DAY 1-#RDBLOGWEEK how do other diagnoses impact your RD and its treatment?

How other Diagnoses Impact my RD and treatment

I Live with Rheumatoid Arthritis, Polymyalgia Rheumatica, Fibromyalgia, Spinal stenosis, Scoliosis and Migraine among other comorbidities.

Sometimes I find it hard to differentiate one Rheumatic Disease from the other and I have neurological diseases aswell which could impact one over the other.

I guess one could say if I have a Migraine with all the nasty symptoms that go along with it then I wouldn’t be able to have my Rheumatoid Arthritis Treatment which is an Actemra Infusion administered by IV every 28 days. If I get an infection like the flu I have to put off my infusion and wait until I am fully recovered and that can have a massive impact on the symptoms of the Rheumatoid Arthritis missing any treatment will put me in a flare.

Spinal Stenosis in my neck can also bring on a Migraine and Rheumatoid Arthritis also can due to associated pain with each of the conditions.

I am in IPain Magazine’s #IPainPatientSpotlight section page 48 and 49.


Hey everyone please check out the latest issue of#IPainLivingMagazinefree to view from the International Pain Foundation. Here is the link to the #IPainPatientPartnerSpotlight which is me on pages 48 and 49.

Please take a look just tap or click the blue. πŸ‘‰Patient Partner Spotlight section of IPain Living Magazine

After checking out the patient spotlight section scroll through from the πŸ‘‰beginning of the IPain Living Magazine Thankyou to the International Pain Foundation for featuring me in your #PatientPartnerSpotlight section and including the #RealLifeDiaries-Living with Rheumatic Diseases book aswell.<b
you would like to purchase the book as a great resource for yourself or a loved one who lives with a Rheumatic Disease please do so her
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http://amzn.to/2n5OSDv

my Task 29 for #NERVEmber

The above is just part of what’s in the full video

Task 29 #NERVEmber

Due to the length of my video I can’t fit it here so please go and see it via this link Thankyou

Follow this link to see the full video for my Task 29

Here is my #NERVEmber Task 29: Done in a creative way I have something special for you today. I have made a karaoke 🎀 video with words with #HopeIsTrue by #IPain and different style butterfly throughout. Please watch to the end and sing along whilst watching the butterfly.🎢 🎡 #IHaveTheNerveToBeHeard for all who live with #ChronicPain conditions.

#NERVEmber Infusion Day 6.11.17 and Supporter of my recently published book project. YEAH!!!!!!

#NERVEmber #ReallifeDiaries #RheumaticDiseases #Infusion
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Today was a great day it was my infusion day I have an Actemra Infusion as a treatment for #RheumatoidArthritis every 28 days.

It is administered by my friend and Infusion Nurse Glenn Allan.(I much prefer it be administered than me trying to do it myself.)
I came in today not only to have my infusion but to also show my book that was recently published Real Life Diaries-Living with Rheumatic Diseases. 
The book is a collection of people who live with Rheumatic Diseases all telling their stories regarding different topics.
Get your copy of the book here: Real Life Diaries: Living with Rheumatic Diseases https://www.amazon.com/dp/1944328696/ref=cm_sw_r_cp_api_AN-.zb20C2X7F
Glenn has been very supportive throughout we can talk about the ups and also the downs of living with these diseases and his support is second to none.(It means a lot) 
He said he wanted to buy the book and is very interested in reading it. I gave him the copy I had with me as I had another copy at home.
 I am very happy I have someone as part of my medical team that both takes the time to listen to any concerns and is able to give friendly and practical info and is very encouraging aswell. 
Thank you I appreciate your support as will Brenda L. Kleinsasser,Lynda Cheldelin Fell,Layne Martin and all the other writers within πŸ™‚ 
I am a big believer in sharing our stories and encouraging hope because hope is healing. #HealingHope #SharingStories #RealStories #RealLifeDiaries #LivingWithRheumaticDiseases
#HopeIsTrue #IHaveTheNerveToBeHeard #PaintTheWorldOrange


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30 Things About My Invisible Illness’


Purchase the Book here Buy the Book on Amazon.

Every Year I usually participate in Invisible Illness Awareness Week however this year that event was cancelled and this year I am posting the 30 Things about my Invisible Illness post for Invisible Disabilities Week Oct 15th-21st

This post is written each year in order to evaluate and see any changes that there may be.

30 Things about my Invisible Illness’

 #IDW17

#InvisibleNoMore

#InvisibleDisabilitiesWeek

#SeeTheInvisible
1. The Invisible Illness’ I live with Are:

  • Rheumatoid Arthritis,
  • Fibromyalgia,
  • Polymyalgia Rheumatica(Rare Disease),
  • General Anxiety Disorder,
  • Agoraphobia,
  • Social Anxiety Disorder
  •  Scoliosis,
  • Migraine,
  • Psoriasis,
  • Tempormandibulor joint Disorder, 
  • Diabetes(updated condition 2017) 
  •  Hypertension(High BP) and 
  • GERD  

2. I was diagnosed with them in the year:

1987 (Migraine)

1996 (Anxiety Disorder but have had the anxiety since childhood),Social Phobia diagnosed but had since childhood and Agoraphobia)

Hypertension I’m unsure of the exact time that began but my sister has more of an idea about incidents of being in an ambulance which I don’t remember so there you go. Apparently the Ambo treating me was a little freaked out by my BP and how high it was and said “that can’t be right” for the age I was.

2012(RA)

2013 (Fibromyalgia)

(2014  GORD and TMJ)

(2017)Diabeties

(2017) Psoriasis

3. I had symptoms since:1987 (Migraine)2010(RA and Fibro) others just came along.

4. The biggest adjustment I’ve had to make is: Not being able to once do what I used to but I’ve adjusted to my new normal and struggling day to day with tasks taking Medications as well as chronic fatigue which is a lot to deal with as it’s more than just being tired.A nap doesn’t really help most of the time. Also not being able to see friends and family as often as I’d like.

5. Most people assume: That I look well but truth is i’m not but I still say thanks and take it as a compliment because they aren’t to know that’s why I am an Advocate to make these diseases visible and bring them out of the shadows. I say things better how I feel when I’m writing or making graphics as I struggle with words face to face. #MyinvisibleFight #InvisibleIllness. Most of the time I smile through the pain and take each day as it comes because it can truly change in an instant.

6. The hardest part about mornings are: Moving and still being fatigued throughout the day. I am often nauseous a lot too and sadly I have become accustomed to it. 

7. My favorite medical TV show is: House other than that I don’t really watch shows of a medical nature.

8. A gadget I couldn’t live without is:My Ipod classic cause it fits thousands of songs on it and helps me to relax. Problem is though I can’t turn my music up loud because loud music is a trigger for my migraines #Phonophobic #photophobic I also enjoy the occasional Netflix and bigpond movies.

9. The hardest part about nights are: Getting enough sleep or getting to sleep #Thestruggleisreal #Fatigued #Painsomnia

10. Each Day I take many Medications and vitamins: including a Biologic treatment given via infusion. #Hope4ACure

I am also on #Methotrexate

 The infusion is to prevent further joint damage or any other damage at the very least to slow the progression of the disease.

11. With Regards to alternative treatments:

I have tried diets and different approaches to eating,I have tried massage aswell. I have an acupuncture mat and a tens machine too.

12. If I had to choose between an invisible illness or visible I would choose: Visible because at least you may not be doubted not having to choose at all would be even better cause some days are pure hell and I wish for nobody to have any illness.

13. Regarding working and career: I am on Disability due to the unpredictability and many issues that come from living with these diseases. Having said that I am a volunteer online and enjoy many things including writing.

14. People would be surprised to know: I like to spend alot of time on my own or maybe that’s not so suprising I don’t know..

15. The hardest thing to accept about my new reality has been: The constant Fatigue and daily chronic pain.The battle with my BP has been hard too.

16. Something I never thought I could do with my illness that I did was: Reach out to others because of my life long social Anxiety but I am super proud of myself for doing so I have really come a long way. I love the people who I have become friends with because we all support each other.

17. Advertisements about my illness always: portray that once u take meds you could basically run a marathon so not true though and it really upsets the community that’s for sure. 

18. Something I really miss doing since I was diagnosed is: Doing more activities with my nieces they mean the world to me and they are my reason for being here and they bring me much joy.

19. It was really hard to have to give up: My studies in IT and Web Design. Cognitive issues have been a big issue and was unable to continue.

20. A new hobby I have taken up since my diagnosis is: Card Making crafts and Adult coloring and writing I have written for a book called Real Life Diaries Living With Rheumatic Disease which was released this world Arthritis Day 12th October 2017.

21. If I could have one day of feeling normal again I would: Dance like nobody is watching and get my fitness on. I would also travel a lot more and to further places in distance I haven’t been. I really want to travel to the USA to meet IPAIN Foundation friends Barby Ingle and her Husband Ken(Sweet yes a real life Barby and Ken They Rock)and I would also love to meet some International Foundation for Autoimmune Arthritis friends and Blue Ribbon Project friends Cathy and Mindy and also the Arthritis National Research Foundation Crew πŸ™‚ I would also love to meet #Dazzle4Rare coordinator and #hesaonline org volunteer Kimberley because she is a strong Advocate for #RareDisease Awareness and I have been happy to take part since #Dazzle4Rare began in 

22. My illness’ have taught me: That I have to live in the moment because no day is the same especially when it’s chronic. I can be fine one day then a total mess the next #ChronicLife that’s just how it is #MynewNormal I’ve accepted it and can’t change what is I can’t control I can only manage with my healthcare team and myself.

23. Want to know a secret? One thing people say that gets under my skin is: You only go online to be part of the pity train(NEWSFLASH to anyone who says this it’s not about pity it’s about Awareness and understanding.

 I also hate so and so has it worse WELL you what it’s not a competition it’s about just being a certain person and I for 1 am gonna be that a person which is a caring and compassionate human being I don’t care if u hurt a little or a lot I SUPPORT u and I have your back. πŸ‘Œ 

 I just believe that we all need to support each other in our times of need and if we did the world would make for a better place that’s why I created United Advocacy. There’s enough hate in this world and I for one am sick to death of it.

 I just want to support everyone so they don’t feel alone no matter what illness someone lives with. 

I volunteer with non profits around the world and support patients and organisations working together to provide resources aswell as awareness about various illness’ I really enjoy being involved in projects from non profits around the globe. 

24. I love it when people: Show support and care about each others causes because together we can all make a difference no needforjudgement that gets nobody anywhere.

25. My favorite motto, scripture or quote that gets me through tough times is: Together we can make a difference. Show u care and spread love not hate.

26. When someone is diagnosed I’d like to tell them: You are not alone I’m here for you if u ever need to talk and I have your back #WEGOTTHIS and we are #StrongerTogether

27. Something that has surprised me about living with an illness is: The amount of people who have connected with me and the new friendships I have made. #ChronicallyFabulous #Spoonies #UnitedTogether #PeoplewithPainMatter

28. The nicest thing someone did for me when I wasn’t feeling well was: let me rest especially during a migraine attack or when I am flaring.

29. I’m involved with Invisible Illness Week and/or invisible Disabilities week because: I think it’s fabulous that we all come together like this as part of a global community #MakingaDifference.

30. The fact that you read this list makes me feel: Special and loved because you took the time to care. Thanks so much if u have read to the end bless you it means a lot.

Let me know you read this to the end via my Facebook page and let’s unite.