It's so important to see a rheumatologist if you have these symptoms because so many conditions have similar symptoms. I have had ME/CFS and Fibromyalgia for around 20 years, but was diagnosed by my rheumatologist with seronegative rheumatoid arthritis a few years ago. With this type of RA the blood tests don't usually show positive for RA so it makes getting diagnosed more difficult. Because many of the symptoms cross with what I already had, it was only when I went to see a new doctor that the additional condition was found. I probably had it for about 4 years before that. Since I already experienced pain from fibro, the additional pain in my hands and having my eyes be drier than usual did not seem like anything to be concerned about. Because my new doctor wanted a complete picture of my condition, we discussed every symptom I had and he did a thorough exam. I feel lucky that it was found and I began treatment before it got too far along.
I have sjogrens, EDS and am now 45. My youngest two children have mitochondrial disease of unknown cause and EDS. I was so healthy before but then it seemed like a chain of events out of nowhere. When I wake up, I often have loss of circulation in at least one hand and foot. I’ve never been overweight and was raised on farm & our own garden. It’s been a journey. And yes, my teeth were lovely most of my life and now are as bad as a person without dental care. 🥴 For my kids and self, we’ve been all over US and never found answers or help. Thank you for your channel! Medical professionals need to know more and not stop learning after school. Diagnosis can only help if you find a knowledgeable & caring Dr & afford the copays. Hard in US
I find that I am forced to find my own information and answers to this disease as my rheumatologist is most unhelpful and has even lied to me directly about blood test results and also by telling me nothing about the drugs she prescribes also saying not to look it up online, all major red flags, but when it's your health you're virtually held hostage over it, more red flags, I look after me though as no one else does. I hope you have worthwhile information to share. ❤
It's really unfortunate to hear about your experience with your rheumatologist. It's so important to have a supportive healthcare provider, and seeking out information for yourself is often necessary. I hope my video provides you with some valuable insights!
I have had dry mouth for many years and no doctor could tell me what it is NOW i know my joints are swelling and extreme pain in my wrists and knees. Thank you for video film.
I'm not even 30 and have had autoimmune issues since the age of 14. I developed them before my dad, who gave me the genetic predisposition! My mental health and emotional state/ environmental irritants have the biggest effect, not medication. When you're stuck in an inescapable and unbearable situation, your immune system turns on you.
@emilyscar6844 well I soaked my feet every medicine I can Epsom salt, alchohol, icy hot,til my doctor finally got medicine for which was to strong,but extra strength tylenol
I only been diagnosed with osteoarthritis. But I’m way worse. WEAK CANT DO ANYTHING. I got Sjrogens. I’m in excruciating pain constantly stiffness. Yea. I break out in rashes. SO WEAK I’m 67. Excruciating pain constantly stiffness. HORRIBLE Horrible Nightmare
I have aunts and uncles with autoimmune diseases. All blood relatives ofc. Rheumatoid Arthritis is one, my oldest uncle has this. And he had uncurable colon cancer, and thanks to him fighting for gene therapy he is now cancer free. He had to fight for it, and he did. And he did have medical personnel in his family, and they fought for him. He got the treatment. And he's healthy ❤😂
Thank you for sharing your uncle's inspiring story! It’s incredible to hear how determination and support can lead to such positive outcomes in the face of adversity.
Unfortunately, rheumatologists are scarce in Nigeria , I go to a very far place to see my doctor and come back late in the night. However, I have changed my diet and it helps a lot.
@@tiwannamincey Did away with gluten and sugar. Although I can't get most of the foods needed for rheumatoid arthritis and we can't do without eating oil here (palm oil) which is not good at all for me but there's no other thing to eat. So I still get pains but not as much as before when I couldn't walk or sleep.
Hi from U.S.A. I’m glad to hear to are able to receive medical care from a Rheumatologist despite having to drive for several hours. You are not alone. After seeing 3 Rheumatologist’s that were all 3 hours drive away, not one Doctor knew what was wrong. The 4th doctor, I like. He is treating me now with some success. This doctor is a 5 hour drive away. Not only in Nigeria are doctors hard to find and many hours drive away. In the U.S.A. this appears to be increasingly normal. It will only get worse as years go on. Peace.
After reading the comments of patients struggling with doctors doing not right diagnosis. I feel blessed and extremely lucky that my first doctor properly diagnosed me at first appointment also i have seronegative RA . He is very experienced. Its sucks though cause im only 22 and this disease hinders my day to day activities and studies which are most important to me. 😢😢
@@Dee-ny5vp I m also 22 and having seronegative arthritis,Can u pls tell what symptoms u have that u reach its diagnosis and pls what medicines are uh taking ?..is it curable or not ..pls tell it would b very helpful for me
@@itss209 swelling in finger joints , constant pain in joints and muscles for over 6 months, hard to get up from bed in morning because of stiffness in muscles, very light fever which goes itself , very bad mental health etc.. they r many more small symptoms. I'm taking methotrexate once a week , leflunumide once a day, and some vitamins and supplements twice a day. Dr also gave painkillers but I don't take them anymore because it messes up with my liver , so I just bear the pain also the pain is significantly less than before after treatment.
I"m trying, but my primary says there's nothing wrong with me. I have Hashimotos, but no longer have high thyroid antibodies so she didn't believe me and wouldn't refer me. I found another Dr to refer me, so I have an appt with a rheumatologist tomorrow.
Very informative! I have all these symptoms. However, I have been diagnosed with Sjogren's. The overlap of these conditions and their symptoms is quite interesting. As a side note, I believe that quite recently the terms primary and secondary associated with Sjogren's has recently been discontinued as has the term syndrome (replaced with the term disease).
But Sjogren's can cause morning in back stiffness that takes all day to work out (although sleeping in a reclining position does help) with dry eyes, dry mouth, and "sand" in your eyes.
While waiting to get into a rheumatologist try the carnivore or ketogenic diet to see if you have a change in symptoms. It could be a food allergy…a lot of people have some success with finding out what foods are triggering
It’s important to remember that this needs treatment. I recently had to tell my family of my diagnosis (I did it also to warn them of their risk) and was told it was just a sign I needed lifestyle changes. I cannot stress how dangerous it is to think like that. You cannot keep up naturally with these symptoms to prevent it entirely without it developing further and you cannot predict the intensity of a flare or the duration. It’s just not possible. We have the treatments, and they’re very safe. I can’t suggest more than to just get it treated.
I'm currently dealing with this. My labs for reuthmatoid where high and it runs in my family. My grandma and mother both have it. I have severe pain in both knees including rashes on my hands, feet, and face and they still won't help smh...
I'm surprised to see more people have similar issues with their doctors when finding care or treatment for RA. I was also very disappointed with my city's only rheumatologist.
I had same issue, suffered for long periods. Ultimately started treatment with steroids and Methotrex, dose and schedule adviced by my rheumatologist. In 5 days, i became normal with no pain. Medicines prooved to be miracle for me. Thank God, thanks to allopathy medicines. I should have started the treatment earlier. 🙏
At 34 I just felt sick and I was so tired. Then the foot pain began first n one foot then the other foot. I felt like I was walking on open wounds. My rheumatologist said my SED and RA Factor and the other test was off the charts. That and my textbook physical symptoms meant that the disease needed to be treated aggressively. Now 30 years later my life changed. I hurt everyday, have deformed feet, and tooth loss. Still the meds that r available today are great and can give RA patients an excellent quality of life.
Finally, I diagnosed by RA and everyday are nightmare. My body is in pain, from morning to night, especially when I worked too much. Medicine is not working yet, I take for 1 month. Because of I have raynaud syndrom too, I asked to my doctor to check my artery, and I am sure I have problem in my feet arteries. Like, I couldn't stand up for long time, hard for walking and tingling everyday.
I'm really sorry to hear that you're going through such a tough time. It sounds incredibly challenging, but it's great that you're actively seeking answers and solutions. I hope you find the right treatment soon!
I’ve had all these symptoms exactly as described and all at the same time and though I still struggle with dry eyes and dry mouth, when I change my diet, all the symptoms go away except the dry eye dry mouth, but it becomes so much more manageable. Mine was related to leaky gut and gut candida and sibo both I got treated…diflucan and rifaximin to resolve it. I’ve gone through this a few times over the years, it comes back due to a have a poor microbiome caused by poor diet, infection, antibiotics.
RA being an autoimmune disorder can be linked to poor gut health (Leaky gut) keeping your micro biome heathy is the first step in preventing and controlling RA.
Absolutely! It's fascinating how our gut health plays such a crucial role in overall well-being, especially when it comes to autoimmune disorders like RA. Thanks for sharing your insights!
Doc, I have deformed fingers in my hand because of RA.. Please help me to remove deformities in my hand? What medicine will I take? What hand exercises will I do..
Get ur d3 checked, you want it in the 50 to 80 range. Mine was 41 after 10 months of 20,000 iu every day. No side affects at all. Also take magnesium dioxide and k2.
I am 28yrs. A teacher by professional for 7 yrs now since I started teaching my shoulder really ache. Nowadays the pain is spread to my hands and legs😢
I have every symptom especially joint pain. My ANA test came back positive and sjogren's ssb was elevated. I definitely thought i was going to be positive for arthritis but nope negative. My rheumatologist seem not to seem to concern but im always in pain. Guess what the diagnosis was??? Fibromyalgia 😭
I’m 40 and I’m afraid I have it. Just recently I’ve started getting very mild stiffness and soreness in my fingers and occasionally my toes. I don’t know what else it could be. The best way to describe the feeling is like I need to crack the knuckles constantly or straighten out the fingers. Not necessarily pain just mild discomfort.
Ive bèen telling my rheumatologist about numb hads for a long time. He just says I have carpal tunnel. I've tried telling him about my chronic exhaustion. He tells me I need to exercise. He's absolutely no help.
My primary dr finally referred me to see a rheumatologist saying it's usually at least 6 months wait to see an RA specialist, and even then they are very selective; you have to have enough evidence that it may be RA for them to consider seeing you. I did not realize it was that difficult to see a specialist. Are there THAT many people needing diagnosis help but not enough RA specialists?
@jskim.9122 i think it depends on where you live. I got an appointment within maybe one month in my small town. I got in quickly with my other appointments too but unfortunately she's the only one in town and she's no longer here. The other ones are at least 40min drive and further 😞
I had blood work done to check thyroid levels. Recently diagnosed with hypothyroidism. My thyroid levels were fine, but i had an ANA of 360. Was referred to a rheumatologist who did more blood work and said that it looks like sjogrens. That was about 2 months ago. My biggest problem right now is the pain in my arms. I can hardly lift my left arm. Pain at night is severe. I have other symptoms of sjogrens, but the arms are the main problem right now. I dont want to take prednisone. I just dont want the mental side effects and the weight gain. Is there another option?
I've read at the NIH that vitamin D receptor defects can be part of the problem, so that even with normal vitamin D levels, the inflammation can rage on anyway.
@@rheumatologistoncall I've seen people say, they could not raise their D3 levels above 30 for years but liposomes took them to 52 and 80 in weeks and months. The changes in their quality of life were something to behold.
My Vitamin D Level Is Low & All The Doctors Say Is My Blood Work Looks Fine But I Have Red Eyes And All Been Having Joint Pain And Numbness For A While
my all blood tests and inflammatory markers are negative but i all joints pain for 3 months and reduced left knee space doctor said its due to anxiety.is this right or i need re evaluation
5:22 I can’t give a thumbs up. It hurts. No, but seriously both my hands hurt badly in the AM and/or when I wake from a nap. I can’t wear my rings anymore because I can’t get them over the finger joint. I’ve also had dry eyes for so long. The ophthalmologist told me the surface of my right eye in particular is badly damaged from dry eye.
ma'am my age is 32 men from Pakistan all blood works are normal ESR 7 CRP .4 rheumatologist says it's not autoimmune disease then kindly tells what causes all joints cracking and stiffness remains same all day plz
@@MuhammadUmar-gh6cz Your CRP is slightly elevated. Normal range is 0.3 or lower so there’s definitely something going on. Just going off of blood tests seems unreliable to me and I’ve been a nurse for over 15 years. Many people will have obvious symptoms but normal serum labs. I hope you get the help you need and I’m sorry to hear you are suffering.
i consulted 5 doctors so far, nobody treat me properly,just gave me antiinflammatory pills,sent me to recovery showers,and other dr. gave me alflutop injection, is this enough?pain is always there, i also have coxatrosys and gonartrosys,all parts of knee,hips,spine crackling n getting worse,swelling all days,is depressing,im only 40yo..all started at 35,i wonder why..
I have it .fingers, can't bend them now have difficulty holding fork ect..in elbows .. shoulders..toes..neck ..well i am assuming the pain in neck is arthritis,but my doctor gives me cocodomol and notjing for inflammatory so i buy my own ..so i had these signs 3 years ago it started in wrists excruciating pain but was given pain killers then and do not have any further help from gp ,so as for saying.. don't ignore these signs..it makes no difference if not really getting anything to relieve it more.
I have a lot of these symptoms but I have thyroid cancer and had 2 RAI treatments and this can cause dry mouth and eyes and affect your salivary glands. My fingers are usually swollen and achy all the time. Had blood work for autoimmune and all negative.
It's very, very hard to get an appointment with a rheumatologist. I have every one symptoms but because my "labs" don't show anything the rheumatologist won't see me. We have one that is within a hour drive and dr has terrible bed side manners.
I was diagnosed with RA even though my only symptoms have so far been only joint pain in my fingers. No pain in my wrist either. I have not had fever, fatigue or any of the other symptoms you mentioned. Even my blood tests only revealed an elevated ESR level. Everything else ( including C-reactive protein) is normal. Should I get a second opinion elsewhere? Kindly advise?
Do you use MRI, CT scan or Ultrasound to diagnose RA? I've had horrible joint pain in hands/wrists for 7 months now and it's spreading to my knees, etc. Aside from a positive ANA test, my other results were "normal". My Rheumatologist refuses to do any type of scan.
I have dry eyes, dry mouth and constant pain in my forth-legs and hands specially my thumbs. My doctor did a bone conduction test and the found severe loss of bone and she diagnosed me with osteoarthritis. However my bones and muscle remain swollen. Should I request a referral for a rheumatologist. Also my adult son and Mother were diagnosed with RA
I have all these symptoms... And my older brother has RA. The knees need replacement, my thumb joints are bad and and i have neck pain and a LOT of foot pain. Dry eyes and mouth ...check.
I have had it for 17 years but years before that the tips of my fingers would randomly become swollen and red and very painful. Then in early 2007 it came on all over with a vengeance. I have been on methotrexate ever since.
@@rheumatologistoncall thankyou yes I'm trying to I can't have antiimflammatory drugs I've tried them only steroids my old doctor gave me them for pain&with codeine,paracetamol I had to change doctors twice since then as I'm not living in the post code area etc so stupid so now everything is al over the place. I am under different hospitals etc. They should be having meetings with me soon so hopefully but this doctor is so stupid. I live in the UK. Everything u say is true so I'm taking notes so I can pull them on it. Thankyou 💜
I am 29 yrs . Have had joint rashes especially on my hand and foot on the same sports way back when I was around 10-15yrs. Have been to hospices and no sign of athlities. What could be the problem I always have shoulder pains when I strain.
I have read that seronegative RA can have worse symptoms. Is this true? Also, can one have carpal tunnel and RA so need surgery? Even with RA meds, my CT is no better and is quite disabling with numbness on waking and often intense pain. Thanks for sharing your expertise.
Thanks somuch for this explanation, everything u said is correct and I am having it all , I am under treatment and taking plaquenil 400 mg every day and I am good 50% but still have pain in my front joint foot it’s not getting better at all I need your help ! I did got injection plasma for it it helped a lot but after 6 months I have pain again , I have taken 3 times the plasma injection! But still I am getting pain , I also have pain in my lower back one side too ! U are so good telling me that the arthritis dosent show in blood test it’s very true , because my Docter said my blood test is good so she gave me triptizol 25 mg tables for 6 months to continue, I am sleeping very well with this tablet! Want to thank you somuch for explaining the arthritis pain which I am going through ! What food I should avoid ? Some say my diet need to change but I never tried pls help me
I'm glad the video was helpful for you! It's great that you're seeking treatment and taking steps to manage your arthritis. I'd recommend discussing your ongoing pain with your doctor to explore other treatment options.
Im 17 and im in agony with my joints and everything, I have every one of these symptoms and its so debilitating especially with it becoming winter the pain becomes so much worse and my joints feel so much more sensitive. It runs in my family.
Thanks for sharing! It's important to understand the differences between conditions like ulnar nerve syndrome and carpal tunnel. Your health journey is unique!
I was just diagnosed with the hla-b27 gene and high inflammation markers. I have been suffering and getting worse for years. What causes the cracking and popping all over like every step or movement causes cracking?
I'm sorry to hear about your diagnosis. It's important to work closely with your healthcare provider to manage your symptoms and explore treatment options.
I am clinically diagnised with Pleural effusion extra pulmonary TB and pneumonia. admitted to hospital with pleural fluid filled in my right lung more than 2/3. i have many of the mentioned symtoms. any chance for RA?
Miałam sztywność stawów skokowych zawsze rano po wstaniu z łóżka ale po odrobaczeniu ten problem znikl.Mam początki Artritis ,ale lekarz przepisze mi Diclo Tabl lub maść i tyle.Jedynie co mnie niepokoi to takie wypukle zgrubienie jak np. polowa jajka na grzbiecie stopy od strony zewnętrznej ,nie boli ale to jest miękkie jak galaretka które powstało od niedawna i na ten problem lekarz ortopeda nie potrafił mi pomóc ,co to jest?😢Moze Pani doktor wie z doświadczenia co to może być.Pozdrawiam z Polski.❤👋🏼👋🏼
Dziękuję za podzielenie się swoją historią! Ważne, aby skonsultować się z lekarzem w sprawie tego zgrubienia. Mam nadzieję, że znajdziesz odpowiedzi, które pozwolą Ci czuć się lepiej.
Even I'm going through the same situation . I had dengu ..post dengu after week my right hand fingers tips r swollen , tingling., inflammation.....in the next 3 days left fingers affected... beginning had bit pain but wt pain killer no pain now ...but swelling, stiffness, inflammation is still there past 24 days....legs fingers also has. Numbness and inflammation....please suggest what it could be....
I have painful eyes that turn into bad headaches a have arthritis in me neck back wrist and knees now a feel my back muscles are tearing apart n my lungs feel heavy when I lay down I can't sleep for it but sleep loads any other time like mostly all-day should I see a specialist (im 40)
Hello mam i got dengue fever 2 mnts ago from onwards my fingers are swelling,and pain, and my hand , foot, elbow are very pain. My ra factor 32 possitive, but ANA negative . Will the pains will go or for life long. Is the rheumathoid arthitis. Doctor suggest only vitamin tablets and pain killer tablets . Plse help me mam
Even I'm going through the same situation . I had dengu ..post dengu after week my right hand fingers tips r swollen , tingling., inflammation.....in the next 3 days left fingers affected... beginning had bit pain but wt pain killer no pain now ...but swelling, stiffness, inflammation is still there past 24 days....legs fingers also has. Numbness and inflammation....please suggest what it could be....
Ive had nine different vials of blood taken and they have all come back as abnormal now i have to wait a month for dr to tell me i kniw what it is so i cancelled him disgusting having to wait that long when im in real pain
I am 30 years old and i am having this carpel tunnel syndromes since 8 months of my pregnancy time and now its been 1 and half years what should i do and to whom i may concern for this?
I have almost all the symptoms since my forties, now I am in my sixties. The pain in the finger joints, wrist and shoulders has become debilitating. I can't move out of my bed in the morning. But my RA factor test always comes negative. Could you advise what to do??
How does RA differ from Connective Tissue Disease? I have already got the diagnosis of PsA as it attacked my knee (seen on an MRi) but I have hand pain in both hands. I also have Raynauds. They say it’s rare to have PsA and RA but I think I have RA too. Currently on Humira which is helping my knee but not doing much for my hands. Humira also normalized my inflammation levels which were so concerning they thought I had blood cancer and sent me to an oncologist/hematologist. Luckily, no blood cancer just tons of inflammation.
Dr my daughter who is 25 years old has been diagnosis with episcleritis. A PET scan was done and everything is normal.Then why does her eyes become red every month
This is caused by inflammation. If it is only happening once a month, maybe it is something that she is eating. Maybe not. Since they don't know what inflammation causes it, then I would try to eat a vegetable diet for a month, raw and cooked, drinking lots of water and nothing else (sugar is an inflammatory food) to see if the inflammation goes down and it stops. Then, you can try introducing new foods every week to see if any of the foods are inflammatory. Sugar, high fructose corn syrup, genetically modified foods, and processed foods are all inflammatory.
I am 47. Both wrists started hurting out of nowhere. Within a week or so became excruciating. Have a rheumatologist appointment in a month after waiting 2 months already. The pain moves around from fingers to thumbs, now forearms and biceps when I twist my wrists. It never has really let up. Probably 5% of the time it doesn’t hurt to just sit. It feels more like tendon pain than joint pain. I’m about 40 lbs. overweight but rarely got sick my entire life. I’m just worried I’ll have someone put me on a ton of meds killing my liver and have worse side effects than the symptoms. Any advice please?
I'm sorry to hear about your wrist pain. It's good that you have a rheumatologist appointment coming up. Remember, it's important to address your health concerns and seek professional advice.
It's so important to see a rheumatologist if you have these symptoms because so many conditions have similar symptoms. I have had ME/CFS and Fibromyalgia for around 20 years, but was diagnosed by my rheumatologist with seronegative rheumatoid arthritis a few years ago. With this type of RA the blood tests don't usually show positive for RA so it makes getting diagnosed more difficult. Because many of the symptoms cross with what I already had, it was only when I went to see a new doctor that the additional condition was found. I probably had it for about 4 years before that. Since I already experienced pain from fibro, the additional pain in my hands and having my eyes be drier than usual did not seem like anything to be concerned about. Because my new doctor wanted a complete picture of my condition, we discussed every symptom I had and he did a thorough exam. I feel lucky that it was found and I began treatment before it got too far along.
@@TerryL421 absolutely
I have sjogrens, EDS and am now 45.
My youngest two children have mitochondrial disease of unknown cause and EDS.
I was so healthy before but then it seemed like a chain of events out of nowhere.
When I wake up, I often have loss of circulation in at least one hand and foot. I’ve never been overweight and was raised on farm & our own garden. It’s been a journey.
And yes, my teeth were lovely most of my life and now are as bad as a person without dental care.
🥴 For my kids and self, we’ve been all over US and never found answers or help.
Thank you for your channel! Medical professionals need to know more and not stop learning after school. Diagnosis can only help if you find a knowledgeable & caring Dr & afford the copays. Hard in US
im thinking whether Covid injections doing this
Probably...injections may affect people differently... it's within our body...pray for good health...
I find that I am forced to find my own information and answers to this disease as my rheumatologist is most unhelpful and has even lied to me directly about blood test results and also by telling me nothing about the drugs she prescribes also saying not to look it up online, all major red flags, but when it's your health you're virtually held hostage over it, more red flags, I look after me though as no one else does. I hope you have worthwhile information to share. ❤
It's really unfortunate to hear about your experience with your rheumatologist. It's so important to have a supportive healthcare provider, and seeking out information for yourself is often necessary. I hope my video provides you with some valuable insights!
I have had dry mouth for many years and no doctor could tell me what it is NOW i know my joints are swelling and extreme pain in my wrists and knees. Thank you for video film.
I'm not even 30 and have had autoimmune issues since the age of 14. I developed them before my dad, who gave me the genetic predisposition! My mental health and emotional state/ environmental irritants have the biggest effect, not medication. When you're stuck in an inescapable and unbearable situation, your immune system turns on you.
Yes ! Correct
@@CosmicGuiltTrip thank you
What have you done to relieve pain?
@emilyscar6844 well I soaked my feet every medicine I can Epsom salt, alchohol, icy hot,til my doctor finally got medicine for which was to strong,but extra strength tylenol
I only been diagnosed with osteoarthritis. But I’m way worse. WEAK CANT DO ANYTHING. I got Sjrogens. I’m in excruciating pain constantly stiffness. Yea. I break out in rashes. SO WEAK I’m 67. Excruciating pain constantly stiffness. HORRIBLE Horrible Nightmare
I have aunts and uncles with autoimmune diseases. All blood relatives ofc. Rheumatoid Arthritis is one, my oldest uncle has this. And he had uncurable colon cancer, and thanks to him fighting for gene therapy he is now cancer free. He had to fight for it, and he did. And he did have medical personnel in his family, and they fought for him. He got the treatment. And he's healthy ❤😂
Thank you for sharing your uncle's inspiring story! It’s incredible to hear how determination and support can lead to such positive outcomes in the face of adversity.
Unfortunately, rheumatologists are scarce in Nigeria , I go to a very far place to see my doctor and come back late in the night. However, I have changed my diet and it helps a lot.
What changes did you make to help you?
@@tiwannamincey Did away with gluten and sugar. Although I can't get most of the foods needed for rheumatoid arthritis and we can't do without eating oil here (palm oil) which is not good at all for me but there's no other thing to eat. So I still get pains but not as much as before when I couldn't walk or sleep.
Hi from U.S.A.
I’m glad to hear to are able to receive medical care from a Rheumatologist despite having to drive for several hours. You are not alone. After seeing 3 Rheumatologist’s that were all 3 hours drive away, not one Doctor knew what was wrong. The 4th doctor, I like. He is treating me now with some success. This doctor is a 5 hour drive away. Not only in Nigeria are doctors hard to find and many hours drive away. In the U.S.A. this appears to be increasingly normal. It will only get worse as years go on.
Peace.
May God help us.@@ladeek35
Your videos are so good thank you!
Ohhh! Thank you for your response!!!!
Wow I have all these for RA
After reading the comments of patients struggling with doctors doing not right diagnosis. I feel blessed and extremely lucky that my first doctor properly diagnosed me at first appointment also i have seronegative RA . He is very experienced. Its sucks though cause im only 22 and this disease hinders my day to day activities and studies which are most important to me. 😢😢
Good for you!!!
what is seronegative RA? My RA factor is normal
@@Dee-ny5vp I m also 22 and having seronegative arthritis,Can u pls tell what symptoms u have that u reach its diagnosis and pls what medicines are uh taking ?..is it curable or not ..pls tell it would b very helpful for me
@@itss209 swelling in finger joints , constant pain in joints and muscles for over 6 months, hard to get up from bed in morning because of stiffness in muscles, very light fever which goes itself , very bad mental health etc.. they r many more small symptoms. I'm taking methotrexate once a week , leflunumide once a day, and some vitamins and supplements twice a day. Dr also gave painkillers but I don't take them anymore because it messes up with my liver , so I just bear the pain also the pain is significantly less than before after treatment.
@@benedictjoseph3832 yes when RA factor is normal and you get diagnosed with rheumatoid arthritis, it is called seronegative RA
I don't have RA, but I really think I have Sjogrens. My dry, horrible eyes are not constant, but intermittent. Lots of other symptoms also.
It's important to listen to your body and seek medical advice if you suspect something isn't right.
I"m trying, but my primary says there's nothing wrong with me. I have Hashimotos, but no longer have high thyroid antibodies so she didn't believe me and wouldn't refer me. I found another Dr to refer me, so I have an appt with a rheumatologist tomorrow.
I am also having issues get a dr to listen to me
Pls I am also having the same issued I don't understand doctor said am ok
Teşekkürler.
Thank you so so much
Very informative! I have all these symptoms. However, I have been diagnosed with Sjogren's. The overlap of these conditions and their symptoms is quite interesting. As a side note, I believe that quite recently the terms primary and secondary associated with Sjogren's has recently been discontinued as has the term syndrome (replaced with the term disease).
A video is coming ❤
Yes the term of Syndrome was replaced by DISEASE
@@christineshields1714 what blood work indicates this?
But Sjogren's can cause morning in back stiffness that takes all day to work out (although sleeping in a reclining position does help) with dry eyes, dry mouth, and "sand" in your eyes.
Yes a video about these two diseases will be published in the next few weeks
While waiting to get into a rheumatologist try the carnivore or ketogenic diet to see if you have a change in symptoms. It could be a food allergy…a lot of people have some success with finding out what foods are triggering
That's a great suggestion! Diet can play a significant role in managing various symptoms.
Yeah I'm from India...even I heard in several videos RA getting -ve wt diet .gluten sugar oil free...and few more things.
It’s important to remember that this needs treatment. I recently had to tell my family of my diagnosis (I did it also to warn them of their risk) and was told it was just a sign I needed lifestyle changes. I cannot stress how dangerous it is to think like that. You cannot keep up naturally with these symptoms to prevent it entirely without it developing further and you cannot predict the intensity of a flare or the duration. It’s just not possible. We have the treatments, and they’re very safe. I can’t suggest more than to just get it treated.
what medications have you found worked best for you?
Thank you for sharing your experience and emphasizing the importance of getting the necessary treatment.
Family only accept if they see visible wounds...sadly. I also have a worst family who thinks im imagining
Menopause can also trigger RA. Hormonal changes
possibly
Yes , agree
I thought so too, what do you think of PCOS causing RA? I have it and always thought my RA was connected to that
I have pcos and my mom had RA@Daynish648
I am 36 years old I have ra last 5 years and my daughter has pcod😢😢😢😢
And if we tell our Drs about this they just dismiss us 😞
It can be frustrating when doctors dismiss our concerns. Keep advocating for yourself and seeking out healthcare providers who will listen.
YES THEY SURE DO! 😡
I highly recommend a direct primary care doctor. It has changed my life as opposed to traditional primary care
I'm currently dealing with this. My labs for reuthmatoid where high and it runs in my family. My grandma and mother both have it. I have severe pain in both knees including rashes on my hands, feet, and face and they still won't help smh...
I'm surprised to see more people have similar issues with their doctors when finding care or treatment for RA. I was also very disappointed with my city's only rheumatologist.
What a lovely genuine caring dr you are. Ty
So nice of you
@@rheumatologistoncall because you are it shows x
I had same issue, suffered for long periods. Ultimately started treatment with steroids and Methotrex, dose and schedule adviced by my rheumatologist. In 5 days, i became normal with no pain. Medicines prooved to be miracle for me. Thank God, thanks to allopathy medicines. I should have started the treatment earlier. 🙏
Thank you for sharing your experience
THank you so much, watching this video and listening to this is a Big help 😇😇😇🙏🙏🙏🥰🥰
You are so welcome
At 34 I just felt sick and I was so tired. Then the foot pain began first n one foot then the other foot. I felt like I was walking on open wounds. My rheumatologist said my SED and RA Factor and the other test was off the charts. That and my textbook physical symptoms meant that the disease needed to be treated aggressively. Now 30 years later my life changed. I hurt everyday, have deformed feet, and tooth loss. Still the meds that r available today are great and can give RA patients an excellent quality of life.
I am so sorry
Thank you Doc for thr information
My pleasure
Finally, I diagnosed by RA and everyday are nightmare. My body is in pain, from morning to night, especially when I worked too much. Medicine is not working yet, I take for 1 month. Because of I have raynaud syndrom too, I asked to my doctor to check my artery, and I am sure I have problem in my feet arteries. Like, I couldn't stand up for long time, hard for walking and tingling everyday.
I'm really sorry to hear that you're going through such a tough time. It sounds incredibly challenging, but it's great that you're actively seeking answers and solutions. I hope you find the right treatment soon!
@rheumatologistoncall thank you. Your videos made me aware of my condition. I hope you will always make educational videos like this ❤️
I’ve had all these symptoms exactly as described and all at the same time and though I still struggle with dry eyes and dry mouth, when I change my diet, all the symptoms go away except the dry eye dry mouth, but it becomes so much more manageable. Mine was related to leaky gut and gut candida and sibo both I got treated…diflucan and rifaximin to resolve it. I’ve gone through this a few times over the years, it comes back due to a have a poor microbiome caused by poor diet, infection, antibiotics.
Thank you for watching my channel!
Thanks for this video. Think I better get checked for this.
I'm glad you found the video helpful! It's always a good idea to stay on top of your health.
RA being an autoimmune disorder can be linked to poor gut health (Leaky gut) keeping your micro biome heathy is the first step in preventing and controlling RA.
Absolutely! It's fascinating how our gut health plays such a crucial role in overall well-being, especially when it comes to autoimmune disorders like RA. Thanks for sharing your insights!
Doc, I have deformed fingers in my hand because of RA.. Please help me to remove deformities in my hand? What medicine will I take? What hand exercises will I do..
Thank you for sharing your concerns. Remember, seeking professional medical help is key to managing RA deformities effectively.
Where will I go doc?
@@AmyDepaz i also have deformations on fingers, I have been to specialist with no luck of fixing them!
Get ur d3 checked, you want it in the 50 to 80 range. Mine was 41 after 10 months of 20,000 iu every day. No side affects at all. Also take magnesium dioxide and k2.
It's important to keep track of your vitamin D levels for overall health!
@@rheumatologistoncall Does Vitamin d deficiency symptoms look like RA
I am 28yrs. A teacher by professional for 7 yrs now since I started teaching my shoulder really ache. Nowadays the pain is spread to my hands and legs😢
Thanks for your valuable advice.
I'm glad you found the advice helpful!
I have every symptom especially joint pain. My ANA test came back positive and sjogren's ssb was elevated. I definitely thought i was going to be positive for arthritis but nope negative. My rheumatologist seem not to seem to concern but im always in pain. Guess what the diagnosis was??? Fibromyalgia 😭
Thank you for sharing!
I would like to thankyou for explaining in detail..
I’m 40 and I’m afraid I have it. Just recently I’ve started getting very mild stiffness and soreness in my fingers and occasionally my toes. I don’t know what else it could be. The best way to describe the feeling is like I need to crack the knuckles constantly or straighten out the fingers. Not necessarily pain just mild discomfort.
It's always a good idea to consult a healthcare professional for any new or concerning symptoms.
@@rheumatologistoncall Does RA manifest overnight
I have sjogrens and have been gaslite for 5 years as my health declines. 😡
I'm sorry to hear that you've been going through this. You're not alone.
Thanks it is very useful for me. Also very important for all.also thanks
You are most welcome
Excellent video
Very informative
Glad you liked it
Ive bèen telling my rheumatologist about numb hads for a long time. He just says I have carpal tunnel. I've tried telling him about my chronic exhaustion. He tells me I need to exercise. He's absolutely no help.
Doctor, thank you so much for the very informative video. ❤ I have a question, can we have RA when the ESR and CRP results are not that high?
Yes you can!
@rheumatologistoncall my CPR and ESR is always high but because of diabetes. Could it be RA as well.
Can you recommend someone in Canada with a similar philosophy to healing RA? 🙏🙏
Unfortunately not, my book will be released soon and you can order it!!!
My primary dr finally referred me to see a rheumatologist saying it's usually at least 6 months wait to see an RA specialist, and even then they are very selective; you have to have enough evidence that it may be RA for them to consider seeing you. I did not realize it was that difficult to see a specialist. Are there THAT many people needing diagnosis help but not enough RA specialists?
There are not enough RA specialists. Look on my website if you are in one of the states where we are seeing patients
Rheumatologistoncall.com
@jskim.9122 i think it depends on where you live. I got an appointment within maybe one month in my small town. I got in quickly with my other appointments too but unfortunately she's the only one in town and she's no longer here. The other ones are at least 40min drive and further 😞
❤❤❤thanks for the info..
You are so welcome
I have had RA for 7YRS. I have just been recently diagnosed with moderate/ severe carpel tunnel
I'm sorry to hear about your diagnosis. It must be challenging to manage both conditions.
I had blood work done to check thyroid levels. Recently diagnosed with hypothyroidism. My thyroid levels were fine, but i had an ANA of 360. Was referred to a rheumatologist who did more blood work and said that it looks like sjogrens. That was about 2 months ago. My biggest problem right now is the pain in my arms. I can hardly lift my left arm. Pain at night is severe. I have other symptoms of sjogrens, but the arms are the main problem right now. I dont want to take prednisone. I just dont want the mental side effects and the weight gain. Is there another option?
thank you
I heard that you have to have a flare up is when you need to be tested. I have them all.
No, you can be tested outside of a flare up
Very informative
thank you
I've read at the NIH that vitamin D receptor defects can be part of the problem, so that even with normal vitamin D levels, the inflammation can rage on anyway.
Thanks for the info!Share with others! Thank you for watching my channel!
@@rheumatologistoncall I've seen people say, they could not raise their D3 levels above 30 for years but liposomes took them to 52 and 80 in weeks and months. The changes in their quality of life were something to behold.
My Vitamin D Level Is Low & All The Doctors Say Is My Blood Work Looks Fine But I Have Red Eyes And All Been Having Joint Pain And Numbness For A While
@@amandaducksworth1981 Read the reviews on Liposomal D3/K2 on the worlds biggest marketplace.
🎉🎉🎉🎉congratulations Dr am from Tanzania
amzn.to/4cxXHNX
my all blood tests and inflammatory markers are negative but i all joints pain for 3 months and reduced left knee space doctor said its due to anxiety.is this right or i need re evaluation
You need a rheumatologist evaluation
@rheumatologistoncall rheumatologist said it's due anxiety .is this right?
Thank you🎉🎉🎉🎉❤❤❤❤
You're very welcome! I'm glad you enjoyed the video!
5:22 I can’t give a thumbs up. It hurts. No, but seriously both my hands hurt badly in the AM and/or when I wake from a nap. I can’t wear my rings anymore because I can’t get them over the finger joint. I’ve also had dry eyes for so long. The ophthalmologist told me the surface of my right eye in particular is badly damaged from dry eye.
thank you for sharing, did you subscribed?
ma'am my age is 32 men from Pakistan all blood works are normal ESR 7 CRP .4 rheumatologist says it's not autoimmune disease then kindly tells what causes all joints cracking and stiffness remains same all day plz
@@MuhammadUmar-gh6cz Your CRP is slightly elevated. Normal range is 0.3 or lower so there’s definitely something going on. Just going off of blood tests seems unreliable to me and I’ve been a nurse for over 15 years. Many people will have obvious symptoms but normal serum labs. I hope you get the help you need and I’m sorry to hear you are suffering.
@@rheumatologistoncall yes
Is golfer's elbow symptoms also a sign of arthritis? Will it ever cure?
Yes it can be!
i consulted 5 doctors so far, nobody treat me properly,just gave me antiinflammatory pills,sent me to recovery showers,and other dr. gave me alflutop injection, is this enough?pain is always there, i also have coxatrosys and gonartrosys,all parts of knee,hips,spine crackling n getting worse,swelling all days,is depressing,im only 40yo..all started at 35,i wonder why..
How is your Vitamin D level? Did you check?
check with another rheumatologist or a second opinion!
@@benedictjoseph3832 i check it,was low,im taking vit d,k, but that doesnt solve my problem,im still in pain!
@@rheumatologistoncall i will, i did, still trying, donno where to go next, maybe recommend me one from bucharest?multumesc!
I have it .fingers, can't bend them now have difficulty holding fork ect..in elbows .. shoulders..toes..neck ..well i am assuming the pain in neck is arthritis,but my doctor gives me cocodomol and notjing for inflammatory so i buy my own ..so i had these signs 3 years ago it started in wrists excruciating pain but was given pain killers then and do not have any further help from gp ,so as for saying.. don't ignore these signs..it makes no difference if not really getting anything to relieve it more.
thanks for watching my videos!
What medicine is good for RA..
you have other videos in my channel
This sounds like me. I've gotten a referral for a rheumatologist made an appointment but they didn't have an opening for 5 months.
Yes that is true all over US, check out our website Rheumatologistoncall.com we might be able to help you!
Mine is over a year away what a joke
I have a lot of these symptoms but I have thyroid cancer and had 2 RAI treatments and this can cause dry mouth and eyes and affect your salivary glands. My fingers are usually swollen and achy all the time. Had blood work for autoimmune and all negative.
It sounds like you've been through a lot with your thyroid cancer and treatments. I hope you're managing your symptoms well.
Does RA always show up in a blood test ?
No
I use a heated wax therapy, at home, for arthritic pain of my hands.
Great! I recommend that all the time to my patients. Did you see my other videos????
If you catch it in the early signs, can you get treatment and live a relatively normal life ? Versus treating it in the later stages?
thnaks
yes!
I wish you were close to our town
It's very, very hard to get an appointment with a rheumatologist. I have every one symptoms but because my "labs" don't show anything the rheumatologist won't see me. We have one that is within a hour drive and dr has terrible bed side manners.
You can see me through telemedicine
Can be RA caused by kidneys disfunction there for metabolic hovoc for wich kidney responsible in body
NO, not by kidney issues!Thank you for watching my videos and supporting my education mission!
I get diagnosed 3 months ago and my hair fall alot i dont take any medicine for arthirits is this from arthritis?
I was diagnosed with RA even though my only symptoms have so far been only joint pain in my fingers. No pain in my wrist either. I have not had fever, fatigue or any of the other symptoms you mentioned. Even my blood tests only revealed an elevated ESR level. Everything else ( including C-reactive protein) is normal. Should I get a second opinion elsewhere? Kindly advise?
Thank you for sharing
@@sunshine2873 do you have joint pain in multiple fingers in both hands? if yes, then it could be RA else i would get a second opinion
Do you use MRI, CT scan or Ultrasound to diagnose RA? I've had horrible joint pain in hands/wrists for 7 months now and it's spreading to my knees, etc. Aside from a positive ANA test, my other results were "normal". My Rheumatologist refuses to do any type of scan.
yes I use MRIs
@@rheumatologistoncall thank you!
I have dry eyes, dry mouth and constant pain in my forth-legs and hands specially my thumbs. My doctor did a bone conduction test and the found severe loss of bone and she diagnosed me with osteoarthritis. However my bones and muscle remain swollen. Should I request a referral for a rheumatologist. Also my adult son and Mother were diagnosed with RA
Thank you
I have all these symptoms... And my older brother has RA. The knees need replacement, my thumb joints are bad and and i have neck pain and a LOT of foot pain. Dry eyes and mouth ...check.
I'm so sorry to hear about your symptoms. It's important to get proper medical attention and support.
Far out I’ve got all of these symptoms and diabetes and low thyroid.
thank you
I have had it for 17 years but years before that the tips of my fingers would randomly become swollen and red and very painful. Then in early 2007 it came on all over with a vengeance. I have been on methotrexate ever since.
GReat!
I've got al this aswel as as&spondylolisthesis etc my doctor takes no notice of me
I am sorry to hear that! Look for a second opinion!
@@rheumatologistoncall thankyou yes I'm trying to I can't have antiimflammatory drugs I've tried them only steroids my old doctor gave me them for pain&with codeine,paracetamol I had to change doctors twice since then as I'm not living in the post code area etc so stupid so now everything is al over the place. I am under different hospitals etc. They should be having meetings with me soon so hopefully but this doctor is so stupid. I live in the UK. Everything u say is true so I'm taking notes so I can pull them on it. Thankyou 💜
I am 29 yrs . Have had joint rashes especially on my hand and foot on the same sports way back when I was around 10-15yrs. Have been to hospices and no sign of athlities. What could be the problem I always have shoulder pains when I strain.
Thank you! Please subscribe to my channel!
I have read that seronegative RA can have worse symptoms. Is this true? Also, can one have carpal tunnel and RA so need surgery? Even with RA meds, my CT is no better and is quite disabling with numbness on waking and often intense pain. Thanks for sharing your expertise.
no, see my video about seronegative RA in my channel
Thanks somuch for this explanation, everything u said is correct and I am having it all , I am under treatment and taking plaquenil 400 mg every day and I am good 50% but still have pain in my front joint foot it’s not getting better at all I need your help ! I did got injection plasma for it it helped a lot but after 6 months I have pain again , I have taken 3 times the plasma injection! But still I am getting pain , I also have pain in my lower back one side too ! U are so good telling me that the arthritis dosent show in blood test it’s very true , because my Docter said my blood test is good so she gave me triptizol 25 mg tables for 6 months to continue, I am sleeping very well with this tablet! Want to thank you somuch for explaining the arthritis pain which I am going through ! What food I should avoid ? Some say my diet need to change but I never tried pls help me
I'm glad the video was helpful for you! It's great that you're seeking treatment and taking steps to manage your arthritis. I'd recommend discussing your ongoing pain with your doctor to explore other treatment options.
Im 17 and im in agony with my joints and everything, I have every one of these symptoms and its so debilitating especially with it becoming winter the pain becomes so much worse and my joints feel so much more sensitive. It runs in my family.
amzn.to/3U89bAn
good video
What happens if you can't get a appointment no doctors in the area has openings.
We see patients in multiple states Rheumatologistoncall.com
I wish it was so easy as just calling a rheumatologist to see you
check my other videos in the channel!
Ma'am. I have RA and my top knuckles turning black recently I consulted a endocrinologist reports ar normal then dermatologist she said melonosis.
Thank you, please subscribe and share it with others!
I have ulna nerves syndrome not carpotunnel
Thanks for sharing! It's important to understand the differences between conditions like ulnar nerve syndrome and carpal tunnel. Your health journey is unique!
After giving birth to my second child I have same symptoms pain in fingers I check my RA factors but my report came negative. Can I go for 2nd opinion
Thank you for watching the videos!
I was just diagnosed with the hla-b27 gene and high inflammation markers. I have been suffering and getting worse for years. What causes the cracking and popping all over like every step or movement causes cracking?
I'm sorry to hear about your diagnosis. It's important to work closely with your healthcare provider to manage your symptoms and explore treatment options.
I am clinically diagnised with Pleural effusion extra pulmonary TB and pneumonia. admitted to hospital with pleural fluid filled in my right lung more than 2/3. i have many of the mentioned symtoms. any chance for RA?
check with rheumatologist
Thank you for watching my channel!
Miałam sztywność stawów skokowych zawsze rano po wstaniu z łóżka ale po odrobaczeniu ten problem znikl.Mam początki Artritis ,ale lekarz przepisze mi Diclo Tabl lub maść i tyle.Jedynie co mnie niepokoi to takie wypukle zgrubienie jak np. polowa jajka na grzbiecie stopy od strony zewnętrznej ,nie boli ale to jest miękkie jak galaretka które powstało od niedawna i na ten problem lekarz ortopeda nie potrafił mi pomóc ,co to jest?😢Moze Pani doktor wie z doświadczenia co to może być.Pozdrawiam z Polski.❤👋🏼👋🏼
Dziękuję za podzielenie się swoją historią! Ważne, aby skonsultować się z lekarzem w sprawie tego zgrubienia. Mam nadzieję, że znajdziesz odpowiedzi, które pozwolą Ci czuć się lepiej.
Even I'm going through the same situation . I had dengu ..post dengu after week my right hand fingers tips r swollen , tingling., inflammation.....in the next 3 days left fingers affected... beginning had bit pain but wt pain killer no pain now ...but swelling, stiffness, inflammation is still there past 24 days....legs fingers also has. Numbness and inflammation....please suggest what it could be....
Sorry to hear that
What if i almost have all symptoms mentioned but only with one side or unilateral CTS (carpal tunnel syndrome ) ?
Thank you
Thank you! Please subscribe to my channel!
U are good
Thank you
I have painful eyes that turn into bad headaches a have arthritis in me neck back wrist and knees now a feel my back muscles are tearing apart n my lungs feel heavy when I lay down I can't sleep for it but sleep loads any other time like mostly all-day should I see a specialist (im 40)
It sounds like you're dealing with a lot. It might be a good idea to consult with a specialist to get a proper diagnosis and treatment plan.
@@rheumatologistoncall I'm there today it's quite scary I'm normally OK on morning but pain is there
Yes my back is killing me
@@rheumatologistoncall I can hardly get up in the morning..my hands and feet have swelling ..not to mention the pain
Hello mam i got dengue fever 2 mnts ago from onwards my fingers are swelling,and pain, and my hand , foot, elbow are very pain. My ra factor 32 possitive, but ANA negative . Will the pains will go or for life long. Is the rheumathoid arthitis. Doctor suggest only vitamin tablets and pain killer tablets . Plse help me mam
Please schedule a visit with a rheumatologist, you need help!
Thanks for watching my videos there is a lot of useful info here!
Even I'm going through the same situation . I had dengu ..post dengu after week my right hand fingers tips r swollen , tingling., inflammation.....in the next 3 days left fingers affected... beginning had bit pain but wt pain killer no pain now ...but swelling, stiffness, inflammation is still there past 24 days....legs fingers also has. Numbness and inflammation....please suggest what it could be....
Hi even I'm going through the same situation....did u recover...pl help what helped u...
@sarithakondal3566
How is ur condition now...im also going through it...whom you consult..
Grazie...soprattutto dei sottotitoli in italiano
Thank you for your kind words!
Ive had nine different vials of blood taken and they have all come back as abnormal now i have to wait a month for dr to tell me i kniw what it is so i cancelled him disgusting having to wait that long when im in real pain
Is it possible to have more pain in one hand than the other? Especially if you are left handed and use your left hand more
YES!!!
Mahal kita 💖
Mahal kita too! Your support means a lot to me!
Hello my RF was positives and l don't get the correct doctor where can l get you
rheumatologistoncall.com/
I am 30 years old and i am having this carpel tunnel syndromes since 8 months of my pregnancy time and now its been 1 and half years what should i do and to whom i may concern for this?
Contact us Rheumatologistoncall.com
I have almost all the symptoms since my forties, now I am in my sixties. The pain in the finger joints, wrist and shoulders has become debilitating. I can't move out of my bed in the morning. But my RA factor test always comes negative. Could you advise what to do??
get an MRI with and without contrast and that will clarify!
Is RA curable ?!
My RA factor is 68. How can I reduce this?!
Thank you!
@@rheumatologistoncall mam, is rhematoid arthritis curable?!
My RA factor is 68.how can I reduce it? Please reply
am i rare to be diagnosed with RA without it passing down with my moms genetics? we tested for genetics and it didnt pass down
Thank you for sharing your experience. It's interesting how genetics can be a mystery sometimes.
What genetic tests did u get done? My mom also has RA
How does RA differ from Connective Tissue Disease?
I have already got the diagnosis of PsA as it attacked my knee (seen on an MRi) but I have hand pain in both hands. I also have Raynauds. They say it’s rare to have PsA and RA but I think I have RA too. Currently on Humira which is helping my knee but not doing much for my hands. Humira also normalized my inflammation levels which were so concerning they thought I had blood cancer and sent me to an oncologist/hematologist. Luckily, no blood cancer just tons of inflammation.
Dr my daughter who is 25 years old has been diagnosis with episcleritis. A PET scan was done and everything is normal.Then why does her eyes become red every month
This is caused by inflammation.
If it is only happening once a month, maybe it is something that she is eating. Maybe not.
Since they don't know what inflammation causes it, then I would try to eat a vegetable diet for a month, raw and cooked, drinking lots of water and nothing else (sugar is an inflammatory food) to see if the inflammation goes down and it stops.
Then, you can try introducing new foods every week to see if any of the foods are inflammatory.
Sugar, high fructose corn syrup, genetically modified foods, and processed foods are all inflammatory.
There could be an autoimmune disease!
What about parasites? Cause these symptoms ?
possibly
I am 47. Both wrists started hurting out of nowhere. Within a week or so became excruciating. Have a rheumatologist appointment in a month after waiting 2 months already. The pain moves around from fingers to thumbs, now forearms and biceps when I twist my wrists. It never has really let up. Probably 5% of the time it doesn’t hurt to just sit. It feels more like tendon pain than joint pain. I’m about 40 lbs. overweight but rarely got sick my entire life. I’m just worried I’ll have someone put me on a ton of meds killing my liver and have worse side effects than the symptoms. Any advice please?
I'm sorry to hear about your wrist pain. It's good that you have a rheumatologist appointment coming up. Remember, it's important to address your health concerns and seek professional advice.