sometimes bother your stomach if it's sensitive like mine, but they can be good quick pick me ups when you really need them).
After 3rd child autoimmune hit me with Hashimotos to Lupus and Sjogrens. It's been 20 years. Periods of remission. Episode of Lyme. Side effects from meds cause secondary problems and toxicity.
I HAVE BEEN SUFFERING WITH R A GOING ON I BELIEVE LIKE 3 YEARS I DO EVERYTHING I CAN WHAT THEY TELL ME TO DO MY DIET BUT WHERE I LIVE AT I HAVE LIMITED RESOURCES I CAN SURE USE YOUR HELP LOOKING FORWARD FROM HEARING FROM ONE OF YOUR TEAM MEMBERS THANK YOU AND GOD BLESS
It sounds like you've been through a lot dealing with RA. Finding resources and support can make a big difference. Speak to us live via text at (503) 647-4568
I hear you, would absolutely love to help you address this! You can get started by live chatting with our team at (503) 647-4568. I would also recommend watching this video on an RN who dealt with both Sjogren's AND lupus and is now in remission th-cam.com/video/CWBpXRqFKdM/w-d-xo.htmlsi=IcOxFub-B5N3CxCu!
Hey Michelle! We would be happy to help you address your symptoms further. You can live chat with our team at (503) 647-4568 to get more specialized help and to learn more about the different solutions to autoimmunity that we offer.
I’m dealing with what I think is lupus. It’s getting worse and I’m seeking answers. My next step is to see a functional doctor. I’m very discouraged. My life has changed so much because of it and not for the better.
I'm sorry to hear about your struggles with what you suspect is lupus. Seeking answers from a functional doctor is a proactive step. Join our Facebook group for additional information: www.drmaggieyu.com/transform, and feel free to message us: m.me/maggieyumd?ref=w14110934. Our community can offer valuable support during your health journey.
I was diagnosed with ra 3 years ago I have been suffering a lot of brain fog many many other things I can sure use someone's help and guidance I live in Oklahoma I have limited resources
If you're dealing with autoimmune issues but don't have digestive symptoms, we focus on understanding and addressing other triggers like stress and inflammation. Have you looked into these areas to support your health? Feel free to text us at (503) 647-4568 if you'd like to learn more!
I have lupus & mixed connective tissue disease, also tested positive for lyme, I live in the country andvtucks are horrible here, I been sick since 2015...I take serrapeptase, nac, and other vitamins & herbs, uts a struggle
Hey Pearl! Thank you for watching and sharing that with us. Dr. Maggie's 5 Pillar approach is going to be crucial for you in addressing these challenges and having tangible solutions. Our team would love to know how we can help. Do send us a message here m.me/maggieyumd?ref=w14110934
The program is designed to turn around all the symptoms that comes along with it so you wont have to suffer anymore regardless. Chat with us to learn more m.me/maggieyumd?ref=w14110934
Hi i was diagnosed with Sjogren's n R,A..i have no pain..my mouth is dry..i have a eye jerk..tinnitus. i use no sugar..eat fish n vegs..but i recently have ibsomnia low apetit.i dont take plaquenil scared of side effects any suggestions for insomnia..n doc wants to put me on SSRI.
Thanks for watching and sharing that with us. I'm sure it hasn't been an easy journey for you. It is so crucial to address the root cause no matter what your diagnosis is. Unfortunately, meds are not the solution, these are just band-aids. We'd love to share more info about this and see how we can help. Please chat with our team to learn more: m.me/maggieyumd?ref=w14110934
Hey Shweta! Meds are definitely not the solution, these are just band-aids and food is just one piece of the puzzle. Would love to learn more about you and get you resources on a root cause approach to end these symptoms you're dealing with. Chat with us here: m.me/maggieyumd?ref=w14110934
I was diagnosed with ra 3 years ago I have been suffering a lot of brain fog many many other things I can sure use someone's help and guidance I live in Oklahoma I have limited resources
I suffer from secondary Sjogren's overlapping rheumatoid arthritis and lupus. My POTS symptoms have caused me to be unable to function without constantly needing to lay down and catch my breath. Heart palpitations, migrain head aches, diarrhea, vomiting, gas, sciatica, fibromyalgia, brain fog. I have not worked in more than 6 months, I live alone and do not have any financial support. I am being evicted and can't pack my house or pay for all my medications. I recently filed for SSDI. it is taking a long time to be awarded. I don't sleep well. It is after 3AM. THIS video was an answered prayer!!!!!
Oh wow, appreciate you sharing this here Jonna for watching our video! We have some many resources about these issues - trainings and case studies. Do make sure to join our group if you're on Facebook for more info www.drmaggieyu.com/transform and send us a message too m.me/maggieyumd?ref=w14110934
For the POTS, if you haven't already, try wearing compression socks even while sitting. That way when you stand, it helps reduce the effects. And also squeeze your hands or a stress ball for at least 20 secs before standing each time. These have both helped me a lot. It also helps to have other electrolytes, not just salt. Ex: cucumbers with lemon and salt, salt and vinegar is better than just salt alone (just a note, these can sometimes bother your stomach if it's sensitive like mine, but they can be good quick pick me ups when you really need them).
What tests did you do for sjogrens?
why dont you guys look into fecal transplants?
My ANA was positive . I then had an extended panel and the centromere antibody was elevated.
After 3rd child autoimmune hit me with Hashimotos to Lupus and Sjogrens. It's been 20 years. Periods of remission. Episode of Lyme. Side effects from meds cause secondary problems and toxicity.
Feel free to text 503-647-4568 with your name to learn more about how we can help
Excellent Program.Thank you Both. You are the best!!!!!
I HAVE BEEN SUFFERING WITH R A GOING ON I BELIEVE LIKE 3 YEARS I DO EVERYTHING I CAN WHAT THEY TELL ME TO DO MY DIET BUT WHERE I LIVE AT I HAVE LIMITED RESOURCES I CAN SURE USE YOUR HELP LOOKING FORWARD FROM HEARING FROM ONE OF YOUR TEAM MEMBERS THANK YOU AND GOD BLESS
It sounds like you've been through a lot dealing with RA. Finding resources and support can make a big difference. Speak to us live via text at (503) 647-4568
Lichen Plano pilaris, late onset lupus, Sjogren’s. I am 52 and also have Bipolar 1.
I hear you, would absolutely love to help you address this! You can get started by live chatting with our team at (503) 647-4568. I would also recommend watching this video on an RN who dealt with both Sjogren's AND lupus and is now in remission th-cam.com/video/CWBpXRqFKdM/w-d-xo.htmlsi=IcOxFub-B5N3CxCu!
This is an infomercial. The only help or advise here is in the comments from viewers.
Hey Michelle! We would be happy to help you address your symptoms further. You can live chat with our team at (503) 647-4568 to get more specialized help and to learn more about the different solutions to autoimmunity that we offer.
I’m dealing with what I think is lupus. It’s getting worse and I’m seeking answers. My next step is to see a functional doctor. I’m very discouraged. My life has changed so much because of it and not for the better.
Feel free to send our team a chat at m.me/maggieyumd?ref=w14110934. We'd love to connect and see how we can assist you.
I'm sorry to hear about your struggles with what you suspect is lupus. Seeking answers from a functional doctor is a proactive step. Join our Facebook group for additional information: www.drmaggieyu.com/transform, and feel free to message us: m.me/maggieyumd?ref=w14110934. Our community can offer valuable support during your health journey.
I was diagnosed with ra 3 years ago I have been suffering a lot of brain fog many many other things I can sure use someone's help and guidance I live in Oklahoma I have limited resources
We are here for you, Carol! Speak to us live via text at (503) 647-4568
what about those with autoimmune disease who do not have gastric/ gut/ digestive issues or symptoms
If you're dealing with autoimmune issues but don't have digestive symptoms, we focus on understanding and addressing other triggers like stress and inflammation. Have you looked into these areas to support your health? Feel free to text us at (503) 647-4568 if you'd like to learn more!
I have lupus & mixed connective tissue disease, also tested positive for lyme, I live in the country andvtucks are horrible here, I been sick since 2015...I take serrapeptase, nac, and other vitamins & herbs, uts a struggle
Hey Pearl! Thank you for watching and sharing that with us. Dr. Maggie's 5 Pillar approach is going to be crucial for you in addressing these challenges and having tangible solutions. Our team would love to know how we can help. Do send us a message here m.me/maggieyumd?ref=w14110934
Omg I couldn’t even imagine this 😢 I have MCTD and it’s been DEBILITATING! I have gastritis and MCTD
@@marygould6357 I just started back on food grade diotematios earth , it's helping tremendously! Not expensive at all either 💗
Dr Maggie what is your advice if the POTS comes from traumatic brain injury or severe concussion? Not auto immune.
The program is designed to turn around all the symptoms that comes along with it so you wont have to suffer anymore regardless. Chat with us to learn more m.me/maggieyumd?ref=w14110934
Hi i was diagnosed with Sjogren's n R,A..i have no pain..my mouth is dry..i have a eye jerk..tinnitus. i use no sugar..eat fish n vegs..but i recently have ibsomnia low apetit.i dont take plaquenil scared of side effects any suggestions for insomnia..n doc wants to put me on SSRI.
Thanks for watching and sharing that with us. I'm sure it hasn't been an easy journey for you. It is so crucial to address the root cause no matter what your diagnosis is. Unfortunately, meds are not the solution, these are just band-aids. We'd love to share more info about this and see how we can help. Please chat with our team to learn more:
m.me/maggieyumd?ref=w14110934
I have the same problem
Hi, I have dry eyes and dry mouth. Do you guys fix with medicine or food?
Hey Shweta! Meds are definitely not the solution, these are just band-aids and food is just one piece of the puzzle. Would love to learn more about you and get you resources on a root cause approach to end these symptoms you're dealing with. Chat with us here: m.me/maggieyumd?ref=w14110934
Do you treat people in other countries? I'm in Australia.
Yes! We are 100% online so you can be anywhere to work with us. For more info, send us a message here m.me/maggieyumd?ref=w14110934
@@DrMaggieYu Thank you.
I have Sjogrens Throid desease brain fog over 30 years I would like to join face book group
Sure thing, you can join us on Facebook here! facebook.com/groups/transformautoimmune/ So exciting! We look forward to seeing you over there
Hola, hello beautiful world God Almighty bless all ❤️I healed from thyroid,it was bad
Kay Dawson
Thanks for sharing Julie! Does anyone else know someone who would benefit from learning this information? Tag their name below
I was diagnosed with ra 3 years ago I have been suffering a lot of brain fog many many other things I can sure use someone's help and guidance I live in Oklahoma I have limited resources