Showing posts with label resources. Show all posts
Showing posts with label resources. Show all posts

Wednesday, September 27, 2017

Why Given Me A Thorn Blog Was Shut Down

Back in May I disabled this blog for several months as I prayed about what to do with it. I had just undergone a solid week of intensive counseling and realized my lifetime mindset, the focus of this blog, had been more about my thorns than about the Rose of Sharron, Jesus Christ. Yes, he has been my Lord since childhood, yet I was more prone to focus on the crashing waves and trying to live my life in a way that would glorify God through the pain, rather than with my eyes firmly set on Jesus Himself and let Him unfold His grace through a life lived for Him, regardless of circumstances. Perhaps this seems like a minor semantical change, but it is a profound heart shift in me!

Starting with the very first day in my week in ministry (and continuing to this day), as I experienced significant and unexpected physical healing in several areas, I was so overwhelmed with God's goodness that I didn't have a heart for this blog anymore. If fact, the "Given Me A Thorn" book title is no longer in my plans at all. Yes, I still plan to write address the times we ask for healing and it does not come (as is still my case in some significant areas), but my title, focus, and perspective has simply been changed by the reality that I am defined by Jesus not by my thorns.

Found on Facebook. Would dearly like to credit the artist if anyone can provide the source, please?
Reminds me of the Butterflies and Battle Boots article I wrote.




I am restoring public viewing of this blog as, within the past week, I have has three needs for public access to some of the health resources previously posted here. The "flavor" of this blog will remain focused on Christians and chronic illness, yet my tone will likely be much more in keeping with my current book title, Harvesting Hope From Heartache.

Please "like" my "Jennifer Saake, author" page at www.facebook.com/HarvestingHope for ongoing updates on all my writing news. :) I need a few thousand likes to demonstate "platform" to potential book publishers and currently only have a few hundred, so please help and pass the need along in your illness support circles!

Why I Wear Combat Boots

Tuesday, December 8, 2015

Book Give-away!


Sorry the cover is backwards. My laptop takes mirror image photos! If there is a way to "flip" them, I sure have never discovered that feature. Keep reading to learn how to enter (once or lots of times)to win a free copy of this book!


Extended Entry Deadline: To enter, please leave a comment (including a valid email address to contact you if you win) on this post prior to Christmas Day, 2015! I'll send out a notification email and post the winner here by Dec.28. You will have 48 hours to respond with your mailing address or I'll need to select a new winner. That's it. EASY. (Keep reading for more chances to enter.)


You can see my dear friend Shelly Benoit Hendricks's correct book cover for her 30 devotional collection for newly diagnosed patients, "You're Chronically Ill...So Now What?" at http://amzn.to/21Mp2T7 or visit the  You're Chronically Ill. Now What? facebook page at https://www.facebook.com/YoureChronicallyIllNowWhat.

For additional enteritis, please share this post widely, on Facebook, pinterest, twitter, your blog, wherever. Leave an additional post each time you do!

Tuesday, June 3, 2014

Mast Cell Activation?


Since childhood, and worsening with age, I have a multitude of allergic type reactions, to bug bites, cigarette smoke, scents, some personal care products (mine or worn by others), perfumes, chemical cleaners, certain animal hairs (wool, rabbits, bears and a few specific cats or dogs) Band-Aids, medical tapes, balloons, freshly repainted buildings, new construction, carpet glues even months after installation, a few specific foods and food additives, herbs, medications (like every narcotic known to man - no "good drugs" for me!), heat, sunlight... Symptoms range from redness, itching, hives, tingling tongue, neurological issues, to migraine headaches and vomiting, to racing heart, tight throat and lungs and even full blown anaphylaxis. For several years now (and under doctor's orders), I've rarely miss a dosage of Zertec every 24 hours. When I forget at bedtime I'm in fullblown reactive mode, without any other trigger, simply to life, by the time I wake up the next morning. I carry Benadryl and an Epi-Pen at all times, because I still have plenty of break through reactivity with various exposures. I have taken a few ambulance rides for more sever reactions.


Allergy testing says I have a true allergy to DUST, that's it. Oh, and to my Albuterol inhaler (that one wasn't a blood test, just the allergist's first hand observation when he had me use it in his office). Arrrgggg! Now don't get me wrong, I'm happy not to be allergic to anything else. But with classic allergies there are usually specific treatment regiments. If I'm not allergic to these things, then doctors aren't quite sure what to do with me. My allergist told me that he believes my anaphylaxis to be phyco-sematic, but since I've even had some of these physical manifestations, visibly witnessed by others, when I've been unconscious, I find this a little hard to accept. I'm more prone to think that, for many doctors, if they don't have a blood test with readable results that they fully understand, in their minds often the illnesses simply "do not exist" because their testing doesn't say so.


I've been offered a variety of explanations, some of which may partially answer the riddle, but nothing that fully satisfies yet. The first explanation has been Multiple Chemical Sensitivity (MCS). After the allergy testing came back without answers, the idea of toxicity was introduced, that rather than being allergic to things, I'm having toxic reactions. I think these two may be on the right track, but don't offer a full answer. Through hours of research (special thank to Danette Hillier-McVeetyof the Ehlers-Danlos (and all related disorders) Support Group, for answering initial questions and pointing me down this investigational pathway!), I personally think we need to investigate Mast Cell Activation Disorder (MCAD) or even perhaps Mastocytosis (the sufferer has too many mast cells to begin with, whereas with MCAS, they are either misshapen and/or release too much histamine and heparin) as it truly seems to me that my own body is overly active in histamine production and it doesn't take much to push it over the edge into full blown reactivity! I'll be addressing these concerns with my doctor this summer. In the meantime, I need one place to list resources I'm finding:


Mast Cell Activation (Always Well, talks about some testing that can be ordered. "In Mastocytosis, the problem can be making too many mast cells or having incorrectly shaped cells.  Very little is understood about Mast Cell Activation Disorder, which shares symptoms with Mastocytosis, but the usual clinical markers are not always present.  It’s theorized that in Mast Cell Activation Disorder, for unknown reasons, one’s mast cells become hypersensitive, ‘behave badly’, and thus are easily triggered to release their contents.
"Mast Cell Disorders are not the same as Multiple Chemical Sensitivity.  But some people with MCS may be incorrectly diagnosed and actually have a mast cell disorder.  In his article called The Role of the Brain and Mast Cells in MCS, Dr. Gunnar Heuser, MD described how he tested a number of his MCS patients for markers that indicate mastocytosis or a mast cell activation disorder. A surprising number turned up positive.  Dr. Heuser postulates, '...that chemical injury can trigger a mast cell disorder which in turn can cause MCS.”)


Allergies, Fibromyalgia or Mast Cell Activation?

Mast Cell Activation Disorders (fromUpToDate)

Mastocytosis Explained

Hyperadrenergic Postural Tachycardia Syndrome (POTS) in Mast Cell Activation Disorders (I "flunked" or "passed", depending on how you look at it, my tilt table test with flying colors, years ago.)

Mast Cell Diseases (Wikipedia)

Mast Cell Activation Disorder and Chronic Illness (Methylation)

MCAS Guide

Diagnosis Histamine Intolerance (scroll down past the adds, yes they are trying to sell their products but the information may still be helpful)

If I understand correctly,  Mastocytosis can only be confirmed with a bone marrow biopsy and MCAS can be confirmed with a blood test.







Monday, September 12, 2011

National Invisible Chronic Illness Week


Welcome to National Invisible Chronic Illness Week (Invisible Illness Week, or IIW for short)! Please join me in watching this video produced by my dear friend, Lisa Copen, founder of both Rest Ministries and IIW.



How will you observe IIW? What can you do to spread awareness, comfort, or simply snuggle into the resources and reality or hope and support extended to you?

Monday, August 8, 2011

Myalgic Encephalomyelitis: International Consensus Criteria

Could "Chronic Fatigue Syndrome" finally be loosing its ambiguous "fatigue" label? We can only hope that this is a step in the right direction!

Myalgic Encephalomyelitis: International Consensus Criteria - Carruthers - Journal of Internal Medicine - Wiley Online Library

Sunday, July 24, 2011

Fibromyalgia

I try not to post identical (or even highly similar) content to two or more of my blogs, but since today's post over at InfertilityMom is more health-related than not, I thought my readers here at GivenMeaThorn might appreciate it as well. For the few of you who happen to subscribe to both, thank you for your patient indulgence in my cross-posting. :)

While it's my personal blog rather than my primary health blog, I am honored to learn today that InfertilityMom has been selected as #22 in the top 100 blogs at 100 Best Sites for Fibromyalgia or Chronic Fatigue Syndrome Information. Thank you! :)


My mom's just completed her 2nd week at week at FibroInnovations. She's sore from all the work they are doing on her, but the results have already been more than we had dared to hope, and she still has another 10 weeks of on site treatment to go before several months of at-home follow-up. After basically falling into this treatment in a way that can only be described as Providential, it truly seems that it is an answer to our prayers for her after over 20 years of pain! Here she is with Dr. Kingston. I will admit that our family was highly skeptical about this program in the beginning, after too many years of "sure cures," but hearing the hope in her voice now makes me feel like this really is going to be a life-altering change for the positive for her.


Speaking of hope and life-altering changes, will you help me keep fighting for change by using your facebook account to join me in daily voting for the Whittemore Peterson Institute? If they can hold onto their current #1 spot in the Pacific region through August 27, they will win $100,000 of desperately needed research funding. If we could move them up from their current 6th place (contest-wide) into first there as well, they would be awarded $250,000. Voting will only take moments from your day and every vote counts! You can learn more about the importance of the Whittemore Peterson Institute in my life by reading back through my many posts on XMRV.

Vivint is giving away $1.25 Million to charities. Help us win!

Saturday, May 21, 2011

Easy Activism

Did you know that 30 seconds of your time could make a $500,000 difference?

If you have a Facebook account (or know someone who does, or you are considering getting one), please keep reading! If you followed this blog very long at all, you've heard me mention the Whittemore Peterson Institute many times. I am so very thankful for this research organization and the hope they bring to not only me personally, but to millions with M.E., CFS, Fibromyalgia, Lyme disease, Gulf War Illness, a-typical MS, Autism, and more.

The Whittemore Peterson Institute (WPI) is 1 out of 100 charities that won a $25,000.00 grant during the first round of Chase Community Giving. Now, WPI is competing for a $500,000.00 grant, and you can help! Please cast your vote, ask your Facebook friends to vote, and spread the word about the important work of WPI. If you have a Facebook account, please cast your vote for WPI by following the instructions below through May 25th at 9 pm PST. (Just under 4 days left!)

STEP-BY-STEP Instructions:
1. From your Facebook page, go to Chase Community Giving: http://www.facebook.com/ChaseCommunityGiving.

2. "Like" Chase Community Giving by clicking on the "Like" button.

3. Now search for Whittemore Peterson Institute for Neuro-Immune Disease.

4. Cast your vote for WPI by clicking the "Vote Now!" button.

5. Please remember our neuro-immune disease community and share in the Love and Giving by voting for other organizations who speak to your heart -- you can vote for up to 5 organizations per Facebook account.

CHASE COMMUNITY GIVING: BIG IDEA
The Whittemore Peterson Institute for Neuro-Immune Disease (WPI) was created to answer a critical need for discovery and medical treatments for those with serious illnesses that impact the body and the brain. These often debilitating and life-long diseases, including M.E., CFS, fibromyalgia, post Lyme disease, GWI and autism, have too few medical solutions. WPI continues to make significant strides through the work of our innovative research program.

Translating novel research into effective patient treatments for millions around the world will begin with the opening of our 10,000 sq. ft. medical facility. Here we can engage in revealing clinical trials and provide on site care to those who are unable to afford care. We require funding for initial expenses and to establish a patient fund. WPI’s commitment to discovery has already inspired much hope worldwide. Now it is time to put hope into action by offering meaningful patient care to these under-served populations.

http://www.wpinstitute.org/help/index.html#chasegiving

Tuesday, May 10, 2011

Explaining Fibromyalgia

I just read a great explanation of Fibromyalgia over on the Faith, Family and Fibromyalgia blog. If you have Fibro, the illustrations will resound with you and possibly give you a simple word picture to use to help explain yourself to others. If you don't have Fibro, this story may give you more understanding for your friend or loved one who does. You'll want to read the whole article in detail, but here's a taste:

Imagine you’re planning a party and expecting about 20 guests. Three or four friends told you they’d come early to help you out. But they don’t show, and instead of 20 guests, you get 100. You’re overwhelmed.
That’s what’s happening with pain signals in someone who has fibromyalgia. The cells send too many pain messages (party guests), up to five times as many as in a healthy person. That can turn mild pressure or even an itch into pain. When those pain signals reach the brain, they’re processed by something called serotonin. People with fibromyalgia, however, don’t have enough serotonin (the friends who didn’t show up to help), leaving the brain overwhelmed.
This is why people with fibromyalgia have pain in tissues that show no sign of damage. It’s not imagined pain; it’s misinterpreted sensation that the brain turns into actual pain. Other substances in the patient’s brain amplify a host of other signals — essentially, “turning up the volume” of everything. That can include light, noise and odor on top of pain, and it can further overload the brain...

Just two more days until Fibromyalgia and Chronic Fatigue Syndrome Awareness Day. The Whittemore Peterson Institute (WPI) is building an international network of Advocates who are dedicated to finding a cure for neuro-immune diseases (NID). Learn about May Awareness at ANIDA.

Thursday, April 28, 2011

Illness and Infertility

Some of you may know that we battled for 13 years to bring home our three living miracles, with infertility, multiple miscarriages and adoption losses along the way. Since I have lived with ME/CFS/XMRV my entire adult life, the issues of chronic illness and infertility were often intertwined with each issue complicating the other on multiple levels, physically, medically, emotionally, spiritually, and just about any other "ally" you can imagine.

Lisa Copen, my dear friend and founder of Rest Ministries, offers some beautiful thoughts on living with chronic illness and facing infertility:
How Do I Know if God Has Motherhood In My Future?

If you find yourself a journey through fertility challenges, you can find additional support on my Hannah's Hope blog and also at the new faith-based blogging community, Held!

Monday, April 4, 2011

$5 book coupon

Rest Ministries is a favorite organization of mine! I'm thrilled to announce that they are re-opening their bookstore full of wonderful resources to keep our eyes on Jesus in the midst of pain. To celebrate, here's a $5 off $25 coupon code to use in their store until April 10, 2011. At checkout, use code:
ap5off25

More information about the RM bookstore can be found here. Please come back and tell me what great finds you chose with your discount! :)

Monday, March 28, 2011

Paws for Comfort

Did you there are tiny, precious "service dogs" trained just for helping out folks with chronic pain? Their gift is heat as they lay across shoulders or other areas of pain for their beloved owners, sharing body heat as a living "heating pad." An organization called Paws for Comfort® "is particularly dedicated to increasing public awareness of under recognized populations of people coping with chronic illnesses, especially invisible conditions, such as Fibromyalgia and Chronic Fatigue Immune Deficiency Syndrome."

Xoloitzcuintli (a rare breed also known as the "Mexican Hairless") can be specifically raised to assist in chronic pain relief. They are tiny so as not to add to pain with too much weight. They are also hairless, a wonderful benefit for those with allergies! Check out Paws for Comfort® to learn more. :)

Wednesday, March 16, 2011

Thorny Situation

Dr. Judy Mikovitz has been an incredible advocate for CFS patients even as she dedicates her life to life to research on our behalf. Here's an in-depth article showing many facets of the political debate surrounding her work in XMRV research. I continue to uphold her in prayer, that God will bring truth to light, and invite you to do the same.
When Judy Mikovits found links between chronic fatigue syndrome and a virus, the world took notice. Now, she's caught between the patients who believe her work and the researchers who don't.
- Virology: Fighting for a Cause

Monday, November 1, 2010

Traveling with "Baggage"

While I am in no condition to travel these days, I have dreams that someday I will be improved enough to consider leaving my own hometown for reasons other than medical needs once again. When living with chronic illness, these kinds of things have to be carefully planned and strategically plotted. You can't just "pack up and go" but need to think through so many things. I remember one cross-country trip several years ago where the airline mangled my wheelchair in their checked baggage handling, then would not cover the damage claiming it didn't qualify as checked baggage in the first place (though they didn't bother warning me before accepting it when we were preparing to board).

I know for some of us (physically or financially) travel is limited only to our dreams. But dream a little with me. Where would you go if you could travel anywhere? Why would you choose that destination? What preparations would you make to make this trip as do-able as you could?

The last fun trip I took was a little over a year ago with my family. We won a week's free RV rental and I learned that taking a "home" on wheels was a fairly workable solution for my travel/health needs. I blogged the entire trip Classic RV Adventures.

What are your best travel tips for navigating away-from-home with chronic health challenges? Do you know of helpful travel websites or resources? I stumbled upon one today called Disability Holidays Guide that prompted this post. Is there are tool or tip you don't leave home without? How do you manage medication, sleep schedules, special transportation needs? Please share!