Dr. Wada is incredibly knowledgeable, a strong patient advocate, and have watched many of her informative presentations. She also oversees the Virtual Sjogren's Summit which features fantastic speakers. I was diagnosed in 2020 during the height of the pandemic. Like Dr. Wada, I had dry eyes at least for 10 yrs and my optometrists blew it off as dryness from wearing contacts and allergies. I was dx'd a few days before my 48th bday and throughout my 40s my flu like symptoms and crashing fatigue were blown off as perimenopausal. I also had GI issues leading up to my dx and GERD was my worst. I have also seen multiple specialists during the past 4 years. I was dx'd through labs and am SSA+ and my severe GI symptoms. Thank you Dr. Girnita and Dr. Wada for sharing your personal story as a physician-patient.
Shared knowledge is a great thing! 😊I was diagnosed with Hypothyroidism when I was young and this year I was diagnosed with Sjogren's. My symptoms were severe joint pain, dry eyes and mouth, stiffness in my fingers and hands, skin and liver symptoms as well. My symptoms seem worse with inactivity. The more active I remain its seems to help with my joint symptoms. I have read where Sjogren's disease is or may be triggered by a virus or bacteria. I have thought in my own case that this could be what triggered my case. I am currently seeing a Rheumatologist. I go for my 3rd visit this month. She prescribed Hydroxychloroquine. I took it for 6 days and had to stop taking it. It made my heart beat faster and made my symptoms worse. I will have to discuss the next line of defense on my next visit. I enjoyed this episode. Thankyou for caring enough to deep dive and discuss autoimmune disorders. It can be such a debilitating disease.
I've been knee deep in the throes of Sjogren's since 2020. When it hit, it hit me hard. Until that point, I was considered quite healthy. Over the last 4 years I've put the pieces together and realize Sjogren's was on a low simmer most of my adult life. For me, the most serious, potentially life-threatening systemic effect has been my 2022 diagnosis of PAH. Thank you for such an enlightening discussion.
@@China-Clay a form of pulmonary hypertension called pulmonary arterial hypertension. Patients with Sjogren’s are at a significant risk of developing pulmonary diseases, especially PAH. That’s why it is recommended that Sjogren’s patients have annual screenings by a pulmonologist.
Yes, two years ago I was diagnosed with a spot on my right lung node. I was told it was Sjogren's related. I was told to use cortisone, which my Diabetes is highly sensitive to too. Two years later, my new pulmanary states that the spot has disappeared butnow states I have CVID ( no IgG -low immunity support). Just another step on the Sjogren's ladder.
I am still looking for answers… I had one ANA positive, but I was told on the low side and could not get in with a rheumatologist. No one seems to be listening to my symptoms. You mentioned being fortunate enough to know what labs to ask for, can you share the labs to ask for? It is hard sometimes not to give up and sit back and accept no diagnosis and this is my life now. Thank you for sharing😘
Can you ask for the ANA to be repeated, as well as the ESR/sed rate and CRP? Given the frequency that sed rate and CRP are ordered in the UK's NHS I assume they must be on the cheaper end
I have really enjoyed this session with both you doctors now I just need to find somebody in my area to help me figure out an appointment to get some help
I don't have any food allergies but discovered that I have been tested 4 times for celiac because I have a chronic rash that "looks" like a celiac rash. Tests are akways negative but doesn't seem to stop them adding a celiac test whenever I need a blood test. Likewise, they keep testing me for RF but it is always negative. Unfortunately that seems to be about as join-the-dots thinking I've ever had. After a one month course of antibiotics for impacted wisdon teeth 30 years ago I've been unable to eat red meat without getting acute diahorrea. My last accidental exposure to beef also caused severe acid and nausea and vomitting.
Your videos are so helpful. I have not been diagnosed with Sjogrens by my rheumatologist. But my ophthalmologist did diagnose me with show grants so they disagree. I feel like my ophthalmologist is right, but have no idea where to go from here.
Hot potato from one doctor to another, was so accurate for me in rural Ohio. My Rheumatologist had to look up what sjogrens was! My nurse practitioner I saw on a whim was the one who asked the questions that got my diagnosis after 7 years!!! I sure would love to have all those tests and bills paid for, but instead, they'll sit where they are. Seeing she had residency at Wexner, which is 45 minutes from me... How can I get ahold of Dr. Wada?
I am almost 69. I never had a dental issue in 60 years of life. I have always kept a good dental regime and appointments q 6 months. Braces in high school but everything else was great. Suddenly, I was diagnosed with dry mouth and several cavities. The next five years my issues increased and I had to have two root canals, capping and also my teeth have been chipping. Because of the chipping, it has become hard to bite into thin sliced round pickle in a sandwich. What a domino effect!!
I had this happen to me. I was tested for a trial. I had one test come back with a false positive. So they kicked me out of the trial. My doctor re tested me and it was fine. I don't understand how one lab says one thing and one says another.
I have had allergic reactions that occurred three hours after contact/ingestion/inoculation. When I have had testing done to confirm this, no one waits around three hours to see the reaction and when I tell them I have one, they dismiss me because if I have a true allergy it will show up within minutes not hours. Is an allergy that shows itself three hours later an immediate hypersensitivity reaction or a delayed hypersensitivity reaction and how can I get it properly diagnosed? I have seen allergists-immunologists with little success.
![I.N "HALLUCINATION" | [Stray Kids : SKZ-PLAYER]](http://i.ytimg.com/vi/n5B5q1Hwt_U/mqdefault.jpg)
Dr. Wada is incredibly knowledgeable, a strong patient advocate, and have watched many of her informative presentations. She also oversees the Virtual Sjogren's Summit which features fantastic speakers. I was diagnosed in 2020 during the height of the pandemic. Like Dr. Wada, I had dry eyes at least for 10 yrs and my optometrists blew it off as dryness from wearing contacts and allergies. I was dx'd a few days before my 48th bday and throughout my 40s my flu like symptoms and crashing fatigue were blown off as perimenopausal. I also had GI issues leading up to my dx and GERD was my worst. I have also seen multiple specialists during the past 4 years. I was dx'd through labs and am SSA+ and my severe GI symptoms. Thank you Dr. Girnita and Dr. Wada for sharing your personal story as a physician-patient.
Thank you for watching and your support!!!
Shared knowledge is a great thing! 😊I was diagnosed with Hypothyroidism when I was young and this year I was diagnosed with Sjogren's. My symptoms were severe joint pain, dry eyes and mouth, stiffness in my fingers and hands, skin and liver symptoms as well. My symptoms seem worse with inactivity. The more active I remain its seems to help with my joint symptoms. I have read where Sjogren's disease is or may be triggered by a virus or bacteria. I have thought in my own case that this could be what triggered my case. I am currently seeing a Rheumatologist. I go for my 3rd visit this month. She prescribed Hydroxychloroquine. I took it for 6 days and had to stop taking it. It made my heart beat faster and made my symptoms worse. I will have to discuss the next line of defense on my next visit. I enjoyed this episode. Thankyou for caring enough to deep dive and discuss autoimmune disorders. It can be such a debilitating disease.
Absolutely!
Thank you Dr. Grinita for these wonderful sessions. They are so informative and helpful.
Glad you like them!
I've been knee deep in the throes of Sjogren's since 2020. When it hit, it hit me hard. Until that point, I was considered quite healthy. Over the last 4 years I've put the pieces together and realize Sjogren's was on a low simmer most of my adult life. For me, the most serious, potentially life-threatening systemic effect has been my 2022 diagnosis of PAH. Thank you for such an enlightening discussion.
PAH?
@@China-Clay a form of pulmonary hypertension called pulmonary arterial hypertension. Patients with Sjogren’s are at a significant risk of developing pulmonary diseases, especially PAH. That’s why it is recommended that Sjogren’s patients have annual screenings by a pulmonologist.
Yes, two years ago I was diagnosed with a spot on my right lung node. I was told it was Sjogren's related. I was told to use cortisone, which my Diabetes is highly sensitive to too. Two years later, my new pulmanary states that the spot has disappeared butnow states I have CVID ( no IgG -low immunity support). Just another step on the Sjogren's ladder.
Thank you for sharing your journey with us. It's important to stay positive and keep moving forward!
@@christineshields1714 wow, thank you! I have lots of tightness in my chest, I think I will check it out asap!
I am still looking for answers… I had one ANA positive, but I was told on the low side and could not get in with a rheumatologist. No one seems to be listening to my symptoms. You mentioned being fortunate enough to know what labs to ask for, can you share the labs to ask for? It is hard sometimes not to give up and sit back and accept no diagnosis and this is my life now. Thank you for sharing😘
I'm sorry to hear about your struggles. It can be frustrating when you feel like no one is listening to your symptoms. Hang in there!
Can you ask for the ANA to be repeated, as well as the ESR/sed rate and CRP? Given the frequency that sed rate and CRP are ordered in the UK's NHS I assume they must be on the cheaper end
I have really enjoyed this session with both you doctors now I just need to find somebody in my area to help me figure out an appointment to get some help
That's great to hear that you found the session helpful! Finding a local professional should be the next step to getting the assistance you need.
I don't have any food allergies but discovered that I have been tested 4 times for celiac because I have a chronic rash that "looks" like a celiac rash. Tests are akways negative but doesn't seem to stop them adding a celiac test whenever I need a blood test. Likewise, they keep testing me for RF but it is always negative. Unfortunately that seems to be about as join-the-dots thinking I've ever had.
After a one month course of antibiotics for impacted wisdon teeth 30 years ago I've been unable to eat red meat without getting acute diahorrea. My last accidental exposure to beef also caused severe acid and nausea and vomitting.
I need your help please🙏🙏🙏🙏
thanks for watching my videos!
Your videos are so helpful. I have not been diagnosed with Sjogrens by my rheumatologist. But my ophthalmologist did diagnose me with show grants so they disagree. I feel like my ophthalmologist is right, but have no idea where to go from here.
It was my ophthalmologist that diagnosed me too. He sent me to a rheumatologist to get tested and BINGO.
Thanks for sharing!
Hot potato from one doctor to another, was so accurate for me in rural Ohio. My Rheumatologist had to look up what sjogrens was! My nurse practitioner I saw on a whim was the one who asked the questions that got my diagnosis after 7 years!!! I sure would love to have all those tests and bills paid for, but instead, they'll sit where they are. Seeing she had residency at Wexner, which is 45 minutes from me... How can I get ahold of Dr. Wada?
thank you for sharing!
Thanks for this brilliant discussion.
Glad you enjoyed it!
I have lived with many of these symptoms all my life. Have there been any studies on Sjogrens and rh negative blood type? I have both.
thanks for sharing
I would love to know your thoughts on LDN!
they will come soon
Thank you for watching my channel!
Great work. Thx. From seatides, tongaat , sa. 1 week since tornado hit
Oh wow!
Yep. I'm 72 and I've been to many .with no help.
It's inspiring to hear about your independence and resilience at 72!
I’m on early stage of Sjögren’s syndrome my mouth very dry and flamy in the morning. So please need your help🙏🙏🙏🙏🙏🙏🙏🙏🙏🙏🙏
What has your dentist said?
thanks for watching my videos!
I am almost 69. I never had a dental issue in 60 years of life. I have always kept a good dental regime and appointments q 6 months. Braces in high school but everything else was great. Suddenly, I was diagnosed with dry mouth and several cavities. The next five years my issues increased and I had to have two root canals, capping and also my teeth have been chipping. Because of the chipping, it has become hard to bite into thin sliced round pickle in a sandwich. What a domino effect!!
Thanks for sharing!!
I had this happen to me. I was tested for a trial. I had one test come back with a false positive. So they kicked me out of the trial. My doctor re tested me and it was fine. I don't understand how one lab says one thing and one says another.
That must have been a frustrating experience. It's always unsettling when different labs provide conflicting results.
In the UK at least we have the problem that a negative test is the end of the road. No retest. But a positive test usually gets a retest
Sizi anlayabilmem için Türkçe altyazı lütfen , teşekkürler.
We will
help me........??
I'm here to help, what do you need assistance with?
I have had allergic reactions that occurred three hours after contact/ingestion/inoculation. When I have had testing done to confirm this, no one waits around three hours to see the reaction and when I tell them I have one, they dismiss me because if I have a true allergy it will show up within minutes not hours. Is an allergy that shows itself three hours later an immediate hypersensitivity reaction or a delayed hypersensitivity reaction and how can I get it properly diagnosed? I have seen allergists-immunologists with little success.
sit in their office for 3 to 4 hours . after a test. 😮
or get another doc.
Thank you!
Genome wide association studies (GWAS) are surprisingly accurate.
Thank you!
❤
Thanks