Bless your heart, I know that pain. I have a Connective Tissue Disease and osteoarthritis. They wreak havoc on my body 24 hrs a day. I wouldn’t wish that pain on my worst enemy. Hoping you have the best results!!!!
I've had RA for 25 years. Trying to describe the pain level is hard. I think we live with it for so long & build up tolerance that our perception is skewed compared to people who don't have autoimmune illnesses. Keep pushing 4ward. U've got this warrior woman!
I am hyperthyroidism and graves disease. Which triggers so many bad things. Right now right foot and ankle is hurting and tingling horribly@celiacandme8916
I relate as I suffer from Lupus and experience severe RA pain on a daily basis. The other day I had my dentist do a root canal without any pain relief or anaesthesia. He was amazed at my high pain tolerance. I think living with pain one becomes accustomed to it.
I have been living with fibro for years. I try so hard to not let it take over my life but some days it just does. People find it hard to believe because when interacting with others, I try to keep a smile on my face and act like I'm fine. Unfortunately I can no longer teach elementary or special education because the strain and stress it put on my body. I pray for a cure. Sometimes I want to scream when people try to tell me how their loved one has it but she still does this, that, or the other, or they do this and are practically cured. Fibro is different for everyone. There is no one size fits all cure! I pray for all my fellow fibro warriors.
Danielle, I'm so glad you're taking care of yourself!! It motivates us other women to do the same! And to feel okay advocating for ourselves ❤ I hope you feel better soon. I'm in the same boat, nice to not be alone.
I understand, and you are a warrior. Chronic pain is exhausting. Yes, I am a warrior too. By the way, thank you for showing real life in caring for Ed. It’s hard. While my mom still lives on her own, for now, I see this day coming. She is starting to have hallucinations and gets confused. Here we go… I love her so much, and yet there are hard days. I get it. Gentle hugs
Hi Danielle, After turning 50 I’m noticing I’m always in extreme discomfort. My whole body hurts and I’m far more sensitive than I ever was. Thanks for being so genuinely authentic and relatable! Glad you’re feeling better! Love ya❤
One person's level 2 may be another person's 10. It is all relative and it can only be relative to yourself. If you are never without pain, that becomes your new normal so you may report a lower level than someone without pain on a regular basis. I prefer to tell the doctor more descriptive phrases than a number. I have had multiple sclerosis for over 60 years so I can relate to both your discomfort (constant) and the pain. I do know that stress is an exacerbater of both discomfort and pain and you have one of the most stressful jobs, caregiver to someone you love. This being said, you are one tough warrior, but do not hesitate to back off and take care of yourself. No one else is walking in your shoes and trying to explain why you need to do whatever may fall on deaf ears. I can tell you are tough and you are stubborn, but do not hesitate to say I just can't right now. Hang in there sweet cheeks! We got your back!
I live in chronic pain as well & have so many areas of pain it’s classified as fibromyalgia -I went through injections of cortisone for the 4 bursa that are in one’s hip region for years -but no longer do that (but it did help for about 2months afterwards) now I have inflammatory pain all over my body but especially legs, hips, feet but can’t take any anti inflammatory like ibuprofen because I had a bleeding ulcer in 2016 & almost died because I’m on blood thinner medication because of afib. Anyway just wanted to say as someone who lives with this everyday & every nightmare of a night in pain you are definitely correct in saying it’s more than just discomfort. I feel for you & understand! ❤️
Have u looked into the Spoon Theory? That can help u to explain your *umpf* factor & not feel so horrible about not being able to do some things. I have MS & think about spoons daily 😂😂
I feel your pain.. it is with me 24/7... Even when I manage to sleep.. my husband says I moan... I wished the injections had worked for me... but they didn't.. I would get home after one and in an hours time the pain got bad again.... I have learned to wrap myself up in an electric blanket and use meditation/rest music to get some relief ... I am not able to take any kind of drugs for it except for Tylenol ... which I don't use... it's like taking candy.. no help at all.... oh and I pray !!! Fibromyalgia and arachnoiditis in my spine is no joke!!!
It took me years to get a diagnosis 😢and the pain is real. The flares are the worse and I thought it was in my head and I punished myself sending prayers
I've been suffering from Fribo for many many years so I know the pain and discomfort that comes from it. But due to other health issues pain meds or cortisone shots I just can't take them. So I have to live like this every day. It stops me from doing so much stuff. I'm very glad for you Danielle that you can find some relief. ❤
I'm praying for you, Danielle...years ago I had horrible neck pain...after a few years, I was completely well...the only thing I have now is an arthritic knee that I have to get some more help for...not too major...as I'm going on 72...🙂
Danielle, I am happy that you finally got a diagnosis that is running throughout your body. Fibromyalgia is harder to the right answer. Its symptoms are signs of so many other issues. Everybody reacts differently so the advice I am giving you is not to listen to others, offering their version of on what you can do or try. Know your body, know the trigger points and relay on your doctor’s care. Family and friends can get ignorant because of constantly saying that you don’t feel right, they just don’t understand until you get the diagnosis. I sure am hoping you get relief because the pain is real. Let’s be positive and hope that all goes well with you. Hugging and loving you deeply. ❤
I feel your pain Danielle, I have Lupus and the pain is unbearable and constant. I was getting injections but my pain is everywhere mostly in my muscles, I use CBD warming cream, if you can get it I highly recommend it. I have mine made. If you can't get it I will send you a jar. Please take care of yourself. I love you and I hate seeing you in pain 🙏🩷
I am so sorry, Danielle. My oldest daughter is just 48 and she too suffers with fibromyalgia. I know that she does cortisone shots as well and she is on a medication called: Lyrica. She told me that it helps but she also does home remedy type things to help her. I will ask her what helps her the most and get back to you. Now that you know what's going on with you - you can put a name to it. I know pain, and I don't wish it on anyone. I really hope treatment works for you and you will began having less pain. OXO Love ya darlin 😘❤
I have had Fibromyalgia for years. Also, it comes from trauma from years of abuse. If you have Fibromyalgia you should get checked for POTS. it has its own set of conditions that aggravates Fibromyalgia.
I'm sitting in my car at the moment. Going in for neck injection. I've been through too much to write here. I was diagnosed in 99.had 8 major lumbar surgeries. Worse every time! Now I'm left seeing a pain management doctor
I'm right there Jane...4 back surgeries, stimulaters, meds, left pretty broken..iam sorry you have gone through so much...just wanted to saw iam there with you....take care
@SharonO-333 Are you in Pain management? I'm in Florida, moved from Connecticut about 2 yrs ago. Getting medication is not as difficult down here. Connecticut stuck to the 90mme! Had trial stimulator, bad for me!
@jane-m4t I'm in Sac, Ca..was in pain management for several years, 61 construction whole life and got really tired of pee in cups and being looked out funny. So, I stopped, I now just go to my PC...I have heard that medication is easier prescribed in Fl.. it's becoming a terrible situation.. had the stimulater put in, and then they removed when he did the fusion..
How to deal with the pain and dealing with the intense care of your father in law. I have a similar problem with RA. Thank u for sharing. Love u too!!! ❤
Ya know, with two auto immune diseases x 30 yrs, I've found myself constantly trying to describe pain or quantify pain when always asked at my doctor's office & wondering why I do that!
When you have fibro you hurt all the time so you start minimalizing pain for discomfort. Also please be careful with the cortisone. I only went when I couldn't stand it anymore but it burnt out my pancreas & now I have Type 1 diabetes
Yeah I like that extreme discomfort because it is pain but it's different than what you think of as pain it's just this ache in your entire body you can't even almost can't pinpoint where because it's coming from everywhere. It's like living with a severe body aches of flu every day of your life and I've had this started 30 years ago so yeah it's just normal and I try to tell myself this is normal so that I can survive it but I feel like looking into what you're taking because it would be nice not to have any or to have less and also the stiffness and also I have hereditary knee problems
You know Danielle, it's strange that you're talking about that, because I went to my chiropractor yesterday, and he said that I was suffering from fibromyalgia, which was caused by emotional trauma. He went through a process on me called QNRT( quantum neurological reset therapy), which goes through things that might have happened in your past that still bother you physically, even though mentally you feel like you're over them, if that makes sense. It's really weird and somewhat unpleasant, but two things came up from past experiences with my parents and afterwards I did feel a huge sense of relief from what in my mind was painful inflammation all over. This might be something you could think about looking into if there are any chiropractors in your area that happen to practice in this field because it's really weird but it seems to help sometimes there's no drugs or anything like that involved in it.
I don't know a lot about this but I know it can be quite painful from what I've heard I sure hope whatever they do to give you some relief hope it works sending prayers and hugs❤
I hear the carnivore diet is like a miracle when it comes to relieving pain. Getting rid of the inflammation that certain foods cause is the key. Try it for a few months, what do you have to lose, but the pain ? 🙂❤🥩
Ihave fibro hurts like crap,My knech and my shoulder alot but it effects other parts of my body, And really the pain meds doesn't help 😢prayers pretty lady 🙏🙏
Hard to express pain, when you're one tough lady like you. Hoping it does the trick. If not, ask your doctor about a cortisone cocktail injection. Doesn't contain anything addictive.
Hey Danielle, I’ve also had fibro for 25 years and understand your version of extreme discomfort. How I rate my pain is on a 1 to 10 scale when I’m describing it to someone else. Example today I’m about a 5 on the pain scale. I thought that might help you! I feel ya girl 🩷
Oh my gosh I have fibromyalgia and I have osteoarthritis and I have degenerative spine and cervical spinal cord compression I could just go on and I cannot take pain medicine cuz it destroys my stomach and gives me ulcers😢😢😢😢 I did not know you had that that is so sad. I'm so sorry because with all the work you do and everything I don't know how you do it oh my gosh because I just have very low energy and I know all you want to do is just kind of lay in bed it's like you have to lay in bed every day just to get the gravity off of your body. So how you do all that running and everything you do is like I don't know it's like a superwoman
Understand.....fibro and RA here, double whammy.....I use pure peppermint essential oil straight rubbed on neck and muscle and joints that are painful. This has worked the best for me over 20 years!! Soak in a tub with epsom salt if you can get in and out okay....will help with minor aches and pains. soft hugs!!
🌿🌸😹Oooooomg oooooomg ooooomg this docor is the worst a eeeeever heard about!a laughiiing how terrible doctor was bescuse a experience the same attitude from doctors,,,Danielle a love how you take the situation! You the queen and a really hope you chabge to a female doctor who understands our body.
5 months ago I had cortisone injection in my neck and left shoulder, I'm needing another one now . Now I'm wondering if I have fibro ? Because I have lower back pain , shoulder, neck and left arm pain Thankyou for your insight x
@ you know the pain i live in manitoba canada it soon be very cold and tons of snow this winter will be bad im already not great i had a hysterectomy full slice open to get a 10 cm fybroid out since then for ladt couple years been bad im 56
Danielle, you should have your own videos, because you only speak of yourself. That way, us that don't want to listen to you at all, can be spared of listening about you. Because , personally, I don't care about you, it's Ed we want to hear and see.
Everybodys version is different...thats why its hard to treat❤❤❤
Bless your heart, I know that pain. I have a Connective Tissue Disease and osteoarthritis. They wreak havoc on my body 24 hrs a day. I wouldn’t wish that pain on my worst enemy. Hoping you have the best results!!!!
thanks girl hang tough.
I've had RA for 25 years. Trying to describe the pain level is hard. I think we live with it for so long & build up tolerance that our perception is skewed compared to people who don't have autoimmune illnesses. Keep pushing 4ward. U've got this warrior woman!
I'm RA and flared up but I try to keep moving . Yesterday napped. So ya if I took a nap I was hurting
I have two autoimmune diseases and truly relate to your comment. Blessings to you.
I am hyperthyroidism and graves disease. Which triggers so many bad things. Right now right foot and ankle is hurting and tingling horribly@celiacandme8916
truth!
I relate as I suffer from Lupus and experience severe RA pain on a daily basis. The other day I had my dentist do a root canal without any pain relief or anaesthesia. He was amazed at my high pain tolerance. I think living with pain one becomes accustomed to it.
I have been living with fibro for years. I try so hard to not let it take over my life but some days it just does. People find it hard to believe because when interacting with others, I try to keep a smile on my face and act like I'm fine. Unfortunately I can no longer teach elementary or special education because the strain and stress it put on my body. I pray for a cure. Sometimes I want to scream when people try to tell me how their loved one has it but she still does this, that, or the other, or they do this and are practically cured. Fibro is different for everyone. There is no one size fits all cure! I pray for all my fellow fibro warriors.
So sorry 🙏
hang tough my fibro warrior.
Former special education teacher here! I get it. CRPS, Fibro, and RA. I finally had to retire early.
@@sherinolan9925 the pain takes over your life!
Danielle, I'm so glad you're taking care of yourself!! It motivates us other women to do the same! And to feel okay advocating for ourselves ❤ I hope you feel better soon. I'm in the same boat, nice to not be alone.
ahhhh thats what I hope with all my words. xoxo
I praying for pain to heal.
I pray for you Mrs Danielle your pain doesn't affect how nice you look for sure
I'm glad to hear you felt like the cortisone was promising for you. Hoping for the very best.💞🙏
I hope so too!
I understand, and you are a warrior. Chronic pain is exhausting. Yes, I am a warrior too. By the way, thank you for showing real life in caring for Ed. It’s hard. While my mom still lives on her own, for now, I see this day coming. She is starting to have hallucinations and gets confused. Here we go… I love her so much, and yet there are hard days. I get it. Gentle hugs
Chronic pain is a new world. Glad you are feeling some relief- hopefully it lasts!!!! ❤
Keeping fingers 🤞🤞Danielle!! TY for keeping us informed. ❤❤❤❤
love u.
🎶 My neck, My back, My 🐱, and My craaaaccck..🎶 😂
I’m happy for you, I need a check up as well. Thanks for the reminder.❤
You are so welcome. and get it girl.
😹🌸✨🩷 Aaaawsome text/song to Danielle GSR🌿
Hi Danielle,
After turning 50 I’m noticing I’m always in extreme discomfort. My whole body hurts and I’m far more sensitive than I ever was. Thanks for being so genuinely authentic and relatable! Glad you’re feeling better! Love ya❤
ugh! im calling this the woman's disease....we push ourselves too much for too long and this is what happens. :)
One person's level 2 may be another person's 10. It is all relative and it can only be relative to yourself. If you are never without pain, that becomes your new normal so you may report a lower level than someone without pain on a regular basis. I prefer to tell the doctor more descriptive phrases than a number. I have had multiple sclerosis for over 60 years so I can relate to both your discomfort (constant) and the pain.
I do know that stress is an exacerbater of both discomfort and pain and you have one of the most stressful jobs, caregiver to someone you love.
This being said, you are one tough warrior, but do not hesitate to back off and take care of yourself. No one else is walking in your shoes and trying to explain why you need to do whatever may fall on deaf ears. I can tell you are tough and you are stubborn, but do not hesitate to say I just can't right now.
Hang in there sweet cheeks! We got your back!
I appreciate it. xoxo
Hugs to you Danielle 🤗
I live in chronic pain as well & have so many areas of pain it’s classified as fibromyalgia -I went through injections of cortisone for the 4 bursa that are in one’s hip region for years -but no longer do that (but it did help for about 2months afterwards) now I have inflammatory pain all over my body but especially legs, hips, feet but can’t take any anti inflammatory like ibuprofen because I had a bleeding ulcer in 2016 & almost died because I’m on blood thinner medication because of afib. Anyway just wanted to say as someone who lives with this everyday & every nightmare of a night in pain you are definitely correct in saying it’s more than just discomfort. I feel for you & understand! ❤️
ugh im sorry. I understand. :)
@@mrsdsalnorcal ❤️
...living w/ chronic pain here.....
booooooo
Me too ..
Have u looked into the Spoon Theory? That can help u to explain your *umpf* factor & not feel so horrible about not being able to do some things. I have MS & think about spoons daily 😂😂
I feel your pain.. it is with me 24/7... Even when I manage to sleep.. my husband says I moan... I wished the injections had worked for me... but they didn't.. I would get home after one and in an hours time the pain got bad again.... I have learned to wrap myself up in an electric blanket and use meditation/rest music to get some relief ... I am not able to take any kind of drugs for it except for Tylenol ... which I don't use... it's like taking candy.. no help at all.... oh and I pray !!! Fibromyalgia and arachnoiditis in my spine is no joke!!!
oh no. hang tough girl. pain sucks.
It took me years to get a diagnosis 😢and the pain is real. The flares are the worse and I thought it was in my head and I punished myself sending prayers
I realize I was also doing this...punishing myself in diff ways. almost like gaslighting myself.
And when im having a Great Day i enjoy my day so much better!
Danielle ❤ sending love & hugs ❤❤❤❤❤❤xxxxxxxxxx
Danielle, so glad you're finding answers. Take care! Have a great weekend. Love you lady!❤😊❤
xoxo
Injections do not repair. Euphoria cm does. Look it up. DMSO can also relieve pain and repair, look it up.
Danielle hope you feel better soon
You're such a dear
Person putting up with pain daily + keeping up with daily activities pets, laundry all that Stuff.
Danielle, I sure hope the cortisone helps you. 🙏🙏. Love from Pennsylvania 💕🌷🐻
I've been suffering from Fribo for many many years so I know the pain and discomfort that comes from it. But due to other health issues pain meds or cortisone shots I just can't take them. So I have to live like this every day. It stops me from doing so much stuff. I'm very glad for you Danielle that you can find some relief. ❤
ugh. im sorry.
@@mrsdsalnorcalThank you ❤
RA and fibro for nearly 3 decades. I can so relate. Bless you😢
Prayers 🎉
I'm praying for you, Danielle...years ago I had horrible neck pain...after a few years, I was completely well...the only thing I have now is an arthritic knee that I have to get some more help for...not too major...as I'm going on 72...🙂
Danielle,
I am happy that you finally got a diagnosis that is running throughout your body.
Fibromyalgia is harder to the right answer. Its symptoms are signs of so many other issues.
Everybody reacts differently so the advice I am giving you is not to listen to others, offering their version of on what you can do or try.
Know your body, know the trigger points and relay on your doctor’s care.
Family and friends can get ignorant because of constantly saying that you don’t feel right, they just don’t understand until you get the diagnosis.
I sure am hoping you get relief because the pain is real. Let’s be positive and hope that all goes well with you.
Hugging and loving you deeply. ❤
thanks girl. im excited and ready to feel as good as I can.
thanks girl. hoping to understand more and start to feel better. xoxo
❤❤❤
You are a warrior, Danielle! 😊. 🙏 for continual relief! ❤
Hope it helps Danielle its not very nice to be on constant pain ❤❤❤❤
Sending big hugs darl. 🤗🥰
Hi Danielle I really hope the treatment works and you soon feel much better.
sounds promising.
❤🙏🤞
Wow, I sure hope you get great relief from the pain now. I can't imagine living with it day in and day out!❤❤
I'm sorry for you but this is something that works for me everybody is different.
Danielle, you keep being a warrior girl look at what you mean my prayers are with you and your family❤🙏🏼Salinger
xoxo
I feel your pain Danielle, I have Lupus and the pain is unbearable and constant. I was getting injections but my pain is everywhere mostly in my muscles, I use CBD warming cream, if you can get it I highly recommend it. I have mine made. If you can't get it I will send you a jar. Please take care of yourself. I love you and I hate seeing you in pain 🙏🩷
ooh. sounds amazing. sorry for your pain.
Yeah I had that pain, for 5 plus years till I finally found treatment cortisone shot, its a new Lease on my Life. Happy for you Danielle.
I hoping for the same luck!
Hun with the menopause and the pain your going through the lady thing you need is Ed you need to rest I know pain.
Prayers for you. I have pain now for five years from my cancer surgery. I’m praying for you.
im sorry.
Hope you feel better
I am sorry, hope you feel better, pain turn to discomfort when it becomes chronic, as the body copes by making that pain a norm
I am so sorry, Danielle. My oldest daughter is just 48 and she too suffers with fibromyalgia. I know that she does cortisone shots as well and she is on a medication called: Lyrica. She told me that it helps but she also does home remedy type things to help her. I will ask her what helps her the most and get back to you. Now that you know what's going on with you - you can put a name to it. I know pain, and I don't wish it on anyone. I really hope treatment works for you and you will began having less pain. OXO
Love ya darlin 😘❤
And there you have it 🎉😊
Had one of those shots in my lower back due my DDD and OA...didnt work for me...glad it helped
I experienced the exact same thing only thing that helped was steroid pill but now unfortunately it has come back.
ugh sorry.
I have had Fibromyalgia for years. Also, it comes from trauma from years of abuse. If you have Fibromyalgia you should get checked for POTS. it has its own set of conditions that aggravates Fibromyalgia.
Prayers for you ❤
"🤞"
Hoping you get relief❤
Yes you explained it,nobody can understand it. I try putting brave face on cause im kinda used to it if that makes since. ❤
same girl same.
I'm sitting in my car at the moment. Going in for neck injection. I've been through too much to write here. I was diagnosed in 99.had 8 major lumbar surgeries. Worse every time! Now I'm left seeing a pain management doctor
I'm right there Jane...4 back surgeries, stimulaters, meds, left pretty broken..iam sorry you have gone through so much...just wanted to saw iam there with you....take care
@SharonO-333 Are you in Pain management? I'm in Florida, moved from Connecticut about 2 yrs ago. Getting medication is not as difficult down here. Connecticut stuck to the 90mme! Had trial stimulator, bad for me!
@jane-m4t I'm in Sac, Ca..was in pain management for several years, 61 construction whole life and got really tired of pee in cups and being looked out funny. So, I stopped, I now just go to my PC...I have heard that medication is easier prescribed in Fl.. it's becoming a terrible situation.. had the stimulater put in, and then they removed when he did the fusion..
im so sorry. hang tough. we are in this together.
@SharonO-333 I'm not happy about pm at all. It's a shit show everywhere. We are fighting though.
Keeping my fingers crossed for you Danielle! I hope you have found relief. Wishing you a pain-free, peaceful, and happy day!🤞❤❤❤😊
thanks.
@mrsdsalnorcal ❤️❤️❤️❣️
How to deal with the pain and dealing with the intense care of your father in law. I have a similar problem with RA. Thank u for sharing. Love u too!!! ❤
Xoxo
Ya know, with two auto immune diseases x 30 yrs, I've found myself constantly trying to describe pain or quantify pain when always asked at my doctor's office & wondering why I do that!
Ugh!
Feel better
I woke up and couldn’t move my neck a couple weeks ago. It was excruciating
oh noooooooooooo. its not fun!
Hope the treatments will make you feel better and pain free. Happy Friday to you all. 🤞❤💜
me too. plus I loved your pic. thanks
I got one last week between L4/L5. Feel lots better this week! Plus i bought a vibration plate a few weeks ago and it’s helping too!
yay.
I pray this works for u Danielle 😊
🤞🤞🤞🤞🤞 sending love Danielle ✌️❤️🌻
Prayers
I sure hope you find an answer! I'm so sorry for all the pain you have! 😢
I had the nerves in my neck burnt so that they don't send pain signals to my brain
🤞Really hope so. Im going next month..
Chronic pain is not fun! Hope it works!!! 😘💝💝💝
When you have fibro you hurt all the time so you start minimalizing pain for discomfort. Also please be careful with the cortisone. I only went when I couldn't stand it anymore but it burnt out my pancreas & now I have Type 1 diabetes
oh no!
@@mrsdsalnorcaltruth please make informed decisions. I understand wanting to ease the pain but this was side effect never disclosed
Ur so funny !! 😂
Pain is the worst
You may find some relief with Castor Oil (Queen of Thrones) and DMSO
Feel better ❤️
Yeah I like that extreme discomfort because it is pain but it's different than what you think of as pain it's just this ache in your entire body you can't even almost can't pinpoint where because it's coming from everywhere. It's like living with a severe body aches of flu every day of your life and I've had this started 30 years ago so yeah it's just normal and I try to tell myself this is normal so that I can survive it but I feel like looking into what you're taking because it would be nice not to have any or to have less and also the stiffness and also I have hereditary knee problems
Yes
You know Danielle, it's strange that you're talking about that, because I went to my chiropractor yesterday, and he said that I was suffering from fibromyalgia, which was caused by emotional trauma. He went through a process on me called QNRT( quantum neurological reset therapy), which goes through things that might have happened in your past that still bother you physically, even though mentally you feel like you're over them, if that makes sense. It's really weird and somewhat unpleasant, but two things came up from past experiences with my parents and afterwards I did feel a huge sense of relief from what in my mind was painful inflammation all over. This might be something you could think about looking into if there are any chiropractors in your area that happen to practice in this field because it's really weird but it seems to help sometimes there's no drugs or anything like that involved in it.
.....I received in my neck epidural steroid injections, 3 times, stair stepped did give me some relief....
I don't know a lot about this but I know it can be quite painful from what I've heard I sure hope whatever they do to give you some relief hope it works sending prayers and hugs❤
thanks friend.
I hear the carnivore diet is like a miracle when it comes to relieving pain. Getting rid of the inflammation that certain foods cause is the key. Try it for a few months, what do you have to lose, but the pain ? 🙂❤🥩
right.
Ihave fibro hurts like crap,My knech and my shoulder alot but it effects other parts of my body, And really the pain meds doesn't help 😢prayers pretty lady 🙏🙏
Ugh sorry.
Hard to express pain, when you're one tough lady like you. Hoping it does the trick. If not, ask your doctor about a cortisone cocktail injection. Doesn't contain anything addictive.
🩷
Hey Danielle, I’ve also had fibro for 25 years and understand your version of extreme discomfort. How I rate my pain is on a 1 to 10 scale when I’m describing it to someone else. Example today I’m about a 5 on the pain scale. I thought that might help you! I feel ya girl 🩷
Danielle feel better
What meds do u get for pain?
just got an injection is some trigger points. hoping that helps. do not want to do daily meds.
Oh my gosh I have fibromyalgia and I have osteoarthritis and I have degenerative spine and cervical spinal cord compression I could just go on and I cannot take pain medicine cuz it destroys my stomach and gives me ulcers😢😢😢😢 I did not know you had that that is so sad. I'm so sorry because with all the work you do and everything I don't know how you do it oh my gosh because I just have very low energy and I know all you want to do is just kind of lay in bed it's like you have to lay in bed every day just to get the gravity off of your body. So how you do all that running and everything you do is like I don't know it's like a superwoman
Just found out. Ugh. Sorry to hear about you.
❤❤❤take. Care. Danille. Love. Prayerd. Take. It. Easy. Have. Dan. Help. U. More. U. Rest🎉🎉😊😊
Understand.....fibro and RA here, double whammy.....I use pure peppermint essential oil straight rubbed on neck and muscle and joints that are painful. This has worked the best for me over 20 years!! Soak in a tub with epsom salt if you can get in and out okay....will help with minor aches and pains. soft hugs!!
oooh love it thanks.
🌿🌸😹Oooooomg oooooomg ooooomg this docor is the worst a eeeeever heard about!a laughiiing how terrible doctor was bescuse a experience the same attitude from doctors,,,Danielle a love how you take the situation! You the queen and a really hope you chabge to a female doctor who understands our body.
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I've suffered over two decades. Gabapentin and lyrica.
ugh. hang tough!
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5 months ago I had cortisone injection in my neck and left shoulder, I'm needing another one now . Now I'm wondering if I have fibro ? Because I have lower back pain , shoulder, neck and left arm pain
Thankyou for your insight x
Me too!
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I can't even take Tylenol because of liver problems.
Boo!
Wait so not everyone has pain all day everyday?
only the specials ones....:)
Do you feel the pain is worse when you exercise Danielle,Or better
The stress is much worse for me.
@@mrsdsalnorcal yeah I understand that
Take care🌷💅🏾🍎🌞❤️✨✨✨
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hi i have fybro too it sucks ❤
Sorry!
@ you know the pain i live in manitoba canada it soon be very cold and tons of snow this winter will be bad im already not great i had a hysterectomy full slice open to get a 10 cm fybroid out since then for ladt couple years been bad im 56
😊hello
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Danielle, you should have your own videos, because you only speak of yourself. That way, us that don't want to listen to you at all, can be spared of listening about you. Because , personally, I don't care about you, it's Ed we want to hear and see.
I know that song 🎵 😂